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Conversion of rat urinary prokallikrein to its active form
Y Takenobu1, M Takaoka, E Suyama
1Department of Pharmacology, Osaka University of Pharmaceutical Sciences, Japan.
Abstract:
A peptide derived from rat urinary prokallikrein by trypsin treatment comprised 7 amino acids, the sequence (Ala-Pro-Pro-Val-Gln-Ser-Arg) of which was identical with that of the N-terminal region in prokallikrein. Thus, with trypsin treatment, rat urinary prokallikrein is converted to the active form with the release of the N-terminal propeptide consisting of 7 amino acids. An Arg-1-Val+1 bond in the prokallikrein was found to be the site of proteolytic cleavage of the propeptide.