Reversible acylation of elastase by gamma-lactam analogues of beta-lactam inhibitors
The reaction of a monocyclic γ-lactam with the serine protease elastase occurs via reversible formation of a hydrolytically labile acyl-enzyme complex; in contrast analogous β-lactam inhibitors irreversibly react to form a relatively stable acyl-enzyme complex.
Main Authors: | Westwood, N, Claridge, T, Edwards, P, Schofield, C |
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Format: | Journal article |
Sprog: | English |
Udgivet: |
1997
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Lignende værker
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Synthesis and evaluation of delta-lactams (piperazones) as elastase inhibitors.
af: Seibel, J, et al.
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'pH-jump' crystallographic analyses of gamma-lactam-porcine pancreatic elastase complexes.
af: Wright, P, et al.
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γ-Lactam analogues of carbapenicillanic acids
af: Baldwin, J, et al.
Udgivet: (1986)