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Andreas Heine

Showing results (71-80 of 134) with videos related to

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Journal of Medicinal Chemistry|October 7, 2011
A small nonrule of 3 compatible fragment library provides high hit rate of endothiapepsin crystal structures with various fragment chemotypesHelene Köster, Tobias Craan, Sascha Brass, et al.
Angewandte Chemie (International Ed. in English)|September 29, 2007
Thermodynamic inhibition profile of a cyclopentyl and a cyclohexyl derivative towards thrombin: the same but for different reasonsChristof Gerlach, Michael Smolinski, Holger Steuber, et al.
Angewandte Chemie (International Ed. in English)|October 12, 2013
Structure of active coagulation factor XIII triggered by calcium binding: basis for the design of next-generation anticoagulantsMartin Stieler, Johannes Weber, Martin Hils, et al.
Virology|May 13, 2019
Structural basis for catalysis and substrate specificity of a 3C-like cysteine protease from a mosquito mesonivirusManuel Kanitz, Sandra Blanck, Andreas Heine, et al.
ACS Omega|December 11, 2023
Crystallographic Fragment Screening on the <i>Shigella</i> Type III Secretion System Chaperone IpgCMarina Gárdonyi, Christian Hasewinkel, Johanna Wallbaum, et al.
ACS Omega|August 5, 2024
Development of a Crystallographic Screening to Identify Sudan Virus VP40 LigandsAnke-Dorothee Werner, Nils Krapoth, Michael J Norris, et al.
Journal of Medicinal Chemistry|July 1, 2016
New Insights into Human 17β-Hydroxysteroid Dehydrogenase Type 14: First Crystal Structures in Complex with a Steroidal Ligand and with a Potent Nonsteroidal InhibitorNicole Bertoletti, Florian Braun, Mahalia Lepage, et al.
Acta Crystallographica. Section D, Biological Crystallography|September 4, 2013
High-affinity inhibitors of Zymomonas mobilis tRNA-guanine transglycosylase through convergent optimizationLuzi Jakob Barandun, Florian Immekus, Philipp C Kohler, et al.
Biomolecules|December 24, 2021
Which Properties Allow Ligands to Open and Bind to the Transient Binding Pocket of Human Aldose Reductase?Anna Sandner, Khang Ngo, Christoph P Sager, et al.
Chemmedchem|August 8, 2006
Unexpected novel binding mode of pyrrolidine-based aspartyl protease inhibitors: design, synthesis and crystal structure in complex with HIV proteaseEdgar Specker, Jark Böttcher, Sascha Brass, et al.
Pageof 14

Showing results (71-80 of 134) with videos related to

Sort By:
Pageof 14
Journal of Medicinal Chemistry|October 7, 2011
A small nonrule of 3 compatible fragment library provides high hit rate of endothiapepsin crystal structures with various fragment chemotypesHelene Köster, Tobias Craan, Sascha Brass, et al.
Angewandte Chemie (International Ed. in English)|September 29, 2007
Thermodynamic inhibition profile of a cyclopentyl and a cyclohexyl derivative towards thrombin: the same but for different reasonsChristof Gerlach, Michael Smolinski, Holger Steuber, et al.
Angewandte Chemie (International Ed. in English)|October 12, 2013
Structure of active coagulation factor XIII triggered by calcium binding: basis for the design of next-generation anticoagulantsMartin Stieler, Johannes Weber, Martin Hils, et al.
Virology|May 13, 2019
Structural basis for catalysis and substrate specificity of a 3C-like cysteine protease from a mosquito mesonivirusManuel Kanitz, Sandra Blanck, Andreas Heine, et al.
ACS Omega|December 11, 2023
Crystallographic Fragment Screening on the <i>Shigella</i> Type III Secretion System Chaperone IpgCMarina Gárdonyi, Christian Hasewinkel, Johanna Wallbaum, et al.
ACS Omega|August 5, 2024
Development of a Crystallographic Screening to Identify Sudan Virus VP40 LigandsAnke-Dorothee Werner, Nils Krapoth, Michael J Norris, et al.
Journal of Medicinal Chemistry|July 1, 2016
New Insights into Human 17β-Hydroxysteroid Dehydrogenase Type 14: First Crystal Structures in Complex with a Steroidal Ligand and with a Potent Nonsteroidal InhibitorNicole Bertoletti, Florian Braun, Mahalia Lepage, et al.
Acta Crystallographica. Section D, Biological Crystallography|September 4, 2013
High-affinity inhibitors of Zymomonas mobilis tRNA-guanine transglycosylase through convergent optimizationLuzi Jakob Barandun, Florian Immekus, Philipp C Kohler, et al.
Biomolecules|December 24, 2021
Which Properties Allow Ligands to Open and Bind to the Transient Binding Pocket of Human Aldose Reductase?Anna Sandner, Khang Ngo, Christoph P Sager, et al.
Chemmedchem|August 8, 2006
Unexpected novel binding mode of pyrrolidine-based aspartyl protease inhibitors: design, synthesis and crystal structure in complex with HIV proteaseEdgar Specker, Jark Böttcher, Sascha Brass, et al.
Pageof 14