Structural Homology-Based Drug Repurposing Approach for Targeting NSP12 SARS-CoV-2.
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ABSTRACT: The severe acute respiratory syndrome coronavirus 2, also known as SARS-CoV-2, is the causative agent of the COVID-19 global pandemic. SARS-CoV-2 has a highly conserved non-structural protein 12 (NSP-12) involved in RNA-dependent RNA polymerase (RdRp) activity. For the identification of potential inhibitors for NSP-12, computational approaches such as the identification of homologous proteins that have been previously targeted by FDA-approved antivirals can be employed. Herein, homologous proteins of NSP-12 were retrieved from Protein DataBank (PDB) and the evolutionary conserved sequence and structure similarity of the active site of the RdRp domain of NSP-12 was characterized. The identified homologous structures of NSP-12 belonged to four viral families: Coronaviridae, Flavivi
SUBMITTER: Aljuaid A
PROVIDER: S-EPMC9694939 | biostudies-literature | 2022 Nov
REPOSITORIES: biostudies-literature
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