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

Synonyms: D-idaric acid

Superclasses: an acid all carboxy acids a carboxylate a dicarboxylate an alpha,omega-dicarboxylate

Chemical Formula: C6H8O8

Molecular Weight: 208.12 Daltons

Monoisotopic Molecular Weight: 210.0375672978 Daltons

D-idarate compound structure

SMILES: C(=O)([O-])C(O)C(O)C(O)C(O)C(=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+/m1/s1


Unification Links: ChEBI:21040 , ChemSpider:5256903 , PubChem:6857567

Standard Gibbs Free Energy of Change 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+

In Reactions of unknown directionality:

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]

Enzymes inhibited by D-idarate, sorted by the type of inhibition, are:

Inhibitor (Mechanism unknown) of: D-glucarate dehydratase [Blumenthal66]


Blumenthal66: Blumenthal H "D-Glucarate Dehydrase." Meth Enz 1966;9:660-665.

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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 SRI International Pathway Tools version 19.0 on Tue Oct 13, 2015, biocyc13.