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Literature summary for 4.1.1.50 extracted from

  • Bitonti, A.J.; Dumont, J.A.; McCann, P.P.
    Characterization of Trypanosoma brucei brucei S-adenosyl-L-methionine decarboxylase and its inhibition by berenil, pentamidine and methylglyoxal bis(guanylhydrazone) (1986), Biochem. J., 237, 685-689.
    View publication on PubMedView publication on EuropePMC

Activating Compound

Activating Compound Comment Organism Structure
putrescine weak stimulation, relatively insensitive to activation as compared with the mammalian enzyme Trypanosoma brucei

Inhibitors

Inhibitors Comment Organism Structure
Berenil irreversible Trypanosoma brucei
methylglyoxal bis(guanylhydrazone) irreversible Trypanosoma brucei
Pentamidine irreversible Trypanosoma brucei

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.03
-
S-adenosyl-L-methionine
-
Trypanosoma brucei

Organism

Organism UniProt Comment Textmining
Trypanosoma brucei
-
brucei
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
S-adenosyl-L-methionine
-
Trypanosoma brucei (5-deoxy-5-adenosyl)(3-aminopropyl)methylsulfonium salt + CO2
-
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