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MmpL3 a potential new target for development of novel anti-tuberculosis drugs

机译:MmpL3是开发新型抗结核药物的潜在新靶标

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Introduction: Tuberculosis (TB) is still a leading cause of mortality in the developing world and there is an unmet clinical need for new drugs with novel mechanism of action. Targeting the complex and unique cell wall of TB-causing pathogen Mycobacterium tuberculosis (Mtb) has been a mainstay of TB drug discovery. Though, the composition of the cell wall of Mtb is well understood, little is known about the assembly process of the cell wall such as the transport of mycolic acids across the cell wall. Areas covered: Recent research demonstrating MmpL3 protein as a transmembrane transporter of mycolic acids is discussed. In addition, MmpL3 has also been implicated in heme transport. Research describing several diverse chemical inhibitors that inhibit MmpL3 is reviewed. Expert opinion: Evidence so far suggests MmpL3 is a transporter of mycolic acids. It has emerged as a novel therapeutic target for Mtb that is essential and for which several small molecule inhibitors have been identified. Identifying the interacting partners, understanding the substrate specificity and the mechanism of transport by MmpL3 are some of the gaps in knowledge that need to be addressed.
机译:简介:结核病(TB)仍是发展中国家死亡的主要原因,临床上对具有新颖作用机制的新药物的需求仍未得到满足。针对引起结核病的病原体结核分枝杆菌(Mtb)的复杂而独特的细胞壁,一直是发现结核病药物的主要手段。虽然,Mtb的细胞壁的组成是众所周知的,但对细胞壁的组装过程(如霉菌酸在细胞壁上的转运)知之甚少。涵盖的领域:最近的研究表明MmpL3蛋白是霉菌酸的跨膜转运蛋白。此外,MmpL3也与血红素转运有关。综述了描述几种抑制MmpL3的多种化学抑制剂的研究。专家意见:迄今为止的证据表明MmpL3是霉菌酸的转运蛋白。它已成为Mtb的新型治疗靶标,这一靶标必不可少,并且已针对该靶标鉴定了几种小分子抑制剂。识别相互作用的伙伴,了解底物特异性和MmpL3的转运机制是需要解决的知识空白。

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