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Plos One
|
May 26, 2010
Synthesis of 5-hydroxyectoine from ectoine: crystal structure of the non-heme iron(II) and 2-oxoglutarate-dependent dioxygenase EctD
Klaus Reuter, Marco Pittelkow, Jan Bursy, et al.
Journal of Molecular Biology
|
June 13, 2009
Think twice: understanding the high potency of bis(phenyl)methane inhibitors of thrombin
Bernhard Baum, Laveena Muley, Andreas Heine, et al.
Proteins
|
March 14, 2014
High resolution crystal structure of Clostridium propionicum β-alanyl-CoA:ammonia lyase, a new member of the "hot dog fold" protein superfamily
Andreas Heine, Gloria Herrmann, Thorsten Selmer, et al.
Chemmedchem
|
November 3, 2022
Boroleucine-Derived Covalent Inhibitors of the ZIKV Protease
Niklas J Braun, Simon Huber, Luna C Schmacke, et al.
Journal of Medicinal Chemistry
|
May 23, 2012
Ligand binding stepwise disrupts water network in thrombin: enthalpic and entropic changes reveal classical hydrophobic effect
Adam Biela, Frank Sielaff, Felix Terwesten, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
May 12, 2016
Changing the selectivity profile - from substrate analog inhibitors of thrombin and factor Xa to potent matriptase inhibitors
Alexander Maiwald, Maya Hammami, Sebastian Wagner, et al.
Journal of Molecular Biology
|
February 17, 2010
Non-additivity of functional group contributions in protein-ligand binding: a comprehensive study by crystallography and isothermal titration calorimetry
Bernhard Baum, Laveena Muley, Michael Smolinski, et al.
Journal of Molecular Biology
|
July 19, 2011
Two solutions for the same problem: multiple binding modes of pyrrolidine-based HIV-1 protease inhibitors
Andreas Blum, Jark Böttcher, Stefanie Dörr, et al.
Journal of Molecular Biology
|
September 6, 2006
Expect the unexpected or caveat for drug designers: multiple structure determinations using aldose reductase crystals treated under varying soaking and co-crystallisation conditions
Holger Steuber, Matthias Zentgraf, Christof Gerlach, et al.
Journal of Molecular Biology
|
May 26, 2007
Crystal structures of tRNA-guanine transglycosylase (TGT) in complex with novel and potent inhibitors unravel pronounced induced-fit adaptations and suggest dimer formation upon substrate binding
Bernhard Stengl, Emmanuel A Meyer, Andreas Heine, et al.
Page
of 14
Search research articles
Search
Showing results (31-40 of 134) with videos related to
Sort By:
Page
of 14
Plos One
|
May 26, 2010
Synthesis of 5-hydroxyectoine from ectoine: crystal structure of the non-heme iron(II) and 2-oxoglutarate-dependent dioxygenase EctD
Klaus Reuter, Marco Pittelkow, Jan Bursy, et al.
Journal of Molecular Biology
|
June 13, 2009
Think twice: understanding the high potency of bis(phenyl)methane inhibitors of thrombin
Bernhard Baum, Laveena Muley, Andreas Heine, et al.
Proteins
|
March 14, 2014
High resolution crystal structure of Clostridium propionicum β-alanyl-CoA:ammonia lyase, a new member of the "hot dog fold" protein superfamily
Andreas Heine, Gloria Herrmann, Thorsten Selmer, et al.
Chemmedchem
|
November 3, 2022
Boroleucine-Derived Covalent Inhibitors of the ZIKV Protease
Niklas J Braun, Simon Huber, Luna C Schmacke, et al.
Journal of Medicinal Chemistry
|
May 23, 2012
Ligand binding stepwise disrupts water network in thrombin: enthalpic and entropic changes reveal classical hydrophobic effect
Adam Biela, Frank Sielaff, Felix Terwesten, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
May 12, 2016
Changing the selectivity profile - from substrate analog inhibitors of thrombin and factor Xa to potent matriptase inhibitors
Alexander Maiwald, Maya Hammami, Sebastian Wagner, et al.
Journal of Molecular Biology
|
February 17, 2010
Non-additivity of functional group contributions in protein-ligand binding: a comprehensive study by crystallography and isothermal titration calorimetry
Bernhard Baum, Laveena Muley, Michael Smolinski, et al.
Journal of Molecular Biology
|
July 19, 2011
Two solutions for the same problem: multiple binding modes of pyrrolidine-based HIV-1 protease inhibitors
Andreas Blum, Jark Böttcher, Stefanie Dörr, et al.
Journal of Molecular Biology
|
September 6, 2006
Expect the unexpected or caveat for drug designers: multiple structure determinations using aldose reductase crystals treated under varying soaking and co-crystallisation conditions
Holger Steuber, Matthias Zentgraf, Christof Gerlach, et al.
Journal of Molecular Biology
|
May 26, 2007
Crystal structures of tRNA-guanine transglycosylase (TGT) in complex with novel and potent inhibitors unravel pronounced induced-fit adaptations and suggest dimer formation upon substrate binding
Bernhard Stengl, Emmanuel A Meyer, Andreas Heine, et al.
Page
of 14