7zxp: Difference between revisions

Line 1:

~~'''Unreleased structure'''~~

~~The entry~~ 7zxp is ~~ON HOLD until Paper Publication~~

==cryo-EM structure of Connexin 32 R22G mutation gap junction channel==

~~Authors~~: Qi, C., ~~Korkhov~~, V.M.

== Structural highlights ==

<table><tr><td colspan='2'>[[7zxp]] 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=7ZXP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7ZXP FirstGlance]. <br>

~~Description~~: ~~cryo~~-~~EM structure of Connexin 32 R22G mutation~~ gap junction ~~channel~~

</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=7zxp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7zxp OCA], [https://pdbe.org/7zxp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7zxp RCSB], [https://www.ebi.ac.uk/pdbsum/7zxp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7zxp ProSAT]</span></td></tr>

[[Category: ~~Unreleased~~ Structures]]

</table>

[[Category: Korkhov~~, V.M~~]]

== Disease ==

[[Category: Qi, C]]

[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]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 7zxp is ON HOLD  until Paper Publication
+==cryo-EM structure of Connexin 32 R22G mutation gap junction channel==
+<StructureSection load='7zxp' size='340' side='right'caption='[[7zxp]], [[Resolution|resolution]] 2.39&Aring;' scene=''>
-Authors: Qi, C., Korkhov, V.M.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[7zxp]] 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=7ZXP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7ZXP FirstGlance]. <br>
-Description: cryo-EM structure of Connexin 32 R22G mutation gap junction channel
+</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=7zxp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7zxp OCA], [https://pdbe.org/7zxp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7zxp RCSB], [https://www.ebi.ac.uk/pdbsum/7zxp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7zxp ProSAT]</span></td></tr>
-[[Category: Unreleased Structures]]
+</table>
-[[Category: Korkhov, V.M]]
+== Disease ==
-[[Category: Qi, C]]
+[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]]