7zxt

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'''Unreleased structure'''
 
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The entry 7zxt is ON HOLD until Paper Publication
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==cryo-EM structure of Connexin 32 W3S mutation hemi channel==
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<StructureSection load='7zxt' size='340' side='right'caption='[[7zxt]], [[Resolution|resolution]] 2.90&Aring;' scene=''>
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Authors: Qi, C., Korkhov, V.M.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7zxt]] is a 6 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=7ZXT OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7ZXT FirstGlance]. <br>
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Description: cryo-EM structure of Connexin 32 W3S mutation hemi channel
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</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=7zxt FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7zxt OCA], [https://pdbe.org/7zxt PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7zxt RCSB], [https://www.ebi.ac.uk/pdbsum/7zxt PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7zxt ProSAT]</span></td></tr>
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[[Category: Unreleased Structures]]
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</table>
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[[Category: Korkhov, V.M]]
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== Disease ==
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[[Category: Qi, C]]
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[https://www.uniprot.org/uniprot/CXB1_HUMAN CXB1_HUMAN] X-linked Charcot-Marie-Tooth disease type 1;X-linked progressive cerebellar ataxia. The disease is caused by mutations affecting the gene represented in this entry. The gene represented in this entry may act as a disease modifier.
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== Function ==
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[https://www.uniprot.org/uniprot/CXB1_HUMAN CXB1_HUMAN] One gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell.
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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: Korkhov VM]]
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[[Category: Qi C]]

Revision as of 05:37, 31 May 2023

cryo-EM structure of Connexin 32 W3S mutation hemi channel

PDB ID 7zxt

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