Identification of Natural Inhibitors Against SARS-CoV-2 Drugable Targets Using Molecular Docking, Molecular Dynamics Simulation, and MM-PBSA Approach

dc.contributor.authorKushwaha, Prem Prakash
dc.contributor.authorSingh, Atul Kumar
dc.contributor.authorBansal, Tanya
dc.contributor.authorYadav, Akansha
dc.contributor.authorPrajapati, Kumari Sunita
dc.contributor.authorShuaib, Mohd
dc.contributor.authorKumar, Shashank
dc.date.accessioned2024-01-16T14:23:10Z
dc.date.accessioned2024-08-13T10:34:07Z
dc.date.available2024-01-16T14:23:10Z
dc.date.available2024-08-13T10:34:07Z
dc.date.issued2021-08-12T00:00:00
dc.description.abstractThe present study explores the SARS-CoV-2 drugable target inhibition efficacy of phytochemicals from Indian medicinal plants using molecular docking, molecular dynamics (MD) simulation, and MM-PBSA analysis. A total of 130 phytochemicals were screened against SARS-CoV-2 Spike (S)-protein, RNA-dependent RNA polymerase (RdRp), and Main protease (Mpro). Result of molecular docking showed that Isoquercetin potentially binds with the active site/protein binding site of the Spike, RdRP, and Mpro targets with a docking score of -8.22, -6.86, and -9.73 kcal/mole, respectively. Further, MS�3, 7-Hydroxyaloin B, 10-Hydroxyaloin A, showed -9.57, -7.07, -8.57 kcal/mole docking score against Spike, RdRP, and Mpro targets respectively. The MD simulation was performed to study the favorable confirmation and energetically stable complex formation ability of Isoquercetin and 10-Hydroxyaloin A phytochemicals in Mpro-unbound/ligand bound/standard inhibitor bound system. The parameters such as RMSD, RMSF, Rg, SASA, Hydrogen-bond formation, energy landscape, principal component analysis showed that the lead phytochemicals form stable and energetically stabilized complex with the target protein. Further, MM-PBSA analysis was performed to compare the Gibbs free energy of the Mpro-ligand bound and standard inhibitor bound complexes. The analysis revealed that the His-41, Cys145, Met49, and Leu27 amino acid residues were majorly responsible for the lower free energy of the complex. Drug likeness and physiochemical properties of the test compounds showed satisfactory results. Taken together, the study concludes that that the Isoquercetin and 10-Hydroxyaloin A phytochemical possess significant efficacy to bind SARS-Cov-2 Mpro active site. The study necessitates further in vitro and in vivo experimental validation of these lead phytochemicals to assess their anti-SARS-CoV-2 potential. � Copyright � 2021 Kushwaha, Singh, Bansal, Yadav, Prajapati, Shuaib and Kumar.en_US
dc.identifier.doi10.3389/fcimb.2021.730288
dc.identifier.issn22352988
dc.identifier.urihttps://doi.org/10.3389/fcimb.2021.730288
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/2858
dc.language.isoen_USen_US
dc.publisherFrontiers Media S.A.en_US
dc.subject10-hydroxyaloin Aen_US
dc.subjectdrugable targetsen_US
dc.subjectin silicoen_US
dc.subjectisoquercetinen_US
dc.subjectSARS-CoV-2en_US
dc.titleIdentification of Natural Inhibitors Against SARS-CoV-2 Drugable Targets Using Molecular Docking, Molecular Dynamics Simulation, and MM-PBSA Approachen_US
dc.title.journalFrontiers in Cellular and Infection Microbiologyen_US
dc.typeArticleen_US
dc.type.accesstypeOpen Accessen_US

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