6n8c: Difference between revisions

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OCA

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-'''Unreleased structure'''
-The entry 6n8c is ON HOLD
+==Structure of the Huntingtin tetramer/dimer mixture determined by paramagnetic NMR==
+<StructureSection load='6n8c' size='340' side='right'caption='[[6n8c]]' scene=''>
+== Structural highlights ==
+<table><tr><td colspan='2'>[[6n8c]] is a 4 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=6N8C OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6N8C FirstGlance]. <br>
+</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'>[https://proteopedia.org/fgij/fg.htm?mol=6n8c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6n8c OCA], [https://pdbe.org/6n8c PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6n8c RCSB], [https://www.ebi.ac.uk/pdbsum/6n8c PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6n8c ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[https://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 ==
+[https://www.uniprot.org/uniprot/HD_HUMAN HD_HUMAN] May play a role in microtubule-mediated transport or vesicle function.
-Authors:
+==See Also==
+*[[Huntingtin|Huntingtin]]
-Description:
+__TOC__
-[[Category: Unreleased Structures]]
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Ceccon A]]
+[[Category: Clore GM]]
+[[Category: Ghirlando R]]
+[[Category: Kotler SA]]
+[[Category: Libich DS]]
+[[Category: Schmidt T]]
+[[Category: Schwieters CD]]