This document discusses in silico drug discovery and development work done by Group A. They used structure-based drug design methods like pharmacophore modeling and FTMap benzene probe mapping to identify optimal drug targets. Specifically, they analyzed the HIV-1 protease protein target using PyMOL and FTMap to map benzene probes and identify four clusters of binding regions that could be used to develop potential drugs through pharmacophore modeling and screening of chemical probes.