Literature DB >> 35562294

SRC homology 3 domains: multifaceted binding modules.

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.
Copyright © 2022 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  SH3 domains; liquid–liquid phase separation; phosphorylation; protein context; protein–protein interactions; signaling

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Substances:

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


  1 in total

1.  Molecular and Functional Characterization of a Short-Type Peptidoglycan Recognition Protein, Ct-PGRP-S1 in the Giant Triton Snail Charonia tritonis.

Authors:  Wenguang Liu; Bing Liu; Gege Zhang; Huixia Jia; Yang Zhang; Xitong Cen; Gaoyou Yao; Maoxian He
Journal:  Int J Mol Sci       Date:  2022-09-21       Impact factor: 6.208

  1 in total

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