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Acyl-coenzyme A synthetase ACSM1, mitochondrial ReactionCatalysis393 ACTIVATION 1.0 ReactionCatalysis394 ACTIVATION CL:0000000 CELL TYPE ONTOLOGY ReactionCatalysis392 ACTIVATION Adenosine triphosphate 1.0 HMDB00250 HMDB C13H16N2O4 Alpha-N-Phenylacetyl-L-glutamine 264.111 CHEBI:1146900 ChEBI Phenylacetyl-CoA AMP BioCyc Mitochondrial Matrix 10181341 ChemSpider C10H14N5O7P Adenosine monophosphate 347.06308 SMILES [O-]P([O-])(=O)OP([O-])([O-])=O 14000-31-8 CAS Phenylacetate Metabolism CHEBI:16027 ChEBI 999 PubChem-compound CO-A BioCyc 34-DIHYDROXYPHENYLACETYL-COA BioCyc ATP BioCyc 5961 PubChem-compound 56-85-9 CAS C21H36N7O16P3S Coenzyme A 767.11523 6816 PubChem-compound 28047-15-6 CAS C07086 KEGG Compound 559142 ChemSpider HMDB00538 HMDB Cell CHEBI:15422 ChEBI 6557 ChemSpider 5746 ChemSpider 7532-39-0 CAS 5742 ChemSpider SMILES NC(=O)CC[C@H](NC(=O)CC1=CC=CC=C1)C(O)=O Acyl-coenzyme A synthetase ACSM2B, mitochondrial 61-19-8 CAS SMILES NC1=C2N=CN([C@@H]3O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]3O)C2=NC=N1 GO:0005829 GENE ONTOLOGY 1.0 C8H8O2 Phenylacetic acid 136.05243 1.0 1.0 Acyl-coenzyme A synthetase ACSM2B, mitochondrial 5858 ChemSpider PW000033 PathWhiz HMDB06503 HMDB HMDB00641 HMDB C10H16N5O13P3 Adenosine triphosphate 506.99576 Alpha-N-Phenylacetyl-L-glutamine Glutamate Metabolism SubPathway Ammonia Recycling SubPathway C00582 KEGG Compound C00064 KEGG Compound Alpha-N-Phenylacetyl-L-glutamine C04148 KEGG Compound HMDB06344 HMDB 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 PPI BioCyc Acyl-coenzyme A synthetase ACSM1, mitochondrial Q68CK6 UniProt 9606 TAXONOMY HMDB01423 HMDB Glycine N-acyltransferase C5H10N2O3 L-Glutamine 146.06914 1.0 92258 PubChem-compound Cytosol 165620 PubChem-compound Q6IB77 UniProt SubPathwayInteraction86 SubPathway86Reaction SubPathwayReaction Adenosine monophosphate SMILES OC(=O)CC1=CC=CC=C1 HMDB00209 HMDB BiologicalState4 L-Glutamine SubPathwayOutput Alpha-N-Phenylacetyl-L-glutamine CHEBI:15537 ChEBI Reaction843 false L-Glutamine + Phenylacetyl-CoA → Alpha-N-Phenylacetyl-L-glutamine + Coenzyme A LEFT_TO_RIGHT SMILES NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O C29H42N7O17P3S Phenylacetyl-CoA 885.15704 Phenylacetic acid CHEBI:18361 ChEBI SubPathwayInteraction85 SubPathway85Reaction SubPathwayReaction C00002 KEGG Compound SMP00072 SMPDB GO:0005759 GENE ONTOLOGY Pyrophosphate CHEBI:30745 ChEBI Coenzyme A GLN BioCyc 6.2.1.2 false 6.2.1.2 Adenosine triphosphate + Coenzyme A + Phenylacetic acid → Adenosine monophosphate + Phenylacetyl-CoA + Pyrophosphate LEFT_TO_RIGHT 1.0 PW000009 PathWhiz Q08AH1 UniProt 83292 ChemSpider SMP00009 SMPDB CHEBI:17884 ChEBI 644102 PubChem-compound SMP00126 SMPDB 6083 PubChem-compound PW000003 PathWhiz C00010 KEGG Compound 1.0 103-82-2 CAS SMILES N[C@@H](CCC(N)=O)C(O)=O CPD-1097 BioCyc C00013 KEGG Compound O7P2 Pyrophosphate 173.91193 PHENYLACETATE BioCyc CHEBI:18050 ChEBI 5957 PubChem-compound 1.0 HMDB00045 HMDB 56-65-5 CAS C00020 KEGG Compound 145148 ChemSpider 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=C(N)N=CN=C12)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)CC1=CC=CC=C1 Glycine N-acyltransferase Transport228 false Alpha-N-Phenylacetyl-L-glutamine (→) Transport: Homo sapiens, Cell, Cytosol to Homo sapiens, Kidney LEFT_TO_RIGHT 85-61-0 CAS 1.0 Acyl-coenzyme A synthetase ACSM1, mitochondrial Glycine N- acyltransferase Acyl-coenzyme A synthetase ACSM2B, mitochondrial L-Glutamine Alpha-N-Phenylacetyl-L- glutamine Phenylacetic acid ATP CoA Phenylacetyl-CoA PP i AMP Alpha-N-Phenylacetyl-L- glutamine CoA ATP CoA PP i AMP Magnesium Magnesium Ammonia Recycling Glutamate Metabolism Intracellular Space Extracellular Space Kidney Mitochondria
Acyl-coenzyme A synthetase ACSM1, mitochondrial ReactionCatalysis393 ACTIVATION 1.0 ReactionCatalysis394 ACTIVATION CL:0000000 CELL TYPE ONTOLOGY ReactionCatalysis392 ACTIVATION Adenosine triphosphate 1.0 HMDB00250 HMDB C13H16N2O4 Alpha-N-Phenylacetyl-L-glutamine 264.111 CHEBI:1146900 ChEBI Phenylacetyl-CoA AMP BioCyc Mitochondrial Matrix 10181341 ChemSpider C10H14N5O7P Adenosine monophosphate 347.06308 SMILES [O-]P([O-])(=O)OP([O-])([O-])=O 14000-31-8 CAS Phenylacetate Metabolism CHEBI:16027 ChEBI 999 PubChem-compound CO-A BioCyc 34-DIHYDROXYPHENYLACETYL-COA BioCyc ATP BioCyc 5961 PubChem-compound 56-85-9 CAS C21H36N7O16P3S Coenzyme A 767.11523 6816 PubChem-compound 28047-15-6 CAS C07086 KEGG Compound 559142 ChemSpider HMDB00538 HMDB Cell CHEBI:15422 ChEBI 6557 ChemSpider 5746 ChemSpider 7532-39-0 CAS 5742 ChemSpider SMILES NC(=O)CC[C@H](NC(=O)CC1=CC=CC=C1)C(O)=O Acyl-coenzyme A synthetase ACSM2B, mitochondrial 61-19-8 CAS SMILES NC1=C2N=CN([C@@H]3O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]3O)C2=NC=N1 GO:0005829 GENE ONTOLOGY 1.0 C8H8O2 Phenylacetic acid 136.05243 1.0 1.0 Acyl-coenzyme A synthetase ACSM2B, mitochondrial 5858 ChemSpider PW000033 PathWhiz HMDB06503 HMDB HMDB00641 HMDB C10H16N5O13P3 Adenosine triphosphate 506.99576 Alpha-N-Phenylacetyl-L-glutamine Glutamate Metabolism SubPathway Ammonia Recycling SubPathway C00582 KEGG Compound C00064 KEGG Compound Alpha-N-Phenylacetyl-L-glutamine C04148 KEGG Compound HMDB06344 HMDB 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 PPI BioCyc Acyl-coenzyme A synthetase ACSM1, mitochondrial Q68CK6 UniProt 9606 TAXONOMY HMDB01423 HMDB Glycine N-acyltransferase C5H10N2O3 L-Glutamine 146.06914 1.0 92258 PubChem-compound Cytosol 165620 PubChem-compound Q6IB77 UniProt SubPathwayInteraction86 SubPathway86Reaction SubPathwayReaction Adenosine monophosphate SMILES OC(=O)CC1=CC=CC=C1 HMDB00209 HMDB BiologicalState4 Homo sapiens, Cell, Mitochondrial Matrix L-Glutamine SubPathwayOutput Alpha-N-Phenylacetyl-L-glutamine CHEBI:15537 ChEBI Reaction843 false L-Glutamine + Phenylacetyl-CoA → Alpha-N-Phenylacetyl-L-glutamine + Coenzyme A LEFT_TO_RIGHT SMILES NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O C29H42N7O17P3S Phenylacetyl-CoA 885.15704 Phenylacetic acid CHEBI:18361 ChEBI SubPathwayInteraction85 SubPathway85Reaction SubPathwayReaction C00002 KEGG Compound http://identifiers.org/smpdb/SMP00072 SMPDB GO:0005759 GENE ONTOLOGY Pyrophosphate CHEBI:30745 ChEBI Coenzyme A GLN BioCyc 6.2.1.2 false 6.2.1.2 Adenosine triphosphate + Coenzyme A + Phenylacetic acid → Adenosine monophosphate + Phenylacetyl-CoA + Pyrophosphate LEFT_TO_RIGHT 1.0 PW000009 PathWhiz Q08AH1 UniProt 83292 ChemSpider http://identifiers.org/smpdb/SMP00009 SMPDB CHEBI:17884 ChEBI 644102 PubChem-compound http://identifiers.org/smpdb/SMP00126 SMPDB 6083 PubChem-compound PW000003 PathWhiz C00010 KEGG Compound 1.0 103-82-2 CAS SMILES N[C@@H](CCC(N)=O)C(O)=O CPD-1097 BioCyc C00013 KEGG Compound O7P2 Pyrophosphate 173.91193 PHENYLACETATE BioCyc CHEBI:18050 ChEBI 5957 PubChem-compound 1.0 HMDB00045 HMDB 56-65-5 CAS C00020 KEGG Compound 145148 ChemSpider 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=C(N)N=CN=C12)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)CC1=CC=CC=C1 Glycine N-acyltransferase Transport228 false Alpha-N-Phenylacetyl-L-glutamine (→) Transport: Homo sapiens, Cell, Cytosol to Homo sapiens, Kidney LEFT_TO_RIGHT 85-61-0 CAS 1.0 Mitochondria ACSM1 GLYAT ACSM2B L-Glutamine Alpha-N- Phenylacetyl- L-glutamine Phenylacetic acid Adenosine triphosphate Coenzyme A Phenylacetyl- CoA Pyrophosphate Adenosine monophosphate Alpha-N- Phenylacetyl- L-glutamine Coenzyme A Adenosine triphosphate Coenzyme A Pyrophosphate Adenosine monophosphate Ammonia Recycling Glutamate Metabolism