A. Mistry

发表

Specificity of antibodies to immunodominant mycobacterial antigens in pulmonary tuberculosis

D. Young, G. Bothamley, J. Ivanyi, 1988, Journal of clinical microbiology.

Sulfoximine-substituted trifluoromethylpyrimidine analogs as inhibitors of proline-rich tyrosine kinase 2 (PYK2) show reduced hERG activity.

Li Xing, Leonard Buckbinder, Amy Baumann, 2009, Bioorganic & medicinal chemistry letters.

Structure of UDP-N-acetylglucosamine enolpyruvyl transferase, an enzyme essential for the synthesis of bacterial peptidoglycan, complexed with substrate UDP-N-acetylglucosamine and the drug fosfomycin.

A. Wonacott, T. Skarzynski, V. Kelly, 1996, Structure.

Crystal structure of cholesteryl ester transfer protein reveals a long tunnel and four bound lipid molecules

Ing-Kae Wang, Xiayang Qiu, Dennis E Danley, 2007, Nature Structural &Molecular Biology.

Crystallographic analysis of triclosan bound to enoyl reductase.

D. Rice, P. Baker, J. Rafferty, 1999, Journal of molecular biology.

Purification and characterization of the herpes simplex virus type 1 ribonucleotide reductase small subunit following expression in Escherichia coli.

M. Weir, H. Marsden, H. Lankinen, 1991, The Journal of general virology.

Purification and characterization of the herpes simplex virus type 1 ribonucleotide reductase small subunit following expression in Escherichia coil

M. Weir, H. Marsden, H. Lankinen, 2007 .

Redesigning and characterizing the substrate specificity and activity of Vibrio fluvialis aminotransferase for the synthesis of imagabalin.

D. Gehlhaar, S. Govindarajan, J. Minshull, 2013, Protein engineering, design & selection : PEDS.

Structural Characterization of Proline-rich Tyrosine Kinase 2 (PYK2) Reveals a Unique (DFG-out) Conformation and Enables Inhibitor Design

Leonard Buckbinder, Daniel P. Walker, L. Buckbinder, 2009, Journal of Biological Chemistry.

Kinetic and structural characteristics of the inhibition of enoyl (acyl carrier protein) reductase by triclosan.

I. Taylor, R. Pauptit, C. Minshull, 1999, Biochemistry.

Phosphorylation of serine residues in histidine-tag sequences attached to recombinant protein kinases: a cause of heterogeneity in mass and complications in function.

P. Lemotte, K. Coleman, K. Geoghegan, 2005, Protein expression and purification.

Trifluoromethylpyrimidine-based inhibitors of proline-rich tyrosine kinase 2 (PYK2): structure-activity relationships and strategies for the elimination of reactive metabolite formation.

Leonard Buckbinder, Jacquelyn Klug-McLeod, Angel Guzman-Perez, 2008, Bioorganic & medicinal chemistry letters.

A new method for bromination of carbazoles, β-carbolines and iminodibenzyls by use of N-bromosuccinimide and silica gel

D. Faulkner, Keith Smith, A. Mistry, 1992 .

Two distinct approaches to crystallization results-recording databases.

A M Hassell, T J Harrocks, E H Dashman, 1994, Acta crystallographica. Section D, Biological crystallography.

Crystal Structures of Cholesteryl Ester Transfer Protein in Complex with Inhibitors

M. Griffor, Shenping Liu, X. Qiu, 2012, The Journal of Biological Chemistry.

Crystal structure of the anti-fungal target N-myristoyl transferase

J. Irwin, I. Taylor, G. Bricogne, 1998, Nature Structural Biology.

Specificity ofAntibodies toImmunodominant Mycobacterial Antigens inPulmonary Tuberculosis

A. Mistry, 1988 .

Characterization of the active site of S. aureus monofunctional glycosyltransferase (Mtg) by site-directed mutation and structural analysis of the protein complexed with moenomycin.

Alita A. Miller, H. Heaslet, A. Mistry, 2009, Journal of structural biology.

The design and synthesis of human branched-chain amino acid aminotransferase inhibitors for treatment of neurodegenerative diseases.

R. T. Carroll, Xiaohong Liu, J. Rubin, 2006, Bioorganic & medicinal chemistry letters.