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Acta Crystallographica. Section D, Biological Crystallography|August 16, 2008
Structures of the wild-type and activated catalytic domains of Brachydanio rerio Polo-like kinase 1 (Plk1): changes in the active-site conformation and interactions with ligandsRobert A Elling, Raymond V Fucini, Michael J RomanowskiThe Biochemical Journal|July 4, 2006
Identification of a novel NADH-specific aldo-keto reductase using sequence and structural homologiesEric Di Luccio, Robert A Elling, David K WilsonStructure (London, England : 1993)|March 15, 2006
Structure-guided engineering of xylitol dehydrogenase cosubstrate specificityAndreas H Ehrensberger, Robert A Elling, David K WilsonBiochemistry|January 28, 2004
Structure of Toxoplasma gondii LDH1: active-site differences from human lactate dehydrogenases and the structural basis for efficient APAD+ useKathryn L Kavanagh, Robert A Elling, David K WilsonBioorganic & Medicinal Chemistry Letters|May 25, 2005
Discovery of selective aldo-keto reductase ligands--an on-bead assay strategySeth Dixon, Lori Robins, Robert A Elling, et al.Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|August 6, 2008
Structure of the Brachydanio rerio Polo-like kinase 1 (Plk1) catalytic domain in complex with an extended inhibitor targeting the adaptive pocket of the enzymeRobert A Elling, Raymond V Fucini, Emily J Hanan, et al.Proceedings of the National Academy of Sciences of the United States of America|September 30, 2016
Structure-guided enzymology of the lipid A acyltransferase LpxM reveals a dual activity mechanismDustin Dovala, Christopher M Rath, Qijun Hu, et al.Bioorganic & Medicinal Chemistry Letters|September 16, 2008
Design and synthesis of 2-amino-isoxazolopyridines as Polo-like kinase inhibitorsEmily J Hanan, Raymond V Fucini, Michael J Romanowski, et al.Protein Expression and Purification|April 17, 2007
Mouse Aurora A: expression in Escherichia coli and purificationRobert A Elling, Bradley T Tangonan, David M Penny, et al.Bioorganic & Medicinal Chemistry Letters|September 17, 2008
Design and synthesis of 2-amino-pyrazolopyridines as Polo-like kinase 1 inhibitorsRaymond V Fucini, Emily J Hanan, Michael J Romanowski, et al.Pageof 2