Updated BioCyc iOS App now
available in iTunes store
Updated BioCyc iOS App now
available in iTunes store
Updated BioCyc iOS App now
available in iTunes store
Updated BioCyc iOS App now
available in iTunes store
Updated BioCyc iOS App now
available in iTunes store
twitter

Escherichia coli K-12 substr. MG1655 Compound: oxamate


Chemical Formula: C2H2NO3

Molecular Weight: 88.043 Daltons

Monoisotopic Molecular Weight: 89.0112929678 Daltons

oxamate compound structure

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 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 Pathway Tools version 19.5 (software by SRI International) on Sat Feb 13, 2016, biocyc14.