8w15: Difference between revisions
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==HTT in complex with HAP40 in the apo state.== | |||
<StructureSection load='8w15' size='340' side='right'caption='[[8w15]], [[Resolution|resolution]] 2.72Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[8w15]] 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=8W15 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8W15 FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.72Å</td></tr> | |||
[[Category: | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8w15 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8w15 OCA], [https://pdbe.org/8w15 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8w15 RCSB], [https://www.ebi.ac.uk/pdbsum/8w15 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8w15 ProSAT]</span></td></tr> | ||
[[Category: Boudet | </table> | ||
[[Category: Doherty | == Disease == | ||
[[Category: Poweleit | [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. | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Boudet J]] | |||
[[Category: Doherty E]] | |||
[[Category: Poweleit N]] | |||
Latest revision as of 13:20, 13 March 2024
HTT in complex with HAP40 in the apo state.
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