Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM008537-10
Application #
6498473
Study Section
National Institute of General Medical Sciences Initial Review Group (BRT)
Program Officer
Rogers, Michael E
Project Start
1993-09-30
Project End
2006-06-30
Budget Start
2002-07-01
Budget End
2003-06-30
Support Year
10
Fiscal Year
2002
Total Cost
$217,144
Indirect Cost
Name
University of Utah
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Woods, Ryan D; O'Shea, Valerie L; Chu, Aurea et al. (2016) Structure and stereochemistry of the base excision repair glycosylase MutY reveal a mechanism similar to retaining glycosidases. Nucleic Acids Res 44:801-10
Watson, Lisa C; Kuchenbecker, Kristopher M; Schiller, Benjamin J et al. (2013) The glucocorticoid receptor dimer interface allosterically transmits sequence-specific DNA signals. Nat Struct Mol Biol 20:876-83
Brinkmeyer, Megan K; Pope, Mary Ann; David, Sheila S (2012) Catalytic contributions of key residues in the adenine glycosylase MutY revealed by pH-dependent kinetics and cellular repair assays. Chem Biol 19:276-86
Heaps, Nicole A; Poulter, C Dale (2011) Synthesis and evaluation of chlorinated substrate analogues for farnesyl diphosphate synthase. J Org Chem 76:1838-43
Nelson, Mary L; Kang, Hyun-Seo; Lee, Gregory M et al. (2010) Ras signaling requires dynamic properties of Ets1 for phosphorylation-enhanced binding to coactivator CBP. Proc Natl Acad Sci U S A 107:10026-31
Meijsing, Sebastiaan H; Pufall, Miles A; So, Alex Y et al. (2009) DNA binding site sequence directs glucocorticoid receptor structure and activity. Science 324:407-10
Workman, Hillary; Flynn, Peter F (2009) Stabilization of RNA oligomers through reverse micelle encapsulation. J Am Chem Soc 131:3806-7
Lee, Gregory M; Pufall, Miles A; Meeker, Charles A et al. (2008) The affinity of Ets-1 for DNA is modulated by phosphorylation through transient interactions of an unstructured region. J Mol Biol 382:1014-30
Rothman, Steven C; Johnston, Jonathan B; Lee, Sungwon et al. (2008) Type II isopentenyl diphosphate isomerase: irreversible inactivation by covalent modification of flavin. J Am Chem Soc 130:4906-13
Van Horn, Wade D; Ogilvie, Mark E; Flynn, Peter F (2008) Use of reverse micelles in membrane protein structural biology. J Biomol NMR 40:203-11

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