8sah
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Huntingtin C-HEAT domain in complex with HAP40== | |
| - | + | <StructureSection load='8sah' size='340' side='right'caption='[[8sah]], [[Resolution|resolution]] 3.20Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[8sah]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8SAH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8SAH FirstGlance]. <br> | |
| - | + | </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=8sah FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8sah OCA], [https://pdbe.org/8sah PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8sah RCSB], [https://www.ebi.ac.uk/pdbsum/8sah PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8sah ProSAT]</span></td></tr> | |
| - | [[Category: | + | </table> |
| - | [[Category: | + | == Disease == |
| - | [[Category: | + | [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. |
| - | [[Category: | + | == Function == |
| - | [[Category: | + | [https://www.uniprot.org/uniprot/HD_HUMAN HD_HUMAN] May play a role in microtubule-mediated transport or vesicle function. |
| - | [[Category: Harding | + | __TOC__ |
| - | [[Category: | + | </StructureSection> |
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Alteen MG]] | ||
| + | [[Category: Arrowsmith CH]] | ||
| + | [[Category: Deme JC]] | ||
| + | [[Category: Harding RJ]] | ||
| + | [[Category: Lea SM]] | ||
Revision as of 17:09, 26 April 2023
Huntingtin C-HEAT domain in complex with HAP40
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