5x8u

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'''Unreleased structure'''
 
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The entry 5x8u is ON HOLD until Paper Publication
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==Crystal Structure of the wild Human ROR gamma Ligand Binding Domain.==
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<StructureSection load='5x8u' size='340' side='right'caption='[[5x8u]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5x8u]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5X8U OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5X8U FirstGlance]. <br>
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</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&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5x8u FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5x8u OCA], [https://pdbe.org/5x8u PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5x8u RCSB], [https://www.ebi.ac.uk/pdbsum/5x8u PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5x8u ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/G1RH57_NOMLE G1RH57_NOMLE]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Retinoid-related orphan receptor gamma (RORgamma) directly controls the differentiation of Th17 cell and the production of interleukin-17, which plays an integral role in autoimmune diseases. To obtain insight into RORgamma, we have determined the first crystal structure of a ternary complex containing RORgamma ligand-binding domain (LBD) bound with a novel synthetic inhibitor and a repressor peptide, 22-mer peptide from silencing mediator of retinoic acid and thyroid hormone receptor (SMRT). Comparison of a binary complex of nonliganded (apo) RORgamma-LBD with a nuclear receptor co-activator (NCoA-1) peptide has shown that our inhibitor displays a unique mechanism different from those caused by natural inhibitor, ursolic acid (UA). The compound unprecedentedly induces indirect disruption of a hydrogen bond between His479 on helix 11 (H11) and Tyr502 on H12, which is crucial for active conformation. This crystallographic study will allow us to develop novel synthetic compounds for autoimmune disease therapy.
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Authors: Noguchi, M., Nomura, A., Murase, K., Doi, S., Yamaguchi, K., Adachi, T.
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Ternary complex of human RORgamma ligand-binding domain, inverse agonist and SMRT peptide shows a unique mechanism of corepressor recruitment.,Noguchi M, Nomura A, Murase K, Doi S, Yamaguchi K, Hirata K, Shiozaki M, Hirashima S, Kotoku M, Yamaguchi T, Katsuda Y, Steensma R, Li X, Tao H, Tse B, Fenn M, Babine R, Bradley E, Crowe P, Thacher S, Adachi T, Kamada M Genes Cells. 2017 Jun;22(6):535-551. doi: 10.1111/gtc.12494. Epub 2017 May 11. PMID:28493531<ref>PMID:28493531</ref>
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Description: Crystal Structure of the wild Human ROR gamma Ligand Binding Domain.
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Doi, S]]
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<div class="pdbe-citations 5x8u" style="background-color:#fffaf0;"></div>
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[[Category: Nomura, A]]
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[[Category: Murase, K]]
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==See Also==
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[[Category: Adachi, T]]
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*[[Nuclear receptor corepressor|Nuclear receptor corepressor]]
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[[Category: Noguchi, M]]
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== References ==
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[[Category: Yamaguchi, K]]
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Adachi T]]
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[[Category: Doi S]]
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[[Category: Murase K]]
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[[Category: Noguchi M]]
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[[Category: Nomura A]]
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[[Category: Yamaguchi K]]

Current revision

Crystal Structure of the wild Human ROR gamma Ligand Binding Domain.

PDB ID 5x8u

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