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SETA is a multifunctional adapter protein with three SH3 domains that binds Grb2, Cbl, and the novel SB1 proteins.
Borinstein, S C; Hyatt, M A; Sykes, V W; Straub, R E; Lipkowitz, S; Boulter, J; Bogler, O.
Affiliation
  • Borinstein SC; Department of Anatomy, Medical College of Virginia, Virginia Commonwealth University, Richmond, VA 23298, USA.
Cell Signal ; 12(11-12): 769-79, 2000 Dec.
Article in En | MEDLINE | ID: mdl-11152963
ABSTRACT
Expression of the src homology 3 (SH3)-encoding, expressed in tumorigenic astrocytes (SETA) gene is associated with astrocyte transformation in culture and tumors in the adult brain. SETA binds to the apoptosis regulator apoptosis-linked gene 2 (ALG-2) interacting protein 1 (AIP1), and modulates apoptosis in astrocytes. The predicted protein structure of SETA revealed two SH3 domains, while related proteins were reported to have three. Here we report the identification of an additional SH3 domain N-terminal to the previously identified SETA sequence. Yeast two-hybrid screening of a p53(-/-) astrocyte cDNA library with this SH3 domain identified a novel gene, SETA binding protein 1 (SB1), with 55% amino acid identity to the renal tumor antigen, NY-REN-45. In vitro confrontation and co-immunoprecipitation experiments confirmed the binding of SB1 to SETA. Evidence that SETA binds to the CD2 protein, the proto-oncogene c-Cbl, and the signal transduction molecule Grb2, and can dimerize via its C-terminal coiled coil (CC) domain is also presented.
Subject(s)
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Database: MEDLINE Main subject: Proteins / Carrier Proteins / Proto-Oncogene Proteins / Src Homology Domains / Ubiquitin-Protein Ligases / Adaptor Proteins, Signal Transducing / Neoplasm Proteins / Nerve Tissue Proteins Type of study: Prognostic_studies Language: En Year: 2000 Type: Article
Search on Google
Database: MEDLINE Main subject: Proteins / Carrier Proteins / Proto-Oncogene Proteins / Src Homology Domains / Ubiquitin-Protein Ligases / Adaptor Proteins, Signal Transducing / Neoplasm Proteins / Nerve Tissue Proteins Type of study: Prognostic_studies Language: En Year: 2000 Type: Article