| Literature DB >> 1530579 |
N P Tomkinson1, I J Galpin, R J Beynon.
Abstract
A series of analogues of chymostatin, including Z-Arg-Leu-Phe-aldehyde (Z-Arg-Leu-Phe-H), have been synthesized. Analysis of the inhibitory potential of these analogues permits identification of residues and interactions that are important for inhibitory activity. Moreover, the structure-function relationship for Z-Arg-Leu-Phe-H and chymostatin inhibition of chymotrypsin and Streptomyces griseus proteinase A (SGPA) was probed further with the aid of molecular mechanics. This analysis identified interactions that provide an explanation for the enhanced activity of the natural product, chymostatin, over the synthetic analogues in the inhibition of chymotrypsin but not SGPA.Entities:
Mesh:
Substances:
Year: 1992 PMID: 1530579 PMCID: PMC1132922 DOI: 10.1042/bj2860475
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857