1005
ChemSpider
6022
PubChem-compound
769
PubChem-compound
439161
PubChem-compound
CPD-8587
BioCyc
BiologicalState304
Bacteria
S-Methylmalonyl-CoA
HMDB0000254
HMDB
SMILES
OC(=O)CCC(O)=O
2.0
17216177
ChemSpider
D-METHYL-MALONYL-COA
BioCyc
HMDB0002310
HMDB
21252287
PubChem-compound
Methylmalonyl-CoA decarboxylase
1.0
HMDB0001341
HMDB
C3H6O2
Propionic acid
74.03678
1.0
C00683
KEGG Compound
HMDB0000538
HMDB
C25H40N7O19P3S
R-Methylmalonyl-CoA
867.1312
C00042
KEGG Compound
C00163
KEGG Compound
ATP
BioCyc
1078
ChemSpider
1.0
C00288
KEGG Compound
1.0
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
Uncharacterized protein ygfH
604-98-8
CAS
Adenosine diphosphate
SMILES
OC([O-])=O
ADP
BioCyc
Propanoyl-CoA Degradation
6.0
CHEBI:15422
ChEBI
HCO3
BioCyc
CHEBI:15380
ChEBI
Escherichia coli
5742
ChemSpider
C25H40N7O19P3S
Succinyl-CoA
867.1312
1038
PubChem-compound
Uncharacterized protein ygfH
1032
PubChem-compound
R-Methylmalonyl-CoA
1.0
Protein sbm
GO:0005829
GENE ONTOLOGY
1.0
274
ChemSpider
CHEBI:15539
ChEBI
C10H16N5O13P3
Adenosine triphosphate
506.99576
PW002057
PathWhiz
CHEBI:16526
ChEBI
C00100
KEGG Compound
O4P
Phosphate
94.95342
SMILES
C[C@H](C(O)=O)C(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP(O)(O)=O)N1C=NC2=C(N)N=CN=C12
SMILES
CCC(O)=O
1010
ChemSpider
CHEBI:16761
ChEBI
methylmalonyl-CoA mutase
439164
PubChem-compound
CHEBI:30768
ChEBI
Succinic acid
methylmalonyl-CoA decarboxylase
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)NCCSC(=O)CCC(O)=O
C24H40N7O17P3S
Propionyl-CoA
823.1414
CHEBI:17544
ChEBI
1.0
Hydrogen Ion
5800
ChemSpider
C01213
KEGG Compound
Cytosol
CO2
Carbon dioxide
43.98983
388310
ChemSpider
1.0
SUC
BioCyc
ReactionCatalysis5968
ACTIVATION
C00080
KEGG Compound
C25H40N7O19P3S
S-Methylmalonyl-CoA
867.1312
110-15-6
CAS
SMILES
[O-]P([O-])([O-])=O
ReactionCatalysis5969
ACTIVATION
73173-92-9
CAS
124-38-9
CAS
1.0
SMP0002069
SMPDB
13628334
ChemSpider
HMDB0001022
HMDB
P52043
UniProt
C00009
KEGG Compound
C00008
KEGG Compound
P52045
UniProt
CHEBI:15378
ChEBI
SMILES
[H+]
14265-44-2
CAS
Succinyl-CoA
Hydrogen Ion
HMDB0001429
HMDB
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
PROPIONYL-COA
BioCyc
Methylmalonyl-CoA decarboxylase
CHEBI:18367
ChEBI
1032
ChemSpider
C00002
KEGG Compound
Phosphate
C00091
KEGG Compound
Protein sbm
METHYL-MALONYL-COA
BioCyc
280
PubChem-compound
ReactionCatalysis5970
ACTIVATION
Hydrogen carbonate
HMDB0001275
HMDB
Succinyl-CoA
PROPIONATE
BioCyc
P27253
UniProt
2
TAXONOMY
CHEBI:15741
ChEBI
1.0
Propionyl-CoA
1.0
73173-91-8
CAS
C00011
KEGG Compound
SMILES
O=C=O
1110
PubChem-compound
SMILES
CCC(=O)SCCNC(=O)CCNC(=O)C(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
Reaction6007
false
S-Methylmalonyl-CoA → R-Methylmalonyl-CoA
LEFT_TO_RIGHT
Reaction6008
false
Hydrogen Ion + R-Methylmalonyl-CoA → Carbon dioxide + Propionyl-CoA
LEFT_TO_RIGHT
HMDB0000595
HMDB
SMILES
C[C@@H](C(O)=O)C(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C(N)N=CN=C12
Reaction6009
false
Propionyl-CoA + Succinic acid ↔ Propionic acid + Succinyl-CoA
REVERSIBLE
HMDB0000237
HMDB
S-Methylmalonyl-CoA
5957
PubChem-compound
3-METHYLBENZYLSUCCINYL-COA
BioCyc
HMDB0002255
HMDB
C4H6O4
Succinic acid
118.02661
562
TAXONOMY
Reaction6005
false
Adenosine triphosphate + Hydrogen carbonate + Propionyl-CoA → Adenosine diphosphate + Hydrogen Ion + Phosphate + S-Methylmalonyl-CoA
LEFT_TO_RIGHT
Reaction6006
false
Succinyl-CoA ↔ R-Methylmalonyl-CoA
REVERSIBLE
H
Hydrogen Ion
1.007825
1061
PubChem-compound
388307
ChemSpider
HMDB0059597
HMDB
1.0
22833590
PubChem-compound
Propionic acid
Carbon dioxide
1.0
HMDB0001967
HMDB
749
ChemSpider
56-65-5
CAS
71-52-3
CAS
Propionyl-CoA
1.0
1.0
317-66-8
CAS
1.0
Adenosine triphosphate
C10H15N5O10P2
Adenosine diphosphate
427.02942
79-09-4
CAS
CHO3
Hydrogen carbonate
60.99257