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Showing 1–5 of 5 results
Advanced filters: Author: Alice Douangamath Clear advanced filters
  • The SARS-CoV-2 main protease is an important target for the development of COVID-19 therapeutics. Here, the authors combine X-ray crystallography and mass spectrometry and performed a large scale fragment screening campaign, which yielded 96 liganded structures of this essential viral protein that are of interest for further drug development efforts.

    • Alice Douangamath
    • Daren Fearon
    • Martin A. Walsh
    ResearchOpen Access
    Nature Communications
    Volume: 11, P: 1-11
  • Fragment-based drug discovery employs screening of small polar compounds typically exhibiting low affinity towards protein targets. Here, the authors combine the use of protein-based binding pharmacophores with the theory of protein hotspots to develop a design protocol for fragment libraries, called SpotXplorer, and validate their approach on common and emerging drug targets.

    • Dávid Bajusz
    • Warren S. Wade
    • György M. Keserű
    ResearchOpen Access
    Nature Communications
    Volume: 12, P: 1-10
  • The SARS-CoV-2 NSP13 helicase is essential for viral replication and of interest as a drug target. Here, the authors present the crystal structures of NSP13 in the apo form and bound to either phosphate or the non-hydrolysable ATP analog AMP-PNP and discuss the helicase mechanism. They also perform a crystallographic fragment screening and identify 65 bound fragments, which could help in the design of new antiviral agents.

    • Joseph A. Newman
    • Alice Douangamath
    • Opher Gileadi
    ResearchOpen Access
    Nature Communications
    Volume: 12, P: 1-11