6kz1
From Proteopedia
(Difference between revisions)
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| - | ==== | + | ==Complex structure of Whirlin and Myosin XVa== |
| - | <StructureSection load='6kz1' size='340' side='right'caption='[[6kz1]]' scene=''> | + | <StructureSection load='6kz1' size='340' side='right'caption='[[6kz1]], [[Resolution|resolution]] 1.69Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id= OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol= FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6kz1]] is a 2 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=6KZ1 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6KZ1 FirstGlance]. <br> |
| - | </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=6kz1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6kz1 OCA], [https://pdbe.org/6kz1 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6kz1 RCSB], [https://www.ebi.ac.uk/pdbsum/6kz1 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6kz1 ProSAT]</span></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.694Å</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=6kz1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6kz1 OCA], [https://pdbe.org/6kz1 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6kz1 RCSB], [https://www.ebi.ac.uk/pdbsum/6kz1 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6kz1 ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/WHRN_HUMAN WHRN_HUMAN] Defects in DFNB31 are the cause of deafness autosomal recessive type 31 (DFNB31) [MIM:[https://omim.org/entry/607084 607084]. DFNB31 is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.<ref>PMID:11973626</ref> <ref>PMID:12833159</ref> <ref>PMID:15841483</ref> Defects in DFNB31 are the cause of Usher syndrome type 2D (USH2D) [MIM:[https://omim.org/entry/611383 611383]. USH is a genetically heterogeneous condition characterized by the association of retinitis pigmentosa and sensorineural deafness. Age at onset and differences in auditory and vestibular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome type 3 (USH3). USH2 is characterized by congenital mild hearing impairment with normal vestibular responses. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/WHRN_HUMAN WHRN_HUMAN] Necessary for elongation and maintenance of inner and outer hair cell stereocilia in the organ of Corti in the inner ear (By similarity). | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Stereocilia, the mechanosensory organelles on the apical surface of hair cells, are necessary to detect sound and carry out mechano-electrical transduction. An electron-dense matrix is located at the distal tips of stereocilia and plays crucial roles in the regulation of stereocilia morphology. Mutations of the components in this tip complex density (TCD) have been associated with profound deafness. However, the mechanism underlying the formation of the TCD is largely unknown. Here, we discover that the specific multivalent interactions among the Whirlin-myosin 15 (Myo15)-Eps8 complex lead to the formation of the TCD-like condensates through liquid-liquid phase separation. The reconstituted TCD-like condensates effectively promote actin bundling. A deafness-associated mutation of Myo15 interferes with the condensates formation and consequently impairs actin bundling. Therefore, our study not only suggests that the TCD in hair cell stereocilia may form via phase separation but it also provides important clues for the possible mechanism underlying hearing loss. | ||
| + | |||
| + | Phase separation-mediated condensation of Whirlin-Myo15-Eps8 stereocilia tip complex.,Lin L, Shi Y, Wang M, Wang C, Lu Q, Zhu J, Zhang R Cell Rep. 2021 Feb 23;34(8):108770. doi: 10.1016/j.celrep.2021.108770. PMID:33626355<ref>PMID:33626355</ref> | ||
| + | |||
| + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
| + | </div> | ||
| + | <div class="pdbe-citations 6kz1" style="background-color:#fffaf0;"></div> | ||
| + | == References == | ||
| + | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: | + | [[Category: Lin L]] |
| + | [[Category: Shi Y]] | ||
| + | [[Category: Wang M]] | ||
| + | [[Category: Zhang R]] | ||
| + | [[Category: Zhu J]] | ||
Current revision
Complex structure of Whirlin and Myosin XVa
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Categories: Homo sapiens | Large Structures | Lin L | Shi Y | Wang M | Zhang R | Zhu J
