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.

Perfetto, L., Gherardini, P., Davey, N., Diella, F., HELMER CITTERICH, M., Cesareni, G. (2013). Exploring the diversity of SPRY/B30.2-mediated interactions. TRENDS IN BIOCHEMICAL SCIENCES, 38(1), 38-46 [10.1016/j.tibs.2012.10.001].

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

Gherardini, P;HELMER CITTERICH, MANUELA;CESARENI, GIOVANNI
2013-01-01

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.
gen-2013
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/18 - GENETICA
Settore BIO/11 - BIOLOGIA MOLECOLARE
English
Con Impact Factor ISI
http://www.sciencedirect.com/science/article/pii/S0968000412001569
Perfetto, L., Gherardini, P., Davey, N., Diella, F., HELMER CITTERICH, M., Cesareni, G. (2013). Exploring the diversity of SPRY/B30.2-mediated interactions. TRENDS IN BIOCHEMICAL SCIENCES, 38(1), 38-46 [10.1016/j.tibs.2012.10.001].
Perfetto, L; Gherardini, P; Davey, N; Diella, F; HELMER CITTERICH, M; Cesareni, G
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/74775
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