S. Fong

Potent, novel in vitro inhibitors of the Pseudomonas aeruginosa deacetylase LpxC.

N. Andersen, C. Raetz, A. Erwin, 2002, Journal of medicinal chemistry.

Directed evolution of D-2-keto-3-deoxy-6-phosphogluconate aldolase to new variants for the efficient synthesis of D- and L-sugars.

C. Mak, S Fong, T D Machajewski, 2000, Chemistry & biology.

Wild-type and mutant bacteriorhodopsins D85N, D96N, and R82Q: purification to homogeneity, pH dependence of pumping, and electron diffraction.

L. Miercke, R. Stroud, A. Mitra, 1991, Biochemistry.

Partitioning of HIV-1 Gag and Gag-related proteins to membranes.

G. Zybarth, S. Scarlata, C. Carter, 1996, Biochemistry.

Structure of a non-peptide inhibitor complexed with HIV-1 protease. Developing a cycle of structure-based drug design.

I D Kuntz, I. Kuntz, P. Furth, 1997, The Journal of biological chemistry.

Wild-type and mutant bacterioopsins D85N, D96N, and R82Q: high-level expression in Escherichia coli.

L. Miercke, R. Stroud, A. Mitra, 1991, Biochemistry.