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The conserved macrodomain encoded as non-structural protein 3 (Nsp3 Mac1) is employed by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to remove host-derived ribosylation, which is a post-translational modification involved in the production of antiviral cytokines. This TEP provides early tools to develop Nsp3 Mac1 inhibitors, including purification protocols of recombinant proteins, reproducible crystallisation condition suitable for X-ray crystallography fragment screening, biophysical (activity and binding) assays and over 200 fragment hits representing a wide range of chemotypes, that are a starting point for the development of more selective and potent compounds.
This document represents version 0 of the TEP datasheet. For more information about TEPs and the TEP Programme, please visit https://www.cmd.ox.ac.uk/resources/teps
disease, structure discovery, infectious disease, chemical probe, NSP3, COVID-19, covid, chemical biology, structural genomics, drug target, drug discovery, target enabling package, genetics, structure, orphan disease, protein
disease, structure discovery, infectious disease, chemical probe, NSP3, COVID-19, covid, chemical biology, structural genomics, drug target, drug discovery, target enabling package, genetics, structure, orphan disease, protein
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