Common junctional plaque protein. The membrane- associated plaques are architectural elements in an important strategic position to influence the arrangement and function of both the cytoskeleton and the cells within the tissue. The presence of plakoglobin in both the desmosomes and in the intermediate junctions suggests that it plays a central role in the structure and function of submembranous plaques. Acts as a substrate for VE-PTP and is required by it to stimulate VE- cadherin function in endothelial cells. Can replace beta-catenin in E-cadherin/catenin adhesion complexes which are proposed to couple cadherins to the actin cytoskeleton. Homodimer. Component of an E-cadherin/ catenin adhesion complex composed of at least E-cadherin/CDH1 and gamma- catenin/JUP, and possibly alpha-catenin/CTNNA1; the complex is located to adherens junctions. The stable association of CTNNA1 is controversial as CTNNA1 was shown not to bind to F-actin when assembled in the complex. Interacts with MUC1. Interacts with CAV1. Interacts with PTPRJ. Interacts with DSC2. Belongs to the beta-catenin family. Note: This description may include information from UniProtKB.
Protein type: Cytoskeletal; Motility/polarity/chemotaxis
Cellular Component: desmosome; internal side of plasma membrane; focal adhesion; apicolateral plasma membrane; intermediate filament; fascia adherens; catenin complex; intercellular junction; cytosol; Z disc; actin cytoskeleton; cell-cell adherens junction; cytoskeleton; membrane; cytoplasm; plasma membrane; nucleus; cell junction; lateral plasma membrane
Molecular Function: protein binding; signal transducer activity; cadherin binding; transcription coactivator activity; structural molecule activity; protein phosphatase binding; protein kinase binding; alpha-catenin binding
Biological Process: skin development; cell migration; cell-cell adhesion; positive regulation of protein import into nucleus; protein heterooligomerization; regulation of cell fate specification; detection of mechanical stimulus; positive regulation of transcription factor activity; cell adhesion; regulation of cell proliferation
LTP: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.