50年代
利奈唑啉
化学
核糖体
蛋白质亚单位
作用机理
活动站点
核糖体RNA
立体化学
组合化学
生物化学
细菌
酶
核糖核酸
生物
遗传学
基因
体外
万古霉素
金黄色葡萄球菌
作者
Joseph A. Ippolito,Z.F. Kanyo,Deping Wang,François Franceschi,Peter B. Moore,Thomas A. Steitz,Erin M. Duffy
摘要
The oxazolidinone antibacterials target the 50S subunit of prokaryotic ribosomes. To gain insight into their mechanism of action, the crystal structure of the canonical oxazolidinone, linezolid, has been determined bound to the Haloarcula marismortui 50S subunit. Linezolid binds the 50S A-site, near the catalytic center, which suggests that inhibition involves competition with incoming A-site substrates. These results provide a structural basis for the discovery of improved oxazolidinones active against emerging drug-resistant clinical strains.
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