7LFV
Crystal structure of the SARS CoV-1 Papain-like protease in complex with peptide inhibitor VIR251
Summary for 7LFV
Entry DOI | 10.2210/pdb7lfv/pdb |
Related PRD ID | PRD_002390 |
Descriptor | papain-like protease, Papain-like protease peptide inhibitor VIR251, ZINC ION, ... (8 entities in total) |
Functional Keywords | covid-19, coronavirus, sars, cov-1, cov-2, papain-like protease, plpro, deubiquitinating enzyme, ubiquitin, activity-based probe, hydrolase-hydrolas inhibitor complex, hydrolase/hydrolas inhibitor |
Biological source | Severe acute respiratory syndrome coronavirus (SARS-CoV) More |
Total number of polymer chains | 4 |
Total formula weight | 76112.03 |
Authors | Olsen, S.K.,Lv, Z. (deposition date: 2021-01-18, release date: 2021-11-10, Last modification date: 2023-11-15) |
Primary citation | Patchett, S.,Lv, Z.,Rut, W.,Bekes, M.,Drag, M.,Olsen, S.K.,Huang, T.T. A molecular sensor determines the ubiquitin substrate specificity of SARS-CoV-2 papain-like protease. Cell Rep, 36:109754-109754, 2021 Cited by PubMed Abstract: The SARS-CoV-2 papain-like protease (PLpro) is a target for antiviral drug development. It is essential for processing viral polyproteins for replication and functions in host immune evasion by cleaving ubiquitin (Ub) and ubiquitin-like protein (Ubl) conjugates. While highly conserved, SARS-CoV-2 and SARS-CoV PLpro have contrasting Ub/Ubl substrate preferences. Using a combination of structural analyses and functional assays, we identify a molecular sensor within the S1 Ub-binding site of PLpro that serves as a key determinant of substrate specificity. Variations within the S1 sensor specifically alter cleavage of Ub substrates but not of the Ubl interferon-stimulated gene 15 protein (ISG15). Significantly, a variant of concern associated with immune evasion carries a mutation in the S1 sensor that enhances PLpro activity on Ub substrates. Collectively, our data identify the S1 sensor region as a potential hotspot of variability that could alter host antiviral immune responses to newly emerging SARS-CoV-2 lineages. PubMed: 34547223DOI: 10.1016/j.celrep.2021.109754 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.23 Å) |
Structure validation
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