| Literature DB >> 22589543 |
Peter Draber1, Ondrej Stepanek, Matous Hrdinka, Ales Drobek, Lukas Chmatal, Linda Mala, Tereza Ormsby, Pavla Angelisova, Vaclav Horejsi, Tomas Brdicka.
Abstract
Transmembrane adaptor proteins are membrane-anchored proteins consisting of a short extracellular part, a transmembrane domain, and a cytoplasmic part with various protein-protein interaction motifs but lacking any enzymatic activity. They participate in the regulation of various signaling pathways by recruiting other proteins to the proximity of cellular membranes where the signaling is often initiated and propagated. In this work, we show that LST1/A, an incompletely characterized protein encoded by MHCIII locus, is a palmitoylated transmembrane adaptor protein. It is expressed specifically in leukocytes of the myeloid lineage, where it localizes to the tetraspanin-enriched microdomains. In addition, it binds SHP-1 and SHP-2 phosphatases in a phosphotyrosine-dependent manner, facilitating their recruitment to the plasma membrane. These data suggest a role for LST1/A in negative regulation of signal propagation.Entities:
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Year: 2012 PMID: 22589543 PMCID: PMC3391116 DOI: 10.1074/jbc.M112.339143
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157