Estrogens: Difference between revisions

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<StructureSection load='1gwr' size='275' side='right' scene='' caption='Human estrogen receptor-ligand binding domain (grey) complex with transcription intermediate factor-2 peptide (pink) and estradiol (PDB code [[1gwr]])'>
<StructureSection load='1gwr' size='275' side='right' scene='' caption='Human estrogen receptor-ligand binding domain (grey) complex with transcription intermediate factor-2 peptide (pink) and estradiol (PDB code [[1gwr]])'>
Estrogens, their receptors and relevant proteins
'''Estrogens, their receptors and relevant proteins.'''
 
There are three major endogenous estrogens that have estrogenic hormonal activity: estrone (E1), estradiol (E2), and estriol (E3). Estradiol, an estrane, is the most potent and prevalent. <scene name='89/895670/Cv/1'>Estradiol</scene> is an important estrogen steroid hormone in both women and men. It is a typical steroid with core four-ring system (ABCD), composed of 17 carbon atoms. Another estrogen called estetrol (E4) is produced only during pregnancy.
*[[Estrogen receptor]]
*[[Estrogen receptor]]
<scene name='Estrogen_receptor/Cv/1'>Click here to see the difference between conformations</scene> of estrogen receptor α complexed with raloxifene and a corepressor peptide (morph was taken from [http://molmovdb.org/cgi-bin/movie.cgi Gallery of Morphs] of the [http://molmovdb.org Yale Morph Server]).
<scene name='Estrogen_receptor/Cv/1'>Click here to see the difference between conformations</scene> of estrogen receptor α complexed with raloxifene and a corepressor peptide (morph was taken from [http://molmovdb.org/cgi-bin/movie.cgi Gallery of Morphs] of the [http://molmovdb.org Yale Morph Server]).
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*[[Aromatase]]
*[[Aromatase]]
*[[Finasteride]]
*[[Finasteride]]
'''Estrone'''
*[[Estrogen receptor 3D structures]]
*[[Estrone sulfatase]]
*[[Sulfatase 3D structures]]
*[[ABC transporter 3D structures]]
*[[ABCG2 multidrug transporter]]
Substrates, such as estrone sulfate, <scene name='83/832932/Cavity_1_-_use2/4'>form hydrogen bonds and stacking interactions</scene> with residues from each subunit in Cavity 1 of ABCG2 multidrug transporter.
*[[Hydroxysteroid dehydrogenase]]
*[[Hydroxysteroid dehydrogenase 3D structures]]
*[[Prostaglandin F synthase]]
'''Estradiol'''
*[[Lipids: structure and classification]]
*[[Estrogen receptor]]
*[[Ivan Koutsopatriy estrogen receptor]]
*[[Estradiol 17-beta-dehydrogenase]]
*[[Student Project 10 for UMass Chemistry 423 Spring 2015]]
*[[Aromatase]]
*[[Sulfotransferase]]
*[[ATPase family AAA domain-containing protein 2]]
*[[Hypoxia-Inducible Factors]]
'''Estriol'''
*[[Cytochrome P450 3D structures]]: [[1x8v]] - MtP450 CYP51 (mutant)+estriol<br />
'''Estetrol'''
*[[3l03]] - Crystal Structure of human Estrogen Receptor alpha Ligand-Binding Domain in complex with a Glucocorticoid Receptor Interacting Protein 1 Nr Box II peptide and Estetrol (Estra-1,3,5(10)-triene-3,15 alpha,16alpha,17beta-tetrol)


</StructureSection>
</StructureSection>


See also:
See also:
*[[Estrogen receptor]]
*[[Nuclear receptors]]
*[[Nuclear receptors]]
*[[Steroid Hormones and their receptors]]


== References ==
== References ==
<references/>
<references/>

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

Alexander Berchansky, Michal Harel