7p5c

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(New page: '''Unreleased structure''' The entry 7p5c is ON HOLD Authors: Description: Category: Unreleased Structures)
Current revision (09:07, 8 September 2021) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 7p5c is ON HOLD
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==Cryo-EM structure of human TTYH3 in Ca2+ and GDN==
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<StructureSection load='7p5c' size='340' side='right'caption='[[7p5c]], [[Resolution|resolution]] 3.20&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7p5c]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7P5C OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7P5C FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr>
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<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">TTYH3, KIAA1691 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=7p5c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7p5c OCA], [https://pdbe.org/7p5c PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7p5c RCSB], [https://www.ebi.ac.uk/pdbsum/7p5c PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7p5c ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[https://www.uniprot.org/uniprot/TTYH3_HUMAN TTYH3_HUMAN]] Probable large-conductance Ca(2+)-activated chloride channel. May play a role in Ca(2+) signal transduction.<ref>PMID:15010458</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The Tweety homologs (TTYHs) are members of a conserved family of eukaryotic membrane proteins that are abundant in the brain. The three human paralogs were assigned to function as anion channels that are either activated by Ca(2+) or cell swelling. To uncover their unknown architecture and its relationship to function, we have determined the structures of human TTYH1-3 by cryo-electron microscopy. All structures display equivalent features of a dimeric membrane protein that contains five transmembrane segments and an extended extracellular domain. As none of the proteins shows attributes reminiscent of an anion channel, we revisited functional experiments and did not find any indication of ion conduction. Instead, we find density in an extended hydrophobic pocket contained in the extracellular domain that emerges from the lipid bilayer, which suggests a role of TTYH proteins in the interaction with lipid-like compounds residing in the membrane.
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Authors:
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Cryo-EM structures of the TTYH family reveal a novel architecture for lipid interactions.,Sukalskaia A, Straub MS, Deneka D, Sawicka M, Dutzler R Nat Commun. 2021 Aug 12;12(1):4893. doi: 10.1038/s41467-021-25106-4. PMID:34385445<ref>PMID:34385445</ref>
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Description:
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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 7p5c" 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>
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[[Category: Human]]
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[[Category: Large Structures]]
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[[Category: Deneka, D]]
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[[Category: Dutzler, R]]
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[[Category: Sawicka, M]]
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[[Category: Straub, M S]]
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[[Category: Sukalskaia, A]]
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[[Category: Lipid metabolism]]
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[[Category: Lipid transport]]
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[[Category: Membrane protein]]

Current revision

Cryo-EM structure of human TTYH3 in Ca2+ and GDN

PDB ID 7p5c

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