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Michael Groll

Showing results (51-60 of 205) with videos related to

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Angewandte Chemie (International Ed. in English)|November 19, 2011
Crystal structure of methylornithine synthase (PylB): insights into the pyrrolysine biosynthesisFelix Quitterer, Anja List, Wolfgang Eisenreich, et al.
Journal of Molecular Biology|December 6, 2011
Crystal structures of mutant IspH proteins reveal a rotation of the substrate's hydroxymethyl group during catalysisIngrid Span, Tobias Gräwert, Adelbert Bacher, et al.
ACS Chemical Biology|November 17, 2025
A Luminescence-Based Screening Platform for Lanthanide-Binding Peptides and ProteinsRobert Klassen, Anna Heider, Hannah Kugler, et al.
Angewandte Chemie (International Ed. in English)|December 20, 2002
The core structure of TMC-95A is a promising lead for reversible proteasome inhibitionMarkus Kaiser, Michael Groll, Christian Renner, et al.
Chemistry & Biology|June 24, 2006
TMC-95-based inhibitor design provides evidence for the catalytic versatility of the proteasomeMichael Groll, Marion Götz, Markus Kaiser, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2006
Inhibitor-binding mode of homobelactosin C to proteasomes: new insights into class I MHC ligand generationMichael Groll, Oleg V Larionov, Robert Huber, et al.
Chembiochem : a European Journal of Chemical Biology|January 29, 2005
Molecular machines for protein degradationMichael Groll, Matthias Bochtler, Hans Brandstetter, et al.
Journal of Molecular Biology|March 5, 2003
Investigations on the maturation and regulation of archaebacterial proteasomesMichael Groll, Hans Brandstetter, Hans Bartunik, et al.
Organic & Biomolecular Chemistry|March 19, 2014
Versatile C(3)-symmetric scaffolds and their use for covalent stabilization of the foldon trimerArne Berthelmann, Johannes Lach, Melissa A Gräwert, et al.
Journal of the American Chemical Society|September 11, 2025
Structure-Guided Engineering of a Bacterial Sesterterpene Synthase for Sesterviridene DiversificationHeng Li, Philip Troycke, Zhiyong Yin, et al.
Pageof 21

Showing results (51-60 of 205) with videos related to

Sort By:
Pageof 21
Angewandte Chemie (International Ed. in English)|November 19, 2011
Crystal structure of methylornithine synthase (PylB): insights into the pyrrolysine biosynthesisFelix Quitterer, Anja List, Wolfgang Eisenreich, et al.
Journal of Molecular Biology|December 6, 2011
Crystal structures of mutant IspH proteins reveal a rotation of the substrate's hydroxymethyl group during catalysisIngrid Span, Tobias Gräwert, Adelbert Bacher, et al.
ACS Chemical Biology|November 17, 2025
A Luminescence-Based Screening Platform for Lanthanide-Binding Peptides and ProteinsRobert Klassen, Anna Heider, Hannah Kugler, et al.
Angewandte Chemie (International Ed. in English)|December 20, 2002
The core structure of TMC-95A is a promising lead for reversible proteasome inhibitionMarkus Kaiser, Michael Groll, Christian Renner, et al.
Chemistry & Biology|June 24, 2006
TMC-95-based inhibitor design provides evidence for the catalytic versatility of the proteasomeMichael Groll, Marion Götz, Markus Kaiser, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2006
Inhibitor-binding mode of homobelactosin C to proteasomes: new insights into class I MHC ligand generationMichael Groll, Oleg V Larionov, Robert Huber, et al.
Chembiochem : a European Journal of Chemical Biology|January 29, 2005
Molecular machines for protein degradationMichael Groll, Matthias Bochtler, Hans Brandstetter, et al.
Journal of Molecular Biology|March 5, 2003
Investigations on the maturation and regulation of archaebacterial proteasomesMichael Groll, Hans Brandstetter, Hans Bartunik, et al.
Organic & Biomolecular Chemistry|March 19, 2014
Versatile C(3)-symmetric scaffolds and their use for covalent stabilization of the foldon trimerArne Berthelmann, Johannes Lach, Melissa A Gräwert, et al.
Journal of the American Chemical Society|September 11, 2025
Structure-Guided Engineering of a Bacterial Sesterterpene Synthase for Sesterviridene DiversificationHeng Li, Philip Troycke, Zhiyong Yin, et al.
Pageof 21