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Literature summary for 3.4.22.38 extracted from

  • Katunuma, N.; Matsui, A.; Inubushi, T.; Murata, E.; Kakegawa, H.; Ohba, Y.; Turk, D.; Turk, V.; Tada, Y.; Asao, T.
    Structure-based development of pyridoxal propionate derivatives as specific inhibitors of cathepsin K in vitro and in vivo (2000), Biochem. Biophys. Res. Commun., 267, 850-854.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
pyridoxal phosphate at 1 mM 85% inhibition Rattus norvegicus

Organism

Organism UniProt Comment Textmining
Rattus norvegicus
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
Z-Phe-Arg-4-methylcoumarin 7-amide + H2O
-
Rattus norvegicus Z-Phe-Arg + 7-amino-4-methylcoumarin
-
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