Article
Overcoming target-mediated quinolone resistance in topoisomerase IV by introducing metal-ion-independent drug-enzyme interactions.
ACS chemical biology - 20 Dec 2013
Aldred Katie J, Schwanz Heidi A, Li Gangqin, McPherson Sylvia A, Turnbough Charles L, Kerns Robert J, Osheroff Neil
Abstract excerpt
Quinolones, which target gyrase and topoisomerase IV, are the most widely prescribed antibacterials worldwide. Unfortunately, their use is threatened by the increasing prevalence of target-mediated drug resistance. Greater than 90% of mutations that confer quinolone resistance act by disrupting enzyme-drug interactions coordinated by a critical water-metal ion bridge. Quinazolinediones are quinolone-like drugs...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
