Scientific Data · 2022 · 25 citations · 62 references
PharmacyBioinformaticsMedicinal ChemistryDrug DesignDrug DiscoveryStructural BiologyBinding Affinity PredictionComputational Drug DiscoveryLigand BindingMolecular DynamicsProtein-ligand DockingProtein-ligand RecognitionMachine Learning Scoring ModelsMolecular Dynamics-based Affinity EstimationProtein - Ligand Affinity PredictionProtein-ligand Binding Affinity PredictionProtein-ligand Binding ModelingProtein-ligand Complex StructureProtein-ligand ComplexesScoring Functions
Computational methods and recently modern machine learning methods have played a key role in structure-based drug design. Though several benchmarking datasets are available for machine learning applications in virtual screening, accurate prediction of binding affinity for a protein-ligand complex remains a major challenge. New datasets that allow for the development of models for predicting binding affinities better than the state-of-the-art scoring functions are important. For the first time, we have developed a dataset, PLAS-5k comprised of 5000 protein-ligand complexes chosen from PDB database. The dataset consists of binding affinities along with energy components like electrostatic, van der Waals, polar and non-polar solvation energy calculated from molecular dynamics simulations using MMPBSA (Molecular Mechanics Poisson-Boltzmann Surface Area) method. The calculated binding affinities outperformed docking scores and showed a good correlation with the available experimental values. The availability of energy components may enable optimization of desired components during machine learning-based drug design. Further, OnionNet model has been retrained on PLAS-5k dataset and is provided as a baseline for the prediction of binding affinities.
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Development and testing of a general amber force field
Junmei Wang, Romain M. Wolf, James W. Caldwell et al. · Journal of Computational Chemistry · 2004 · 19.6K citations