MetaCyc Compound: α-D-ribose-1-methylphosphonate 5-phosphate

Citations: [Kamat11]

Chemical Formula: C6H11O10P2

Molecular Weight: 305.09 Daltons

Monoisotopic Molecular Weight: 308.00621969040003 Daltons

α-D-ribose-1-methylphosphonate 5-phosphate compound structure

SMILES: CP([O-])(=O)OC1(C(C(C(O1)COP(=O)([O-])[O-])O)O)

InChI: InChI=1S/C6H14O10P2/c1-17(9,10)16-6-5(8)4(7)3(15-6)2-14-18(11,12)13/h3-8H,2H2,1H3,(H,9,10)(H2,11,12,13)/p-3/t3-,4-,5-,6-/m1/s1


Unification Links: ChEBI:68686, PubChem:70678984

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -454.09625Inferred by computational analysis [Latendresse13]

Reactions known to consume the compound:

methylphosphonate degradation I , methylphosphonate degradation II :
α-D-ribose-1-methylphosphonate 5-phosphate → 5-phospho-α-D-ribose 1,2-cyclic phosphate + methane

Reactions known to produce the compound:

methylphosphonate degradation I , methylphosphonate degradation II :
α-D-ribose-1-methylphosphonate-5-triphosphate + H2O → α-D-ribose-1-methylphosphonate 5-phosphate + diphosphate + H+

Created in EcoCyc 22-Nov-2011 by Keseler I, SRI International
Imported from EcoCyc 20-Dec-2011 by Keseler I, SRI International


Kamat11: Kamat SS, Williams HJ, Raushel FM (2011). "Intermediates in the transformation of phosphonates to phosphate by bacteria." Nature 480(7378);570-3. PMID: 22089136

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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