细胞色素
细胞色素c氧化酶
呼吸链
辅酶Q-细胞色素c还原酶
电子传递复合物IV
生物化学
细胞色素b
电子传输链
结核分枝杆菌
化学
细胞色素C1
细胞色素c
生物
线粒体
肺结核
医学
酶
病理
基因
线粒体DNA
作者
Thangaraj Sindhu,Debnath Pal
出处
期刊:Current Molecular Pharmacology
[Bentham Science]
日期:2022-04-01
卷期号:15 (2): 380-392
被引量:5
标识
DOI:10.2174/1874467214666210928152512
摘要
: The cytochrome bc1-aa3 supercomplex plays an essential role in the cellular respiratory system of Mycobacterium Tuberculosis. It transfers electrons from menaquinol to cytochrome aa3 (Complex IV) via cytochrome bc1 (Complex III), which reduces the oxygen. The electron transfer from a variety of donors into oxygen through the respiratory electron transport chain is essential to pump protons across the membrane creating an electrochemical transmembrane gradient (proton motive force, PMF) that regulates the synthesis of ATP via the oxidative phosphorylation process. Cytochrome bc1-aa3 supercomplex in M. tuberculosis is, therefore, a major drug target for antibiotic action. In recent years, several respiratory chain components have been targeted for developing new candidate drugs, illustrating the therapeutic potential of obstructing energy conversion of M. tuberculosis. The recently available cryo-EM structure of mycobacterial cytochrome bc1-aa3 supercomplex with open and closed conformations has opened new avenues for understanding its structure and function for developing more effective, new therapeutics against pulmonary tuberculosis. In this review, we discuss the role and function of several components, subunits, and drug targeting elements of the supercomplex cytochrome bc1-aa3 and its potential inhibitors in detail.
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