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6022 PubChem-compound 79-83-4 CAS Aspartate metabolism SubPathway HMDB00250 HMDB HMDB01341 HMDB 1.0 AMP BioCyc aspartate 1-decarboxylase 1.0 C10H14N5O7P Adenosine monophosphate 347.06308 Pyrophosphate 1.0 SMILES [O-]P([O-])(=O)OP([O-])([O-])=O 14000-31-8 CAS CHEBI:16027 ChEBI C6H11O4 (R)-pantoate 147.06628 239 PubChem-compound B-ALANINE BioCyc ATP BioCyc SubPathwayInteraction1335 SubPathway1335Reaction SubPathwayReaction C00049 KEGG Compound 8.0 128 ChemSpider SMILES NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O Beta-Alanine 1.0 1.0 559142 ChemSpider HMDB00538 HMDB ADP BioCyc CHEBI:7916 ChEBI C3H7NO2 Beta-Alanine 89.047676 Pantothenate synthetase 1.0 CHEBI:15422 ChEBI 1.0 5745 ChemSpider HMDB00191 HMDB 5742 ChemSpider 1038 PubChem-compound L-ASPARTATE BioCyc C9H18NO8P D-4'-Phosphopantothenate 299.077 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 1.0 ReactionCatalysis2956 ACTIVATION HMDB59597 HMDB Aspartate 1-decarboxylase 274 ChemSpider Adenosine monophosphate P31663 UniProt 5858 ChemSpider 2.0 C00864 KEGG Compound C10H16N5O13P3 Adenosine triphosphate 506.99576 CHEBI:16526 ChEBI C9H17NO5 Pantothenic acid 219.11067 CHEBI:17053 ChEBI 1010 ChemSpider 131 PubChem-compound CHEBI:16761 ChEBI 2.7.1.33 false 2.7.1.33 Adenosine triphosphate + Pantothenic acid → Adenosine diphosphate + D-4'-Phosphopantothenate LEFT_TO_RIGHT ReactionCatalysis2968 ACTIVATION PPI BioCyc HMDB01967 HMDB SMILES NCCC(O)=O 2.0 HMDB00056 HMDB HMDB00210 HMDB 1.0 PANTOTHENATE BioCyc PW000787 PathWhiz Unknown Hydrogen Ion 5800 ChemSpider Pantothenic acid CO2 Carbon dioxide 43.98983 SMILES CC(C)(COP(O)(O)=O)C(O)C(=O)NCCC(O)=O Adenosine triphosphate C00080 KEGG Compound 4-P-PANTOTHENATE BioCyc SMILES CC(C)(CO)C(O)C(=O)NCCC(O)=O 124-38-9 CAS C00008 KEGG Compound D-4'-Phosphopantothenate CHEBI:15378 ChEBI SMILES [H+] PW000896 PathWhiz 58-64-0 CAS 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 CHEBI:18361 ChEBI SMP00915 SMPDB Pantothenate synthetase C00002 KEGG Compound 963 ChemSpider pantothenate synthetase L-Aspartic acid 280 PubChem-compound C4H7NO4 L-Aspartic acid 133.0375 107-95-9 CAS 1.0 (R)-pantoate 644102 PubChem-compound 988 PubChem-compound 6083 PubChem-compound 44367445 PubChem-compound SMP00809 SMPDB C00011 KEGG Compound SMILES O=C=O C00099 KEGG Compound P0A790 UniProt CHEBI:15980 ChEBI C00013 KEGG Compound C03492 KEGG Compound O7P2 Pyrophosphate 173.91193 234 ChemSpider 5957 PubChem-compound 1.0 HMDB00045 HMDB H Hydrogen Ion 1.007825 HMDB01016 HMDB SMILES CC(C)(CO)C(O)C([O-])=O Carbon dioxide 56-84-8 CAS Unknown 56-65-5 CAS C00020 KEGG Compound Pantothenate kinase 1 Aspartate 1-decarboxylase Adenosine diphosphate Reaction3364 false Hydrogen Ion + L-Aspartic acid → Beta-Alanine + Carbon dioxide LEFT_TO_RIGHT 6.3.2.1 false 6.3.2.1 (R)-pantoate + Adenosine triphosphate + Beta-Alanine → Adenosine monophosphate + Hydrogen Ion + Pantothenic acid + Pyrophosphate LEFT_TO_RIGHT C10H15N5O10P2 Adenosine diphosphate 427.02942 SMILES N[C@@H](CC(O)=O)C(O)=O CHEBI:16958 ChEBI Beta-Alanine Metabolism CHEBI:15905 ChEBI ReactionCatalysis3333 ACTIVATION Aspartate 1-decarboxylase Pantothenate synthetase Unknown L-Aspartic acid H + CO 2 Beta-Alanine ATP (R)-pantoate AMP PP i H + Pantothenic acid ATP D-4'- Phosphopantothenate ADP Aspartate metabolism
6022 PubChem-compound 79-83-4 CAS HMDB00250 HMDB HMDB01341 HMDB 1.0 AMP BioCyc aspartate 1-decarboxylase 1.0 C10H14N5O7P Adenosine monophosphate 347.06308 Pyrophosphate 1.0 SMILES [O-]P([O-])(=O)OP([O-])([O-])=O 14000-31-8 CAS CHEBI:16027 ChEBI C6H11O4 (R)-pantoate 147.06628 239 PubChem-compound B-ALANINE BioCyc ATP BioCyc SubPathwayInteraction1335 SubPathway1335Reaction SubPathwayReaction C00049 KEGG Compound 8.0 128 ChemSpider SMILES NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O Beta-Alanine 1.0 1.0 559142 ChemSpider HMDB00538 HMDB ADP BioCyc CHEBI:7916 ChEBI C3H7NO2 Beta-Alanine 89.047676 Pantothenate synthetase 1.0 CHEBI:15422 ChEBI 1.0 5745 ChemSpider HMDB00191 HMDB 5742 ChemSpider 1038 PubChem-compound L-ASPARTATE BioCyc C9H18NO8P D-4'-Phosphopantothenate 299.077 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 1.0 ReactionCatalysis2956 ACTIVATION HMDB59597 HMDB Aspartate 1-decarboxylase 274 ChemSpider Adenosine monophosphate P31663 UniProt 5858 ChemSpider 2.0 C00864 KEGG Compound C10H16N5O13P3 Adenosine triphosphate 506.99576 CHEBI:16526 ChEBI C9H17NO5 Pantothenic acid 219.11067 CHEBI:17053 ChEBI 1010 ChemSpider 131 PubChem-compound CHEBI:16761 ChEBI 2.7.1.33 false 2.7.1.33 Adenosine triphosphate + Pantothenic acid → Adenosine diphosphate + D-4'-Phosphopantothenate LEFT_TO_RIGHT ReactionCatalysis2968 ACTIVATION PPI BioCyc HMDB01967 HMDB SMILES NCCC(O)=O 2.0 Aspartate metabolism SubPathway HMDB00056 HMDB HMDB00210 HMDB 1.0 PANTOTHENATE BioCyc PW000787 PathWhiz Unknown Hydrogen Ion 5800 ChemSpider Pantothenic acid CO2 Carbon dioxide 43.98983 SMILES CC(C)(COP(O)(O)=O)C(O)C(=O)NCCC(O)=O Adenosine triphosphate C00080 KEGG Compound 4-P-PANTOTHENATE BioCyc SMILES CC(C)(CO)C(O)C(=O)NCCC(O)=O 124-38-9 CAS C00008 KEGG Compound D-4'-Phosphopantothenate CHEBI:15378 ChEBI SMILES [H+] PW000896 PathWhiz 58-64-0 CAS 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 CHEBI:18361 ChEBI http://identifiers.org/smpdb/SMP00915 SMPDB Pantothenate synthetase C00002 KEGG Compound 963 ChemSpider pantothenate synthetase L-Aspartic acid 280 PubChem-compound C4H7NO4 L-Aspartic acid 133.0375 107-95-9 CAS 1.0 (R)-pantoate 644102 PubChem-compound 988 PubChem-compound 6083 PubChem-compound 44367445 PubChem-compound http://identifiers.org/smpdb/SMP00809 SMPDB C00011 KEGG Compound SMILES O=C=O C00099 KEGG Compound P0A790 UniProt CHEBI:15980 ChEBI C00013 KEGG Compound C03492 KEGG Compound O7P2 Pyrophosphate 173.91193 234 ChemSpider 5957 PubChem-compound 1.0 HMDB00045 HMDB H Hydrogen Ion 1.007825 HMDB01016 HMDB SMILES CC(C)(CO)C(O)C([O-])=O Carbon dioxide 56-84-8 CAS Unknown 56-65-5 CAS C00020 KEGG Compound Pantothenate kinase 1 Aspartate 1-decarboxylase Adenosine diphosphate Reaction3364 false Hydrogen Ion + L-Aspartic acid → Beta-Alanine + Carbon dioxide LEFT_TO_RIGHT 6.3.2.1 false 6.3.2.1 (R)-pantoate + Adenosine triphosphate + Beta-Alanine → Adenosine monophosphate + Hydrogen Ion + Pantothenic acid + Pyrophosphate LEFT_TO_RIGHT C10H15N5O10P2 Adenosine diphosphate 427.02942 SMILES N[C@@H](CC(O)=O)C(O)=O CHEBI:16958 ChEBI Beta-Alanine Metabolism CHEBI:15905 ChEBI ReactionCatalysis3333 ACTIVATION panD panC Unknown L-Aspartic acid Hydrogen Ion Carbon dioxide Beta-Alanine Adenosine triphosphate (R)-pantoate Adenosine monophosphate Pyrophosphate Hydrogen Ion Pantothenic acid Adenosine triphosphate D-4'- Phosphopantothenate Adenosine diphosphate Aspartate metabolism