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7MHF

Crystal Structure of SARS-CoV-2 Main Protease (Mpro) at 100 K

Summary for 7MHF
Entry DOI10.2210/pdb7mhf/pdb
Related7MHG 7MHH 7MHI 7MHJ 7MHK 7MHL 7MHM 7MHN 7MHO 7MHP 7MHQ
Descriptor3C-like proteinase, DIMETHYL SULFOXIDE, ZINC ION, ... (4 entities in total)
Functional Keywordssars-cov-2, coronavirus, main protease, 3clpro, mpro, 100 k, hydrolase, temperature, temperature series, multitemperature, multiconformer
Biological sourceSevere acute respiratory syndrome coronavirus 2
Total number of polymer chains1
Total formula weight34281.62
Authors
Ebrahim, A.,Riley, B.T.,Kumaran, D.,Andi, B.,Fuchs, M.R.,McSweeney, S.,Keedy, D.A. (deposition date: 2021-04-15, release date: 2021-05-12, Last modification date: 2023-10-25)
Primary citationEbrahim, A.,Riley, B.T.,Kumaran, D.,Andi, B.,Fuchs, M.R.,McSweeney, S.,Keedy, D.A.
The tem-per-ature-dependent conformational ensemble of SARS-CoV-2 main protease (M pro ).
Iucrj, 9:682-694, 2022
Cited by
PubMed Abstract: The COVID-19 pandemic, instigated by the SARS-CoV-2 coronavirus, continues to plague the globe. The SARS-CoV-2 main protease, or M, is a promising target for the development of novel antiviral therapeutics. Previous X-ray crystal structures of M were obtained at cryogenic tem-per-ature or room tem-per-ature only. Here we report a series of high-resolution crystal structures of unliganded M across multiple tem-per-atures from cryogenic to physiological, and another at high humidity. We inter-rogate these data sets with parsimonious multiconformer models, multi-copy ensemble models, and isomorphous difference density maps. Our analysis reveals a perturbation-dependent conformational landscape for M, including a mobile zinc ion inter-leaved between the catalytic dyad, mercurial conformational heterogeneity at various sites including a key substrate-binding loop, and a far-reaching intra-molecular network bridging the active site and dimer inter-face. Our results may inspire new strategies for antiviral drug development to aid preparation for future coronavirus pandemics.
PubMed: 36071812
DOI: 10.1107/S2052252522007497
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.55 Å)
Structure validation

226707

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