4lnw: Difference between revisions
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==Crystal structure of TR-alpha bound to T3 in a second site== | ==Crystal structure of TR-alpha bound to T3 in a second site== | ||
<StructureSection load='4lnw' size='340' side='right' caption='[[4lnw]], [[Resolution|resolution]] 1.90Å' scene=''> | <StructureSection load='4lnw' size='340' side='right'caption='[[4lnw]], [[Resolution|resolution]] 1.90Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[4lnw]] is a 1 chain structure with sequence from [ | <table><tr><td colspan='2'>[[4lnw]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4LNW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4LNW FirstGlance]. <br> | ||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CAS:S-(DIMETHYLARSENIC)CYSTEINE'>CAS</scene>, <scene name='pdbligand=T3:3,5,3TRIIODOTHYRONINE'>T3</scene></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4lnw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4lnw OCA], [https://pdbe.org/4lnw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4lnw RCSB], [https://www.ebi.ac.uk/pdbsum/4lnw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4lnw ProSAT]</span></td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | |||
</table> | </table> | ||
== Disease == | == Disease == | ||
[ | [https://www.uniprot.org/uniprot/THA_HUMAN THA_HUMAN] Defects in THRA are the cause of congenital hypothyroidism non-goitrous type 6 (CHNG6) [MIM:[https://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 == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/THA_HUMAN THA_HUMAN] Nuclear hormone receptor. High affinity receptor for triiodothyronine. | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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</div> | </div> | ||
<div class="pdbe-citations 4lnw" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 4lnw" style="background-color:#fffaf0;"></div> | ||
==See Also== | |||
*[[Thyroid hormone receptor|Thyroid hormone receptor]] | |||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: | [[Category: Large Structures]] | ||
[[Category: | [[Category: Aparicio R]] | ||
[[Category: | [[Category: Polikarpov I]] | ||
[[Category: | [[Category: Puhl AC]] | ||