...
首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Peptide deformylase inhibitors of Mycobacterium tuberculosis: synthesis, structural investigations, and biological results.
【24h】

Peptide deformylase inhibitors of Mycobacterium tuberculosis: synthesis, structural investigations, and biological results.

机译:结核分枝杆菌的肽脱甲酰基酶抑制剂:合成,结构研究和生物学结果。

获取原文
获取原文并翻译 | 示例
           

摘要

Bacterial peptide deformylase (PDF) belongs to a subfamily of metalloproteases catalyzing the removal of the N-terminal formyl group from newly synthesized proteins. We report the synthesis and biological activity of highly potent inhibitors of Mycobacterium tuberculosis (Mtb) PDF enzyme as well as the first X-ray crystal structure of Mtb PDF. Structure-activity relationship and crystallographic data clarified the structural requirements for high enzyme potency and cell based potency. Activities against single and multi-drug-resistant Mtb strains are also reported.
机译:细菌肽去甲酰基化酶(PDF)属于金属蛋白酶的一个亚家族,催化从新合成的蛋白质中去除N末端甲酰基。我们报告了结核分枝杆菌(Mtb)PDF酶的高效抑制剂的合成和生物学活性,以及​​Mtb PDF的第一个X射线晶体结构。结构-活性关系和晶体学数据阐明了对高酶效能和基于细胞的效能的结构要求。还报道了针对单一和多重耐药性Mtb菌株的活性。

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