摘要：Enzymes are one of the most important groups of drug targets, and identifying possible ligand-enzyme interactions is of major importance in many drug discovery processes. Novel computational methods have been developed that can apply the information from the increasing number of resolved and available ligand-enzyme complexes to model new unknown interactions and therefore contribute to answer open questions in the field of drug discovery like the identification of unknown protein functions, off-target binding, ligand 3D homology modeling and induced-fit simulations.
关键词：Unknown protein fuctions ; Off-target binding ; Drug repositioning ; Ligand 3D homolgy modeling ; Induced-fit simulations ; ProBiS-ligands web server
