ZO-2, SH3 domain (IPR035598)
Short name: ZO-2_SH3
Overlapping homologous superfamilies
- SH3-like domain superfamily (IPR036028)
- SH3 domain (IPR001452)
- ZO-2, SH3 domain (IPR035598)
This entry represents the SH3 domain of ZO-2.
The zona occuldens proteins (ZO-1, ZO-2 and ZO-3) are a family of tight junction associated proteins that function as cross-linkers, anchoring the TJ strand proteins to the actin-based cytoskeleton [PMID: 9214391]. Each protein contains three PDZ (postsynaptic density, disc-large, ZO-1) domains, a single SH3 (Src Homology-3) domain and a catalytically inactive GK (guanylate kinase) domain, the presence of which identifies them as members of the membrane-associated guanylate kinase (MAGUK) protein family. The signature PDZ-SH3-GuK tandem of MAGUKs may form a structural supramodule with three domains interacting with each other to assemble into an integral structural unit [PMID: 21965684, PMID: 22030391].
They also share an acidic domain at the C-terminal region of the molecules not found in other MAGUK proteins. It has been demonstrated that the first PDZ domain is involved in binding the C-terminal -Y-V motif of claudins [PMID: 10601346]. By contrast, the occludin-binding domain of ZO-1 has been shown to lie in the GK and acidic domains [PMID: 9792688]. Although the precise location of the actin-binding motif has not been elucidated, it appears to be within the C-terminal half of the molecules, since transfection of this region into fibroblasts induces co-localisation of ZO-1 and ZO-2 with actin fibres.
- cd12027 (SH3_ZO-2)