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9BRV

SARS-CoV-2 Papain-like Protease (PLpro) with Fragment 5

This is a non-PDB format compatible entry.
Summary for 9BRV
Entry DOI10.2210/pdb9brv/pdb
DescriptorPapain-like protease nsp3, N-[2-(dimethylamino)ethyl]-N'-(3-methylphenyl)thiourea, ZINC ION, ... (6 entities in total)
Functional Keywordsplpro, sars-cov-2, drug discovery, inhibitor, viral protein, hydrolase
Biological sourceSevere acute respiratory syndrome coronavirus 2 (2019-nCoV, SARS-CoV-2)
Total number of polymer chains2
Total formula weight73482.88
Authors
Amporndanai, K.,Zhao, B.,Fesik, S.W. (deposition date: 2024-05-11, release date: 2024-07-31, Last modification date: 2024-09-04)
Primary citationTaylor, A.J.,Amporndanai, K.,Rietz, T.A.,Zhao, B.,Thiruvaipati, A.,Wei, Q.,South, T.M.,Crow, M.M.,Apakama, C.,Sensintaffar, J.L.,Phan, J.,Lee, T.,Fesik, S.W.
Fragment-Based Screen of SARS-CoV-2 Papain-like Protease (PL pro ).
Acs Med.Chem.Lett., 15:1351-1357, 2024
Cited by
PubMed Abstract: Coronaviruses have been responsible for numerous viral outbreaks in the past two decades due to the high transmission rate of this family of viruses. The deadliest outbreak is the recent Covid-19 pandemic, which resulted in over 7 million deaths worldwide. SARS-CoV-2 papain-like protease (PL) plays a key role in both viral replication and host immune suppression and is highly conserved across the coronavirus family, making it an ideal drug target. Herein we describe a fragment-based screen against PL using protein-observed NMR experiments, identifying 77 hit fragments. Analyses of NMR perturbation patterns and X-ray cocrystallized structures reveal fragments bind to two distinct regions of the protein. Importantly none of the fragments identified belong to the same chemical class as the few reported inhibitors, allowing for the discovery of a novel class of PL inhibitors.
PubMed: 39140055
DOI: 10.1021/acsmedchemlett.4c00238
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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