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分枝杆菌InhA是合理药物设计的合适靶点吗?

Is Mycobacterial InhA a Suitable Target for Rational Drug Design?

作者信息

Rizet Julien, Maveyraud Laurent, Rengel David, Guillet Valérie, Publicola Gabriel, Rodriguez Frédéric, Lherbet Christian, Mourey Lionel

机构信息

Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, Université Toulouse III - Paul Sabatier (UT3), 205 route de Narbonne, BP 64182, 31077, Toulouse Cedex 4, France.

Synthèse et Physico-Chimie de Molécules d'Intérêt Biologique (SPCMIB), Université de Toulouse, CNRS, Université Toulouse III - Paul Sabatier (UT3), 118 route de Narbonne, 31062, Toulouse Cedex 09, France.

出版信息

ChemMedChem. 2025 Jul 1;20(13):e202500079. doi: 10.1002/cmdc.202500079. Epub 2025 Apr 29.

Abstract

InhA, an NAD-dependent enoyl-acyl carrier protein reductase, is involved in the biosynthesis of mycolic acids, specific lipids to mycobacteria. InhA is the target of isoniazid, a first-line antituberculosis drug used since the 1950s. Isoniazid is a prodrug that needs to be activated by the catalase-peroxidase KatG. Due to resistance problems, a substantial amount of work has been carried out to identify or design direct inhibitors of InhA, demonstrating that this enzyme is still considered a relevant target for the discovery of new antituberculosis drugs. Much of this work included the resolution of crystallographic structures. Indeed, over a hundred structures have been deposited in the Protein Data Bank for different forms of the enzyme (apo, holo, and complexes), demonstrating a real crystalline polymorphism. Taken together, these structures constitute a valuable dataset. However, the complete decoding of the enzyme's properties and its inhibition literally comes up against its molecular plasticity at the level of a motif essential to the definition of the active site: the substrate-binding loop. In this article, a detailed analysis of this structural dataset is proposed, describing in particular the different families of inhibitors and attempting to establish structural links of causality.

摘要

InhA是一种依赖NAD的烯酰-酰基载体蛋白还原酶,参与分枝菌酸(分枝杆菌特有的脂质)的生物合成。InhA是异烟肼的作用靶点,异烟肼是自20世纪50年代以来使用的一线抗结核药物。异烟肼是一种前体药物,需要过氧化氢酶-过氧化物酶KatG激活。由于耐药性问题,人们开展了大量工作来鉴定或设计InhA的直接抑制剂,这表明该酶仍然被认为是发现新型抗结核药物的一个相关靶点。这项工作大部分包括晶体结构的解析。事实上,蛋白质数据库中已经存放了一百多个该酶不同形式(无配体、结合辅酶以及复合物)的结构,显示出真正的晶体多态性。这些结构合在一起构成了一个有价值的数据集。然而,要完全解读该酶的特性及其抑制作用,实际上在活性位点定义至关重要的一个基序水平上遇到了其分子可塑性问题:底物结合环。本文对这个结构数据集进行了详细分析,特别描述了不同的抑制剂家族,并试图建立因果关系的结构联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d8c/12221120/fc4221ff9b34/CMDC-20-e202500079-g004.jpg

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