Loading Pathway...
CHEBI:16015 ChEBI SMP00824 SMPDB 30572 ChemSpider Reaction2902 true 2-Aminoacrylic acid → 2-iminopropanoate LEFT_TO_RIGHT C23H38N7O17P3S Acetyl-CoA 809.1258 Reaction2903 true 2-iminopropanoate + Hydrogen Ion + Water → Ammonium + Pyruvic acid LEFT_TO_RIGHT P00909 UniProt 937 ChemSpider Anthranilate synthase component II Tryptophan biosynthesis protein trpCF HMDB00250 HMDB 123991 PubChem-compound NADH Anthranilate synthase component 1 439153 PubChem-compound SMILES O 4.2.1.20 false 4.2.1.20 Indole + L-Serine → L-Tryptophan + Water LEFT_TO_RIGHT 4.1.99.1 false 4.1.99.1 L-Tryptophan → 2-Aminoacrylic acid + Hydrogen Ion + Indole LEFT_TO_RIGHT Pyrophosphate 1.0 HMDB00929 HMDB SMP00835 SMPDB HMDB01112 HMDB CHEBI:17115 ChEBI HMDB00148 HMDB 120-72-9 CAS 2-Aminoacrylic acid NAD 5961 PubChem-compound CHEBI:17111 ChEBI H4N Ammonium 18.034374 1.2.4.1 false 1.2.4.1 Coenzyme A + NAD + Pyruvic acid → Acetyl-CoA + Carbon dioxide + NADH LEFT_TO_RIGHT 1.0 SMILES N1C=CC2=C1C=CC=C2 6816 PubChem-compound 1.0 Pyruvic acid 559142 ChemSpider CHEBI:15846 ChEBI C3H4O3 Pyruvic acid 88.016045 ReactionCatalysis2542 ACTIVATION 5746 ChemSpider HMDB01206 HMDB SMILES OC1C(O)C(NC2=C(C=CC=C2)C([O-])=O)OC1COP([O-])([O-])=O 1.0 1038 PubChem-compound SMILES CC(=N)C([O-])=O SMILES OC(COP([O-])([O-])=O)C(O)C1=CNC2=C1C=CC=C2 SMILES O[C@H](COP([O-])([O-])=O)[C@@H](O)C(=O)CNC1=CC=CC=C1C([O-])=O SMILES O[C@@H]1C=CC(=C[C@H]1OC(=C)C(O)=O)C(O)=O 7540-64-9 CAS HMDB59597 HMDB 274 ChemSpider HMDB00902 HMDB CHEBI:16908 ChEBI HMDB00243 HMDB C00108 KEGG Compound 5736 ChemSpider 1.0 709 ChemSpider C00463 KEGG Compound Acetyl-CoA CHEBI:17333 ChEBI 1010 ChemSpider SER BioCyc SMILES CC(C)(COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N)C(O)C(=O)NCCC(=O)NCCS 73-22-3 CAS 1948-56-7 CAS HMDB41827 HMDB PPI BioCyc C00119 KEGG Compound C3H7O6P D-Glyceraldehyde 3-phosphate 169.99803 HMDB01423 HMDB Ammonium C5H10N2O3 L-Glutamine 146.06914 Hydrogen Ion 1.0 C11H12N2O2 L-Tryptophan 204.08987 C12H13NO9P N-(5-phosphoribosyl)-anthranilate 346.03442 C12H13NO9P 1-(o-carboxyphenylamino)-1'-deoxyribulose 5'-phosphate 346.03442 218 ChemSpider C11H12NO6P (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate 285.04132 C3H4NO2 2-iminopropanoate 86.02475 58-68-4 CAS L-Glutamic acid C5H13O14P3 Phosphoribosyl pyrophosphate 389.9518 2.0 124-38-9 CAS PW000779 PathWhiz 798 PubChem-compound C7H7NO2 2-Aminobenzoic acid 137.04768 1.0 Tryptophan biosynthesis protein trpCF C00001 KEGG Compound Anthranilate synthase component II 1.0 Anthranilate synthase component 1 CHEBI:18361 ChEBI C00004 KEGG Compound C00003 KEGG Compound 1031 ChemSpider ReactionCatalysis2864 ACTIVATION 1.0 4.0 ReactionCatalysis2866 ACTIVATION ReactionCatalysis2865 ACTIVATION ReactionCatalysis2867 ACTIVATION GLN BioCyc PW000769 PathWhiz GLT BioCyc 1.0 HMDB03609 HMDB ReactionCatalysis2860 ACTIVATION ReactionCatalysis2862 ACTIVATION ReactionCatalysis2861 ACTIVATION 1.0 C3H5NO2 2-Aminoacrylic acid 87.03203 SMP00802 SMPDB TCA cycle SubPathway C21H28N7O14P2 NAD 664.11694 227 PubChem-compound C00011 KEGG Compound SMILES O=C=O C01342 KEGG Compound 7339 PubChem-compound CHEBI:28938 ChEBI C00010 KEGG Compound C00251 KEGG Compound CHEBI:17123 ChEBI 5951 PubChem-compound D-Glutamine and D-Glutamate Metabolism SubPathway 2-Aminobenzoic acid C00013 KEGG Compound O7P2 Pyrophosphate 173.91193 Tryptophan synthase beta chain C21H29N7O14P2 NADH 665.12476 1.0 CHEBI:16828 ChEBI Tryptophanase Tryptophan synthase alpha chain Phosphoribosyl pyrophosphate CHEBI:17138 ChEBI H Hydrogen Ion 1.007825 D-Glyceraldehyde 3-phosphate L-Glutamine C00022 KEGG Compound Unknown L-Tryptophan 53-84-9 CAS SubPathwayInteraction1671 SubPathway1671Reaction SubPathwayReaction C00025 KEGG Compound Unknown 6066 ChemSpider C00024 KEGG Compound SubPathwayInteraction1672 SubPathway1672Reaction SubPathwayReaction SMILES N[C@@H](CO)C(O)=O P00904 UniProt 222 ChemSpider SMILES NC(=C)C(O)=O 1.0 C02218 KEGG Compound SubPathwayInteraction1168 SubPathwayReaction SubPathway1168Reaction SMILES NC(=O)C1=C[N+](=CC=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O 6305 PubChem-compound 2.0 CHEBI:58613 ChEBI CHEBI:18277 ChEBI 5682 ChemSpider 776 ChemSpider tryptophan synthase, β subunit dimer Unknown SMILES NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C(N)N=CN=C23)[C@@H](O)[C@H]1O CHEBI:1146900 ChEBI Water tryptophanase / L-cysteine desulfhydrase SMILES [O-]P([O-])(=O)OP([O-])([O-])=O 14000-31-8 CAS 2.0 CO-A BioCyc C10H10O6 Chorismate 226.04774 CHEBI:58866 ChEBI 72-89-9 CAS 56-85-9 CAS HMDB12199 HMDB Coenzyme A 7062 ChemSpider 1.0 P0A853 UniProt C21H36N7O16P3S Coenzyme A 767.11523 SMILES N[C@@H](CC1=CNC2=CC=CC=C12)C(O)=O 14798-03-9 CAS TRP BioCyc 24.0 11542 ChemSpider SMP00792 SMPDB 6557 ChemSpider SMILES CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N 1.0 7732-18-5 CAS 388299 ChemSpider Chorismate 591-59-3 CAS Tryptophan synthase beta chain 617-12-9 CAS Tryptophan synthase alpha chain 127-17-3 CAS 1.0 2-iminopropanoate 56-86-0 CAS Tryptophanase P00895 UniProt C5H9NO4 L-Glutamic acid 147.05316 33032 PubChem-compound SMILES [NH4+] HMDB00641 HMDB 1.0 CHEBI:16526 ChEBI N-(5-phosphoribosyl)-anthranilate 1-(o-carboxyphenylamino)-1'-deoxyribulose 5'-phosphate C00065 KEGG Compound C00064 KEGG Compound (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate 1.0 1.0 CHEBI:16881 ChEBI SMILES CC(=O)C(O)=O P0A877 UniProt P0A879 UniProt HMDB01967 HMDB 962 PubChem-compound CPD-9517 BioCyc INDOLE BioCyc Unknown Unknown C8H7N Indole 117.057846 392413 ChemSpider C00078 KEGG Compound ANTHRANILATE BioCyc CO2 Carbon dioxide 43.98983 5893 PubChem-compound HMDB02111 HMDB CHEBI:30754 ChEBI C00080 KEGG Compound CHEBI:77456 ChEBI Pyruvate dehydrogenase complex 729 PubChem-compound SMILES N[C@@H](CCC(O)=O)C(O)=O CHEBI:32816 ChEBI PW000815 PathWhiz 1.0 CHEBI:15377 ChEBI CHEBI:15378 ChEBI SMILES [H+] PYRUVATE BioCyc 56-45-1 CAS 60.0 Unknown HMDB00187 HMDB 1.0 1.0 280 PubChem-compound L-Serine Reaction2898 false 1-(o-carboxyphenylamino)-1'-deoxyribulose 5'-phosphate + Hydrogen Ion → (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate + Carbon dioxide + Water LEFT_TO_RIGHT 4.2.1.20 false 4.2.1.20 (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate → D-Glyceraldehyde 3-phosphate + Indole LEFT_TO_RIGHT HMDB00738 HMDB 4.1.1.48 false 4.1.1.48 N-(5-phosphoribosyl)-anthranilate → 1-(o-carboxyphenylamino)-1'-deoxyribulose 5'-phosphate LEFT_TO_RIGHT C3H7NO3 L-Serine 105.042595 4.1.3.27 false 4.1.3.27 Chorismate + L-Glutamine → 2-Aminobenzoic acid + Hydrogen Ion + L-Glutamic acid + Pyruvic acid LEFT_TO_RIGHT 4.1.3.27 false 4.1.3.27 2-Aminobenzoic acid + Phosphoribosyl pyrophosphate → N-(5-phosphoribosyl)-anthranilate + Pyrophosphate LEFT_TO_RIGHT 1.0 PW000803 PathWhiz HMDB01487 HMDB HMDB01123 HMDB 644102 PubChem-compound 444493 PubChem-compound 16741146 PubChem-compound SMILES N[C@@H](CCC(N)=O)C(O)=O SMILES OC(COP(O)(O)=O)C=O PRPP BioCyc 1.0 ACETYL-COA BioCyc CHEBI:18050 ChEBI 60.0 H2O Water 18.010565 SMILES O[C@H]1[C@@H](O)[C@@H](O[P@](O)(=O)OP(O)(O)=O)O[C@@H]1COP(O)(O)=O NADH BioCyc NAD BioCyc 1060 PubChem-compound GAP BioCyc SMILES NC1=CC=CC=C1C(O)=O Carbon dioxide C00661 KEGG Compound HMDB00280 HMDB Indole CHEBI:15351 ChEBI 12039 PubChem-compound tRNA Charging 2 SubPathway 110510 ChemSpider 118-92-3 CAS anthranilate synthase 85-61-0 CAS tryptophan metabolism Anthranilate synthase component 1 Anthranilate synthase component II Anthranilate synthase component II Tryptophan biosynthesis protein trpCF Tryptophan biosynthesis protein trpCF Tryptophan synthase alpha chain Tryptophan synthase beta chain Tryptophanase Unknown Unknown Unknown Chorismate L-Glutamine L-Glutamic acid Pyruvic acid H + 2-Aminobenzoic acid Phosphoribosyl pyrophosphate PP i N-(5- phosphoribosyl)- anthranilate 1-(o- carboxyphenylamino)- 1'- deoxyribulose 5'-phosphate H + H 2 O CO 2 (1S,2R)-1-C- (indol-3- yl)glycerol 3-phosphate D- Glyceraldehyde 3-phosphate Indole L-Serine H 2 O L-Tryptophan H + Indole 2-Aminoacrylic acid 2- iminopropanoate H 2 O H + Ammonium Pyruvic acid CoA NAD Acetyl-CoA CO 2 NADH tRNA Charging 2 TCA cycle D-Glutamine and D-Glutamate Metabolism Unknown
CHEBI:16015 ChEBI http://identifiers.org/smpdb/SMP00824 SMPDB 30572 ChemSpider Reaction2902 true 2-Aminoacrylic acid → 2-iminopropanoate LEFT_TO_RIGHT C23H38N7O17P3S Acetyl-CoA 809.1258 Reaction2903 true 2-iminopropanoate + Hydrogen Ion + Water → Ammonium + Pyruvic acid LEFT_TO_RIGHT P00909 UniProt 937 ChemSpider Anthranilate synthase component II Tryptophan biosynthesis protein trpCF HMDB00250 HMDB 123991 PubChem-compound NADH Anthranilate synthase component 1 439153 PubChem-compound SMILES O 4.2.1.20 false 4.2.1.20 Indole + L-Serine → L-Tryptophan + Water LEFT_TO_RIGHT 4.1.99.1 false 4.1.99.1 L-Tryptophan → 2-Aminoacrylic acid + Hydrogen Ion + Indole LEFT_TO_RIGHT Pyrophosphate 1.0 HMDB00929 HMDB http://identifiers.org/smpdb/SMP00835 SMPDB HMDB01112 HMDB D-Glutamine and D-Glutamate Metabolism SubPathway CHEBI:17115 ChEBI HMDB00148 HMDB 120-72-9 CAS 2-Aminoacrylic acid NAD 5961 PubChem-compound CHEBI:17111 ChEBI H4N Ammonium 18.034374 1.2.4.1 false 1.2.4.1 Coenzyme A + NAD + Pyruvic acid → Acetyl-CoA + Carbon dioxide + NADH LEFT_TO_RIGHT 1.0 SMILES N1C=CC2=C1C=CC=C2 6816 PubChem-compound 1.0 Pyruvic acid 559142 ChemSpider CHEBI:15846 ChEBI C3H4O3 Pyruvic acid 88.016045 ReactionCatalysis2542 ACTIVATION 5746 ChemSpider HMDB01206 HMDB SMILES OC1C(O)C(NC2=C(C=CC=C2)C([O-])=O)OC1COP([O-])([O-])=O 1.0 1038 PubChem-compound SMILES CC(=N)C([O-])=O SMILES OC(COP([O-])([O-])=O)C(O)C1=CNC2=C1C=CC=C2 SMILES O[C@H](COP([O-])([O-])=O)[C@@H](O)C(=O)CNC1=CC=CC=C1C([O-])=O SMILES O[C@@H]1C=CC(=C[C@H]1OC(=C)C(O)=O)C(O)=O 7540-64-9 CAS HMDB59597 HMDB 274 ChemSpider HMDB00902 HMDB CHEBI:16908 ChEBI HMDB00243 HMDB C00108 KEGG Compound 5736 ChemSpider 1.0 709 ChemSpider C00463 KEGG Compound Acetyl-CoA CHEBI:17333 ChEBI 1010 ChemSpider SER BioCyc SMILES CC(C)(COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N)C(O)C(=O)NCCC(=O)NCCS 73-22-3 CAS 1948-56-7 CAS HMDB41827 HMDB PPI BioCyc TCA cycle SubPathway C00119 KEGG Compound C3H7O6P D-Glyceraldehyde 3-phosphate 169.99803 HMDB01423 HMDB Ammonium C5H10N2O3 L-Glutamine 146.06914 Hydrogen Ion 1.0 C11H12N2O2 L-Tryptophan 204.08987 C12H13NO9P N-(5-phosphoribosyl)-anthranilate 346.03442 C12H13NO9P 1-(o-carboxyphenylamino)-1'-deoxyribulose 5'-phosphate 346.03442 218 ChemSpider C11H12NO6P (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate 285.04132 C3H4NO2 2-iminopropanoate 86.02475 58-68-4 CAS L-Glutamic acid C5H13O14P3 Phosphoribosyl pyrophosphate 389.9518 2.0 124-38-9 CAS PW000779 PathWhiz 798 PubChem-compound C7H7NO2 2-Aminobenzoic acid 137.04768 1.0 Tryptophan biosynthesis protein trpCF C00001 KEGG Compound Anthranilate synthase component II 1.0 Anthranilate synthase component 1 CHEBI:18361 ChEBI C00004 KEGG Compound C00003 KEGG Compound 1031 ChemSpider ReactionCatalysis2864 ACTIVATION 1.0 4.0 ReactionCatalysis2866 ACTIVATION ReactionCatalysis2865 ACTIVATION ReactionCatalysis2867 ACTIVATION GLN BioCyc PW000769 PathWhiz GLT BioCyc 1.0 HMDB03609 HMDB ReactionCatalysis2860 ACTIVATION ReactionCatalysis2862 ACTIVATION ReactionCatalysis2861 ACTIVATION 1.0 C3H5NO2 2-Aminoacrylic acid 87.03203 http://identifiers.org/smpdb/SMP00802 SMPDB C21H28N7O14P2 NAD 664.11694 227 PubChem-compound C00011 KEGG Compound SMILES O=C=O C01342 KEGG Compound 7339 PubChem-compound CHEBI:28938 ChEBI C00010 KEGG Compound C00251 KEGG Compound CHEBI:17123 ChEBI 5951 PubChem-compound 2-Aminobenzoic acid C00013 KEGG Compound O7P2 Pyrophosphate 173.91193 Tryptophan synthase beta chain C21H29N7O14P2 NADH 665.12476 1.0 CHEBI:16828 ChEBI Tryptophanase Tryptophan synthase alpha chain Phosphoribosyl pyrophosphate CHEBI:17138 ChEBI H Hydrogen Ion 1.007825 D-Glyceraldehyde 3-phosphate L-Glutamine C00022 KEGG Compound Unknown L-Tryptophan 53-84-9 CAS SubPathwayInteraction1671 SubPathway1671Reaction SubPathwayReaction C00025 KEGG Compound Unknown 6066 ChemSpider C00024 KEGG Compound SubPathwayInteraction1672 SubPathway1672Reaction SubPathwayReaction SMILES N[C@@H](CO)C(O)=O P00904 UniProt 222 ChemSpider SMILES NC(=C)C(O)=O 1.0 C02218 KEGG Compound SubPathwayInteraction1168 SubPathwayReaction SubPathway1168Reaction SMILES NC(=O)C1=C[N+](=CC=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O 6305 PubChem-compound 2.0 CHEBI:58613 ChEBI CHEBI:18277 ChEBI 5682 ChemSpider 776 ChemSpider tryptophan synthase, β subunit dimer Unknown SMILES NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C(N)N=CN=C23)[C@@H](O)[C@H]1O CHEBI:1146900 ChEBI Water tryptophanase / L-cysteine desulfhydrase SMILES [O-]P([O-])(=O)OP([O-])([O-])=O 14000-31-8 CAS 2.0 tRNA Charging 2 SubPathway CO-A BioCyc C10H10O6 Chorismate 226.04774 CHEBI:58866 ChEBI 72-89-9 CAS 56-85-9 CAS HMDB12199 HMDB Coenzyme A 7062 ChemSpider 1.0 P0A853 UniProt C21H36N7O16P3S Coenzyme A 767.11523 SMILES N[C@@H](CC1=CNC2=CC=CC=C12)C(O)=O 14798-03-9 CAS TRP BioCyc 24.0 11542 ChemSpider http://identifiers.org/smpdb/SMP00792 SMPDB 6557 ChemSpider SMILES CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N 1.0 7732-18-5 CAS 388299 ChemSpider Chorismate 591-59-3 CAS Tryptophan synthase beta chain 617-12-9 CAS Tryptophan synthase alpha chain 127-17-3 CAS 1.0 2-iminopropanoate 56-86-0 CAS Tryptophanase P00895 UniProt C5H9NO4 L-Glutamic acid 147.05316 33032 PubChem-compound SMILES [NH4+] HMDB00641 HMDB 1.0 CHEBI:16526 ChEBI N-(5-phosphoribosyl)-anthranilate 1-(o-carboxyphenylamino)-1'-deoxyribulose 5'-phosphate C00065 KEGG Compound C00064 KEGG Compound (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate 1.0 1.0 CHEBI:16881 ChEBI SMILES CC(=O)C(O)=O P0A877 UniProt P0A879 UniProt HMDB01967 HMDB 962 PubChem-compound CPD-9517 BioCyc INDOLE BioCyc Unknown Unknown C8H7N Indole 117.057846 392413 ChemSpider C00078 KEGG Compound ANTHRANILATE BioCyc CO2 Carbon dioxide 43.98983 5893 PubChem-compound HMDB02111 HMDB CHEBI:30754 ChEBI C00080 KEGG Compound CHEBI:77456 ChEBI Pyruvate dehydrogenase complex 729 PubChem-compound SMILES N[C@@H](CCC(O)=O)C(O)=O CHEBI:32816 ChEBI PW000815 PathWhiz 1.0 CHEBI:15377 ChEBI CHEBI:15378 ChEBI SMILES [H+] PYRUVATE BioCyc 56-45-1 CAS 60.0 Unknown HMDB00187 HMDB 1.0 1.0 280 PubChem-compound L-Serine Reaction2898 false 1-(o-carboxyphenylamino)-1'-deoxyribulose 5'-phosphate + Hydrogen Ion → (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate + Carbon dioxide + Water LEFT_TO_RIGHT 4.2.1.20 false 4.2.1.20 (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate → D-Glyceraldehyde 3-phosphate + Indole LEFT_TO_RIGHT HMDB00738 HMDB 4.1.1.48 false 4.1.1.48 N-(5-phosphoribosyl)-anthranilate → 1-(o-carboxyphenylamino)-1'-deoxyribulose 5'-phosphate LEFT_TO_RIGHT C3H7NO3 L-Serine 105.042595 4.1.3.27 false 4.1.3.27 Chorismate + L-Glutamine → 2-Aminobenzoic acid + Hydrogen Ion + L-Glutamic acid + Pyruvic acid LEFT_TO_RIGHT 4.1.3.27 false 4.1.3.27 2-Aminobenzoic acid + Phosphoribosyl pyrophosphate → N-(5-phosphoribosyl)-anthranilate + Pyrophosphate LEFT_TO_RIGHT 1.0 PW000803 PathWhiz HMDB01487 HMDB HMDB01123 HMDB 644102 PubChem-compound 444493 PubChem-compound 16741146 PubChem-compound SMILES N[C@@H](CCC(N)=O)C(O)=O SMILES OC(COP(O)(O)=O)C=O PRPP BioCyc 1.0 ACETYL-COA BioCyc CHEBI:18050 ChEBI 60.0 H2O Water 18.010565 SMILES O[C@H]1[C@@H](O)[C@@H](O[P@](O)(=O)OP(O)(O)=O)O[C@@H]1COP(O)(O)=O NADH BioCyc NAD BioCyc 1060 PubChem-compound GAP BioCyc SMILES NC1=CC=CC=C1C(O)=O Carbon dioxide C00661 KEGG Compound HMDB00280 HMDB Indole CHEBI:15351 ChEBI 12039 PubChem-compound 110510 ChemSpider 118-92-3 CAS anthranilate synthase 85-61-0 CAS tryptophan metabolism trpE trpD trpD trpC trpC trpA trpB tnaA Unknown Unknown Unknown Chorismate L-Glutamine L-Glutamic acid Pyruvic acid Hydrogen Ion 2-Aminobenzoic acid Phosphoribosyl pyrophosphate Pyrophosphate N-(5- phosphoribosyl)- anthranilate 1-(o- carboxyphenylamino)- 1'- deoxyribulose 5'-phosphate Hydrogen Ion Water Carbon dioxide (1S,2R)-1-C- (indol-3- yl)glycerol 3-phosphate D- Glyceraldehyde 3-phosphate Indole L-Serine Water L-Tryptophan Hydrogen Ion Indole 2-Aminoacrylic acid 2- iminopropanoate Water Hydrogen Ion Ammonium Pyruvic acid Coenzyme A NAD Acetyl-CoA Carbon dioxide NADH tRNA Charging 2 TCA cycle D-Glutamine and D-Glutamate Metabolism Unknown