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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:L-tyrosine residue
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Accession:CHEBI:46858 term browser browse the term
Synonyms:related_synonym: Formula=C9H9NO2;   L-tyrosine;   L-tyrosine acid residue;   L-tyrosyl;   SMILES=O=C(*)[C@@H](N*)CC=1C=CC(=CC1)O;   Tyr;   Y
 alt_id: CHEBI:29975;   CHEBI:46207
 xref: PDBeChem:TYR_LL;   RESID:AA0019
 cyclic_relationship: is_enantiomer_of CHEBI:29976


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Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 503
    role 503
      application 459
        pharmaceutical 454
          drug 454
            nutraceutical 21
              L-tyrosine 0
                L-tyrosine residue 0
                  3-bromo-L-tyrosine residue 0
                  L-tyrosine amide residue 0
                  L-tyrosine-O-phosphate(2-) residue 0
                  L-tyrosine-O-sulfate(1-) residue 0
                  O-(ADP-D-ribosyl)-L-tyrosine(2-) residue 0
                  O-[5'-(adenyl-(5'->3')-adenyl)]-L-tyrosine(2-) residue 0
                  O-[5'-(adenyl-(5'->3')-adenyl-(5'->3')-adenyl)]-L-tyrosine(3-) residue 0
                  O-adenyl-L-tyrosine residue 0
                  O-adenyl-L-tyrosine(1-) residue 0
                  O-guanylyl-L-tyrosine(1-) residue 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 503
    subatomic particle 503
      composite particle 503
        hadron 503
          baryon 503
            nucleon 503
              atomic nucleus 503
                atom 503
                  main group element atom 496
                    p-block element atom 496
                      carbon group element atom 485
                        carbon atom 484
                          organic molecular entity 484
                            heteroorganic entity 478
                              organochalcogen compound 430
                                organooxygen compound 428
                                  carbon oxoacid 368
                                    carboxylic acid 368
                                      carboacyl group 308
                                        univalent carboacyl group 308
                                          formyl group 4
                                            aldehyde 4
                                              amino aldehyde 0
                                                L-tyrosinal 0
                                                  L-tyrosine 0
                                                    L-tyrosine residue 0
                                                      3-bromo-L-tyrosine residue 0
                                                      L-tyrosine amide residue 0
                                                      L-tyrosine-O-phosphate(2-) residue 0
                                                      L-tyrosine-O-sulfate(1-) residue 0
                                                      O-(ADP-D-ribosyl)-L-tyrosine(2-) residue 0
                                                      O-[5'-(adenyl-(5'->3')-adenyl)]-L-tyrosine(2-) residue 0
                                                      O-[5'-(adenyl-(5'->3')-adenyl-(5'->3')-adenyl)]-L-tyrosine(3-) residue 0
                                                      O-adenyl-L-tyrosine residue 0
                                                      O-adenyl-L-tyrosine(1-) residue 0
                                                      O-guanylyl-L-tyrosine(1-) residue 0
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