Department of Pharmaceutical Sciences, Division of Pharmaceutical Chemistry, University of Vienna, Josef-Holaubek-Platz 2, 1090 Vienna, Austria.
NeGeMac Research Platform, Department of Pharmaceutical Sciences, Division of Pharmaceutical Chemistry, University of Vienna, Josef-Holaubek-Platz 2, 1090 Vienna, Austria.
J Chem Inf Model. 2023 Sep 11;63(17):5549-5570. doi: 10.1021/acs.jcim.3c00563. Epub 2023 Aug 25.
Knowledge of the putative bound-state conformation of a molecule is an essential prerequisite for the successful application of many computer-aided drug design methods that aim to assess or predict its capability to bind to a particular target receptor. An established approach to predict bioactive conformers in the absence of receptor structure information is to sample the low-energy conformational space of the investigated molecules and derive representative conformer ensembles that can be expected to comprise members closely resembling possible bound-state ligand conformations. The high relevance of such conformer generation functionality led to the development of a wide panel of dedicated commercial and open-source software tools throughout the last decades. Several published benchmarking studies have shown that open-source tools usually lag behind their commercial competitors in many key aspects. In this work, we introduce the open-source conformer ensemble generator CONFORGE, which aims at delivering state-of-the-art performance for all types of organic molecules in drug-like chemical space. The ability of CONFORGE and several well-known commercial and open-source conformer ensemble generators to reproduce experimental 3D structures as well as their computational efficiency and robustness has been assessed thoroughly for both typical drug-like molecules and macrocyclic structures. For small molecules, CONFORGE clearly outperformed all other tested open-source conformer generators and performed at least equally well as the evaluated commercial generators in terms of both processing speed and accuracy. In the case of macrocyclic structures, CONFORGE achieved the best average accuracy among all benchmarked generators, with RDKit's generator coming close in second place.
对分子的假设结合态构象的了解是许多旨在评估或预测其与特定靶受体结合能力的计算机辅助药物设计方法成功应用的必要前提。在没有受体结构信息的情况下预测生物活性构象的一种既定方法是对研究分子的低能构象空间进行采样,并得出代表性的构象集合,这些构象集合可以预期包含与可能的结合态配体构象密切相似的成员。这种构象生成功能的高度相关性导致了过去几十年中广泛的专用商业和开源软件工具的发展。多项已发表的基准研究表明,开源工具在许多关键方面通常落后于其商业竞争对手。在这项工作中,我们介绍了开源构象集合生成器 CONFORGE,它旨在为药物样化学空间中的所有类型的有机分子提供最先进的性能。我们对 CONFORGE 以及几个知名的商业和开源构象集合生成器对实验 3D 结构的重现能力及其计算效率和鲁棒性进行了全面评估,包括典型的药物样分子和大环结构。对于小分子,CONFORGE 明显优于所有其他测试的开源构象生成器,并且在处理速度和准确性方面与评估的商业生成器至少同样出色。在大环结构的情况下,CONFORGE 在所有基准生成器中实现了最佳的平均准确性,RDKit 的生成器紧随其后排名第二。