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6n8c

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'''Unreleased structure'''
 
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The entry 6n8c is ON HOLD until Paper Publication
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==Structure of the Huntingtin tetramer/dimer mixture determined by paramagnetic NMR==
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<StructureSection load='6n8c' size='340' side='right' caption='[[6n8c]], [[NMR_Ensembles_of_Models | 10 NMR models]]' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6n8c]] is a 4 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6N8C OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6N8C FirstGlance]. <br>
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Description:
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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=6n8c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6n8c OCA], [http://pdbe.org/6n8c PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6n8c RCSB], [http://www.ebi.ac.uk/pdbsum/6n8c PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6n8c ProSAT]</span></td></tr>
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[[Category: Unreleased Structures]]
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</table>
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== Disease ==
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[[http://www.uniprot.org/uniprot/HD_HUMAN HD_HUMAN]] Juvenile Huntington disease;Huntington disease. The disease is caused by mutations affecting the gene represented in this entry.
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== Function ==
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[[http://www.uniprot.org/uniprot/HD_HUMAN HD_HUMAN]] May play a role in microtubule-mediated transport or vesicle function.
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__TOC__
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</StructureSection>
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[[Category: Ceccon, A]]
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[[Category: Clore, G M]]
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[[Category: Ghirlando, R]]
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[[Category: Kotler, S A]]
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[[Category: Libich, D S]]
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[[Category: Schmidt, T]]
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[[Category: Schwieters, C D]]
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[[Category: Dimer of dimer]]
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[[Category: Tetramer]]
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[[Category: Unknown function]]

Revision as of 09:36, 13 February 2019

Structure of the Huntingtin tetramer/dimer mixture determined by paramagnetic NMR

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