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7BZF

COVID-19 RNA-dependent RNA polymerase post-translocated catalytic complex

Summary for 7BZF
Entry DOI10.2210/pdb7bzf/pdb
EMDB information30252
DescriptorRNA-directed RNA polymerase, Non-structural protein 8, Non-structural protein 7, ... (6 entities in total)
Functional Keywordscovid-19, 2019-ncov, sars-cov-2, virus, rdrp, nsp12, nsp7, nsp8, rtc, cryo-em, viral protein, rna polymerase, drug target, antiviral, replication transcription complex, viral protein-rna complex, viral protein/rna
Biological sourceSevere acute respiratory syndrome coronavirus 2 (2019-nCoV)
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Total number of polymer chains6
Total formula weight175832.92
Authors
Wang, Q.,Gao, Y.,Ji, W.,Mu, A.,Rao, Z. (deposition date: 2020-04-27, release date: 2020-06-03, Last modification date: 2024-03-27)
Primary citationWang, Q.,Wu, J.,Wang, H.,Gao, Y.,Liu, Q.,Mu, A.,Ji, W.,Yan, L.,Zhu, Y.,Zhu, C.,Fang, X.,Yang, X.,Huang, Y.,Gao, H.,Liu, F.,Ge, J.,Sun, Q.,Yang, X.,Xu, W.,Liu, Z.,Yang, H.,Lou, Z.,Jiang, B.,Guddat, L.W.,Gong, P.,Rao, Z.
Structural Basis for RNA Replication by the SARS-CoV-2 Polymerase.
Cell, 182:417-428.e13, 2020
Cited by
PubMed Abstract: Nucleotide analog inhibitors, including broad-spectrum remdesivir and favipiravir, have shown promise in in vitro assays and some clinical studies for COVID-19 treatment, this despite an incomplete mechanistic understanding of the viral RNA-dependent RNA polymerase nsp12 drug interactions. Here, we examine the molecular basis of SARS-CoV-2 RNA replication by determining the cryo-EM structures of the stalled pre- and post- translocated polymerase complexes. Compared with the apo complex, the structures show notable structural rearrangements happening to nsp12 and its co-factors nsp7 and nsp8 to accommodate the nucleic acid, whereas there are highly conserved residues in nsp12, positioning the template and primer for an in-line attack on the incoming nucleotide. Furthermore, we investigate the inhibition mechanism of the triphosphate metabolite of remdesivir through structural and kinetic analyses. A transition model from the nsp7-nsp8 hexadecameric primase complex to the nsp12-nsp7-nsp8 polymerase complex is also proposed to provide clues for the understanding of the coronavirus transcription and replication machinery.
PubMed: 32526208
DOI: 10.1016/j.cell.2020.05.034
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.26 Å)
Structure validation

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