6n8c: Difference between revisions
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==Structure of the Huntingtin tetramer/dimer mixture determined by paramagnetic NMR== | ==Structure of the Huntingtin tetramer/dimer mixture determined by paramagnetic NMR== | ||
<StructureSection load='6n8c' size='340' side='right' caption='[[6n8c | <StructureSection load='6n8c' size='340' side='right'caption='[[6n8c]]' scene=''> | ||
== Structural highlights == | == 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 [ | <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='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | </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> | </table> | ||
== Disease == | == 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 == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/HD_HUMAN HD_HUMAN] May play a role in microtubule-mediated transport or vesicle function. | ||
==See Also== | |||
*[[Huntingtin|Huntingtin]] | |||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: | [[Category: Large Structures]] | ||
[[Category: | [[Category: Ceccon A]] | ||
[[Category: Clore GM]] | |||
[[Category: | [[Category: Ghirlando R]] | ||
[[Category: | [[Category: Kotler SA]] | ||
[[Category: | [[Category: Libich DS]] | ||
[[Category: | [[Category: Schmidt T]] | ||
[[Category: | [[Category: Schwieters CD]] | ||
[[Category: | |||
Latest revision as of 10:36, 1 May 2024
Structure of the Huntingtin tetramer/dimer mixture determined by paramagnetic NMRStructure of the Huntingtin tetramer/dimer mixture determined by paramagnetic NMR
Structural highlights
DiseaseHD_HUMAN Juvenile Huntington disease;Huntington disease. The disease is caused by mutations affecting the gene represented in this entry. FunctionHD_HUMAN May play a role in microtubule-mediated transport or vesicle function. See Also |
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