Nature Communications (Jun 2020)

Structural plasticity of SARS-CoV-2 3CL Mpro active site cavity revealed by room temperature X-ray crystallography

  • Daniel W. Kneller,
  • Gwyndalyn Phillips,
  • Hugh M. O’Neill,
  • Robert Jedrzejczak,
  • Lucy Stols,
  • Paul Langan,
  • Andrzej Joachimiak,
  • Leighton Coates,
  • Andrey Kovalevsky

DOI
https://doi.org/10.1038/s41467-020-16954-7
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 6

Abstract

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The SARS-CoV-2 3CL main protease (3CL Mpro) is a chymotrypsin-like protease that facilitates the production of non-structural proteins, which are essential for viral replication and is therefore of great interest as a drug target. Here, the authors present the 2.30 Å room temperature crystal structure of ligand-free 3CL Mpro and compare it with the earlier determined low-temperature ligand-free and inhibitor-bound crystal structures.