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Outbreaks of human epidemic nonbacterial gastroenteritis are mainly caused by noroviruses. Viral replication requires a 3C-like cysteine protease (3CL<sup>pro</sup>) which processes the 200 kDa viral polyprotein into six functional proteins. The 3CL<sup>pro</sup> has attracted much interest due to its potential as a target for antiviral drugs. A system for growing high-quality crystals of native Southampton norovirus 3CL<sup>pro</sup> (SV3CP) has been established, allowing the ligand-free crystal structure to be determined to 1.3 Å in a tetrameric state. This also allowed crystal-based fragment screening to be performed with various compound libraries, ultimately to guide drug discovery for SV3CP. A total of 19 fragments were found to bind to the protease out of the 844 which were screened. Two of the hits were located at the active site of SV3CP and showed good inhibitory activity in kinetic assays. Another 5 were found at the enzyme's putative RNA-binding site and a further 11 were located in the symmetric central cavity of the tetramer.

Original publication

DOI

10.1016/j.yjsbx.2020.100031

Type

Journal article

Journal

Journal of structural biology: X

Publication Date

01/2020

Volume

4

Addresses

Division of Medicine, UCL, Gower Street, London WC1E 6BT, UK.