In this study, we demonstrate the utility of our method to identify the possible mechanism of adverse effect of commercial drugs by combining functional site similarity searching on a structural proteome wide scale, small molecule screening, and conventional protein ligand docking free samples of priligy
In this study, we demonstrate the utility of our method to identify the possible mechanism of adverse effect of commercial drugs by combining functional site similarity searching on a structural proteome wide scale, small molecule screening, and conventional protein ligand docking free samples of priligy