7roj
From Proteopedia
(Difference between revisions)
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==Amyloid-related segment of alphaB-crystallin residues 90-100 with G95W mutation== | ==Amyloid-related segment of alphaB-crystallin residues 90-100 with G95W mutation== | ||
| - | <StructureSection load='7roj' size='340' side='right'caption='[[7roj]]' scene=''> | + | <StructureSection load='7roj' size='340' side='right'caption='[[7roj]], [[Resolution|resolution]] 1.60Å' 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=7ROJ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7ROJ FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[7roj]] is a 12 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7ROJ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7ROJ 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=7roj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7roj OCA], [https://pdbe.org/7roj PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7roj RCSB], [https://www.ebi.ac.uk/pdbsum/7roj PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7roj ProSAT]</span></td></tr> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=TFA:TRIFLUOROACETIC+ACID'>TFA</scene></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=7roj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7roj OCA], [https://pdbe.org/7roj PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7roj RCSB], [https://www.ebi.ac.uk/pdbsum/7roj PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7roj ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == 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 == | ||
| + | [[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. | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Atomic structures of amyloid oligomers that capture the neurodegenerative disease pathology are essential to understand disease-state causes and finding cures. Here we investigate the G6W mutation of the cytotoxic, hexameric amyloid model KV11. The mutation results into an asymmetric dodecamer composed of a pair of 30 degrees twisted antiparallel beta-sheets. The complete break between adjacent beta-strands is unprecedented among amyloid fibril crystal structures and supports that our structure is an oligomer. The poor shape complementarity between mated sheets reveals an interior channel for binding lipids, suggesting that the toxicity may be due to a perturbation of lipid transport rather than a direct disruption of membrane integrity. Viability assays on mouse suprachiasmatic nucleus, anterior hypothalamus, and cerebral cortex demonstrated selective regional vulnerability consistent with Alzheimer's disease. Neuropeptides released from the brain slices may provide clues to how G6W initiates cellular injury. | ||
| + | |||
| + | Atomic view of an amyloid dodecamer exhibiting selective cellular toxic vulnerability in acute brain slices.,Gray ALH, Sawaya MR, Acharyya D, Lou J, Edington EM, Best MD, Prosser RA, Eisenberg DS, Do TD Protein Sci. 2021 Dec 26. doi: 10.1002/pro.4268. PMID:34954854<ref>PMID:34954854</ref> | ||
| + | |||
| + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
| + | </div> | ||
| + | <div class="pdbe-citations 7roj" style="background-color:#fffaf0;"></div> | ||
| + | == References == | ||
| + | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Do | + | [[Category: Do, T D]] |
| - | [[Category: Eisenberg | + | [[Category: Eisenberg, D S]] |
| - | [[Category: Sawaya | + | [[Category: Sawaya, M R]] |
| + | [[Category: Amyloid oligomer]] | ||
| + | [[Category: Protein fibril]] | ||
Revision as of 07:31, 2 March 2022
Amyloid-related segment of alphaB-crystallin residues 90-100 with G95W mutation
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