Centro de Bioinformática y Simulación Molecular (CBSM), Universidad de Talca, 1 Poniente No. 1141, Casilla 721, Talca, Chile.
J Comput Aided Mol Des. 2018 Dec;32(12):1315-1336. doi: 10.1007/s10822-018-0173-3. Epub 2018 Oct 26.
In the last decades, human protein kinases (PKs) have been relevant as targets in the development of novel therapies against many diseases, but the study of Mycobacterium tuberculosis PKs (MTPKs) involved in tuberculosis pathogenesis began much later and has not yet reached an advanced stage of development. To increase knowledge of these enzymes, in this work we studied the structural features of MTPKs, with focus on their ATP-binding sites and their interactions with inhibitors. PknA, PknB, and PknG are the most studied MTPKs, which were previously crystallized; ATP-competitive inhibitors have been designed against them in the last decade. In the current work, reported PknA, PknB, and PknG inhibitors were extracted from literature and their orientations inside the ATP-binding site were proposed by using docking method. With this information, interaction fingerprints were elaborated, which reveal the more relevant residues for establishing chemical interactions with inhibitors. The non-crystallized MTPKs PknD, PknF, PknH, PknJ, PknK, and PknL were also studied; their three-dimensional structural models were developed by using homology modeling. The main characteristics of MTPK ATP-binding sites (the non-crystallized and crystallized MTPKs, including PknE and PknI) were accounted; schemes of the main polar and nonpolar groups inside their ATP-binding sites were constructed, which are suitable for a major understanding of these proteins as antituberculotic targets. These schemes could be used for establishing comparisons between MTPKs and human PKs in order to increase selectivity of MTPK inhibitors. As a key tool for guiding medicinal chemists interested in the design of novel MTPK inhibitors, our work provides a map of the structural elements relevant for the design of more selective ATP-competitive MTPK inhibitors.
在过去的几十年中,人类蛋白激酶(PKs)已成为开发针对许多疾病的新型疗法的重要靶点,但对结核分枝杆菌蛋白激酶(MTPKs)的研究直到后来才开始,并且尚未达到高级开发阶段。为了增加对这些酶的了解,在这项工作中,我们研究了 MTPKs 的结构特征,重点研究了它们的 ATP 结合位点及其与抑制剂的相互作用。PknA、PknB 和 PknG 是研究最深入的 MTPKs,它们之前已经结晶;在过去十年中,针对它们设计了 ATP 竞争性抑制剂。在当前的工作中,从文献中提取了报道的 PknA、PknB 和 PknG 抑制剂,并通过对接方法提出了它们在 ATP 结合位点内的取向。利用这些信息,制定了相互作用指纹,揭示了与抑制剂建立化学相互作用更相关的残基。还研究了未结晶的 MTPKs PknD、PknF、PknH、PknJ、PknK 和 PknL;通过同源建模开发了它们的三维结构模型。MTPK ATP 结合位点的主要特征(包括 PknE 和 PknI 的未结晶和结晶 MTPKs)得到了说明;构建了它们的 ATP 结合位点内主要极性和非极性基团的方案,这有助于对这些蛋白作为抗结核靶点的主要理解。这些方案可用于在 MTPKs 和人类 PKs 之间建立比较,以提高 MTPK 抑制剂的选择性。作为指导对设计新型 MTPK 抑制剂感兴趣的药物化学家的关键工具,我们的工作提供了与设计更具选择性的 ATP 竞争性 MTPK 抑制剂相关的结构元素图谱。