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Current Opinion in Chemical Biology|June 24, 2008
New ways to target old receptorsAdrian Whitty, Thomas V RieraMethods in Molecular Biology (Clifton, N.J.)|June 19, 2016
Characterization of Inhibitor Binding Through Multiple Inhibitor Analysis: A Novel Local Fitting MethodThomas V Riera, Tim J Wigle, Robert A CopelandBiochemistry|July 23, 2008
A kinetic alignment of orthologous inosine-5'-monophosphate dehydrogenasesThomas V Riera, Wen Wang, Helen R Josephine, 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.Biochemistry|August 30, 2011
Allosteric activation via kinetic control: potassium accelerates a conformational change in IMP dehydrogenaseThomas V Riera, Lianqing Zheng, Helen R Josephine, et al.Biochemistry|February 6, 2016
CARM1 Preferentially Methylates H3R17 over H3R26 through a Random Kinetic MechanismSuzanne L Jacques, Katrina P Aquino, Jodi Gureasko, et al.Journal of the American Chemical Society|January 8, 2010
The structural basis of Cryptosporidium -specific IMP dehydrogenase inhibitor selectivityIain S Macpherson, Sivapriya Kirubakaran, Suresh Kumar Gorla, et al.The Journal of Biological Chemistry|January 31, 2015
Quantitative analysis of receptor tyrosine kinase-effector coupling at functionally relevant stimulus levelsSimin Li, Devayani Bhave, Jennifer M Chow, et al.Bioorganic & Medicinal Chemistry|June 24, 2004
Analogs of 1-phosphonooxy-2,2-dihydroxy-3-oxo-5-(methylthio)pentane, an acyclic intermediate in the methionine salvage pathway: a new preparation and characterization of activity with E1 enolase/phosphatase from Klebsiella oxytocaYalin Zhang, Melissa H Heinsen, Milka Kostic, et al.Chemistry & Biology|January 25, 2008
Targeting a prokaryotic protein in a eukaryotic pathogen: identification of lead compounds against cryptosporidiosisNwakaso N Umejiego, Deviprasad Gollapalli, Lisa Sharling, et al.Pageof 2