1nav
From Proteopedia
m (Protected "1nav" [edit=sysop:move=sysop]) |
|||
Line 1: | Line 1: | ||
- | [[Image:1nav.png|left|200px]] | ||
- | |||
- | <!-- | ||
- | The line below this paragraph, containing "STRUCTURE_1nav", creates the "Structure Box" on the page. | ||
- | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
- | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
- | or leave the SCENE parameter empty for the default display. | ||
- | --> | ||
{{STRUCTURE_1nav| PDB=1nav | SCENE= }} | {{STRUCTURE_1nav| PDB=1nav | SCENE= }} | ||
- | |||
===Thyroid Receptor Alpha in complex with an agonist selective for Thyroid Receptor Beta1=== | ===Thyroid Receptor Alpha in complex with an agonist selective for Thyroid Receptor Beta1=== | ||
+ | {{ABSTRACT_PUBMED_12699376}} | ||
+ | ==Disease== | ||
+ | [[http://www.uniprot.org/uniprot/THA_HUMAN THA_HUMAN]] Defects in THRA are the cause of congenital hypothyroidism non-goitrous type 6 (CHNG6) [MIM:[http://omim.org/entry/614450 614450]]. A disease characterized by growth retardation, developmental retardation, skeletal dysplasia, borderline low thyroxine levels and high triiodothyronine levels. There is differential sensitivity to thyroid hormone action, with retention of hormone responsiveness in the hypothalamic pituitary axis and liver but skeletal, gastrointestinal, and myocardial resistance.<ref>PMID:22168587</ref> | ||
- | + | ==Function== | |
- | + | [[http://www.uniprot.org/uniprot/THA_HUMAN THA_HUMAN]] Nuclear hormone receptor. High affinity receptor for triiodothyronine. | |
- | + | ||
- | + | ||
- | + | ||
==About this Structure== | ==About this Structure== | ||
Line 22: | Line 13: | ||
==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID:012699376</ref><references group="xtra"/> | + | <ref group="xtra">PMID:012699376</ref><references group="xtra"/><references/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Bladh, L G.]] | [[Category: Bladh, L G.]] |
Revision as of 06:14, 25 March 2013
Contents |
Thyroid Receptor Alpha in complex with an agonist selective for Thyroid Receptor Beta1
Template:ABSTRACT PUBMED 12699376
Disease
[THA_HUMAN] Defects in THRA are the cause of congenital hypothyroidism non-goitrous type 6 (CHNG6) [MIM:614450]. A disease characterized by growth retardation, developmental retardation, skeletal dysplasia, borderline low thyroxine levels and high triiodothyronine levels. There is differential sensitivity to thyroid hormone action, with retention of hormone responsiveness in the hypothalamic pituitary axis and liver but skeletal, gastrointestinal, and myocardial resistance.[1]
Function
[THA_HUMAN] Nuclear hormone receptor. High affinity receptor for triiodothyronine.
About this Structure
1nav is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Ye L, Li YL, Mellstrom K, Mellin C, Bladh LG, Koehler K, Garg N, Garcia Collazo AM, Litten C, Husman B, Persson K, Ljunggren J, Grover G, Sleph PG, George R, Malm J. Thyroid receptor ligands. 1. Agonist ligands selective for the thyroid receptor beta1. J Med Chem. 2003 Apr 24;46(9):1580-8. PMID:12699376 doi:http://dx.doi.org/10.1021/jm021080f
- ↑ Bochukova E, Schoenmakers N, Agostini M, Schoenmakers E, Rajanayagam O, Keogh JM, Henning E, Reinemund J, Gevers E, Sarri M, Downes K, Offiah A, Albanese A, Halsall D, Schwabe JW, Bain M, Lindley K, Muntoni F, Vargha-Khadem F, Dattani M, Farooqi IS, Gurnell M, Chatterjee K. A mutation in the thyroid hormone receptor alpha gene. N Engl J Med. 2012 Jan 19;366(3):243-9. doi: 10.1056/NEJMoa1110296. Epub 2011 Dec, 14. PMID:22168587 doi:10.1056/NEJMoa1110296
Categories: Homo sapiens | Bladh, L G. | Collazo, A M.Garcia. | Garg, N. | George, R. | Grover, G. | Husman, B. | Koehler, K. | Li, Y L. | Litten, C. | Ljunggren, J. | Malm, J. | Mellin, C. | Mellstrom, K. | Persson, K. | Sleph, P G. | Ye, L. | Complex | Ligand | Membrane protein | Nuclear receptor | Thyroid receptor