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Literature summary for 4.1.1.38 extracted from

  • Willard, J.M.; Rose, I.A.
    Formation of enolpyruvate in the phosphoenolpyruvate carboxytransphosphorylase reaction (1973), Biochemistry, 12, 5241-5246.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
Imidodiphosphate competitive with respect to diphosphate Propionibacterium freudenreichii subsp. shermanii
Methylene diphosphonate competitive with respect to diphosphate Propionibacterium freudenreichii subsp. shermanii

Organism

Organism UniProt Comment Textmining
Propionibacterium freudenreichii subsp. shermanii
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-
-

Reaction

Reaction Comment Organism Reaction ID
diphosphate + oxaloacetate = phosphate + phosphoenolpyruvate + CO2 in the reverse direction the addition of CO2 is only to the si face of phosphoenolpyruvate Propionibacterium freudenreichii subsp. shermanii

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
phosphate + phosphoenolpyruvate + CO2
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Propionibacterium freudenreichii subsp. shermanii diphosphate + oxaloacetate
-
?
phosphoenolpyruvate + phosphate the addition of a proton to yield pyruvate is nonstereospecific, suggesting that enolpyruvate is ketonized after leaving the enzyme Propionibacterium freudenreichii subsp. shermanii pyruvate + diphosphate
-
?