Protein Structure and Function Prediction of SARS-CoV 2: Prospective Antivirus Active Drug Binding Sites

Today a newly emerged corona-virus known as SARS-CoV 2 has become cause of global health concern and took away the lives large number people throughout world. Corona-viruses are enveloped virus with positive single stranded genome 26.4 to 31.7 kb. Envelop is made up four structural proteins namely envelop protein (E), membrane (M), spike (S) nucleocapsid (N). These responsible for overall shape size (structure virus). forms ion channels, virus, entering inside target host cell by binding receptor binds RNA forming multiple copies. We investigate reliability homogeneity among all species such MERS CoV, Bat-CoV HKU4, Transmissible gastro-enteritis coronavirus (TGEV), Porcine epidemic diarrhea (PEDV), HCoV-229E Whale-CoV SW1, M-CoV, Hedgehog 1, Bulbul-CoV HKU11 etc, using binary graph which helpful in findings sequence reliability, secondary tertiary structure model prediction advanced builder, we build various protein/gene products selecting them from SARS-COV 2, further finding target-ligand future therapeutic applications. Consequently modeling bring into being that have pentameric lipid pores allow transportation were able depict active drug sites.