Nuclear receptors: Difference between revisions
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== 3-Ketosteroid receptors== | == 3-Ketosteroid receptors== | ||
===[[Androgen receptor]]=== | ===[[Androgen receptor]]=== | ||
=[[Glucocorticoid receptor]]= | ===[[Glucocorticoid receptor]]=== | ||
=[[Vitamin D receptor]]= | =[[Vitamin D receptor]]= | ||
</StructureSection> | </StructureSection> | ||
== References == | == References == | ||
<references/> | <references/> |
Revision as of 20:53, 25 January 2021
Under development!!! Nuclear receptor structure is composed of 5 domains - A/B: N-terminal regulatory domain contains activation function 1 (residues 101-370), activation function 5 (residues 360-485) and dimerization surface (residues 1-36 and 370-494). Thyroid Hormone Receptor-likePeroxisome Proliferator-Activated ReceptorsPPARγ
Estrogen Receptor-likeEstrogen receptorEstrogen receptor alpha
Estrogen receptor beta3-Ketosteroid receptorsAndrogen receptorGlucocorticoid receptorVitamin D receptor |
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ReferencesReferences
- ↑ Bohl CE, Wu Z, Chen J, Mohler ML, Yang J, Hwang DJ, Mustafa S, Miller DD, Bell CE, Dalton JT. Effect of B-ring substitution pattern on binding mode of propionamide selective androgen receptor modulators. Bioorg Med Chem Lett. 2008 Oct 15;18(20):5567-70. Epub 2008 Sep 5. PMID:18805694 doi:10.1016/j.bmcl.2008.09.002
- ↑ Li MJ, Greenblatt HM, Dym O, Albeck S, Pais A, Gunanathan C, Milstein D, Degani H, Sussman JL. Structure of estradiol metal chelate and estrogen receptor complex: The basis for designing a new class of selective estrogen receptor modulators. J Med Chem. 2011 Apr 7. PMID:21473635 doi:10.1021/jm200192y