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Escherichia coli K-12 substr. MG1655 Compound: carbamate

Synonyms: carbamic acid, aminoformic acid

Superclasses: an acid all carboxy acids a carboxylate an amino acid
an amino acid or its derivative an amino acid

Chemical Formula: CH2NO2

Molecular Weight: 60.032 Daltons

Monoisotopic Molecular Weight: 61.016378345700005 Daltons

carbamate compound structure

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

InChI: InChI=1S/CH3NO2/c2-1(3)4/h2H2,(H,3,4)/p-1

InChIKey: InChIKey=KXDHJXZQYSOELW-UHFFFAOYSA-M

Unification Links: ChEBI:13941 , ChemSpider:270 , HMDB:HMDB03551 , KEGG:C01563 , PubChem:276

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -95.36

Reactions known to consume the compound:

cyanate degradation , uracil degradation III :
carbamate + 2 H+ → ammonium + CO2

Reactions known to produce the compound:

cyanate degradation :
cyanate + hydrogen carbonate + H+carbamate + CO2

uracil degradation III :
(Z)-3-ureidoacrylate peracid + H2O → carbamate + (Z)-3-peroxyaminoacrylate + H+

Not in pathways:
3-ureidoacrylate + H2O → carbamate + aminoacrylate + H+
(Z)-2-methylureidoacrylate peracid + H2O → (Z)-2-methyl-peroxyaminoacrylate + carbamate + H+

Not in pathways:
a carboxylic ester + H2O → an alcohol + a carboxylate + H+
an aldehyde + NADP+ + H2O → a carboxylate + NADPH + 2 H+
an acyl phosphate + H2O → a carboxylate + phosphate + H+
an acyl-CoA + H2O → a carboxylate + coenzyme A + H+
a 1-acyl 2-lyso-phosphatidylcholine + H2O → a carboxylate + sn-glycero-3-phosphocholine + H+

In Reactions of unknown directionality:

Not in pathways:
a 5-L-glutamyl-[peptide][periplasmic space] + an amino acid[periplasmic space] = a 5-L-glutamyl-amino acid[periplasmic space] + a peptide[periplasmic space]

Not in pathways:
a 2-acyl 1-lyso-phosphatidylcholine + H2O = a carboxylate + sn-glycero-3-phosphocholine + H+
an aldehyde[periplasmic space] + FAD[periplasmic space] + H2O[periplasmic space] = a carboxylate[periplasmic space] + FADH2[periplasmic space]


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 19.0 on Fri Aug 28, 2015, BIOCYC14B.