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Literature summary for 3.4.22.38 extracted from

  • Bossard, M.J.; Tomaszek, T.A.; Levy, M.A.; Ijames, C.F.; Huddleston, M.J.; Briand, J.; Thompson, S.; Halpert, S.; Veber, D.F.; Carr, S.A.; Meek, T.D.; Tew, D.G.
    Mechanism of inhibition of cathepsin K by potent, selective 1,5-Diacylcarbohydrazides: A new class of mechanism-based inhibitors of thiol proteases (1999), Biochemistry, 38, 15893-15902.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
2,2'-N,N'-bis(benzyloxycarbonyl)-L-leucinylcarbohydrazide
-
Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
benzyloxycarbonyl-Leu-Arg-4-methylcoumarin 7-amide + H2O
-
Homo sapiens benzyloxycarbonyl-Leu-Arg + 7-amino-4-methylcoumarin
-
?

Turnover Number [1/s]

Turnover Number Minimum [1/s] Turnover Number Maximum [1/s] Substrate Comment Organism Structure
0.00011
-
2,2'-N,N'-bis(benzyloxycarbonyl)-L-leucinylcarbohydrazide pH 5.5, room temperature Homo sapiens

Ki Value [mM]

Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
0.0000027
-
2,2'-N,N'-bis(benzyloxycarbonyl)-L-leucinylcarbohydrazide pH 5.5, room temperature Homo sapiens