8sah: Difference between revisions
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==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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