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Identification and Characterization of a Novel SH3-Domain Binding Protein, Sab, Which Preferentially Associates with Bruton's Tyrosine Kinase (Btk)

Authors :
Matsushita, Masato
Yamadori, Tomoki
Kato, Seishi
Takemoto, Yoshihiro
Inazawa, Jouji
Baba, Yoshihiro
Hashimoto, Shoji
Sekine, Shingo
Arai, Shigeyuki
Kunikata, Toshio
Kurimoto, Masashi
Kishimoto, Tadamitsu
Tsukada, Satoshi
Source :
Biochemical and Biophysical Research Communications; April 1998, Vol. 245 Issue: 2 p337-343, 7p
Publication Year :
1998

Abstract

Protein interaction cloning method was used to identify a novel molecule, Sab, which binds to the SH3 domain of Bruton's tyrosine kinase (Btk), the deficient cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia and murine X-linked immunodeficiency. Immunoprecipitation using the anti-Sab antibody identified the protein product of the gene as a 70 kDa molecule. While Sab does not have a proline-rich sequence, it was shown to bind to Btk through the commonly conserved structure among SH3 domains. Remarkably, Sab exhibited a high preference for binding to Btk rather than to other cytoplasmic tyrosine kinases, which suggests a unique role of Sab in the Btk signal transduction pathway.

Details

Language :
English
ISSN :
0006291X and 10902104
Volume :
245
Issue :
2
Database :
Supplemental Index
Journal :
Biochemical and Biophysical Research Communications
Publication Type :
Periodical
Accession number :
ejs674158
Full Text :
https://doi.org/10.1006/bbrc.1998.8420