9es2: Difference between revisions

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'''Unreleased structure'''


The entry 9es2 is ON HOLD  until Paper Publication
==ATP-bound human mitochondrial Hsp60 double-ring complex==
 
<StructureSection load='9es2' size='340' side='right'caption='[[9es2]], [[Resolution|resolution]] 2.44&Aring;' scene=''>
Authors: Lopez-Alonso, J.P., Tascon, I., Ubarretxena-Belandia, I.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9es2]] is a 14 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=9ES2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9ES2 FirstGlance]. <br>
Description: ATP-bound human mitochondrial Hsp60 double-ring complex
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.44&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ATP:ADENOSINE-5-TRIPHOSPHATE'>ATP</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr>
[[Category: Lopez-Alonso, J.P]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9es2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9es2 OCA], [https://pdbe.org/9es2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9es2 RCSB], [https://www.ebi.ac.uk/pdbsum/9es2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9es2 ProSAT]</span></td></tr>
[[Category: Tascon, I]]
</table>
[[Category: Ubarretxena-Belandia, I]]
== Disease ==
[https://www.uniprot.org/uniprot/CH60_HUMAN CH60_HUMAN] Autosomal dominant spastic paraplegia type 13;Pelizaeus-Merzbacher-like disease due to HSPD1 mutation. The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/CH60_HUMAN CH60_HUMAN] Implicated in mitochondrial protein import and macromolecular assembly. May facilitate the correct folding of imported proteins. May also prevent misfolding and promote the refolding and proper assembly of unfolded polypeptides generated under stress conditions in the mitochondrial matrix.
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Lopez-Alonso JP]]
[[Category: Tascon I]]
[[Category: Ubarretxena-Belandia I]]

Latest revision as of 07:59, 9 April 2025

ATP-bound human mitochondrial Hsp60 double-ring complex

9es2, resolution 2.44Å

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