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C01144 Isophenoxazine Benzoate degradation via hydroxylation Xanthurenic 3-Hydroxy- L-kynurenine 4,6-Dihydroxyquinoline 2,3-Dihydroxyindole N-Methyltryptamine Glycolysis / Gluconeogenesis Indolelactate 5-Hydroxykynurenamine 6-Hydroxykynurenate 3-Methyldioxyindole 4,8-Dihydroxyquinoline Cinnavalininate Anthranilate Anthranilate Oxaloacetate 5-Hydroxyindoleacetaldehyde 4-(2-Aminophenyl)-2,4-dioxobutanoate C00527 2-Formamino benzoylacetate 5-(3'-Carboxy-3'-oxopropyl) -4,6-dihydroxypicolinate 5-(2'-Carboxyethyl)-4,6-dihydroxypicolinate Indole-3-acetate 7,8-Dihydro-7,8-dihydroxykynurenate 2-Formylaminobenzaldehyde 4-(2-Amino-5-hydroxyphenyl) -2,4-dioxobutanoate (Z)-5-Oxohex-2-enedioate 3-Hydroxykynurenamine C00877 3-(2-Aminoethyl) -1H-indol-5-ol N-Methylserotonin 5-Hydroxy-N-formylkynurenine 5-Hydroxy -L-tryptophan Quinolinate Formyl-5-hydroxykynurenamine 5-(2'-Formylethyl)-4,6-dihydroxypicolinate 2-Aminomuconate L-Tryptophanyl-tRNA Melatonin 5-(3'-Carboxy-3'-oxopropenyl)-4,6-dihydroxypicolin 3-Methoxyanthranilate 3-Methylindolepyruvate Glucobrassicin C00332 3-Indoleglycolaldehyde 2-Aminomuconate PhenylAla, Tyr and Trp biosynthesis 2-Amino-3-carboxymuconate 5-Hydroxyindolepyruvate 4-(2-Amino-3-hydroxyphenyl) -2,4-dioxobutanoate 2-Oxoglutarate Indole-3-acetaldoxime 3-Hydroxyanthranilate Nicotinate and nicotinamide metabolism Kynurenate 5-Hydroxyindoleacetate 6-Hydroxyindolelactate Indole-3-ethanol 8-Methoxykynurenate Indole-3-acetaldehyde 2-Oxoadipate N-Acetylindoxyl 5-Methoxyindoleacetate Benzoate degradation via hydroxylation Indolepyruvate Formylanthranilate 7,8-Dihydroxykynurenate 5-Hydroxyindoleacetylglycine Formyl-N-acetyl-5- methoxykynurenamine Ido1 Tdo2 N-Acetylisatin Cyp2f4 1.13.12.3 Prmt1 Aldh3a2 1.13.11.23 2.1.1.49 Aldh3a2 Kynu Rnf25 Acat1 Tryptamine Ddc 2-Aminophenol 1.1.1.190 Aadat L-Tryptophan CYPC12 Cyp2d2 N-Acetylserotonin Formylkynurenine 1.1.1.191 3.2.1.147 3-Indoleacetonitrile Tph1 3.5.1.9 3.5.1.4 L-Kynurenine Maob Aldh1a2 Kynu Aox1 Prmt1 1.14.16.3 ALDH1A4 Dhcr24 Maob Ogdh 2.6.1.27 1.5.1.- Gcdh Cyp2a1 Aadat 4.1.99.1 Asmt Abp1 Mdm2 Cyp1a1 Cyp1a2 4.1.1.43 Maob 1.7.3.2 1.1.1.110 Aldh2 1.13.11.17 Aldh1a1 3.5.1.49 1.14.13.9 Ido1 Asmt 3.5.5.1 6-Hydroxymelatonin Echs1 Hadh 1.14.99.2 Ido1 Indole Ddc Prmt1 Inmt 1.13.11.10 5-Hydroxykynurenine 3.5.99.5 5-Methoxytryptamine Cyp2c80 1.3.1.18 1.13.11.- Mdm2 1.2.1.32 2.1.1.47 Aldh1a1 Indole-3-acetamide Aldh9a1 Cyp4f1 1.2.3.7 Kynu Cyp19a1 Cyp7b1 Haao Dd5 Cyp2b15 Aldh2 Cyp2j4 Ube3a Mdm2 Aldh1a2 4.2.1.84 Wars 4.1.1.- 1.13.99.3 Acetyl-CoA 2.6.1.27 AFMID Ube3a Maob Cyp2a2 Aldh9a1 Cat Cyp1b1 CYP3A4 1.4.3.2 Rnf25 Hsd17b10 Gcdh Ddc 2.6.1.27 Aanat CYP2A13 Acmsd 1.2.1.- 1.10.3.4 1.14.16.- Cyp2e1 Aldh1a4
Description
This pathway describes the metabolism of tryptophan, an essential amino acid.
This pathway was originally converted from rat to human, using ortholog information. Original pathway was created by Sebastien Burel.
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