View source for 8csw


==Local refinement of protein 4.2 in Class 2 of erythrocyte ankyrin-1 complex==
<StructureSection load='8csw' size='340' side='right'caption='[[8csw]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[8csw]] is a 1 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=8CSW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8CSW FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.5&#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=8csw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8csw OCA], [https://pdbe.org/8csw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8csw RCSB], [https://www.ebi.ac.uk/pdbsum/8csw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8csw ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN] Hereditary spherocytosis. The disease is caused by variants affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN] Probably plays an important role in the regulation of erythrocyte shape and mechanical properties.
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Cali T]]
[[Category: Clarke OB]]
[[Category: Johnston JD]]
[[Category: Kim K]]
[[Category: Noble AJ]]
[[Category: Vallese F]]
[[Category: Yen LY]]