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Literature summary for 4.2.3.3 extracted from

  • Yuan, P.M.; Gracy, R.W.; Hartman, F.C.
    Haloacetol phosphates as affinity labels for methylglyoxal synthase (1977), Biochem. Biophys. Res. Commun., 74, 1007-1013.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
3-bromoacetol phosphate irreversible inactivation by reacting with a nucleophilic group located in the active center, dihydroxyacetone phosphate or phosphate protects Proteus vulgaris
3-chloroacetol phosphate competitive Proteus vulgaris
3-iodoacetol phosphate irreversible inactivation by reacting with a nucleophilic group located in the active center, dihydroxyacetone phosphate or phosphate protects Proteus vulgaris
additional information no inactivation by iodoacetate or p-mercuribenzoate Proteus vulgaris

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.22
-
dihydroxyacetone phosphate
-
Proteus vulgaris

Organism

Organism UniProt Comment Textmining
Proteus vulgaris
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
dihydroxyacetone phosphate
-
Proteus vulgaris methylglyoxal + phosphate
-
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