MGP Database

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MGP003066

Ontology/Pathway Information

Entrez Gene ID6898
Gene Nametyrosine aminotransferase
Gene Symbol TAT
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005829 TAS:ReactomeCcytosol
GO:0005739 IEA:EnsemblCmitochondrion
GO:0016597 IEA:EnsemblFamino acid binding
GO:0080130 IEA:UniProtKB-ECFL-phenylalanine:2-oxoglutarate aminotransferase activity
GO:0004838 IDA:UniProtKBFL-tyrosine:2-oxoglutarate aminotransferase activity
GO:0030170 IEA:InterProFpyridoxal phosphate binding
GO:0006103 IDA:UniProtKBP2-oxoglutarate metabolic process
GO:0009058 IEA:InterProPbiosynthetic process
GO:0034641 TAS:ReactomePcellular nitrogen compound metabolic process
GO:0006536 IDA:UniProtKBPglutamate metabolic process
GO:0006559 TAS:ReactomePL-phenylalanine catabolic process
GO:0051384 IEA:EnsemblPresponse to glucocorticoid
GO:0046689 IEA:EnsemblPresponse to mercury ion
GO:0006979 IEA:EnsemblPresponse to oxidative stress
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0006572 IDA:UniProtKBPtyrosine catabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_111217Metabolism
REACT_13Metabolism of amino acids and derivatives
REACT_1786Phenylalanine and tyrosine catabolism
SMP Pathway Links
SMP IDDescription
SMP00169Alkaptonuria
SMP00429Disulfiram Action Pathway
SMP00498Dopamine beta-hydroxylase deficiency
SMP00190Hawkinsinuria
SMP00533Monoamine oxidase-a deficiency (MAO-A)
SMP00008Phenylalanine and Tyrosine Metabolism
SMP00206Phenylketonuria
SMP00006Tyrosine Metabolism
SMP00494Tyrosinemia, transient, of the newborn
SMP00369Tyrosinemia Type 2 (or Richner-Hanhart syndrome)
SMP00370Tyrosinemia Type 3 (TYRO3)
SMP00218Tyrosinemia Type I
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