View source for 6dv5


==Oligomeric complex of a Hsp27 24-mer at 3.6 A resolution==
<StructureSection load='6dv5' size='340' side='right'caption='[[6dv5]], [[Resolution|resolution]] 3.58&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6dv5]] is a 24 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=6DV5 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6DV5 FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.58&#8491;</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=6dv5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6dv5 OCA], [https://pdbe.org/6dv5 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6dv5 RCSB], [https://www.ebi.ac.uk/pdbsum/6dv5 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6dv5 ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/HSPB1_HUMAN HSPB1_HUMAN] Autosomal dominant Charcot-Marie-Tooth disease type 2F;Distal hereditary motor neuropathy type 2. 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 ==
[https://www.uniprot.org/uniprot/HSPB1_HUMAN HSPB1_HUMAN] Involved in stress resistance and actin organization.

==See Also==
*[[Heat Shock Protein structures|Heat Shock Protein structures]]
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Aguda AH]]
[[Category: Brayer GD]]