8gts

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (09:35, 1 March 2024) (edit) (undo)
 
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 8gts is ON HOLD until 2025-03-08
+
==CryoEM structure of human Pannexin1 with R217H congenital mutation.==
-
 
+
<StructureSection load='8gts' size='340' side='right'caption='[[8gts]], [[Resolution|resolution]] 3.87&Aring;' scene=''>
-
Authors:
+
== Structural highlights ==
-
 
+
<table><tr><td colspan='2'>[[8gts]] is a 7 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=8GTS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8GTS FirstGlance]. <br>
-
Description:
+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.87&#8491;</td></tr>
-
[[Category: Unreleased Structures]]
+
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8gts FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8gts OCA], [https://pdbe.org/8gts PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8gts RCSB], [https://www.ebi.ac.uk/pdbsum/8gts PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8gts ProSAT]</span></td></tr>
 +
</table>
 +
== Function ==
 +
[https://www.uniprot.org/uniprot/PANX1_HUMAN PANX1_HUMAN] Structural component of the gap junctions and the hemichannels. May play a role as a Ca(2+)-leak channel to regulate ER Ca(2+) homeostasis.<ref>PMID:16908669</ref> <ref>PMID:20829356</ref>
 +
== References ==
 +
<references/>
 +
__TOC__
 +
</StructureSection>
 +
[[Category: Homo sapiens]]
 +
[[Category: Large Structures]]
 +
[[Category: Hussain N]]
 +
[[Category: Penmatsa A]]

Current revision

CryoEM structure of human Pannexin1 with R217H congenital mutation.

PDB ID 8gts

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools