John F. Vickrey

“Wide-Open” 1.3 Å Structure of a Multidrug-Resistant HIV-1 Protease as a Drug Target

Philip D. Martin, John F. Vickrey, Gheorghe Proteasa et al. · Structure · 2005 · 98 citations · Full text

å Structure, Drug Target, Biochemistry +8

Crystal Structures of a Multidrug-Resistant Human Immunodeficiency Virus Type 1 Protease Reveal an Expanded Active-Site Cavity

B.C. Logsdon, John F. Vickrey, Philip D. Martin et al. · Journal of Virology · 2004 · 79 citations · Full text

Crystal Structure, Structural Bioinformatics, Biomolecular Structure Prediction +20

Aspartate transcarbamoylase genes of Pseudomonas putida: requirement for an inactive dihydroorotase for assembly into the dodecameric holoenzyme

Michael J. Schurr, John F. Vickrey, Amar Kumar et al. · Journal of Bacteriology · 1995 · 51 citations · Full text

Aldo-keto Reductase, Escherichia Coli, P. Putida Atcase +16

Contribution of the 80s loop of HIV-1 protease to the multidrug-resistance mechanism: crystallographic study of MDR769 HIV-1 protease variants

Ravikiran S. Yedidi, Georghe Proteasa, Jorge L. Martinez et al. · Acta Crystallographica Section D Biological Crystallography · 2011 · 33 citations · Full text

Crystal Structure, Protein Assembly, Biomolecular Structure Prediction +20

Pseudomonas aeruginosa Aspartate Transcarbamoylase

John F. Vickrey, Guy Hervé, David R. Evans · Journal of Biological Chemistry · 2002 · 25 citations · Full text