2n7i

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m (Protected "2n7i" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 2n7i is ON HOLD until Paper Publication
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==NMR structure of the prolactin receptor transmembrane domain==
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<StructureSection load='2n7i' size='340' side='right' caption='[[2n7i]], [[NMR_Ensembles_of_Models | 10 NMR models]]' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[2n7i]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2N7I OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2N7I FirstGlance]. <br>
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</td></tr><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=2n7i FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2n7i OCA], [http://pdbe.org/2n7i PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2n7i RCSB], [http://www.ebi.ac.uk/pdbsum/2n7i PDBsum]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/PRLR_HUMAN PRLR_HUMAN]] This is a receptor for the anterior pituitary hormone prolactin (PRL). Isoform 4 is unable to transduce prolactin signaling. Isoform 6 is unable to transduce prolactin signaling.<ref>PMID:12580759</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The prolactin receptor is an archetype member of the class I cytokine receptor family, comprising receptors with fundamental functions in biology as well as key drug targets. Structurally, each of these receptors represent an intriguing diversity, providing an exceptionally challenging target for structural biology. Here, we access the molecular architecture of the monomeric human prolactin receptor by combining experimental and computational efforts. We solve the NMR structure of its transmembrane domain in micelles and collect structural data on overlapping fragments of the receptor with small-angle X-ray scattering, native mass spectrometry and NMR spectroscopy. Along with previously published data, these are integrated by molecular modelling to generate a full receptor structure. The result provides the first full view of a class I cytokine receptor, exemplifying the architecture of more than 40 different receptor chains, and reveals that the extracellular domain is merely the tip of a molecular iceberg.
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Authors: Bugge, K., Kragelund, B.B.
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A combined computational and structural model of the full-length human prolactin receptor.,Bugge K, Papaleo E, Haxholm GW, Hopper JT, Robinson CV, Olsen JG, Lindorff-Larsen K, Kragelund BB Nat Commun. 2016 May 13;7:11578. doi: 10.1038/ncomms11578. PMID:27174498<ref>PMID:27174498</ref>
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Description: NMR structure of the prolactin receptor transmembrane 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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<div class="pdbe-citations 2n7i" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
[[Category: Bugge, K]]
[[Category: Bugge, K]]
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[[Category: Kragelund, B.B]]
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[[Category: Kragelund, B B]]
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[[Category: Hormone receptor]]
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[[Category: Membrane protein]]
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[[Category: Receptor]]
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[[Category: Transmembrane domain]]

Revision as of 08:22, 1 June 2016

NMR structure of the prolactin receptor transmembrane domain

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