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Chemical Biology & Drug Design|February 12, 2009
CREDO: a protein-ligand interaction database for drug discoveryAdrian Schreyer, Tom BlundellJournal of Cheminformatics|November 8, 2012
USRCAT: real-time ultrafast shape recognition with pharmacophoric constraintsAdrian M Schreyer, Tom BlundellProteins|September 30, 2005
Functional restraints on the patterns of amino acid substitutions: application to sequence-structure homology recognitionVijayalakshmi Chelliah, Tom Blundell, Kenji MizuguchiJournal of Chemical Information and Modeling|February 18, 2014
Does a more precise chemical description of protein-ligand complexes lead to more accurate prediction of binding affinity?Pedro J Ballester, Adrian Schreyer, Tom L BlundellJournal of Computer-Aided Molecular Design|April 6, 2010
Annular tautomerism: experimental observations and quantum mechanics calculationsAurora J Cruz-Cabeza, Adrian Schreyer, William R PittChemical Biology & Drug Design|June 13, 2009
On the origins of enzyme inhibitor selectivity and promiscuity: a case study of protein kinase binding to staurosporineDuangrudee Tanramluk, Adrian Schreyer, William R Pitt, et al.International Journal of Biological Macromolecules|September 29, 2025
Crystal structure of dihydrodipicolinate synthase from Mycobacterium tuberculosis in complex with pyruvate and insights into allosteric regulationLuis Victor Santana Rosa, Beata Blaszczyk, Tom Blundell, et al.Plos One|December 15, 2012
What can we learn from the evolution of protein-ligand interactions to aid the design of new therapeutics?Alicia P Higueruelo, Adrian Schreyer, G Richard J Bickerton, et al.Chemical Biology & Drug Design|October 9, 2009
Atomic interactions and profile of small molecules disrupting protein-protein interfaces: the TIMBAL databaseAlícia P Higueruelo, Adrian Schreyer, G Richard J Bickerton, et al.Cancer Research|June 3, 2009
Targeting LMO2 with a peptide aptamer establishes a necessary function in overt T-cell neoplasiaAlex Appert, Chang-Hoon Nam, Natividad Lobato, et al.Pageof 2