3sgo: Difference between revisions

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[[Image:3sgo.jpg|left|200px]]


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==Amyloid-related segment of alphaB-crystallin residues 90-100==
The line below this paragraph, containing "STRUCTURE_3sgo", creates the "Structure Box" on the page.
<StructureSection load='3sgo' size='340' side='right'caption='[[3sgo]], [[Resolution|resolution]] 2.56&Aring;' scene=''>
You may change the PDB parameter (which sets the PDB file loaded into the applet)
== Structural highlights ==
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
<table><tr><td colspan='2'>[[3sgo]] 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=3SGO OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3SGO FirstGlance]. <br>
or leave the SCENE parameter empty for the default display.
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.557&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3sgo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3sgo OCA], [https://pdbe.org/3sgo PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3sgo RCSB], [https://www.ebi.ac.uk/pdbsum/3sgo PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3sgo ProSAT]</span></td></tr>
{{STRUCTURE_3sgo|  PDB=3sgo  |  SCENE=  }}
</table>
 
== Disease ==
===Amyloid-related segment of alphaB-crystallin residues 90-100===
[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.
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
{{ABSTRACT_PUBMED_22403391}}
[[Category: Cascio D]]
 
[[Category: Eisenberg D]]
==About this Structure==
[[Category: Laganowsky A]]
[[3sgo]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3SGO OCA].  
[[Category: Sawaya MR]]
 
==Reference==
<ref group="xtra">PMID:022403391</ref><references group="xtra"/>
[[Category: Cascio, D.]]
[[Category: Eisenberg, D.]]
[[Category: Laganowsky, A.]]
[[Category: Sawaya, M R.]]
[[Category: Amyloid]]
[[Category: Amyloid oligomer]]
[[Category: Beta cylindrin]]
[[Category: Protein fibril]]

Latest revision as of 12:50, 1 March 2024

Amyloid-related segment of alphaB-crystallin residues 90-100Amyloid-related segment of alphaB-crystallin residues 90-100

Structural highlights

3sgo is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:X-ray diffraction, Resolution 2.557Å
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Disease

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

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.

3sgo, resolution 2.56Å

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OCA