MetaCyc Compound: (2R)-3-sulfolactate

Synonyms: (R)-3-sulfolactic acid, (R)-sulfolactate, (2R)-2-hydroxy-3-sulfopropanoate, L-sulfolactate

Superclasses: an organosulfur compounda sulfonate3-sulfolactate

Chemical Formula: C3H4O6S

Molecular Weight: 168.12 Daltons

Monoisotopic Molecular Weight: 169.9885086152 Daltons

(2<i>R</i>)-3-sulfolactate compound structure

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

InChI: InChI=1S/C3H6O6S/c4-2(3(5)6)1-10(7,8)9/h2,4H,1H2,(H,5,6)(H,7,8,9)/p-2/t2-/m0/s1


Unification Links: ChEBI:58738, KEGG:C11537, PubChem:25246047

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -176.46376Inferred by computational analysis [Latendresse13]

Reactions known to consume the compound:

(R)-cysteate degradation , sulfolactate degradation I :
(2R)-3-sulfolactate → pyruvate + sulfite + H+

sulfolactate degradation II , sulfolactate degradation III :
3-sulfolactate + an oxidized unknown electron acceptor → 3-sulfopyruvate + an reduced unknown electron acceptor

Reactions known to produce the compound:

2,3-dihydroxypropane-1-sulfonate degradation :
(R)-2,3-dihydroxypropane 1-sulfonate + 2 NAD+ + H2O → (2R)-3-sulfolactate + 2 NADH + 3 H+

coenzyme M biosynthesis I :
(2R)-phospho-3-sulfolactate + H2O → (2R)-3-sulfolactate + phosphate

sulfoquinovose degradation II :
3-sulfolactaldehyde + NAD(P)+ + H2O → 3-sulfolactate + NAD(P)H + 2 H+

Reactions known to both consume and produce the compound:

(R)-cysteate degradation , coenzyme M biosynthesis I :
(2R)-3-sulfolactate + NAD+ ↔ 3-sulfopyruvate + NADH + H+

sulfolactate degradation I :
(2R)-3-sulfolactate + NADP+ ↔ 3-sulfopyruvate + NADPH + H+

Not in pathways:
(2R)-3-sulfolactate + NAD(P)+ ↔ 3-sulfopyruvate + NAD(P)H + H+

Revised 11-Sep-2009 by Caspi R, SRI International


Latendresse13: Latendresse M. (2013). "Computing Gibbs Free Energy of Compounds and Reactions in MetaCyc."

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Please cite the following article in publications resulting from the use of MetaCyc: Caspi et al, Nucleic Acids Research 42:D459-D471 2014
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