Cysteinyl peptide inhibitors of Bacillus cereus zinc beta-lactamase
- PMID: 11249142
- DOI: 10.1016/s0968-0896(00)00257-1
Cysteinyl peptide inhibitors of Bacillus cereus zinc beta-lactamase
Abstract
Several cysteinyl peptides have been synthesised and shown to be reversible competitive inhibitors of the Bacillus cereus metallo-beta-lactamase. The pH dependence of pKi indicates that the thiol anion displaces hydroxide ion from the active site zinc(II). D,D-Peptides bind to the enzyme better than other diastereoisomers, which is compatible with the predicted stereochemistry of the active site.
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