7zxo: Difference between revisions
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==cryo-EM structure of Connexin 32 gap junction channel== | |||
<StructureSection load='7zxo' size='340' side='right'caption='[[7zxo]], [[Resolution|resolution]] 2.50Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[7zxo]] is a 12 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=7ZXO OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7ZXO FirstGlance]. <br> | |||
</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=7zxo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7zxo OCA], [https://pdbe.org/7zxo PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7zxo RCSB], [https://www.ebi.ac.uk/pdbsum/7zxo PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7zxo ProSAT]</span></td></tr> | |||
[[Category: | </table> | ||
[[Category: Korkhov | == Disease == | ||
[[Category: Qi | [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. | ||
== Function == | |||
[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. | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Korkhov VM]] | |||
[[Category: Qi C]] | |||
Revision as of 05:37, 31 May 2023
cryo-EM structure of Connexin 32 gap junction channel
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