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Current Opinion in Structural Biology|December 15, 2000
AB(5) toxins: structures and inhibitor designE Fan, E A Merritt, C L Verlinde, et al.Acta Crystallographica. Section D, Biological Crystallography|August 10, 2000
Structure of m-carboxyphenyl-alpha-D-galactopyranoside complexed to heat-labile enterotoxin at 1.3 A resolution: surprising variations in ligand-binding modesW E Minke, J Pickens, E A Merritt, et al.Journal of Molecular Biology|January 15, 1999
Structure-based discovery of a pore-binding ligand: towards assembly inhibitors for cholera and related AB5 toxinsB T Hovey, C L Verlinde, E A Merritt, et al.Structure (London, England : 1993)|July 15, 1994
Structure-based drug design: progress, results and challengesC L Verlinde, W G HolThe Journal of Biological Chemistry|November 24, 1999
Using a galactose library for exploration of a novel hydrophobic pocket in the receptor binding site of the Escherichia coli heat-labile enterotoxinW E Minke, F Hong, C L Verlinde, et al.Journal of Computer-Aided Molecular Design|April 1, 1992
In search of new lead compounds for trypanosomiasis drug design: a protein structure-based linked-fragment approachC L Verlinde, G Rudenko, W G HolBiochemistry|May 8, 1999
Structure-based exploration of the ganglioside GM1 binding sites of Escherichia coli heat-labile enterotoxin and cholera toxin for the discovery of receptor antagonistsW E Minke, C Roach, W G Hol, et al.Journal of Medicinal Chemistry|May 29, 1999
The role of waters in docking strategies with incremental flexibility for carbohydrate derivatives: heat-labile enterotoxin, a multivalent test caseW E Minke, D J Diller, W G Hol, et al.Journal of Medicinal Chemistry|November 21, 1998
Selective tight binding inhibitors of trypanosomal glyceraldehyde-3-phosphate dehydrogenase via structure-based drug designA M Aronov, C L Verlinde, W G Hol, et al.Pageof 32