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Proceedings of the National Academy of Sciences of the United States of America|October 9, 2012
Fragment-guided design of subnanomolar β-lactamase inhibitors active in vivoOliv Eidam, Chiara Romagnoli, Guillaume Dalmasso, et al.
Chemmedchem|January 21, 2025
Binding-Site Switch for Protein Kinase CK2 InhibitorsDylan Grenier, Muriel Gelin, Yinshan Yang, et al.
Journal of Medicinal Chemistry|March 23, 2007
NMR screening applied to the fragment-based generation of inhibitors of creatine kinase exploiting a new interaction proximate to the ATP binding siteAnne-Sophie Bretonnet, Anne Jochum, Olivier Walker, et al.
ACS Chemical Biology|May 9, 2014
Increasing chemical space coverage by combining empirical and computational fragment screensSarah Barelier, Oliv Eidam, Inbar Fish, et al.
The Journal of Biological Chemistry|August 19, 2006
Glutathionylation induces the dissociation of 1-Cys D-peroxiredoxin non-covalent homodimerValérie Noguera-Mazon, Jérôme Lemoine, Olivier Walker, et al.
Analytica Chimica Acta|April 29, 2020
Miniaturized weak affinity chromatography for ligand identification of nanodiscs-embedded G-protein coupled receptorsLucile Lecas, Lucie Hartmann, Lydia Caro, et al.
FEBS Letters|July 31, 2012
Competitive binding of UBPY and ubiquitin to the STAM2 SH3 domain revealed by NMRAnja Lange, Mouhamad-Baligh Ismail, Gwladys Rivière, et al.
Biochemical and Biophysical Research Communications|July 21, 2011
Aspartate 458 of human glutathione synthetase is important for cooperativity and active site structureTeresa R Brown, Michael L Drummond, Sarah Barelier, et al.
Nucleosides, Nucleotides & Nucleic Acids|April 25, 2006
F-ara-AMP is a substrate of cytoplasmic 5'-nucleotidase II (cN-II): HPLC and NMR studies of enzymatic dephosphorylationLars P Jordheim, Emeline Cros, Carlos M Galmarini, et al.
European Journal of Medicinal Chemistry|July 16, 2022
A fragment-based drug discovery strategy applied to the identification of NDM-1 β-lactamase inhibitorsJérémy Caburet, Benjamin Boucherle, Sofiane Bourdillon, et al.
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