...
首页> 外文期刊>Molecular cell >Localization of the ribosomal protection protein Tet(O) on the ribosome and the mechanism of tetracycline resistance.
【24h】

Localization of the ribosomal protection protein Tet(O) on the ribosome and the mechanism of tetracycline resistance.

机译:核糖体保护蛋白Tet(O)在核糖体上的定位和四环素抗性的机制。

获取原文
获取原文并翻译 | 示例
           

摘要

Tet(O) belongs to a class of ribosomal protection proteins that mediate tetracycline resistance. It is a G protein that shows significant sequence similarity to elongation factor EF-G. Here we present a cryo-electron microscopic reconstruction, at 16 A resolution, of its complex with the E. coli 70S ribosome. Tet(O) was bound in the presence of a noncleavable GTP analog to programmed ribosomal complexes carrying fMet-tRNA in the P site. Tet(O) is directly visible as a mass close to the A-site region, similar in shape and binding position to EF-G. However, there are important differences. One of them is the different location of the tip of domain IV, which in the Tet(O) case, does not overlap with the ribosomal A site but is directly adjacent to the primary tetracycline binding site. Our findings give insights into the mechanism of tetracycline resistance.
机译:Tet(O)属于一类核糖体保护蛋白,可介导四环素抗性。它是一种G蛋白,与延伸因子EF-G具有显着的序列相似性。在这里,我们介绍了其与大肠杆菌70S核糖体的复合物在16 A分辨率下的低温电子显微镜重建。 Tet(O)在不可裂解的GTP类似物的存在下与在P位点携带fMet-tRNA的程序化核糖体复合物结合。 Tet(O)可以直接看到靠近A部位区域的质量,其形状和结合位置与EF-G相似。但是,有重要的区别。其中之一是结构域IV尖端的不同位置,在Tet(O)情况下,该区域不与核糖体A位点重叠,而是直接与一级四环素结合位点相邻。我们的发现为四环素耐药性机制提供了见识。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号