DNA旋转酶
结核分枝杆菌
抗生素
肺结核
抗药性
药品
医学
计算生物学
药理学
生物
微生物学
遗传学
基因
大肠杆菌
病理
作者
Swetarka Das,Tanu Garg,Srinivas Nanduri,Amitava Dasgupta,Sidharth Chopra
标识
DOI:10.2174/1568026619666190304130218
摘要
DNA gyrase is a clinically validated drug target, currently targeted only by fluoroquinolone class of antibacterials. However, owing to increasing drug resistance as well as a concomitant reduction in the availability of newer classes of antibiotics, fluoroquinolones are increasingly being over-utilized in order to treat serious infections, including multi-drug resistant tuberculosis. This, in turn, increases the probability of resistance to fluoroquinolones, which is mediated by a single amino acid change in gyrA, leading to class-wide resistance. In this review, we provide an overview of the recent progress in identifying novel scaffolds which target DNA gyrase and provide an update on their discovery and development status.
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