6pfm
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of GDC-0927 bound to estrogen receptor alpha== | |
| - | + | <StructureSection load='6pfm' size='340' side='right'caption='[[6pfm]], [[Resolution|resolution]] 2.84Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[6pfm]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6PFM OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6PFM FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=OGJ:(2S)-2-(4-{2-[3-(fluoromethyl)azetidin-1-yl]ethoxy}phenyl)-3-(3-hydroxyphenyl)-4-methyl-2H-1-benzopyran-6-ol'>OGJ</scene></td></tr> | |
| - | [[Category: | + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6pet|6pet]]</td></tr> |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6pfm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6pfm OCA], [http://pdbe.org/6pfm PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6pfm RCSB], [http://www.ebi.ac.uk/pdbsum/6pfm PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6pfm ProSAT]</span></td></tr> |
| - | [[Category: Labadie, S | + | </table> |
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/ESR1_HUMAN ESR1_HUMAN]] Nuclear hormone receptor. The steroid hormones and their receptors are involved in the regulation of eukaryotic gene expression and affect cellular proliferation and differentiation in target tissues. Ligand-dependent nuclear transactivation involves either direct homodimer binding to a palindromic estrogen response element (ERE) sequence or association with other DNA-binding transcription factors, such as AP-1/c-Jun, c-Fos, ATF-2, Sp1 and Sp3, to mediate ERE-independent signaling. Ligand binding induces a conformational change allowing subsequent or combinatorial association with multiprotein coactivator complexes through LXXLL motifs of their respective components. Mutual transrepression occurs between the estrogen receptor (ER) and NF-kappa-B in a cell-type specific manner. Decreases NF-kappa-B DNA-binding activity and inhibits NF-kappa-B-mediated transcription from the IL6 promoter and displace RELA/p65 and associated coregulators from the promoter. Recruited to the NF-kappa-B response element of the CCL2 and IL8 promoters and can displace CREBBP. Present with NF-kappa-B components RELA/p65 and NFKB1/p50 on ERE sequences. Can also act synergistically with NF-kappa-B to activate transcription involving respective recruitment adjacent response elements; the function involves CREBBP. Can activate the transcriptional activity of TFF1. Also mediates membrane-initiated estrogen signaling involving various kinase cascades. Isoform 3 is involved in activation of NOS3 and endothelial nitric oxide production. Isoforms lacking one or several functional domains are thought to modulate transcriptional activity by competitive ligand or DNA binding and/or heterodimerization with the full length receptor. Isoform 3 can bind to ERE and inhibit isoform 1.<ref>PMID:7651415</ref> <ref>PMID:10970861</ref> <ref>PMID:9328340</ref> <ref>PMID:10681512</ref> <ref>PMID:10816575</ref> <ref>PMID:11477071</ref> <ref>PMID:11682626</ref> <ref>PMID:15078875</ref> <ref>PMID:16043358</ref> <ref>PMID:15891768</ref> <ref>PMID:16684779</ref> <ref>PMID:18247370</ref> <ref>PMID:17932106</ref> <ref>PMID:19350539</ref> <ref>PMID:20705611</ref> <ref>PMID:21937726</ref> <ref>PMID:21330404</ref> <ref>PMID:22083956</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Kiefer, J R]] | ||
| + | [[Category: Labadie, S S]] | ||
| + | [[Category: Li, J]] | ||
| + | [[Category: Liang, J]] | ||
[[Category: Ortwine, D]] | [[Category: Ortwine, D]] | ||
| - | + | [[Category: Ray, N C]] | |
| - | + | [[Category: Vinogradova, M]] | |
| - | + | ||
| - | [[Category: Ray, N | + | |
| - | [[Category: | + | |
[[Category: Wang, X]] | [[Category: Wang, X]] | ||
| - | [[Category: | + | [[Category: Zbieg, J R]] |
| + | [[Category: Zhang, B]] | ||
| + | [[Category: Antagonist]] | ||
| + | [[Category: Breast cancer]] | ||
| + | [[Category: Ligand]] | ||
| + | [[Category: Nuclear protein]] | ||
Revision as of 10:49, 17 July 2019
Crystal structure of GDC-0927 bound to estrogen receptor alpha
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Categories: Large Structures | Kiefer, J R | Labadie, S S | Li, J | Liang, J | Ortwine, D | Ray, N C | Vinogradova, M | Wang, X | Zbieg, J R | Zhang, B | Antagonist | Breast cancer | Ligand | Nuclear protein
