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Journal of Medicinal Chemistry|December 2, 1999
Vancomycin binding to low-affinity ligands: delineating a minimum set of interactions necessary for high-affinity bindingP J Loll, J Kaplan, B S Selinsky, et al.Journal of Medicinal Chemistry|May 18, 2001
The role of sugar residues in molecular recognition by vancomycinJ Kaplan, B D Korty, P H Axelsen, et al.Annual Review of Biophysics and Biomolecular Structure|August 15, 2000
The structural biology of molecular recognition by vancomycinP J Loll, P H AxelsenBiochemistry|April 25, 2001
Structural analysis of NSAID binding by prostaglandin H2 synthase: time-dependent and time-independent inhibitors elicit identical enzyme conformationsB S Selinsky, K Gupta, C T Sharkey, et al.Chemistry & Biology|May 14, 1998
A ligand-mediated dimerization mode for vancomycinP J Loll, R Miller, C M Weeks, et al.Protein Science : a Publication of the Protein Society|September 7, 2000
Static light scattering studies of OmpF porin: implications for integral membrane protein crystallizationC Hitscherich, J Kaplan, M Allaman, et al.Molecular Pharmacology|November 28, 2001
O-acetylsalicylhydroxamic acid, a novel acetylating inhibitor of prostaglandin H2 synthase: structural and functional characterization of enzyme-inhibitor interactionsP J Loll, C T Sharkey, S J O'Connor, et al.Acta Crystallographica. Section D, Biological Crystallography|June 22, 2001
De novo structure determination of vancomycin aglycon using the anomalous scattering of chlorineP J LollBiochemistry|January 16, 1990
Effects of potassium on lipid-protein interactions in light sarcoplasmic reticulumB S Selinsky, P L YeagleBiochimica Et Biophysica Acta|February 28, 1985
Phospholipid exchange between restricted and nonrestricted domains in sarcoplasmic reticulum vesiclesB S Selinsky, P L YeaglePageof 185