Aug 2026· Journal of Chemical Theory and Computation· Vol 22, pp. 9188 - 9198· 0 citations· 32 references
Medicine
TL;DR
An enhanced local optimization strategy based on curved line search (CLS) is introduced and integrated into AutoDock Vina, resulting in Vina_CLS, demonstrating that improved local optimization can substantially enhance docking performance.
Abstract
Physics-based protein–ligand docking critically depends on efficient pose sampling, yet established sampling and local refinement algorithms can be inefficient and unstable in the highly nonconvex energy landscapes characteristic of protein–ligand interactions. To address this limitation, we introduce an enhanced local optimization strategy based on curved line search (CLS) and integrate it into AutoDock Vina, resulting in Vina_CLS. The proposed method enables more flexible step-size selection during local refinement and improves convergence in challenging regions of the energy landscape. Across benchmarks on the PDBbind refined set and the LEADS-PEP data set, Vina_CLS consistently outperforms the baseline, exhibiting greater robustness by solving more docking problems, as well as improved efficiency through reduced function and gradient evaluations and shorter runtimes. These gains translate into practical benefits, including more frequent identification of difficult-to-access local minima, enhanced redocking accuracy, and increased recovery of near-native poses. Together, these results demonstrate that improved local optimization can substantially enhance docking performance, highlighting an important, underexplored opportunity to advance structure-based drug discovery.
PandaDock’s empirical scoring function ranks 8th of 25 methods evaluated, ahead of every AutoDock Vina and Vinardo configuration tested, while the GNN scores below Vina, consistent with the within-target ceiling identified on SAIR.
Assessment of pose prediction methods when the bound structure of a reference ligand is known and the likely binding mode(s) of a related compound are needed, and this work focuses on cases where the new compound has multiple potential binding modes.
Ažbeta Kubincová, S. S. Çınaroğlu, Jianna Ongsioco et al.· Journal of Chemical Informat...· 0 citations
Structural investigation of re-docked actives showed that re-ranked poses were more native-like, with improved binding-site occupancy, reduced centroid displacement, and greater recovery of co-crystal interactions.
L. Le, Thanh-An Pham, Ngoc Nguyen Tran et al.· bioRxiv· 0 citations
Structure-based virtual screening (VS) is widely used for the computational selection of drug candidates from compound libraries. Protein–ligand docking calculations are often performed as key steps in the early stages of this process. However, current docking calculations have limited accuracy. Thus, improvements are needed to more efficiently identify promising drug candidates. In this study, we performed mixed-solvent molecular dynamics (MSMD) simulations using four types of probe molecules to improve the accuracy of large-scale VS. We proposed a method for the modification of the docking scoring function for five selected atom classifications (XS_types). This approach integrated the grid free energy derived from the relevant atoms across the probe molecules. VS experiments conducted on nine target proteins showed improved accuracy, with the average EF1% increasing from 6.65 to 7.36. Our method may facilitate drug discovery with higher accuracy than that of conventional methods.
Unknown authors· Journal of Chemical Informat...· 0 citations
Structure-based virtual screening of chemical libraries is an established and widely used strategy for identifying novel ligands for G-protein-coupled receptors. An enhancement based on integrating protein–ligand interaction with docking has previously been proposed, but its actual impact on improving screening outcomes has remained unclear. Here, we present a comprehensive assessment based on systematic benchmarking using a diverse set of class A G-protein-coupled receptors and different approaches to represent protein–ligand, including dynamic patterns extracted from molecular dynamics simulations. Our results demonstrate that the combined approach overall improves the efficacy bias of selected ligands as compared to docking alone (ranking by scoring function). All tested variations prove broadly functional; however, the most sophisticated one─incorporating simulation and a learning model─emerges as the most robust alternative for a prospective setting. The analysis of two prospective cases, the design of both agonists and antagonists of CNR1 and the more challenging search for CXCR4 nonpeptidic agonist, reveals both great potential and inherent structural limitations, highlighting the need for an accurate and suitable three-dimensional structure.
Luca Chiesa, G. Bret, Severine Schneider et al.· Journal of Chemical Informat...· 0 citations
This work proposes a method to compute accurate kinetics for general ligand-unbinding problems at modest computational expense and minimal fine tuning, building on the AIMMD path sampling framework and opting for modelling the committor with a single descriptor-free, equivariant graph neural network shared across all systems.
Simon M. Lichtinger, Roberto Covino· 0 citations
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