拓扑异构酶
计算生物学
业务
化学
药理学
医学
生物
生物化学
酶
作者
Paul Toth,Steven C. Ratigan,Joshua W. Powell,Sydney R Cassel,Jack C. Yalowich,Craig A. McElroy,Steffen Lindert,Charles E. Bell,Mark J. Mitton‐Fry
标识
DOI:10.1021/acsmedchemlett.5c00060
摘要
Novel bacterial topoisomerase inhibitors (NBTIs) targeting DNA gyrase and topoisomerase IV constitute a new antibacterial class for deadly pathogens such as MRSA. While most NBTIs induce gyrase-mediated single-strand DNA breaks, a subset of amide NBTIs induces both single-strand and double-strand DNA breaks. Here, we report the X-ray crystal structures of two such amide NBTIs, 148 and 185, and demonstrate an unusual binding mode characterized by engagement of both GyrA D83 and R122. The synthesis of two isosteric triazole NBTIs is also described, one of which (342) affords only single-strand DNA breaks, while the other (276) also induces both single- and double-strand DNA breaks. A combination of docking and molecular dynamics simulations is employed to further investigate the potential structural underpinnings of differences in DNA cleavage.
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