tryptophan metabolism Gene Set

Dataset KEGG Pathways
Category structural or functional annotations
Type pathway
Description The chemical reactions and pathways involving tryptophan, the chiral amino acid 2-amino-3-(1H-indol-3-yl)propanoic acid. (Gene Ontology, GO_0006568)
External Link http://www.genome.jp/kegg/pathway/hsa/hsa00380.html
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Genes

57 proteins participating in the tryptophan metabolism pathway from the KEGG Pathways dataset.

Symbol Name
AADAT aminoadipate aminotransferase
AANAT aralkylamine N-acetyltransferase
ACAT1 acetyl-CoA acetyltransferase 1
ACAT2 acetyl-CoA acetyltransferase 2
ACMSD aminocarboxymuconate semialdehyde decarboxylase
AFMID arylformamidase
ALDH1A3 aldehyde dehydrogenase 1 family, member A3
ALDH1B1 aldehyde dehydrogenase 1 family, member B1
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial)
ALDH3A1 aldehyde dehydrogenase 3 family, member A1
ALDH3A2 aldehyde dehydrogenase 3 family, member A2
ALDH7A1 aldehyde dehydrogenase 7 family, member A1
ALDH9A1 aldehyde dehydrogenase 9 family, member A1
AOC2 amine oxidase, copper containing 2 (retina-specific)
AOC3 amine oxidase, copper containing 3
AOX1 aldehyde oxidase 1
ASMT acetylserotonin O-methyltransferase
CARM1 coactivator-associated arginine methyltransferase 1
CAT catalase
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
DDC dopa decarboxylase (aromatic L-amino acid decarboxylase)
ECHS1 enoyl CoA hydratase, short chain, 1, mitochondrial
EHHADH enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase
GCDH glutaryl-CoA dehydrogenase
HAAO 3-hydroxyanthranilate 3,4-dioxygenase
HADH hydroxyacyl-CoA dehydrogenase
HADHA hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
HEMK1 HemK methyltransferase family member 1
HSD17B10 hydroxysteroid (17-beta) dehydrogenase 10
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
INMT indolethylamine N-methyltransferase
KMO kynurenine 3-monooxygenase (kynurenine 3-hydroxylase)
KYNU kynureninase
LCMT1 leucine carboxyl methyltransferase 1
LCMT2 leucine carboxyl methyltransferase 2
LNX1 ligand of numb-protein X 1, E3 ubiquitin protein ligase
MAOA monoamine oxidase A
MAOB monoamine oxidase B
METTL2B methyltransferase like 2B
METTL6 methyltransferase like 6
NFX1 nuclear transcription factor, X-box binding 1
OGDH oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)
OGDHL oxoglutarate dehydrogenase-like
PRMT2 protein arginine methyltransferase 2
PRMT3 protein arginine methyltransferase 3
PRMT5 protein arginine methyltransferase 5
PRMT6 protein arginine methyltransferase 6
PRMT7 protein arginine methyltransferase 7
PRMT8 protein arginine methyltransferase 8
TDO2 tryptophan 2,3-dioxygenase
TPH1 tryptophan hydroxylase 1
TPH2 tryptophan hydroxylase 2
WARS tryptophanyl-tRNA synthetase
WARS2 tryptophanyl tRNA synthetase 2, mitochondrial
WBSCR22 Williams Beuren syndrome chromosome region 22