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2n3j

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m (Protected "2n3j" [edit=sysop:move=sysop])
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'''Unreleased structure'''
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==Solution Structure of the alpha-crystallin domain from the redox-sensitive chaperone, HSPB1==
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<StructureSection load='2n3j' size='340' side='right' caption='[[2n3j]], [[NMR_Ensembles_of_Models | 10 NMR models]]' scene=''>
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The entry 2n3j is ON HOLD
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== Structural highlights ==
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<table><tr><td colspan='2'>[[2n3j]] is a 2 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2N3J OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2N3J FirstGlance]. <br>
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Authors: Rajagopal, P., Shi, L., Klevit, R.E.
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</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2n3j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2n3j OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2n3j RCSB], [http://www.ebi.ac.uk/pdbsum/2n3j PDBsum]</span></td></tr>
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</table>
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Description: Solution Structure of the alpha_crystallin domain from the redox chaperone, HSPB1
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== Disease ==
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[[Category: Unreleased Structures]]
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[[http://www.uniprot.org/uniprot/HSPB1_HUMAN HSPB1_HUMAN]] Autosomal dominant Charcot-Marie-Tooth disease type 2F;Distal hereditary motor neuropathy type 2. 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.
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[[Category: Klevit, R.E]]
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== Function ==
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[[Category: Shi, L]]
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[[http://www.uniprot.org/uniprot/HSPB1_HUMAN HSPB1_HUMAN]] Involved in stress resistance and actin organization.
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__TOC__
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</StructureSection>
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[[Category: Klevit, R E]]
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[[Category: Liu, Y]]
[[Category: Rajagopal, P]]
[[Category: Rajagopal, P]]
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[[Category: Shi, L]]
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[[Category: Chaperone]]
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[[Category: Crystallin]]
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[[Category: Redox-sensitive chaperone]]
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[[Category: Small heat shock protein]]

Revision as of 12:16, 20 August 2015

Solution Structure of the alpha-crystallin domain from the redox-sensitive chaperone, HSPB1

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