9rkx: Difference between revisions
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The entry | ==Atomic model of Cx43 gap junction channel rigid-body fitted to the in situ structure of the human Cx43 gap junction== | ||
<StructureSection load='9rkx' size='340' side='right'caption='[[9rkx]], [[Resolution|resolution]] 14.00Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[9rkx]] 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=9RKX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9RKX FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 14Å</td></tr> | |||
[[Category: | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9rkx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9rkx OCA], [https://pdbe.org/9rkx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9rkx RCSB], [https://www.ebi.ac.uk/pdbsum/9rkx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9rkx ProSAT]</span></td></tr> | ||
</table> | |||
== Disease == | |||
[https://www.uniprot.org/uniprot/CXA1_HUMAN CXA1_HUMAN] Autosomal recessive non-syndromic sensorineural deafness type DFNB;Hypoplastic left heart syndrome;Oculodentodigital dysplasia;Craniometaphyseal dysplasia;Syndactyly type 3. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease may be caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. | |||
== Function == | |||
[https://www.uniprot.org/uniprot/CXA1_HUMAN CXA1_HUMAN] Gap junction protein that acts as a regulator of bladder capacity. A 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. May play a critical role in the physiology of hearing by participating in the recycling of potassium to the cochlear endolymph. Negative regulator of bladder functional capacity: acts by enhancing intercellular electrical and chemical transmission, thus sensitizing bladder muscles to cholinergic neural stimuli and causing them to contract (By similarity). | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Eshriew E]] | |||
[[Category: Huiskonen JT]] | |||
[[Category: Kumpula E-P]] | |||
[[Category: Teli S]] | |||
Latest revision as of 09:29, 15 April 2026
Atomic model of Cx43 gap junction channel rigid-body fitted to the in situ structure of the human Cx43 gap junction
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