Suppr超能文献

细菌组氨酸激酶作为新型抗菌药物靶点

Bacterial histidine kinases as novel antibacterial drug targets.

作者信息

Bem Agnieszka E, Velikova Nadya, Pellicer M Teresa, Baarlen Peter van, Marina Alberto, Wells Jerry M

机构信息

Host-Microbe Interactomics, Wageningen University , De Elst 1, 6708 WD Wageningen, The Netherlands.

出版信息

ACS Chem Biol. 2015 Jan 16;10(1):213-24. doi: 10.1021/cb5007135. Epub 2014 Dec 26.

Abstract

Bacterial histidine kinases (HKs) are promising targets for novel antibacterials. Bacterial HKs are part of bacterial two-component systems (TCSs), the main signal transduction pathways in bacteria, regulating various processes including virulence, secretion systems and antibiotic resistance. In this review, we discuss the biological importance of TCSs and bacterial HKs for the discovery of novel antibacterials, as well as published TCS and HK inhibitors that can be used as a starting point for structure-based approaches to develop novel antibacterials.

摘要

细菌组氨酸激酶(HKs)是新型抗菌药物的有前景的靶点。细菌HKs是细菌双组分系统(TCSs)的一部分,TCSs是细菌主要的信号转导途径,调节包括毒力、分泌系统和抗生素耐药性在内的各种过程。在本综述中,我们讨论了TCSs和细菌HKs对于发现新型抗菌药物的生物学重要性,以及已发表的可作为基于结构的方法开发新型抗菌药物起点的TCS和HK抑制剂。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验