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==HSPB5 alpha-crystallin domain mutant R120G-ACD== | ==HSPB5 alpha-crystallin domain mutant R120G-ACD== | ||
<StructureSection load='6bp9' size='340' side='right' caption='[[6bp9 | <StructureSection load='6bp9' size='340' side='right'caption='[[6bp9]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6bp9]] is a 2 chain structure with sequence from [ | <table><tr><td colspan='2'>[[6bp9]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6BP9 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6BP9 FirstGlance]. <br> | ||
</td></tr> | </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=6bp9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6bp9 OCA], [https://pdbe.org/6bp9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6bp9 RCSB], [https://www.ebi.ac.uk/pdbsum/6bp9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6bp9 ProSAT]</span></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | |||
</table> | </table> | ||
== Disease == | == Disease == | ||
[ | [https://www.uniprot.org/uniprot/CRYAB_HUMAN CRYAB_HUMAN] Posterior polar cataract;Alpha-crystallinopathy;Zonular cataract;Familial isolated dilated cardiomyopathy;Fatal infantile hypertonic myofibrillar myopathy. 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. 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 == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/CRYAB_HUMAN CRYAB_HUMAN] May contribute to the transparency and refractive index of the lens. Has chaperone-like activity, preventing aggregation of various proteins under a wide range of stress conditions. | ||
==See Also== | |||
*[[Crystallin 3D structures|Crystallin 3D structures]] | |||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: | [[Category: Large Structures]] | ||
[[Category: | [[Category: Klevit RE]] | ||
[[Category: | [[Category: Rajagopal P]] | ||
Latest revision as of 13:38, 14 June 2023
HSPB5 alpha-crystallin domain mutant R120G-ACDHSPB5 alpha-crystallin domain mutant R120G-ACD
Structural highlights
DiseaseCRYAB_HUMAN Posterior polar cataract;Alpha-crystallinopathy;Zonular cataract;Familial isolated dilated cardiomyopathy;Fatal infantile hypertonic myofibrillar myopathy. 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. 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. FunctionCRYAB_HUMAN May contribute to the transparency and refractive index of the lens. Has chaperone-like activity, preventing aggregation of various proteins under a wide range of stress conditions. See Also |
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