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The entry | ==Crystal Structure of Human Protocadherin-15 EC2-3 V250N== | ||
<StructureSection load='6eb5' size='340' side='right'caption='[[6eb5]], [[Resolution|resolution]] 2.60Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[6eb5]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EB5 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EB5 FirstGlance]. <br> | |||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene></td></tr> | |||
[[Category: | <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=6eb5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6eb5 OCA], [http://pdbe.org/6eb5 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6eb5 RCSB], [http://www.ebi.ac.uk/pdbsum/6eb5 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6eb5 ProSAT]</span></td></tr> | ||
</table> | |||
== Disease == | |||
[[http://www.uniprot.org/uniprot/PCD15_HUMAN PCD15_HUMAN]] Usher syndrome type 1;Autosomal recessive non-syndromic sensorineural deafness type DFNB. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting distinct genetic loci, including 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/PCD15_HUMAN PCD15_HUMAN]] Calcium-dependent cell-adhesion protein. Essential for maintenance of normal retinal and cochlear function. | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Large Structures]] | |||
[[Category: Choudhary, D]] | |||
[[Category: Sotomayor, M]] | |||
[[Category: Calcium-binding protein]] | |||
[[Category: Cell adhesion]] | |||
[[Category: Hair cell]] | |||
[[Category: Mechanotransduction]] | |||
[[Category: Stereocilia]] | |||
[[Category: Tip link]] | |||
Revision as of 08:49, 21 August 2019
Crystal Structure of Human Protocadherin-15 EC2-3 V250NCrystal Structure of Human Protocadherin-15 EC2-3 V250N
Structural highlights
Disease[PCD15_HUMAN] Usher syndrome type 1;Autosomal recessive non-syndromic sensorineural deafness type DFNB. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting distinct genetic loci, including the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. Function[PCD15_HUMAN] Calcium-dependent cell-adhesion protein. Essential for maintenance of normal retinal and cochlear function. |
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