Abstract |
In this study, the binding strength of 32 diastereomers of nelfinavir, a proposed drug for the treatment of COVID-19, was considered against main protease. Molecular docking was used to determine the most potent diastereomers. The top three diastereomers along with apo form of protein were then considered via molecular dynamics simulation and MM-GBSA method. During the simulation, the structural consideration of four proteins considered was carried out using RMSD, RMSF, Rg and hydrogen bond analysis tools. Our data demonstrated that the effect of nelfinavir RSRSR stereoisomer on protein stability and compactness is higher than the other. We also found from the hydrogen bond analysis that this important diastereomer form three hydrogen bonds with the residues of Glu166, Gly143 and Hie41. MM/GBSA analysis showed that the binding strength of RSRSR is more than other stereoisomers and that the main contributions to binding energy are vdW and electronic terms. The nelfinavir RSRSR stereoisomer introduced in this study may be effective in the treatment of COVID-19.
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Authors | Mohsen Sargolzaei |
Journal | Journal of molecular graphics & modelling
(J Mol Graph Model)
Vol. 103
Pg. 107803
(03 2021)
ISSN: 1873-4243 [Electronic] United States |
PMID | 33333424
(Publication Type: Journal Article)
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Copyright | Copyright © 2020 Elsevier Inc. All rights reserved. |
Chemical References |
- Antiviral Agents
- Apoproteins
- Protease Inhibitors
- Coronavirus 3C Proteases
- Nelfinavir
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Topics |
- Antiviral Agents
(chemistry, metabolism)
- Apoproteins
(antagonists & inhibitors, chemistry, metabolism)
- Binding Sites
- Coronavirus 3C Proteases
(antagonists & inhibitors, chemistry, metabolism)
- Hydrogen Bonding
- Kinetics
- Molecular Docking Simulation
- Molecular Dynamics Simulation
- Nelfinavir
(chemistry, metabolism)
- Protease Inhibitors
(chemistry, metabolism)
- Protein Binding
- Protein Conformation, alpha-Helical
- Protein Conformation, beta-Strand
- Protein Interaction Domains and Motifs
- SARS-CoV-2
(chemistry, enzymology)
- Stereoisomerism
- Thermodynamics
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