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Plos Computational Biology
|
February 24, 2015
Selectivity by small-molecule inhibitors of protein interactions can be driven by protein surface fluctuations
David K Johnson, John Karanicolas
Protein Science : a Publication of the Protein Society
|
September 19, 2002
The origins of asymmetry in the folding transition states of protein L and protein G
John Karanicolas, Charles L Brooks
Plos Computational Biology
|
March 19, 2013
Druggable protein interaction sites are more predisposed to surface pocket formation than the rest of the protein surface
David K Johnson, John Karanicolas
Journal of Chemical Information and Modeling
|
January 5, 2016
Ultra-High-Throughput Structure-Based Virtual Screening for Small-Molecule Inhibitors of Protein-Protein Interactions
David K Johnson, John Karanicolas
Nature Methods
|
March 2, 2010
Atomic accuracy in predicting and designing noncanonical RNA structure
Rhiju Das, John Karanicolas, David Baker
Plos One
|
July 17, 2015
DARC 2.0: Improved Docking and Virtual Screening at Protein Interaction Sites
Ragul Gowthaman, Sergey Lyskov, John Karanicolas
Plos One
|
August 27, 2013
Fast docking on graphics processing units via Ray-Casting
Karen R Khar, Lukasz Goldschmidt, John Karanicolas
Journal of Chemical Information and Modeling
|
July 25, 2013
Structural properties of non-traditional drug targets present new challenges for virtual screening
Ragul Gowthaman, Eric J Deeds, John Karanicolas
Plos One
|
October 21, 2015
Enhancements to the Rosetta Energy Function Enable Improved Identification of Small Molecules that Inhibit Protein-Protein Interactions
Andrea Bazzoli, Simon P Kelow, John Karanicolas
Journal of Computational Chemistry
|
October 25, 2016
Optimal allosteric stabilization sites using contact stabilization analysis
Alex Dickson, Christopher T Bailey, John Karanicolas
Page
of 8
Search research articles
Search
Showing results (11-20 of 78) with videos related to
Sort By:
Page
of 8
Plos Computational Biology
|
February 24, 2015
Selectivity by small-molecule inhibitors of protein interactions can be driven by protein surface fluctuations
David K Johnson, John Karanicolas
Protein Science : a Publication of the Protein Society
|
September 19, 2002
The origins of asymmetry in the folding transition states of protein L and protein G
John Karanicolas, Charles L Brooks
Plos Computational Biology
|
March 19, 2013
Druggable protein interaction sites are more predisposed to surface pocket formation than the rest of the protein surface
David K Johnson, John Karanicolas
Journal of Chemical Information and Modeling
|
January 5, 2016
Ultra-High-Throughput Structure-Based Virtual Screening for Small-Molecule Inhibitors of Protein-Protein Interactions
David K Johnson, John Karanicolas
Nature Methods
|
March 2, 2010
Atomic accuracy in predicting and designing noncanonical RNA structure
Rhiju Das, John Karanicolas, David Baker
Plos One
|
July 17, 2015
DARC 2.0: Improved Docking and Virtual Screening at Protein Interaction Sites
Ragul Gowthaman, Sergey Lyskov, John Karanicolas
Plos One
|
August 27, 2013
Fast docking on graphics processing units via Ray-Casting
Karen R Khar, Lukasz Goldschmidt, John Karanicolas
Journal of Chemical Information and Modeling
|
July 25, 2013
Structural properties of non-traditional drug targets present new challenges for virtual screening
Ragul Gowthaman, Eric J Deeds, John Karanicolas
Plos One
|
October 21, 2015
Enhancements to the Rosetta Energy Function Enable Improved Identification of Small Molecules that Inhibit Protein-Protein Interactions
Andrea Bazzoli, Simon P Kelow, John Karanicolas
Journal of Computational Chemistry
|
October 25, 2016
Optimal allosteric stabilization sites using contact stabilization analysis
Alex Dickson, Christopher T Bailey, John Karanicolas
Page
of 8