2ll2: Difference between revisions

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 ==Structure of the Cx43 C-terminal domain bound to tubulin==
-<StructureSection load='2ll2' size='340' side='right' caption='[[2ll2]], [[NMR_Ensembles_of_Models | 10 NMR models]]' scene=''>
+<StructureSection load='2ll2' size='340' side='right'caption='[[2ll2]]' scene=''>
 == Structural highlights ==
-<table><tr><td colspan='2'>[[2ll2]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LL2 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2LL2 FirstGlance]. <br>
+<table><tr><td colspan='2'>[[2ll2]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LL2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LL2 FirstGlance]. <br>
-</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2ll2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ll2 OCA], [http://pdbe.org/2ll2 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2ll2 RCSB], [http://www.ebi.ac.uk/pdbsum/2ll2 PDBsum]</span></td></tr>
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</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=2ll2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ll2 OCA], [https://pdbe.org/2ll2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ll2 RCSB], [https://www.ebi.ac.uk/pdbsum/2ll2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ll2 ProSAT]</span></td></tr>
 </table>
 == Disease ==
-[[http://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.
+[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 ==
-[[http://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).
+[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).
 <div style="background-color:#fffaf0;">
 == Publication Abstract from PubMed ==
@@ Line 18: / Line 20: @@
 </div>
 <div class="pdbe-citations 2ll2" style="background-color:#fffaf0;"></div>
+==See Also==
+*[[Connexin 3D structure|Connexin 3D structure]]
 == References ==
 <references/>
 __TOC__
 </StructureSection>
-[[Category: Adjadj, E]]
+[[Category: Homo sapiens]]
-[[Category: Benmansour, K]]
+[[Category: Large Structures]]
-[[Category: Brikci-Nigassa, A Saidi]]
+[[Category: Adjadj E]]
-[[Category: Clement, M]]
+[[Category: Benmansour K]]
-[[Category: Curmi, P A]]
+[[Category: Clement M]]
-[[Category: Ha-Duong, T]]
+[[Category: Curmi PA]]
-[[Category: Pastre, D]]
+[[Category: Ha-Duong T]]
-[[Category: Ziani, L]]
+[[Category: Pastre D]]
-[[Category: Membrane protein]]
+[[Category: Saidi Brikci-Nigassa A]]
+[[Category: Ziani L]]