Bem Agnieszka E, Velikova Nadya, Pellicer M Teresa, Baarlen Peter van, Marina Alberto, Wells Jerry M
Host-Microbe Interactomics, Wageningen University , De Elst 1, 6708 WD Wageningen, The Netherlands.
ACS Chem Biol. 2015 Jan 16;10(1):213-24. doi: 10.1021/cb5007135. Epub 2014 Dec 26.
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.
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。