6n8c: Difference between revisions

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'''Unreleased structure'''


The entry 6n8c is ON HOLD  until Paper Publication
==Structure of the Huntingtin tetramer/dimer mixture determined by paramagnetic NMR==
 
<StructureSection load='6n8c' size='340' side='right' caption='[[6n8c]], [[NMR_Ensembles_of_Models | 10 NMR models]]' scene=''>
Authors:  
== Structural highlights ==
 
<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>
Description:  
</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>
[[Category: Unreleased Structures]]
</table>
== Disease ==
[[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.
== Function ==
[[http://www.uniprot.org/uniprot/HD_HUMAN HD_HUMAN]] May play a role in microtubule-mediated transport or vesicle function.
__TOC__
</StructureSection>
[[Category: Ceccon, A]]
[[Category: Clore, G M]]
[[Category: Ghirlando, R]]
[[Category: Kotler, S A]]
[[Category: Libich, D S]]
[[Category: Schmidt, T]]
[[Category: Schwieters, C D]]
[[Category: Dimer of dimer]]
[[Category: Tetramer]]
[[Category: Unknown function]]