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CHEBI ONTOLOGY - ANNOTATIONS

The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/. The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/). For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.

Term:Glu-Thr-Thr-Tyr
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Accession:CHEBI:73489 term browser browse the term
Definition:A tetrapeptide composed of L-glutamic acid, two L-threonine units and L-tyrosine joined in sequence by peptide linkages.
Synonyms:exact_synonym: L-alpha-glutamyl-L-threonyl-L-threonyl-L-tyrosine
 related_synonym: E-T-T-Y;   ETTY;   Formula=C22H32N4O10;   InChI=1S/C22H32N4O10/c1-10(27)17(20(33)24-15(22(35)36)9-12-3-5-13(29)6-4-12)26-21(34)18(11(2)28)25-19(32)14(23)7-8-16(30)31/h3-6,10-11,14-15,17-18,27-29H,7-9,23H2,1-2H3,(H,24,33)(H,25,32)(H,26,34)(H,30,31)(H,35,36)/t10-,11-,14+,15+,17+,18+/m1/s1;   InChIKey=UQULNJAARAXSPO-ZCWPNWOLSA-N;   L-Glu-L-Thr-L-Thr-L-Tyr;   SMILES=C[C@@H](O)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O


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  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            Glu-Thr-Thr-Tyr 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 0
    subatomic particle 0
      composite particle 0
        hadron 0
          baryon 0
            nucleon 0
              atomic nucleus 0
                atom 0
                  main group element atom 0
                    p-block element atom 0
                      carbon group element atom 0
                        carbon atom 0
                          organic molecular entity 0
                            heteroorganic entity 0
                              organochalcogen compound 0
                                organooxygen compound 0
                                  carbon oxoacid 0
                                    carboxylic acid 0
                                      carboacyl group 0
                                        univalent carboacyl group 0
                                          formyl group 0
                                            aldehyde 0
                                              amino aldehyde 0
                                                L-tyrosinal 0
                                                  L-tyrosine 0
                                                    Glu-Thr-Thr-Tyr 0
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