结合拓扑相似性、分子动力学、MMGBSA 和 SiteMap 分析鉴定登革热 NS2B-NS3 蛋白酶的新型抑制剂

Sheikh Murtuja, Mohd Usman Mohd Siddique, Kumar Pratyush Srivastava, Yogeeta O Agarwal, Sakshi Wagh, Sabina Yasmin, Azim Ansari, Mohd Sayeed Shaikh, Md Saquib Hasnain, Sameer N Goyal
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引用次数: 0

摘要

简介:根据我们团队报告的参考分子 4-(1,3-二氧代异吲哚啉-2-基)-N-(4-乙基苯基)苯磺酰胺设计了 DENV NS2B-NS3 蛋白酶抑制剂,目的是通过合理的方法优化先导化合物。我们发现了锌id为ZINC23504872、ZINC48412318、ZINC00413269、ZINC13998032和ZINC75249613的五个得分最高的分子,它们带有 "嘧啶-4(3H)-酮 "基本支架,是抗DENV蛋白酶的有希望的候选化合物:发现已鉴定的 HITs 与参考分子之间的形状和静电互补性分别为 Tanimotoshape 0.453、0.690、0.680、0.685 和 0.672,Tanimotoelectrostatic 0.211、0.211、0.441、0.442、0.442 和 0.442。分子对接研究表明,已鉴定的 HIT 与活性位点残基的相互作用良好,结合能较低。通过 MD 模拟研究评估了对接复合物的稳定性。所有前五位 HITs 的蛋白质骨架 RMSD 值(1.6779、3.1563、3.3634、3.3893 和 3.0960 Å)和蛋白质骨架 RMSF 值(分别为 1.0126、1.0834、1.0890、0.9974 和 1.0080 Å)都很稳定,在整个 100ns MD 运行期间,分子没有从活性口袋中波动:可药用性 Dscore 低于 1 表明配体与活性位点结合紧密。发现 ZINC23504872 的 Dscore 为 1.084,而第二类化合物 ZINC48412318、ZINC00413269、ZINC13998032 和 ZINC75249613 的 Dscore 分别为 0.503、0.484、0.487 和 0.501。硅内 ADMET 计算结果表明,这五种 HITs 都具有药物相似性,并且没有违反利宾斯基的五人规则:综上所述,这些在实验室中生成的数据表明,所发现的含有嘧啶-4(3H)-酮的分子很有希望成为 DENV 蛋白酶抑制剂的支架。然而,还需要实验结果来证明所获得的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identifying Novel Inhibitors for Dengue NS2B-NS3 Protease by Combining Topological similarity, Molecular Dynamics, MMGBSA and SiteMap Analysis.

Introduction: DENV NS2B-NS3 protease inhibitors were designed based upon the reference molecule, 4-(1,3-dioxoisoindolin-2-yl)-N-(4-ethylphenyl) benzenesulfonamide, reported by our team with the aim to optimize lead compound via rational approach. Top five best scoring molecules with zinc ids ZINC23504872, ZINC48412318, ZINC00413269, ZINC13998032 and ZINC75249613 bearing 'pyrimidin-4(3H)-one' basic scaffold have been identified as a promising candidate against DENV protease enzyme.

Methods: The shape and electrostatic complementary between identified HITs and reference molecules were found to be Tanimotoshape 0.453, 0.690, 0.680, 0.685 & 0.672 respectively and Tanimotoelectrostatic 0.211, 0.211, 0.441, 0.442, 0.442 and 0.442 respectively. The molecular docking studies suggested that the identified HITs displayed the good interactions with active site residues and lower binding energies. The stability of docked complexes was assessed by MD simulations studies. The RMSD values of protein backbone (1.6779, 3.1563, 3.3634, 3.3893 & 3.0960 Å) and protein backbone RMSF values (1.0126, 1.0834, 1.0890, 0.9974 & 1.0080 Å respectively) for all top five HITs were stable and molecules did not fluctuate from the active pocket during entire 100ns MD run.

Results: The druggability Dscore below 1 indicate the tightly binding of ligand at the active site. Dscore for ZINC23504872 was found to be 1.084 while for the second class of compounds ZINC48412318, ZINC00413269, ZINC13998032 and ZINC75249613, 0.503, 0.484, 0.487 and 0.501 Dscores were observed. In-silico ADMET calculations suggested that all five HITs were possessed the drug likeliness properties and did not violate the Lipinski's rule of five.

Conclusion: Summing up, these in-silico generated data suggested that the identified molecules bearing pyrimidin-4(3H)-one would be promising scaffold for DENV protease inhibitors. However, experimental results are needed to prove the obtained results.

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