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The S2 Pocket Governs the Genus-Specific Substrate Selectivity of Coronavirus 3C-Like Protease.
- Source :
-
Advanced science (Weinheim, Baden-Wurttemberg, Germany) [Adv Sci (Weinh)] 2024 Nov; Vol. 11 (44), pp. e2407766. Date of Electronic Publication: 2024 Oct 08. - Publication Year :
- 2024
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Abstract
- Coronavirus 3C-like protease (CoV 3CL <superscript>pro</superscript> ) is essential for viral replication, providing an attractive target for monitoring the evolution of CoV and developing anti-CoV drugs. Here, the substrate-binding modes of 3CL <superscript>pro</superscript> s from four CoV genera are analyzed and found that the S2 pocket in 3CL <superscript>pro</superscript> is highly conserved within each genus but differs between genera. Functionally, the S2 pocket, in conjunction with S4 and S1' pockets, governs the genus-specific substrate selectivity of 3CL <superscript>pro</superscript> . Resurrected ancestral 3CL <superscript>pro</superscript> s from four CoV genera validate the genus-specific divergence of S2 pocket. Drawing upon the genus-specific S2 pocket as evolutionary marker, eight newly identified 3CL <superscript>pro</superscript> s uncover the ancestral state of modern 3CL <superscript>pro</superscript> and elucidate the possible evolutionary process for CoV. It is also demonstrated that the S2 pocket is highly correlated with the genus-specific inhibitory potency of PF-07321332 (an FDA-approved drug against COVID-19) on different CoV 3CL <superscript>pro</superscript> s. This study on 3CL <superscript>pro</superscript> provides novel insights to inform evolutionary mechanisms for CoV and develop genera-specific or broad-spectrum drugs against CoVs.<br /> (© 2024 The Author(s). Advanced Science published by Wiley‐VCH GmbH.)
- Subjects :
- Substrate Specificity
SARS-CoV-2 genetics
SARS-CoV-2 enzymology
SARS-CoV-2 drug effects
SARS-CoV-2 metabolism
Humans
COVID-19 virology
COVID-19 metabolism
Betacoronavirus genetics
Betacoronavirus enzymology
Binding Sites
Coronavirus 3C Proteases genetics
Coronavirus 3C Proteases metabolism
Coronavirus 3C Proteases chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 2198-3844
- Volume :
- 11
- Issue :
- 44
- Database :
- MEDLINE
- Journal :
- Advanced science (Weinheim, Baden-Wurttemberg, Germany)
- Publication Type :
- Academic Journal
- Accession number :
- 39377200
- Full Text :
- https://doi.org/10.1002/advs.202407766