1nav | pdb_00001nav
From Proteopedia
Thyroid Receptor Alpha in complex with an agonist selective for Thyroid Receptor Beta1
| ||||||||||||
Structural highlights
DiseaseTHA_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] FunctionTHA_HUMAN Nuclear hormone receptor. High affinity receptor for triiodothyronine. Evolutionary Conservation![]() Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. See AlsoReferences
| ||||||||||||||||||||
This page was last modified 07:54, 14 February 2024.