MetaCyc Compound: all-trans-decaprenyl diphosphate

Superclasses: a lipid an isoprenoid an isoprenoid phosphate an isoprenoid diphosphate an all-trans-polyisoprenyl diphosphate

For polyisoprenols and polyisoprenyl phosphates nomenclature, see an isoprenoid.

Chemical Formula: C50H81O7P2

Molecular Weight: 856.13 Daltons

Monoisotopic Molecular Weight: 858.5692280710999 Daltons


InChI: InChI=1S/C50H84O7P2/c1-41(2)21-12-22-42(3)23-13-24-43(4)25-14-26-44(5)27-15-28-45(6)29-16-30-46(7)31-17-32-47(8)33-18-34-48(9)35-19-36-49(10)37-20-38-50(11)39-40-56-59(54,55)57-58(51,52)53/h21,23,25,27,29,31,33,35,37,39H,12-20,22,24,26,28,30,32,34,36,38,40H2,1-11H3,(H,54,55)(H2,51,52,53)/p-3/b42-23+,43-25+,44-27+,45-29+,46-31+,47-33+,48-35+,49-37+,50-39+


Unification Links: ChEBI:60721 , HMDB:HMDB59616 , KEGG:C17432 , PubChem:25245574

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): 642.7823 Inferred by computational analysis [Latendresse13]

Reactions known to consume the compound:

menaquinol-10 biosynthesis :
all-trans-decaprenyl diphosphate + 1,4-dihydroxy-2-naphthoate + H+ → demethylmenaquinol-10 + CO2 + diphosphate

ubiquinol-10 biosynthesis (eukaryotic) , ubiquinol-10 biosynthesis (prokaryotic) :
all-trans-decaprenyl diphosphate + 4-hydroxybenzoate → 3-decaprenyl-4-hydroxybenzoate + diphosphate

linoleate biosynthesis I (plants) :
oleoyl-CoA + a lipid + H+ → a lipid oleoyl-group + coenzyme A

Reactions known to produce the compound:

glutathione redox reactions I :
a lipid hydroperoxide + 2 glutathione + H+a lipid + glutathione disulfide + 2 H2O

In Reactions of unknown directionality:

all-trans-decaprenyl diphosphate biosynthesis :
(2E,6E)-farnesyl diphosphate + 7 isopentenyl diphosphate = all-trans-decaprenyl diphosphate + 7 diphosphate

Not in pathways:
an all-trans-polyisoprenyl diphosphate + 1,4-dihydroxy-2-naphthoate + H+ = a demethylmenaquinol + CO2 + diphosphate

an isoprenoid diphosphate + 4-hydroxybenzoate = a 4-hydroxy-3-polyprenylbenzoate + diphosphate


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 38:D473-D479 2010
Page generated by SRI International Pathway Tools version 18.0 on Thu Oct 30, 2014, biocyc14.