Metabolic Modeling Tutorial
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Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
12/28 - 12/31
for maintenance.
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
12/28 - 12/31
for maintenance.
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
12/28 - 12/31
for maintenance.
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
12/28 - 12/31
for maintenance.
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Escherichia coli K-12 substr. MG1655 Compound: oxamate

Chemical Formula: C2H2NO3

Molecular Weight: 88.043 Daltons

Monoisotopic Molecular Weight: 89.0112929678 Daltons

SMILES: C(C([O-])=O)(=O)N

InChI: InChI=1S/C2H3NO3/c3-1(4)2(5)6/h(H2,3,4)(H,5,6)/p-1

InChIKey: InChIKey=SOWBFZRMHSNYGE-UHFFFAOYSA-M

Unification Links: CAS:471-47-6 , ChEBI:58363 , ChemSpider:2285344 , IAF1260:37602 , KEGG:C01444 , PubChem:3017661

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -121.3

Reactions known to produce the compound:

allantoin degradation IV (anaerobic) :
oxamate + carbamoyl-phosphate ← oxalurate + phosphate

Enzymes inhibited by oxamate, sorted by the type of inhibition, are:

Inhibitor (Competitive) of: D-lactate dehydrogenase [Kaczorowski78]


References

Kaczorowski78: Kaczorowski G, Kohn LD, Kaback HR (1978). "Purification and properties of D-lactate dehydrogenase from Escherichia coli ML 308-225." Methods Enzymol 1978;53;519-27. PMID: 362128


Report Errors or Provide Feedback
Please cite the following article in publications resulting from the use of EcoCyc: Nucleic Acids Research 41:D605-12 2013
Page generated by SRI International Pathway Tools version 18.5 on Sat Dec 20, 2014, BIOCYC13B.