2n0k: Difference between revisions
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==Chemical shift assignments and structure of the alpha-crystallin domain from human, HSPB5== | ==Chemical shift assignments and structure of the alpha-crystallin domain from human, HSPB5== | ||
<StructureSection load='2n0k' size='340' side='right' caption='[[2n0k | <StructureSection load='2n0k' size='340' side='right'caption='[[2n0k]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2n0k]] is a 2 chain structure with sequence from [ | <table><tr><td colspan='2'>[[2n0k]] 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=2N0K OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2N0K FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2n0k FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2n0k OCA], [https://pdbe.org/2n0k PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2n0k RCSB], [https://www.ebi.ac.uk/pdbsum/2n0k PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2n0k ProSAT]</span></td></tr> | ||
</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. | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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</div> | </div> | ||
<div class="pdbe-citations 2n0k" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 2n0k" style="background-color:#fffaf0;"></div> | ||
==See Also== | |||
*[[Crystallin 3D structures|Crystallin 3D structures]] | |||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Baker | [[Category: Large Structures]] | ||
[[Category: Klevit | [[Category: Baker D]] | ||
[[Category: Rajagopal | [[Category: Klevit RE]] | ||
[[Category: Shi | [[Category: Rajagopal P]] | ||
[[Category: Shi L]] | |||