A New Covalent Inhibitor of Class C β-Lactamases Reveals Extended Active Site Specificity
Author:
Affiliation:
1. Department of Chemistry, Wesleyan University, Middletown, Connecticut 06459, United States
2. Department of Chemistry, University of Texas at Austin, Austin, Texas 78712-1224, United States
Funder
National Institute of Allergy and Infectious Diseases
Division of Chemistry
Welch Foundation
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.biochem.5b01149
Reference35 articles.
1. Proliferation and significance of clinically relevant β-lactamases
2. Three Decades of β-Lactamase Inhibitors
3. O-Aryloxycarbonyl Hydroxamates: New β-Lactamase Inhibitors That Cross-Link the Active Site
4. Kinetics and Mechanism of Inhibition of a Serine β-Lactamase by O-Aryloxycarbonyl Hydroxamates
5. SERINE β-LACTAMASES AND PENICILLIN-BINDING PROTEINS
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