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APPL1 is a multifunctional endosomal signaling adaptor protein
Author(s) -
Nicole L. Diggins,
Donna J. Webb
Publication year - 2017
Publication title -
biochemical society transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.562
H-Index - 144
eISSN - 1470-8752
pISSN - 0300-5127
DOI - 10.1042/bst20160191
Subject(s) - signal transducing adaptor protein , pleckstrin homology domain , phosphotyrosine binding domain , endosome , microbiology and biotechnology , signal transduction , amphiphysin , biology , endocytosis , receptor , biochemistry , proto oncogene tyrosine protein kinase src , sh2 domain , intracellular , dynamin
Endosomal adaptor proteins are important regulators of signaling pathways underlying many biological processes. These adaptors can integrate signals from multiple pathways via localization to specific endosomal compartments, as well as through multiple protein–protein interactions. One such adaptor protein that has been implicated in regulating signaling pathways is the adaptor protein containing a pleckstrin homology (PH) domain, phosphotyrosine-binding (PTB) domain, and leucine zipper motif 1 (APPL1). APPL1 localizes to a subset of Rab5-positive endosomes through its Bin–Amphiphysin–Rvs and PH domains, and it coordinates signaling pathways through its interaction with many signaling receptors and proteins through its PTB domain. This review discusses our current understanding of the role of APPL1 in signaling and trafficking, as well as highlights recent work into the function of APPL1 in cell migration and adhesion.

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