Research Topics
| Justin AshworthSummaryAffiliation: University of Washington Country: USA Publications
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Detail Information
Publications
Computational redesign of endonuclease DNA binding and cleavage specificityJustin Ashworth
Howard Hughes Medical Institute and Department of Biochemistry, University of Washington, Seattle, Washington 98195, USA
Nature 441:656-9. 2006..These results suggest that computational protein design methods can have an important role in the creation of novel highly specific endonucleases for gene therapy and other applications...
Assessment of the optimization of affinity and specificity at protein-DNA interfacesJustin Ashworth
Department of Biochemistry, University of Washington, Seattle, WA 98195, USA
Nucleic Acids Res 37:e73. 2009..The approach provides a complement to traditional methods of mutational analysis, and should be useful for rapidly formulating hypotheses about the roles of amino acid residues in protein-DNA interfaces...
Computational reprogramming of homing endonuclease specificity at multiple adjacent base pairsJustin Ashworth
Department of Biochemistry, University of Washington, Seattle, WA 98195, USA
Nucleic Acids Res 38:5601-8. 2010....
Exploitation of binding energy for catalysis and designSummer B Thyme
Department of Biochemistry, University of Washington, Seattle, Washington 98195, USA
Nature 461:1300-4. 2009..Our results illustrate how classical enzymology and modern protein design can each inform the other...
RosettaScripts: a scripting language interface to the Rosetta macromolecular modeling suiteSarel J Fleishman
Department of Biochemistry, University of Washington, Seattle, Washington, United States of America
PLoS ONE 6:e20161. 2011....
Thermodynamics of DNA target site recognition by homing endonucleasesJennifer H Eastberg
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, A3 025 Seattle, WA 98109, USA
Nucleic Acids Res 35:7209-21. 2007....
Slow-onset inhibition of fumarylacetoacetate hydrolase by phosphinate mimics of the tetrahedral intermediate: kinetics, crystal structure and pharmacokineticsRaynard L Bateman
Arthur F Scott Laboratory of Chemistry, Reed College, 3203 SE Woodstock Blvd, Portland, OR 97202, USA
Biochem J 402:251-60. 2007..These potent inhibitors provide a means to chemically phenocopy the metabolic defects of either HT1 or FAH knockout mice and promise future pharmacological utility for hepatocyte transplantation...
