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10.1016/j.isci.2020.101258

http://scihub22266oqcxt.onion/10.1016/j.isci.2020.101258
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suck abstract from ncbi


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pmid32592996      iScience 2020 ; 23 (7): 101258
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  • Crystal Structure of the SARS-CoV-2 Non-structural Protein 9, Nsp9 #MMPMID32592996
  • Littler DR; Gully BS; Colson RN; Rossjohn J
  • iScience 2020[Jul]; 23 (7): 101258 PMID32592996show ga
  • Many of the SARS-CoV-2 proteins have related counterparts across the Severe Acute Respiratory Syndrome (SARS-CoV) family. One such protein is non-structural protein 9 (Nsp9), which is thought to mediate viral replication, overall virulence, and viral genomic RNA reproduction. We sought to better characterize the SARS-CoV-2 Nsp9 and subsequently solved its X-ray crystal structure, in an apo form and, unexpectedly, in a peptide-bound form with a sequence originating from a rhinoviral 3C protease sequence (LEVL). The SARS-CoV-2 Nsp9 structure revealed the high level of structural conservation within the Nsp9 family. The exogenous peptide binding site is close to the dimer interface and impacted the relative juxtapositioning of the monomers within the homodimer. We have established a protocol for the production of SARS-CoV-2 Nsp9, determined its structure, and identified a peptide-binding site that warrants further study to understanding Nsp9 function.
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