Escherichia coli K-12 substr. MG1655 Compound: L-idarate

Synonyms: L-idaric acid

Superclasses: an acidall carboxy acidsa carboxylatea dicarboxylatean alpha,omega-dicarboxylate

Chemical Formula: C6H8O8

Molecular Weight: 208.12 Daltons

Monoisotopic Molecular Weight: 210.0375672978 Daltons

L-idarate compound structure

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

InChI: InChI=1S/C6H10O8/c7-1(3(9)5(11)12)2(8)4(10)6(13)14/h1-4,7-10H,(H,11,12)(H,13,14)/p-2/t1-,2-,3+,4+/m0/s1


Unification Links: ChEBI:21332, ChemSpider:5256788, PubChem:6857451

Standard Gibbs Free Energy of Formation (ΔfG in kcal/mol): -311.88

Reactions known to produce the compound:

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+

Reactions known to both consume and produce the compound:

Not in pathways:
L-idarate ↔ D-glucarate

In Reactions of unknown directionality:

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

This compound has been characterized as an alternative substrate of the following enzymes: D-glucarate dehydratase

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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 Wed May 4, 2016, biocyc13.