Literature DB >> 23164942

Exploring the diversity of SPRY/B30.2-mediated interactions.

Livia Perfetto1, Pier Federico Gherardini, Norman E Davey, Francesca Diella, Manuela Helmer-Citterich, Gianni Cesareni.   

Abstract

The SPla/Ryanodine receptor (SPRY)/B30.2 domain is one of the most common folds in higher eukaryotes. The human genome encodes 103 SPRY/B30.2 domains, several of which are involved in the immune response. Approximately 45% of human SPRY/B30.2-containing proteins are E3 ligases. The role and function of the majority of SPRY/B30.2 domains are still poorly understood, however, in several cases mutations in this domain have been linked to congenital disorders. The recent characterization of SPRY/B30.2-mediated protein interactions has provided evidence for a role of this domain as an adaptor module to assemble macromolecular complexes, analogous to Src homology (SH)2, SH3, and WW domains. However, functional and structural evidence suggests that SPRY/B30.2 is a more versatile fold, allowing a wide range of binding modes.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 23164942     DOI: 10.1016/j.tibs.2012.10.001

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  30 in total

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