Heterologous production, purification and crystallization of 24C-sterol methyltransferase fromCandida albicans
Mpontshane NS. et al, (2025)
High-throughput crystallographic fragment screening of Zika virus NS3 Helicase.
Godoy AS. et al, (2024)
Accelerating Drug Discovery With High-Throughput Crystallographic Fragment Screening and Structural Enablement
Fearon D. et al, (2024), Applied Research
Open science discovery of potent noncovalent SARS-CoV-2 main protease inhibitors.
Boby ML. et al, (2023), Science, 382
Allosteric regulation and crystallographic fragment screening of SARS-CoV-2 NSP15 endoribonuclease.
Godoy AS. et al, (2023), Nucleic Acids Res, 51, 5255 - 5270
Turning high-throughput structural biology into predictive inhibitor design.
Saar KL. et al, (2023), Proc Natl Acad Sci U S A, 120
Simultaneous identification of viruses and viral variants with programmable DNA nanobait.
Bošković F. et al, (2023), Nat Nanotechnol
Simultaneous identification of viruses and SARS-CoV-2 variants with programmable DNA nanobait
Bošković F. et al, (2021)
Deliberately Losing Control of C-H Activation Processes in the Design of Small-Molecule-Fragment Arrays Targeting Peroxisomal Metabolism.
Khan Tareque R. et al, (2020), ChemMedChem, 15, 2513 - 2520
Open Science Discovery of Potent Non-Covalent SARS-CoV-2 Main Protease Inhibitors
Boby ML. et al, (2020)
Crystallographic and electrophilic fragment screening of the SARS-CoV-2 main protease.
Douangamath A. et al, (2020), Nat Commun, 11
Demonstration of the utility of DOS-derived fragment libraries for rapid hit derivatisation in a multidirectional fashion.
Kidd SL. et al, (2020), Chem Sci, 11, 10792 - 10801