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FEBS Letters|January 14, 2026
Cell wall target fragment discovery using a low-cost, minimal fragment libraryKaizhou Yan, Mathew Stanley, Olawale Raimi, et al.
The EMBO Journal|March 17, 2006
Structural insights into the mechanism and inhibition of eukaryotic O-GlcNAc hydrolysisFrancesco V Rao, Helge C Dorfmueller, Fabrizio Villa, et al.
Amino Acids|July 20, 2010
Substrate and product analogues as human O-GlcNAc transferase inhibitorsHelge C Dorfmueller, Vladimir S Borodkin, David E Blair, et al.
Acta Crystallographica. Section D, Biological Crystallography|August 8, 2012
Structural and biochemical characterization of a trapped coenzyme A adduct of Caenorhabditis elegans glucosamine-6-phosphate N-acetyltransferase 1Helge C Dorfmueller, Wenxia Fang, Francesco V Rao, et al.
Chemistry & Biology|November 25, 2010
Cell-penetrant, nanomolar O-GlcNAcase inhibitors selective against lysosomal hexosaminidasesHelge C Dorfmueller, Vladimir S Borodkin, Marianne Schimpl, et al.
Journal of the American Chemical Society|December 21, 2006
GlcNAcstatin: a picomolar, selective O-GlcNAcase inhibitor that modulates intracellular O-glcNAcylation levelsHelge C Dorfmueller, Vladimir S Borodkin, Marianne Schimpl, et al.
Open Biology|October 4, 2013
Structure of a bacterial putative acetyltransferase defines the fold of the human O-GlcNAcase C-terminal domainFrancesco V Rao, Alexander W Schüttelkopf, Helge C Dorfmueller, et al.
The Biochemical Journal|November 22, 2013
Bisubstrate UDP-peptide conjugates as human O-GlcNAc transferase inhibitorsVladimir S Borodkin, Marianne Schimpl, Mehmet Gundogdu, et al.
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