首页> 外文期刊>Journal of the American Chemical Society >Molecular Dynamics Simulations of the 30S Ribosomal Subunit Reveal a Preferred Tetracyciine Binding Site
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Molecular Dynamics Simulations of the 30S Ribosomal Subunit Reveal a Preferred Tetracyciine Binding Site

机译:30S核糖体亚基的分子动力学模拟揭示了优选的替西米西结合位点。

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摘要

Tetracyciine (Tc) and its analogues are important antibiotics affecting both gram-positive and gram-negative bacteria.12 Tc inhibits protein synthesis by binding to the 30S subunit of the bacterial ribosome, preventing tRNA binding to the A-site. Clinical use has led to several resistance mechanisms, including export of Tc from the cell and mutations in the bacterial rRNA. Much effort is being made to develop new Tcs that can evade resistance while effectively inhibiting protein synthesis.
机译:Tetracyciine(Tc)及其类似物是影响革兰氏阳性和革兰氏阴性细菌的重要抗生素。12Tc通过与细菌核糖体的30S亚基结合来抑制蛋白质合成,从而阻止tRNA与A位点结合。临床使用已导致多种耐药机制,包括Tc从细胞中输出和细菌rRNA中的突变。人们正在付出很大的努力来开发新的Tcs,它们可以逃避耐药性,同时有效地抑制蛋白质的合成。

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