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Molecules (Basel, Switzerland)
|
June 27, 2024
Three-Dimensional Interaction Homology: Deconstructing Residue-Residue and Residue-Lipid Interactions in Membrane Proteins
Glen E Kellogg
American Journal of Botany
|
June 29, 2011
The structure and function of RuBisCO and their implications for systematic studies
E Kellogg, N Juliano
Current Topics in Medicinal Chemistry
|
November 26, 2009
Hydrophobicity--shake flasks, protein folding and drug discovery
Aurijit Sarkar, Glen E Kellogg
Proteins
|
October 23, 2009
A novel and efficient tool for locating and characterizing protein cavities and binding sites
Ashutosh Tripathi, Glen E Kellogg
Journal of Molecular Graphics
|
December 1, 1992
KEY, LOCK, and LOCKSMITH: complementary hydropathic map predictions of drug structure from a known receptor-receptor structure from known drugs
G E Kellogg, D J Abraham
Protein Science : a Publication of the Protein Society
|
August 1, 1996
Differences in hydropathic properties of ligand binding at four independent sites in wheat germ agglutinin-oligosaccharide crystal complexes
C S Wright, G E Kellogg
Journal of Computer-Aided Molecular Design
|
February 1, 1994
The effect of physical organic properties on hydrophobic fields
D J Abraham, G E Kellogg
Proteins
|
November 12, 2013
Intuitive, but not simple: including explicit water molecules in protein-protein docking simulations improves model quality
Hardik I Parikh, Glen E Kellogg
Frontiers in Molecular Biosciences
|
November 22, 2021
3D Interaction Homology: Computational Titration of Aspartic Acid, Glutamic Acid and Histidine Can Create pH-Tunable Hydropathic Environment Maps
Noah B Herrington, Glen E Kellogg
Journal of Computer-Aided Molecular Design
|
August 3, 2005
A computational tool to optimize ligand selectivity between two similar biomacromolecular targets
Deliang L Chen, Glen E Kellogg
Page
of 17
Search research articles
Search
Showing results (1-10 of 168) with videos related to
Sort By:
Page
of 17
Molecules (Basel, Switzerland)
|
June 27, 2024
Three-Dimensional Interaction Homology: Deconstructing Residue-Residue and Residue-Lipid Interactions in Membrane Proteins
Glen E Kellogg
American Journal of Botany
|
June 29, 2011
The structure and function of RuBisCO and their implications for systematic studies
E Kellogg, N Juliano
Current Topics in Medicinal Chemistry
|
November 26, 2009
Hydrophobicity--shake flasks, protein folding and drug discovery
Aurijit Sarkar, Glen E Kellogg
Proteins
|
October 23, 2009
A novel and efficient tool for locating and characterizing protein cavities and binding sites
Ashutosh Tripathi, Glen E Kellogg
Journal of Molecular Graphics
|
December 1, 1992
KEY, LOCK, and LOCKSMITH: complementary hydropathic map predictions of drug structure from a known receptor-receptor structure from known drugs
G E Kellogg, D J Abraham
Protein Science : a Publication of the Protein Society
|
August 1, 1996
Differences in hydropathic properties of ligand binding at four independent sites in wheat germ agglutinin-oligosaccharide crystal complexes
C S Wright, G E Kellogg
Journal of Computer-Aided Molecular Design
|
February 1, 1994
The effect of physical organic properties on hydrophobic fields
D J Abraham, G E Kellogg
Proteins
|
November 12, 2013
Intuitive, but not simple: including explicit water molecules in protein-protein docking simulations improves model quality
Hardik I Parikh, Glen E Kellogg
Frontiers in Molecular Biosciences
|
November 22, 2021
3D Interaction Homology: Computational Titration of Aspartic Acid, Glutamic Acid and Histidine Can Create pH-Tunable Hydropathic Environment Maps
Noah B Herrington, Glen E Kellogg
Journal of Computer-Aided Molecular Design
|
August 3, 2005
A computational tool to optimize ligand selectivity between two similar biomacromolecular targets
Deliang L Chen, Glen E Kellogg
Page
of 17