Small-molecules bind to proteins within surface cavities. The prediction of these interactions is done through docking simulations. Structure-based virtual screening (molecular docking) has been used to discover new ligands based on target structures. Docking methods are widely applied and accepted nowadays in drug design. Two approaches are particularly popular within the molecular docking community. One approach uses a matching technique that describes the protein and the ligand as complementary surfaces. The second approach simulates the actual docking process in which the ligand-protein pairwise interaction energies are calculated. Both approaches have significant advantages as well as some limitations. molecular docking software https://www.computabio.com/molecular-docking-software.html
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Small-molecules bind to proteins within surface cavities. The prediction of these interactions is done through docking simulations. Structure-based virtual screening (molecular docking) has been used to discover new ligands based on target structures. Docking methods are widely applied and accepted nowadays in drug design. Two approaches are particularly popular within the molecular docking community. One approach uses a matching technique that describes the protein and the ligand as complementary surfaces. The second approach simulates the actual docking process in which the ligand-protein pairwise interaction energies are calculated. Both approaches have significant advantages as well as some limitations. molecular docking software https://www.computabio.com/molecular-docking-software.html

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