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Acta Crystallographica. Section D, Biological Crystallography
|
March 25, 1999
Rapid automated molecular replacement by evolutionary search
C R Kissinger, D K Gehlhaar, D B Fogel
Acta Crystallographica. Section D, Biological Crystallography
|
September 22, 2001
Molecular replacement by evolutionary search
C R Kissinger, D K Gehlhaar, B A Smith, et al.
Proteins
|
July 1, 1996
Exploring the energy landscapes of molecular recognition by a genetic algorithm: analysis of the requirements for robust docking of HIV-1 protease and FKBP-12 complexes
G M Verkhivker, P A Rejto, D K Gehlhaar, et al.
Journal of Medicinal Chemistry
|
February 3, 1995
De novo design of enzyme inhibitors by Monte Carlo ligand generation
D K Gehlhaar, K E Moerder, D Zichi, et al.
Chemistry & Biology
|
May 1, 1995
Molecular recognition of the inhibitor AG-1343 by HIV-1 protease: conformationally flexible docking by evolutionary programming
D K Gehlhaar, G M Verkhivker, P A Rejto, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
June 25, 1999
Thermodynamics and kinetics of ligand-protein binding studied with the weighted histogram analysis method and simulated annealing
D Bouzida, S Arthurs, A B Colson, et al.
Journal of Computer-Aided Molecular Design
|
December 29, 2000
Deciphering common failures in molecular docking of ligand-protein complexes
G M Verkhivker, D Bouzida, D K Gehlhaar, et al.
Journal of Molecular Recognition : JMR
|
December 28, 1999
Towards understanding the mechanisms of molecular recognition by computer simulations of ligand-protein interactions
G M Verkhivker, P A Rejto, D Bouzida, et al.
Proteins
|
December 18, 2001
Hierarchy of simulation models in predicting molecular recognition mechanisms from the binding energy landscapes: structural analysis of the peptide complexes with SH2 domains
G M Verkhivker, D Bouzida, D K Gehlhaar, et al.
Journal of Medicinal Chemistry
|
July 5, 1996
Bis tertiary amide inhibitors of the HIV-1 protease generated via protein structure-based iterative design
M Melnick, S H Reich, K K Lewis, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
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Acta Crystallographica. Section D, Biological Crystallography
|
March 25, 1999
Rapid automated molecular replacement by evolutionary search
C R Kissinger, D K Gehlhaar, D B Fogel
Acta Crystallographica. Section D, Biological Crystallography
|
September 22, 2001
Molecular replacement by evolutionary search
C R Kissinger, D K Gehlhaar, B A Smith, et al.
Proteins
|
July 1, 1996
Exploring the energy landscapes of molecular recognition by a genetic algorithm: analysis of the requirements for robust docking of HIV-1 protease and FKBP-12 complexes
G M Verkhivker, P A Rejto, D K Gehlhaar, et al.
Journal of Medicinal Chemistry
|
February 3, 1995
De novo design of enzyme inhibitors by Monte Carlo ligand generation
D K Gehlhaar, K E Moerder, D Zichi, et al.
Chemistry & Biology
|
May 1, 1995
Molecular recognition of the inhibitor AG-1343 by HIV-1 protease: conformationally flexible docking by evolutionary programming
D K Gehlhaar, G M Verkhivker, P A Rejto, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
June 25, 1999
Thermodynamics and kinetics of ligand-protein binding studied with the weighted histogram analysis method and simulated annealing
D Bouzida, S Arthurs, A B Colson, et al.
Journal of Computer-Aided Molecular Design
|
December 29, 2000
Deciphering common failures in molecular docking of ligand-protein complexes
G M Verkhivker, D Bouzida, D K Gehlhaar, et al.
Journal of Molecular Recognition : JMR
|
December 28, 1999
Towards understanding the mechanisms of molecular recognition by computer simulations of ligand-protein interactions
G M Verkhivker, P A Rejto, D Bouzida, et al.
Proteins
|
December 18, 2001
Hierarchy of simulation models in predicting molecular recognition mechanisms from the binding energy landscapes: structural analysis of the peptide complexes with SH2 domains
G M Verkhivker, D Bouzida, D K Gehlhaar, et al.
Journal of Medicinal Chemistry
|
July 5, 1996
Bis tertiary amide inhibitors of the HIV-1 protease generated via protein structure-based iterative design
M Melnick, S H Reich, K K Lewis, et al.
Page
of 1