This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


4wj7

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
'''Unreleased structure'''
+
==CCM2 PTB domain in complex with KRIT1 NPxY/F3==
-
 
+
<StructureSection load='4wj7' size='340' side='right' caption='[[4wj7]], [[Resolution|resolution]] 2.75&Aring;' scene=''>
-
The entry 4wj7 is ON HOLD until Paper Publication
+
== Structural highlights ==
-
 
+
<table><tr><td colspan='2'>[[4wj7]] is a 8 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4WJ7 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4WJ7 FirstGlance]. <br>
-
Authors: Fisher, O.S., Liu, W., Zhang, R., Stiegler, A.L., Boggon, T.J.
+
</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4wj7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4wj7 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4wj7 RCSB], [http://www.ebi.ac.uk/pdbsum/4wj7 PDBsum]</span></td></tr>
-
 
+
</table>
-
Description:
+
== Disease ==
 +
[[http://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 ==
 +
[[http://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: Boggon, T J]]
 +
[[Category: Fisher, O S]]
 +
[[Category: Liu, W]]
 +
[[Category: Stiegler, A L]]
 +
[[Category: Zhang, R]]
 +
[[Category: Complex]]
 +
[[Category: Npxy motif]]
 +
[[Category: Ptb domain]]

Revision as of 11:15, 24 December 2014

CCM2 PTB domain in complex with KRIT1 NPxY/F3

4wj7, resolution 2.75Å

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools