6y2h
From Proteopedia
(Difference between revisions)
Line 3: | Line 3: | ||
<StructureSection load='6y2h' size='340' side='right'caption='[[6y2h]], [[Resolution|resolution]] 2.15Å' scene=''> | <StructureSection load='6y2h' size='340' side='right'caption='[[6y2h]], [[Resolution|resolution]] 2.15Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[6y2h]] is a 4 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[6y2h]] is a 4 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=6Y2H OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6Y2H FirstGlance]. <br> |
- | </td></tr><tr id=' | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.154Å</td></tr> |
- | <tr id=' | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=SCN:THIOCYANATE+ION'>SCN</scene></td></tr> |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6y2h FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6y2h OCA], [https://pdbe.org/6y2h PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6y2h RCSB], [https://www.ebi.ac.uk/pdbsum/6y2h PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6y2h ProSAT]</span></td></tr> |
</table> | </table> | ||
== Disease == | == Disease == | ||
- | [ | + | [https://www.uniprot.org/uniprot/CLIC5_HUMAN CLIC5_HUMAN] Autosomal recessive non-syndromic sensorineural deafness type DFNB. The disease is caused by mutations affecting the gene represented in this entry. |
== Function == | == Function == | ||
- | [ | + | [https://www.uniprot.org/uniprot/CLIC5_HUMAN CLIC5_HUMAN] Required for normal hearing (PubMed:24781754). It is necessary for the formation of stereocilia in the inner ear and normal development of the organ of Corti (By similarity). Can insert into membranes and form poorly selective ion channels that may also transport chloride ions. May play a role in the regulation of transepithelial ion absorption and secretion. Is required for the development and/or maintenance of the proper glomerular endothelial cell and podocyte architecture (PubMed:15184393, PubMed:18028448, PubMed:20335315). Plays a role in formation of the lens suture in the eye, which is important for normal optical properties of the lens (By similarity).[UniProtKB:Q8BXK9]<ref>PMID:15184393</ref> <ref>PMID:18028448</ref> <ref>PMID:20335315</ref> <ref>PMID:24781754</ref> |
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
Line 28: | Line 28: | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: Ferofontov | + | [[Category: Ferofontov A]] |
- | [[Category: Giladi | + | [[Category: Giladi M]] |
- | [[Category: Haitin | + | [[Category: Haitin Y]] |
- | + | ||
- | + | ||
- | + | ||
- | + |
Current revision
The crystal structure of human chloride intracellular channel protein 5
|