Polyoxometalate HIV-1 Protease Inhibitors. A New Mode of Protease Inhibition

Author:

Judd Deborah A.1,Nettles James H.1,Nevins Neysa1,Snyder James P.1,Liotta Dennis C.1,Tang Jordan1,Ermolieff Jacques1,Schinazi Raymond F.1,Hill Craig L.1

Affiliation:

1. Contribution from the Department of Chemistry, Emory University, Atlanta, Georgia 30322, Veterans Affairs Medical Center and Laboratory of Biochemical Pharmacology, Department of Pediatrics, Emory University School of Medicine, Decatur, Georgia 30033, and the Protein Studies Program, Oklahoma Medical Research Foundation and Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Reference105 articles.

1. Human immunodeficiency virus protease expressed in Escherichia coli exhibits autoprocessing and specific maturation of the gag precursor.

2. Abdel-Meguid, S.; Zhao, B.; Murthy, K. H. M.; Winborne, E.; Choi, J. K.; Desjarlais, R. L.; Minnich, M. D.; Culp, J. S.; Debouck, C.; Tomaszek, T. A., Jr.; Meek, T. D.; Dreyer, G. B. 1995, unpublished results.

3. Structure and evolution of a human erythroid transcription factor

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