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Literature summary for 3.4.22.1 extracted from

  • Gilmore, B.F.; Harriott, P.; Walker, B.
    The inactivation of bovine cathepsin B by novel N-chloro-acetyl-dipeptides: application of the Houghten tea bag methodology to inhibitor synthesis (2005), Biochem. Biophys. Res. Commun., 333, 1284-1288.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
additional information no inhibition with N-chloroacetyl-Gly-Gly-OH Bos taurus
N-chloroacetyl-Gly-Leu-OH
-
Bos taurus
N-chloroacetyl-Leu-Leu-OH
-
Bos taurus
N-chloroacetyl-Leu-Leu-OMe
-
Bos taurus
N-chloroacetyl-Lys-Leu-OH
-
Bos taurus
N-chloroacetyl-Phe-Leu-OH
-
Bos taurus
N-chloroacetyl-Phe-Met-OH
-
Bos taurus
N-chloroacetyl-Ser-Leu-OH
-
Bos taurus

Organism

Organism UniProt Comment Textmining
Bos taurus P07688
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
5-dimethylaminonaphthalene-1-sulfonyl-Phe-Arg-Phe(NO2)-Leu + H2O pH 6.4, 37°C, 2 mM cysteine, 1 mM EDTA Bos taurus ?
-
?

Synonyms

Synonyms Comment Organism
cathepsin B
-
Bos taurus