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CDOCKER and λ-dynamics for prospective prediction in D3R Grand Challenge 2

机译:D3R Grand Challenge 2中的DOCKER和λ动力学用于前瞻性预测

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摘要

The opportunity to prospectively predict ligand bound poses and free energies of binding to the Farnesoid X Receptor in the D3R Grand Challenge 2 provided a useful exercise to evaluate CHARMM based docking (CDOCKER) and λ-dynamics methodologies for use in “real-world” applications in computer aided drug design. In addition to measuring their current performance, several recent methodological developments have been analyzed retrospectively to highlight best procedural practices in future applications. For pose prediction with CDOCKER, when the protein structure used for rigid receptor docking was close to the crystallographic holo structure, reliable poses were obtained. Benzimidazoles, with a known holo receptor structure, were successfully docked with an average RMSD of 0.97 Å. Other non-benzimidazole ligands displayed less accuracy largely because the receptor structures we chose for docking were too different from the experimental holo structures. However, retrospective analysis has shown that when these ligands were re-docked into their holo structures, the average RMSD dropped to 1.18 Å for all ligands. When sulfonamides and spiros were docked with the apo structure, which agrees more with their holo structure than the structures we chose, 5 out of 6 ligands were correctly docked. These docking results emphasize the need for flexible receptor docking approaches. For λ-dynamics techniques, including multisite λ-dynamics (MSλD), reasonable agreement with experiment was observed for the 33 ligands investigated; root mean square errors of 2.08 and 1.67 kcal/mol were obtained for free energy sets 1 and 2, respectively. Retrospectively, soft-core potentials, adaptive landscape flattening, and biasing potential replica exchange (BP-REX) algorithms were critical to model large substituent perturbations with sufficient precision and within restrictive timeframes, such as was required with participation in Grand Challenge 2. These developments, their associated benefits, and proposed procedures for their use in future applications are discussed.
机译:在D3R Grand Challenge 2中前瞻性地预测配体结合姿势和与Farnesoid X受体结合的自由能的机会,为评估基于CHARMM的对接(CDOCKER)和λ动力学方法在“现实世界”应用中的应用提供了有用的练习。在计算机辅助药物设计中。除了衡量其当前性能外,还对一些最新的方法学发展进行了回顾性分析,以突出未来应用中的最佳程序实践。对于使用CDOCKER进行姿势预测,当用于刚性受体对接的蛋白质结构接近晶体全息结构时,可获得可靠的姿势。具有已知全受体结构的苯并咪唑已成功对接,平均RMSD为0.97。其他非苯并咪唑配体显示的准确性较低,主要是因为我们选择用于对接的受体结构与实验性整体结构差异太大。然而,回顾性分析表明,当这些配体重新对接进入其整体结构时,所有配体的平均RMSD均降至1.18。当磺酰胺和螺环与载脂蛋白结构对接时,与我们选择的结构相比,它们与它们的整体结构更吻合,所以6个配体中有5个正确对接了。这些对接结果强调了对灵活的受体对接方法的需求。对于包括多位点λ动力学(MSλD)在内的λ动力学技术,观察到了33种配体与实验的合理吻合。自由能集1和2的均方根误差分别为2.08和1.67 kcal / mol。回顾性地,软核电势,自适应景观展平和偏置电势副本交换(BP-REX)算法对于以足够的精度和在有限的时间范围内建模大型取代基扰动至关重要,例如参与大挑战2所需。讨论了它们的相关好处以及在将来的应用中使用它们的建议过程。

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