E. Winborne

发表

The crystal structures at 2.2-A resolution of hydroxyethylene-based inhibitors bound to human immunodeficiency virus type 1 protease show that the inhibitors are present in two distinct orientations.

K. Murthy, E. Winborne, M. Minnich, 1994 .

Rational design, synthesis, and crystallographic analysis of a hydroxyethylene-based HIV-1 protease inhibitor containing a heterocyclic P1'--P2' amide bond isostere.

R. DesJarlais, K. Murthy, E. Winborne, 1994, Journal of medicinal chemistry.

A check on rational drug design: crystal structure of a complex of human immunodeficiency virus type 1 protease with a novel gamma-turn mimetic inhibitor.

R. DesJarlais, E. Winborne, B. Zhao, 1995, Journal of medicinal chemistry.

2.9 Å crystal structure of ligand-free tryptophanyl-tRNA synthetase

C. Carter, E. Winborne, V. Ilyin, 1996 .

The three‐dimensional structure of recombinant bovine chymosin at 2.3 Å resolution

A. Wlodawer, E. Winborne, G. Gilliland, 1990, Proteins.

Inhibition of human immunodeficiency virus-1 protease by a C2-symmetric phosphinate. Synthesis and crystallographic analysis.

R. DesJarlais, K. Murthy, E. Winborne, 1993, Biochemistry.

A metal‐mediated hydride shift mechanism for xylose isomerase based on the 1.6 Å Streptomycs rubiginosus structure with xylitol and D‐xylose

T. Poulos, E. Winborne, G. Gilliland, 1991, Proteins.

CRYSTALLOGRAPHY OF BIOLOGICAL MACROMOLECULES

Stanislav, Cusack, C. Carter, 2005 .

Polymorphous crystallization and diffraction of threonine deaminase from Escherichia coli.

E. Winborne, G. Gilliland, E. Eisenstein, 1998, Acta crystallographica. Section D, Biological crystallography.

Crystallization and preliminary x-ray diffraction studies of subtilisin GX from Bacillus sp. GX6644.

D. R. Durham, T. Poulos, E. Winborne, 1987, The Journal of biological chemistry.

A preliminary crystallographic study of recombinant human interleukin 1 beta.

E. Winborne, G. Gilliland, Y. Hirai, 1987, The Journal of biological chemistry.

Three-dimensional structure of a simian immunodeficiency virus protease/inhibitor complex. Implications for the design of human immunodeficiency virus type 1 and 2 protease inhibitors.

Baoguang Zhao, E. Winborne, M. Minnich, 1993, Biochemistry.

Binding interactions of human interleukin 5 with its receptor alpha subunit. Large scale production, structural, and functional studies of Drosophila-expressed recombinant proteins.

S. Carr, M. Doyle, Baoguang Zhao, 1995, The Journal of biological chemistry.

An orally bioavailable HIV-1 protease inhibitor containing an imidazole-derived peptide bond replacement: crystallographic and pharmacokinetic analysis.

R. DesJarlais, Baoguang Zhao, K. Murthy, 1994, Biochemistry.