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Biochemistry|July 23, 2008
A kinetic alignment of orthologous inosine-5'-monophosphate dehydrogenasesThomas V Riera, Wen Wang, Helen R Josephine, et al.Journal of Chemical Information and Modeling|July 10, 2012
Relationship between hot spot residues and ligand binding hot spots in protein-protein interfacesBrandon S Zerbe, David R Hall, Sandor Vajda, et al.Chemical Science|June 24, 2021
Defining and navigating macrocycle chemical spaceLauren A Viarengo-Baker, Lauren E Brown, Anna A Rzepiela, et al.Journal of Medicinal Chemistry|July 21, 2022
Conformational Effects on the Passive Membrane Permeability of Synthetic MacrocyclesAnna A Rzepiela, Lauren A Viarengo-Baker, Victor Tatarskii, et al.Drug Discovery Today|February 20, 2016
Quantifying the chameleonic properties of macrocycles and other high-molecular-weight drugsAdrian Whitty, Mengqi Zhong, Lauren Viarengo, et al.Analytical Biochemistry|May 29, 2013
Determining the affinity and stoichiometry of interactions between unmodified proteins in solution using BiacoreEric S Day, Allan D Capili, Christopher W Borysenko, et al.Molecules (Basel, Switzerland)|April 28, 2015
Inhibition of Oncogenic Transcription Factor REL by the Natural Product Derivative Calafianin Monomer 101 Induces Proliferation Arrest and Apoptosis in Human B-Lymphoma Cell LinesAlan T Yeo, Spandan Chennamadhavuni, Adrian Whitty, et al.Biochemistry|April 14, 2004
Substitution of the conserved Arg-Tyr dyad selectively disrupts the hydrolysis phase of the IMP dehydrogenase reactionYollete V Guillén Schlippe, Thomas V Riera, Mohammad R Seyedsayamdost, et al.Journal of Medicinal Chemistry|August 1, 2015
New Frontiers in DruggabilityDima Kozakov, David R Hall, Raeanne L Napoleon, et al.Journal of Biomolecular Screening|August 12, 2005
Adopting a practical statistical approach for evaluating assay agreement in drug discoveryDongyu Sun, Adrian Whitty, James Papadatos, et al.Pageof 8