| Literature DB >> 35562294 |
Ugo Dionne1, Lily J Percival2, François J M Chartier1, Christian R Landry3, Nicolas Bisson4.
Abstract
The assembly of complexes following the detection of extracellular signals is often controlled by signaling proteins comprising multiple peptide binding modules. The SRC homology (SH)3 family represents the archetypical modular protein interaction module, with ~300 annotated SH3 domains in humans that regulate an impressive array of signaling processes. We review recent findings regarding the allosteric contributions of SH3 domains host protein context, their phosphoregulation, and their roles in phase separation that challenge the simple model in which SH3s are considered to be portable domains binding to specific proline-rich peptide motifs.Entities:
Keywords: SH3 domains; liquid–liquid phase separation; phosphorylation; protein context; protein–protein interactions; signaling
Mesh:
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Year: 2022 PMID: 35562294 DOI: 10.1016/j.tibs.2022.04.005
Source DB: PubMed Journal: Trends Biochem Sci ISSN: 0968-0004 Impact factor: 14.264