C L Verlinde

Structure-based drug design: progress, results and challenges.

C L Verlinde, W G Hol, C. Verlinde, 1994, Structure.

Crystallographic and molecular modeling studies on trypanosomal triosephosphate isomerase: a critical assessment of the predicted and observed structures of the complex with 2-phosphoglycerate.

C L Verlinde, M. Noble, C. Verlinde, 1991, Journal of medicinal chemistry.

Structure of the complex between trypanosomal triosephosphate isomerase and N‐hydroxy‐4‐phosphono‐butanamide: Binding at the active site despite an “open” flexible loop conformation

C L Verlinde, F. Opperdoes, C. Verlinde, 1992, Protein science : a publication of the Protein Society.

Structure of m-carboxyphenyl-alpha-D-galactopyranoside complexed to heat-labile enterotoxin at 1.3 A resolution: surprising variations in ligand-binding modes.

E A Merritt, C L Verlinde, W G Hol, 2000, Acta crystallographica. Section D, Biological crystallography.

Anion binding at the active site of trypanosomal triosephosphate isomerase. Monohydrogen phosphate does not mimic sulphate.

C L Verlinde, M. Noble, C. Verlinde, 1991, European journal of biochemistry.

Structure-based exploration of the ganglioside GM1 binding sites of Escherichia coli heat-labile enterotoxin and cholera toxin for the discovery of receptor antagonists.

C L Verlinde, C. Verlinde, W. Hol, 1999, Biochemistry.

Crystal structure of glycosomal glyceraldehyde-3-phosphate dehydrogenase from Leishmania mexicana: implications for structure-based drug design and a new position for the inorganic phosphate binding site.

C L Verlinde, W G Hol, C. Verlinde, 1995, Biochemistry.

Glycolysis as a target for the design of new anti-trypanosome drugs.

C L Verlinde, F. Opperdoes, M. Gelb, 2001, Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy.

The role of waters in docking strategies with incremental flexibility for carbohydrate derivatives: heat-labile enterotoxin, a multivalent test case.

C L Verlinde, D J Diller, C. Verlinde, 1999, Journal of medicinal chemistry.