9pvg: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
New page: '''Unreleased structure''' The entry 9pvg is ON HOLD until Paper Publication Authors: Fisher, O.S., Boggon, T.J. Description: Co-crystal structure of two CCM2 PTB domains bound to a KR...
 
OCA (talk | contribs)
No edit summary
 
(One intermediate revision by the same user not shown)
Line 1: Line 1:
'''Unreleased structure'''


The entry 9pvg is ON HOLD  until Paper Publication
==Co-crystal structure of two CCM2 PTB domains bound to a KRIT1 peptide encompassing NPxF2 and NPxF3==
 
<StructureSection load='9pvg' size='340' side='right'caption='[[9pvg]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
Authors: Fisher, O.S., Boggon, T.J.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9pvg]] is a 6 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=9PVG OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9PVG FirstGlance]. <br>
Description: Co-crystal structure of two CCM2 PTB domains bound to a KRIT1 peptide encompassing NPxF2 and NPxF3
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3&#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=9pvg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9pvg OCA], [https://pdbe.org/9pvg PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9pvg RCSB], [https://www.ebi.ac.uk/pdbsum/9pvg PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9pvg ProSAT]</span></td></tr>
[[Category: Boggon, T.J]]
</table>
[[Category: Fisher, O.S]]
== Disease ==
[https://www.uniprot.org/uniprot/CCM2_HUMAN CCM2_HUMAN] Hereditary cerebral cavernous malformation. The disease is caused by mutations affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/CCM2_HUMAN CCM2_HUMAN] Component of the CCM signaling pathway which is a crucial regulator of heart and vessel formation and integrity. May act through the stabilization of endothelial cell junctions (By similarity). May function as a scaffold protein for MAP2K3-MAP3K3 signaling. Seems to play a major role in the modulation of MAP3K3-dependent p38 activation induced by hyperosmotic shock (By similarity).
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Boggon TJ]]
[[Category: Fisher OS]]