Articles
The 1.9 Å structure of human α-N-acetylgalactosaminidase The molecular basis of Schindler and Kanzaki diseases (with Nathaniel E. Clark), Journal of Molecular Biology (2010)
alpha-N-acetylgalactosaminidase (alpha-NAGAL; E.C. 3.2.1.49) is a lysosomal exoglycosidase that cleaves terminal alpha-N-acetylgalactosamine residues from glycopeptides...
Mutant α-galactosidase A enzymes identified in Fabry disease patients with residual enzyme activity: biochemical characterization and restoration of normal intracellular processing by 1-deoxygalactonojirimycin (with Satoshi Ishii, Hui-Hwa Chang, Kunito Kawasaki, Kayo Yasuda, Hui-Li Wu, and Jian-Qiang Fan), Biochemical Journal (2007)
Fabry disease is a lysosomal storage disorder caused by the deficiency of alpha-Gal A (alpha-galactosidase...
The 1.51-Angstrom structure of the poxvirus L1 protein, a target of potent neutralizing antibodies. (with Timothy J. Allison, Christiana Fogg, Bernard Moss, and David N. Garboczi), Proceedings of the National Academy of Sciences, USA (2005)
Although eradicated from nature more than two decades ago, the threat of smallpox has reemerged...