PARD6A
Domain
The pseudo-CRIB domain together with the PDZ domain is required for the interaction with Rho small GTPases.
The PB1 domain mediates interactions with MAP2K5.
The PDZ domain mediates the interaction with CRB3.
Function
Adapter protein involved in asymmetrical cell division and cell polarization processes. Probably involved in the formation of epithelial tight junctions. Association with PARD3 may prevent the interaction of PARD3 with F11R/JAM1, thereby preventing tight junction assembly. The PARD6-PARD3 complex links GTP-bound Rho small GTPases to atypical protein kinase C proteins (PubMed:10873802). Regulates centrosome organization and function. Essential for the centrosomal recruitment of key proteins that control centrosomal microtubule organization (PubMed:20719959).
Post-translational modifications
Phosphorylated by the TGF-beta receptor.
Sequence Similarities
Belongs to the PAR6 family.
Tissue Specificity
Expressed in pancreas, skeletal muscle, brain and heart. Weakly expressed in kidney and placenta.
Cellular localization
- Cytoplasm
- Cell membrane
- Cell projection
- Ruffle
- Cell junction
- Tight junction
- Cytoplasm
- Cytoskeleton
- Microtubule organizing center
- Centrosome
- Centriolar satellite
- Cytoplasm
- Cytoskeleton
- Microtubule organizing center
- Centrosome
- Colocalizes with GTP-bound CDC42 or RAC1 at membrane ruffles and with PARD3 and PRKCI at epithelial tight junctions. Recruited to the centrosome by a microtubule and dynein-dynactin-dependent mechanism.
Alternative names
PAR6A, PARD6A, Partitioning defective 6 homolog alpha, PAR-6, PAR-6 alpha, PAR-6A, PAR6C, Tax interaction protein 40, TIP-40