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Bioorganic & Medicinal Chemistry|April 23, 2003
Non-thiol farnesyltransferase inhibitors: N-(4-acylamino-3-benzoylphenyl)-3-[5-(4-nitrophenyl)-2-furyl]acrylic acid amidesKatja Kettler, Jacek Sakowski, Katrin Silber, et al.Archiv Der Pharmazie|September 7, 2007
Novel deoxyxylulosephosphate-reductoisomerase inhibitors: fosmidomycin derivatives with spacious acyl residuesRegina Ortmann, Jochen Wiesner, Katrin Silber, et al.Journal of Medicinal Chemistry|May 28, 2004
Assessing scoring functions for protein-ligand interactionsPhilippe Ferrara, Holger Gohlke, Daniel J Price, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|September 12, 2009
High-affinity inhibitors of tRNA-guanine transglycosylase replacing the function of a structural water clusterPhilipp C Kohler, Tina Ritschel, W Bernd Schweizer, et al.Journal of the American Society for Mass Spectrometry|August 8, 2012
Quantifying protein-ligand binding constants using electrospray ionization mass spectrometry: a systematic binding affinity study of a series of hydrophobically modified trypsin inhibitorsDragana Cubrilovic, Adam Biela, Frank Sielaff, et al.Journal of Medicinal Chemistry|May 23, 2012
Ligand binding stepwise disrupts water network in thrombin: enthalpic and entropic changes reveal classical hydrophobic effectAdam Biela, Frank Sielaff, Felix Terwesten, et al.Journal of Medicinal Chemistry|February 4, 2020
Protein-Induced Change in Ligand Protonation during Trypsin and Thrombin Binding: Hint on Differences in Selectivity Determinants of Both Proteins?Khang Ngo, Chelsey Collins-Kautz, Stefan Gerstenecker, et al.Journal of Molecular Biology|July 19, 2011
Two solutions for the same problem: multiple binding modes of pyrrolidine-based HIV-1 protease inhibitorsAndreas 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 conditionsHolger 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 bindingBernhard Stengl, Emmanuel A Meyer, Andreas Heine, et al.Pageof 25