9l8p

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (05:54, 1 October 2025) (edit) (undo)
 
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 9l8p is ON HOLD until Paper Publication
+
==in situ structure of mtHsp60-Hsp10==
-
 
+
<StructureSection load='9l8p' size='340' side='right'caption='[[9l8p]], [[Resolution|resolution]] 7.30&Aring;' scene=''>
-
Authors: Jung, M., Roh, S.
+
== Structural highlights ==
-
 
+
<table><tr><td colspan='2'>[[9l8p]] is a 28 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=9L8P OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9L8P FirstGlance]. <br>
-
Description: in situ structure of mtHsp60-Hsp10
+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 7.3&#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></td></tr>
-
[[Category: Jung, M]]
+
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9l8p FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9l8p OCA], [https://pdbe.org/9l8p PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9l8p RCSB], [https://www.ebi.ac.uk/pdbsum/9l8p PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9l8p ProSAT]</span></td></tr>
-
[[Category: Roh, S]]
+
</table>
 +
== 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: Jung M]]
 +
[[Category: Roh S]]

Current revision

in situ structure of mtHsp60-Hsp10

PDB ID 9l8p

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools