Abstract
According to WHO, the current Coronavirus disease situation is 8,506,107 confirmed
and 455,231 death cases in approx 216 Countries, areas, or territories. For the treatment of Severe acute respiratory
syndrome coronavirus 2 (SARS-CoV-2) drug repurposing seems to be an effective
strategy as it could shorten the time and reduce the cost compared to de novo
drug discovery. For that, we need to identify target binding sites. Thus, we
have reported for the first time structural druggability assessment for
SARS-CoV-2 proteome a pan-druggability prediction based on the open-source
pocket detection code fpocket and rank them on the basis of druggability score.
We have identified in a total of 433 pockets on the SARS-CoV-2 proteome and
characterized by physicochemical descriptors. In which, 47 pockets identified
as druggable and 71 as potential drug-binding pockets.