4fqn

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (11:23, 1 March 2024) (edit) (undo)
 
(3 intermediate revisions not shown.)
Line 1: Line 1:
-
[[Image:4fqn.png|left|200px]]
 
-
{{STRUCTURE_4fqn| PDB=4fqn | SCENE= }}
+
==Crystal structure of the CCM2 C-terminal Harmonin Homology Domain (HHD)==
-
 
+
<StructureSection load='4fqn' size='340' side='right'caption='[[4fqn]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
-
===Crystal structure of the CCM2 C-terminal Harmonin Homology Domain (HHD)===
+
== Structural highlights ==
-
 
+
<table><tr><td colspan='2'>[[4fqn]] is a 4 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=4FQN OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4FQN FirstGlance]. <br>
-
{{ABSTRACT_PUBMED_23266514}}
+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.9&#8491;</td></tr>
-
 
+
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4fqn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4fqn OCA], [https://pdbe.org/4fqn PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4fqn RCSB], [https://www.ebi.ac.uk/pdbsum/4fqn PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4fqn ProSAT]</span></td></tr>
-
==About this Structure==
+
</table>
-
[[4fqn]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4FQN OCA].
+
== 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: Homo sapiens]]
-
[[Category: Boggon, T J.]]
+
[[Category: Large Structures]]
-
[[Category: Fisher, O S.]]
+
[[Category: Boggon TJ]]
-
[[Category: Li, X.]]
+
[[Category: Fisher OS]]
-
[[Category: Murphy, J W.]]
+
[[Category: Li X]]
-
[[Category: Zhang, R.]]
+
[[Category: Murphy JW]]
-
[[Category: Harmonin-homology domain]]
+
[[Category: Zhang R]]
-
[[Category: Helical domain]]
+
-
[[Category: Homo-dimer]]
+
-
[[Category: Protein binding]]
+
-
[[Category: Protein-protein interaction]]
+

Current revision

Crystal structure of the CCM2 C-terminal Harmonin Homology Domain (HHD)

PDB ID 4fqn

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools