Our research has been addressed in developing subtype-selective ligands for the Thyroid Hormone Receptor (TR). The lead compound we synthesized, GC-1, revealed interesting and potentially useful thyromimetic properties. This new compound, structurally related to the natural hormone T3, is a high affinity ligand for the TR and shows subtype selectivity for TR-beta over TR-alpha in both receptor binding and ligand-activation function. T3 is not subtype selective. The crystal structure of TR-beta ligand binding domain (LDB) bound with GC-1, TR-beta LDB bound with T3 and TR-alpha-1 LBD bound with T3 have been solved Visual inspection of these structure with the program MidasPlus and using the Computer Graphics Laboratory facilities has been essential in understanding the molecular basis for GC-1 subtype selectivity.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001081-22
Application #
6119127
Study Section
Project Start
1999-07-01
Project End
2000-06-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
22
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Kozak, John J; Gray, Harry B; Garza-López, Roberto A (2018) Relaxation of structural constraints during Amicyanin unfolding. J Inorg Biochem 179:135-145
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Kozak, John J; Gray, Harry B; Garza-López, Roberto A (2016) Cytochrome unfolding pathways from computational analysis of crystal structures. J Inorg Biochem 155:44-55
Amlong, Corey A; Perkins, Mark G; Houle, Timothy T et al. (2016) Contrasting Effects of the ?-Aminobutyric Acid Type A Receptor ?3 Subunit N265M Mutation on Loss of Righting Reflexes Induced by Etomidate and the Novel Anesthetic Barbiturate R-mTFD-MPAB. Anesth Analg 123:1241-1246

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