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Results: 1-17 |
Results: 17
Conformational changes in Leishmania mexicana glyceraldehyde-3-phosphate dehydrogenase induced by designed inhibitors
Authors: Suresh, S Bressi, JC Kennedy, KJ Verlinde, CLMJ Gelb, MH Hol, WGJ
Citation: S. Suresh et al., Conformational changes in Leishmania mexicana glyceraldehyde-3-phosphate dehydrogenase induced by designed inhibitors, J MOL BIOL, 309(2), 2001, pp. 423-435
Adenosine analogues as selective inhibitors of glyceraldehyde-3-phosphate dehydrogenase of Trypanosomatidae via structure-based drug design
Authors: Bressi, JC Verlinde, CLMJ Aronov, AM Le Shaw, M Shin, SS Nguyen, LN Suresh, S Buckner, FS Van Voorhis, WC Kuntz, ID Hol, WGJ Gelb, MH
Citation: Jc. Bressi et al., Adenosine analogues as selective inhibitors of glyceraldehyde-3-phosphate dehydrogenase of Trypanosomatidae via structure-based drug design, J MED CHEM, 44(13), 2001, pp. 2080-2093
AB(5) toxins: structures and inhibitor design
Authors: Fan, EK Merritt, EA Verlinde, CLMJ Hol, WGJ
Citation: Ek. Fan et al., AB(5) toxins: structures and inhibitor design, CURR OP STR, 10(6), 2000, pp. 680-686
Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man
Authors: Cideciyan, AV Haeseleer, F Fariss, RN Aleman, TS Jang, GF Verlinde, CLMJ Marmor, MF Jacobson, SG Palczewski, K
Citation: Av. Cideciyan et al., Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man, VIS NEUROSC, 17(5), 2000, pp. 667-678
Structure of m-carboxyphenyl-alpha-D-galactopyranoside complexed to heat-labile enterotoxin at 1.3 angstrom resolution: surprising variations in ligand-binding modes
Authors: Minke, WE Pickens, J Merritt, EA Fan, EK Verlinde, CLMJ Hol, WGJ
Citation: We. Minke et al., Structure of m-carboxyphenyl-alpha-D-galactopyranoside complexed to heat-labile enterotoxin at 1.3 angstrom resolution: surprising variations in ligand-binding modes, ACT CRYST D, 56, 2000, pp. 795-804
Ca2+-binding proteins in the retina: from discovery to etiology of human disease
Authors: Sokal, I Li, N Verlinde, CLMJ Haeseleer, F Baehr, W Palczewski, K
Citation: I. Sokal et al., Ca2+-binding proteins in the retina: from discovery to etiology of human disease, BBA-MOL CEL, 1498(2-3), 2000, pp. 233-251
Adenosine analogues as inhibitors of Trypanosoma brucei phosphoglycerate kinase: Elucidation of a novel binding mode for a 2-amino-N-6-substituted adenosine
Authors: Bressi, JC Choe, J Hough, MT Buckner, FS Van Voorhis, WC Verlinde, CLMJ Hol, WGJ Gelb, MH
Citation: Jc. Bressi et al., Adenosine analogues as inhibitors of Trypanosoma brucei phosphoglycerate kinase: Elucidation of a novel binding mode for a 2-amino-N-6-substituted adenosine, J MED CHEM, 43(22), 2000, pp. 4135-4150
Five members of a novel Ca2+-binding protein (CABP) subfamily with similarity to calmodulin
Authors: Haeseleer, F Sokal, I Verlinde, CLMJ Erdjument-Bromage, H Tempst, P Pronin, AN Benovic, JL Fariss, RN Palczewski, K
Citation: F. Haeseleer et al., Five members of a novel Ca2+-binding protein (CABP) subfamily with similarity to calmodulin, J BIOL CHEM, 275(2), 2000, pp. 1247-1260
High-affinity pentavalent ligands of Escherichia coli heat-labile enterotoxin by modular structure-based design
Authors: Fan, EK Zhang, ZS Minke, WE Hou, Z Verlinde, CLMJ Hol, WGJ
Citation: Ek. Fan et al., High-affinity pentavalent ligands of Escherichia coli heat-labile enterotoxin by modular structure-based design, J AM CHEM S, 122(11), 2000, pp. 2663-2664
Structure-based reevaluation of the mechanism of class I fructose-1,6-bisphosphate aldolase
Authors: Verlinde, CLMJ Quigley, PM
Citation: Clmj. Verlinde et Pm. Quigley, Structure-based reevaluation of the mechanism of class I fructose-1,6-bisphosphate aldolase, J MOL MODEL, 5(3), 1999, pp. 37-45
A critical evaluation of several global optimization algorithms for the purpose of molecular docking
Authors: Diller, DJ Verlinde, CLMJ
Citation: Dj. Diller et Clmj. Verlinde, A critical evaluation of several global optimization algorithms for the purpose of molecular docking, J COMPUT CH, 20(16), 1999, pp. 1740-1751
Structure-based design of submicromolar, biologically active inhibitors oftrypanosomatid glyceraldehyde-3-phosphate dehydrogenase
Authors: Aronov, AM Suresh, S Buckner, FS Van Voorhis, WC Verlinde, CLMJ Opperdoes, FR Hol, WGJ Gelb, MH
Citation: Am. Aronov et al., Structure-based design of submicromolar, biologically active inhibitors oftrypanosomatid glyceraldehyde-3-phosphate dehydrogenase, P NAS US, 96(8), 1999, pp. 4273-4278
Structure-based discovery of a pore-binding ligand: Towards assembly inhibitors for cholera and related AB(5) toxins
Authors: Hovey, BT Verlinde, CLMJ Merritt, EA Hol, WGJ
Citation: Bt. Hovey et al., Structure-based discovery of a pore-binding ligand: Towards assembly inhibitors for cholera and related AB(5) toxins, J MOL BIOL, 285(3), 1999, pp. 1169-1178
The role of waters in docking strategies with incremental flexibility for carbohydrate derivatives: Heat-labile enterotoxin, a multivalent test case
Authors: Minke, WE Diller, DJ Hol, WGJ Verlinde, CLMJ
Citation: We. Minke et al., The role of waters in docking strategies with incremental flexibility for carbohydrate derivatives: Heat-labile enterotoxin, a multivalent test case, J MED CHEM, 42(10), 1999, pp. 1778-1788
Using a galactose library for exploration of a novel hydrophobic pocket inthe receptor binding site of the Escherichia coli heat-labile enterotoxin
Authors: Minke, WE Hong, F Verlinde, CLMJ Hol, WGJ Fan, E
Citation: We. Minke et al., Using a galactose library for exploration of a novel hydrophobic pocket inthe receptor binding site of the Escherichia coli heat-labile enterotoxin, J BIOL CHEM, 274(47), 1999, pp. 33469-33473
Conformational changes in guanylyl cyclase-activating protein 1 (GCAP1) and its tryptophan mutants as a function of calcium concentration
Authors: Sokal, I Otto-Bruc, AE Surgucheva, I Verlinde, CLMJ Wang, CK Baehr, W Palczewski, K
Citation: I. Sokal et al., Conformational changes in guanylyl cyclase-activating protein 1 (GCAP1) and its tryptophan mutants as a function of calcium concentration, J BIOL CHEM, 274(28), 1999, pp. 19829-19837
Structure-based exploration of the ganglioside GM1 binding sites of Escherichia coli heat-labile enterotoxin and cholera toxin for the discovery of receptor antagonists
Authors: Minke, WE Roach, C Hol, WGJ Verlinde, CLMJ
Citation: We. Minke et al., Structure-based exploration of the ganglioside GM1 binding sites of Escherichia coli heat-labile enterotoxin and cholera toxin for the discovery of receptor antagonists, BIOCHEM, 38(18), 1999, pp. 5684-5692
Risultati: 1-17 |