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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-histidyl group
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Accession:CHEBI:32514 term browser browse the term
Synonyms:exact_synonym: (2S)-2-amino-3-(1H-imidazol-4-yl)propanoyl;   L-histidyl
 related_synonym: Formula=C6H8N3O;   His-;   SMILES=C=1(N=CNC1)C[C@@H](C(*)=O)N
 cyclic_relationship: is_enantiomer_of CHEBI:32522


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Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 5066
    role 5030
      biological role 5030
        biochemical role 4951
          metabolite 4939
            histidine 0
              L-histidine 0
                L-histidyl group 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 5066
    subatomic particle 5057
      composite particle 5057
        hadron 5057
          baryon 5057
            nucleon 5057
              atomic nucleus 5057
                atom 5057
                  main group element atom 5026
                    main group molecular entity 5025
                      s-block molecular entity 4957
                        hydrogen molecular entity 4950
                          hydrides 4555
                            inorganic hydride 405
                              pnictogen hydride 401
                                nitrogen hydride 401
                                  azane 393
                                    ammonia 393
                                      organic amino compound 286
                                        amino acid 181
                                          alpha-amino acid 151
                                            alpha-amino-acid residue 0
                                              proteinogenic amino-acid residue 0
                                                N-terminal proteinogenic amino-acid residue 0
                                                  L-histidyl group 0
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