4dma
From Proteopedia
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- | [[Image:4dma.jpg|left|200px]] | ||
- | < | + | ==Crystal structure of ERa LBD in complex with RU100132== |
- | + | <StructureSection load='4dma' size='340' side='right'caption='[[4dma]], [[Resolution|resolution]] 2.30Å' scene=''> | |
- | + | == Structural highlights == | |
- | or the | + | <table><tr><td colspan='2'>[[4dma]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4DMA OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4DMA FirstGlance]. <br> |
- | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.3Å</td></tr> | |
- | --> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=0L8:2-BROMO-6-(FURAN-3-YL)-4-(HYDROXYMETHYL)BIPHENYL-4-OL'>0L8</scene></td></tr> |
- | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4dma FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4dma OCA], [https://pdbe.org/4dma PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4dma RCSB], [https://www.ebi.ac.uk/pdbsum/4dma PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4dma ProSAT]</span></td></tr> | |
+ | </table> | ||
+ | == Function == | ||
+ | [https://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> | ||
- | == | + | ==See Also== |
- | + | *[[Estrogen receptor 3D structures|Estrogen receptor 3D structures]] | |
- | + | == References == | |
- | + | <references/> | |
- | + | __TOC__ | |
- | + | </StructureSection> | |
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
- | [[Category: Bourguet | + | [[Category: Large Structures]] |
- | [[Category: Brelivet | + | [[Category: Mus musculus]] |
- | [[Category: Cura | + | [[Category: Bourguet W]] |
- | [[Category: Eiler | + | [[Category: Brelivet Y]] |
- | [[Category: Moras | + | [[Category: Cura V]] |
- | [[Category: Osz | + | [[Category: Eiler S]] |
- | [[Category: Peluso-Iltis | + | [[Category: Moras D]] |
- | [[Category: Rochel | + | [[Category: Osz J]] |
- | [[Category: Ruff | + | [[Category: Peluso-Iltis C]] |
- | + | [[Category: Rochel N]] | |
- | + | [[Category: Ruff M]] | |
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Current revision
Crystal structure of ERa LBD in complex with RU100132
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Categories: Homo sapiens | Large Structures | Mus musculus | Bourguet W | Brelivet Y | Cura V | Eiler S | Moras D | Osz J | Peluso-Iltis C | Rochel N | Ruff M