8vlx
From Proteopedia
(Difference between revisions)
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<table><tr><td colspan='2'>[[8vlx]] 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=8VLX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8VLX FirstGlance]. <br> | <table><tr><td colspan='2'>[[8vlx]] 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=8VLX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8VLX 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]] 2.6Å</td></tr> | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.6Å</td></tr> | ||
| - | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1ACS: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1ACS:1-[(1~{S},2~{R})-2-(phenylmethyl)cyclopentyl]-3-[1-[(1~{S})-1-pyridin-4-ylethyl]piperidin-4-yl]urea'>A1ACS</scene></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=8vlx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8vlx OCA], [https://pdbe.org/8vlx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8vlx RCSB], [https://www.ebi.ac.uk/pdbsum/8vlx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8vlx ProSAT]</span></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=8vlx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8vlx OCA], [https://pdbe.org/8vlx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8vlx RCSB], [https://www.ebi.ac.uk/pdbsum/8vlx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8vlx ProSAT]</span></td></tr> | ||
</table> | </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. | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
Current revision
HTT in complex with HAP40 and a small molecule.
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