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Journal of Medicinal Chemistry
|
September 1, 1991
Crystallographic and molecular modeling studies on trypanosomal triosephosphate isomerase: a critical assessment of the predicted and observed structures of the complex with 2-phosphoglycerate
M E Noble, C L Verlinde, H Groendijk, et al.
Journal of Molecular Biology
|
May 24, 2001
Conformational changes in Leishmania mexicana glyceraldehyde-3-phosphate dehydrogenase induced by designed inhibitors
S Suresh, J C Bressi, K J Kennedy, et al.
Acta Crystallographica. Section C, Crystal Structure Communications
|
February 15, 1990
Structure of the neuroleptic drug 4-amino-N-1-[(1-ethyl-2-pyrrolidinyl)methyl]-5-(ethylsulfonyl)-2- methoxybenzamide (amisulpride)
H L De Winter, C L Verlinde, N M Blaton, et al.
The Journal of Biological Chemistry
|
July 3, 1999
Conformational changes in guanylyl cyclase-activating protein 1 (GCAP1) and its tryptophan mutants as a function of calcium concentration
I Sokal, A E Otto-Bruc, I Surgucheva, et al.
Protein Science : a Publication of the Protein Society
|
December 1, 1992
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, C J Witmans, T Pijning, et al.
The Journal of Biological Chemistry
|
January 8, 2000
Five members of a novel Ca(2+)-binding protein (CABP) subfamily with similarity to calmodulin
F Haeseleer, I Sokal, C L Verlinde, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 14, 1999
Structure-based design of submicromolar, biologically active inhibitors of trypanosomatid glyceraldehyde-3-phosphate dehydrogenase
A M Aronov, S Suresh, F S Buckner, et al.
Journal of Medicinal Chemistry
|
October 14, 1994
Selective inhibition of trypanosomal glyceraldehyde-3-phosphate dehydrogenase by protein structure-based design: toward new drugs for the treatment of sleeping sickness
C L Verlinde, M Callens, S Van Calenbergh, et al.
Journal of Medicinal Chemistry
|
November 7, 2000
Adenosine analogues as inhibitors of Trypanosoma brucei phosphoglycerate kinase: elucidation of a novel binding mode for a 2-amino-N(6)-substituted adenosine
J C Bressi, J Choe, M T Hough, et al.
Journal of Medicinal Chemistry
|
September 15, 1995
Synthesis and structure-activity relationships of analogs of 2'-deoxy-2'-(3-methoxybenzamido)adenosine, a selective inhibitor of trypanosomal glycosomal glyceraldehyde-3-phosphate dehydrogenase
S Van Calenbergh, C L Verlinde, J Soenens, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
Journal of Medicinal Chemistry
|
September 1, 1991
Crystallographic and molecular modeling studies on trypanosomal triosephosphate isomerase: a critical assessment of the predicted and observed structures of the complex with 2-phosphoglycerate
M E Noble, C L Verlinde, H Groendijk, et al.
Journal of Molecular Biology
|
May 24, 2001
Conformational changes in Leishmania mexicana glyceraldehyde-3-phosphate dehydrogenase induced by designed inhibitors
S Suresh, J C Bressi, K J Kennedy, et al.
Acta Crystallographica. Section C, Crystal Structure Communications
|
February 15, 1990
Structure of the neuroleptic drug 4-amino-N-1-[(1-ethyl-2-pyrrolidinyl)methyl]-5-(ethylsulfonyl)-2- methoxybenzamide (amisulpride)
H L De Winter, C L Verlinde, N M Blaton, et al.
The Journal of Biological Chemistry
|
July 3, 1999
Conformational changes in guanylyl cyclase-activating protein 1 (GCAP1) and its tryptophan mutants as a function of calcium concentration
I Sokal, A E Otto-Bruc, I Surgucheva, et al.
Protein Science : a Publication of the Protein Society
|
December 1, 1992
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, C J Witmans, T Pijning, et al.
The Journal of Biological Chemistry
|
January 8, 2000
Five members of a novel Ca(2+)-binding protein (CABP) subfamily with similarity to calmodulin
F Haeseleer, I Sokal, C L Verlinde, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 14, 1999
Structure-based design of submicromolar, biologically active inhibitors of trypanosomatid glyceraldehyde-3-phosphate dehydrogenase
A M Aronov, S Suresh, F S Buckner, et al.
Journal of Medicinal Chemistry
|
October 14, 1994
Selective inhibition of trypanosomal glyceraldehyde-3-phosphate dehydrogenase by protein structure-based design: toward new drugs for the treatment of sleeping sickness
C L Verlinde, M Callens, S Van Calenbergh, et al.
Journal of Medicinal Chemistry
|
November 7, 2000
Adenosine analogues as inhibitors of Trypanosoma brucei phosphoglycerate kinase: elucidation of a novel binding mode for a 2-amino-N(6)-substituted adenosine
J C Bressi, J Choe, M T Hough, et al.
Journal of Medicinal Chemistry
|
September 15, 1995
Synthesis and structure-activity relationships of analogs of 2'-deoxy-2'-(3-methoxybenzamido)adenosine, a selective inhibitor of trypanosomal glycosomal glyceraldehyde-3-phosphate dehydrogenase
S Van Calenbergh, C L Verlinde, J Soenens, et al.
Page
of 4