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Author Details

Sarah Barelier
CNRS, Aix-Marseille University
2009
17
11
Nevan J Krogan (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36197115Direct capture, inhibition and crystal structure of HsaD (Rv3569c) from M.â¿¿tuberculosis.FEBS J2023
37192550Structure-guided optimization of adenosine mimetics as selective and potent inhibitors of coronavirus nsp14 N7-methyltransferases.Eur J Med Chem2023
36206736The long-awaited structure of human fucosidase FucA1 opens novel avenues for the treatment of fucosidosis.Structure2022
35398351Molecular basis for substrate recognition and septum cleavage by AtlA, the major N-acetylglucosaminidase of Enterococcus faecalis.J Biol Chem2022
25981045Lineage-Specific Viral Hijacking of Non-canonical E3 Ubiquitin Ligase Cofactors in the Evolution of Vif Anti-APOBEC3 Activity.Cell Rep2015
26421501The Recognition of Identical Ligands by Unrelated Proteins.ACS Chem Biol2015
24791931Substrate deconstruction and the nonadditivity of enzyme recognition.J Am Chem Soc2014
24807704Increasing chemical space coverage by combining empirical and computational fragment screens.ACS Chem Biol2014
23874896Roles for ordered and bulk solvent in ligand recognition and docking in two related cavities.PLoS One2013
23043117Fragment-guided design of subnanomolar β-lactamase inhibitors active in vivo.Proc Natl Acad Sci U S A2012
21411360Ligand specificity, privileged substructures and protein druggability from fragment-based screening.Curr Opin Chem Biol2011
21771585Aspartate 458 of human glutathione synthetase is important for cooperativity and active site structure.Biochem Biophys Res Commun2011
20305821Discovery of fragment molecules that bind the human peroxiredoxin 5 active site.PLoS One2010
20800579The role of the glycine triad in human glutathione synthetase.Biochem Biophys Res Commun2010
20575554Ligand specificity in fragment-based drug design.J Med Chem2010
20192224Fragment-based deconstruction of Bcl-xL inhibitors.J Med Chem2010
19118006Tumor protein 53-induced nuclear protein 1 is a major mediator of p53 antioxidant function.Cancer Res2009
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Collaborators

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Institute for Experimental Pathology, University of Iceland
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Boston University
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University of California, USA Quantitative Biosciences Institute (QBI) san francisco
Co-authored papers 1
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