肺结核
聚酮合酶
聚酮
结核分枝杆菌
药物发现
毒力
抗药性
化学
酶
计算生物学
生物合成
微生物学
生物
医学
生物化学
基因
病理
作者
Fei Xia,Haoling Zhang,Huanaoyu Yang,Mingming Zheng,Wenjian Min,Chengliang Sun,Kai Yuan,Peng Yang
标识
DOI:10.1016/j.ejmech.2023.115702
摘要
Tuberculosis (TB) is one of the most threatening diseases for humans, however, the drug treatment strategy for TB has been stagnant and inadequate, which could not meet current treatment needs. TB is caused by Mycobacterial tuberculosis, which has a unique cell wall that plays a crucial role in its growth, virulence, and drug resistance. Polyketide synthase 13 (Pks13) is an essential enzyme that catalyzes the biosynthesis of the cell wall and its critical role is only found in Mycobacteria. Therefore, Pks13 is a promising target for developing novel anti-TB drugs. In this review, we first introduced the mechanism of targeting Pks13 for TB treatment. Subsequently, we focused on summarizing the recent advance of Pks13 inhibitors, including the challenges encountered during their discovery and the rational design strategies employed to overcome these obstacles, which could be helpful for the development of novel Pks13 inhibitors in the future.
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