Progesterone receptor: Difference between revisions

From Proteopedia
Jump to navigationJump to search
Michal Harel (talk | contribs)
New page: <StructureSection load='1p6o' size='350' side='right' caption='Structure of yeast cytosine deaminase complex with pyrimidine-based inhibitor, acetate, Ca+2 (green) and Zn+2 (grey) ions (PD...
 
Michal Harel (talk | contribs)
No edit summary
 
(15 intermediate revisions by 2 users not shown)
Line 1: Line 1:
<StructureSection load='1p6o' size='350' side='right' caption='Structure of yeast cytosine deaminase complex with pyrimidine-based inhibitor, acetate, Ca+2 (green) and Zn+2 (grey) ions (PDB entry [[1p6o]])' scene='55/551217/Cv/1'>
<StructureSection load='2w8y' size='350' side='right' caption='Structure of human progesterone receptor ligand-binding domain complex with RU486 and sulfate (PDB entry [[2w8y]])' scene='78/780972/Cv/2'>


<ref>PMID:21638687</ref>
== Function ==


== Function ==
'''Progesterone receptor''' (PR) binds to DNA and inhibits transcription. It is [[Nuclear receptors|nuclear receptor]]. The inhibition terminates when progesterone binds to PR.  The ovarian steroid progesterone which is essential for breast development and reproductive behavior, is mediated by PR<ref>PMID:19072517</ref>.


== Disease ==
See also [[Intracellular receptors]]


== Relevance ==
== Relevance ==
The response to hormone therapy in breast cancer correlates with PR.  PR absence in breast tumor cells predicts resistance to hormone therapy <ref>PMID:16234531</ref>.  [[Mometasone]] is a potent agonist of PR<ref>PMID:15189034</ref>.


== Structural highlights ==
== Structural highlights ==


 
The structure of the complex of the ligand-binding domain of PR with RU486 - an abortion-inducing drug - shows the ligand bound at a similar location to other agonists or partial agonists with a flexible loop of PR being a possible entry route to the <scene name='78/780972/Cv/4'>binding site and several PR-RU486 interactions</scene><ref>PMID:19372222</ref>. Water molecules are shown as red spheres. <scene name='89/895670/Cv/8'>Human progesterone receptor ligand-binding domain bound with progesterone</scene> ([[1a28]]).
</StructureSection>
</StructureSection>
== 3D Structures of progesterone receptor ==
== 3D Structures of progesterone receptor ==
Line 17: Line 19:
Updated on {{REVISIONDAY2}}-{{MONTHNAME|{{REVISIONMONTH}}}}-{{REVISIONYEAR}}
Updated on {{REVISIONDAY2}}-{{MONTHNAME|{{REVISIONMONTH}}}}-{{REVISIONYEAR}}
{{#tree:id=OrganizedByTopic|openlevels=0|
{{#tree:id=OrganizedByTopic|openlevels=0|
* Progesterone receptor residues 1-125
**[[1ejf]] – hPR - human<br />
* Progesterone receptor residues 72-195
**[[4x8y]] – hPR<br />


* Progesterone receptor DNA-binding domain residues 399-476
* Progesterone receptor DNA-binding domain residues 399-476


**[[2c7a]] – hPR DBD + DNA - human<br />
**[[2c7a]] – hPR DBD + DNA<br />


* Progesterone receptor ligand-binding domain residues 673-933
* Progesterone receptor ligand-binding domain residues 673-933

Latest revision as of 09:29, 18 January 2024

Structure of human progesterone receptor ligand-binding domain complex with RU486 and sulfate (PDB entry 2w8y)

Drag the structure with the mouse to rotate

3D Structures of progesterone receptor

Updated on 18-January-2024

References

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky