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The Cbl proteins are binding partners for the Cool/Pix family of p21-activated kinase-binding proteins
- Source :
- FEBS Letters. (1-3):119-123
- Publisher :
- Published by Elsevier B.V.
-
Abstract
- Members of the Cool protein family contain SH3, Dbl, and pleckstrin homology domains and are binding partners for the p21-activated kinase (PAK). Using the yeast two-hybrid screen, we identified Cbl-b as a Cool family binding partner. We co-immunoprecipitated endogenous Cool and Cbl-b from a variety of breast cancer cell lines. The Cool–Cbl-b interaction requires the SH3 domain of Cool and competes with the binding of PAK to Cool proteins. Expression of Cbl-b effectively blocks the ability of Cool-2 to stimulate PAK, thus providing an additional mechanism, aside from catalyzing receptor ubiquitination, by which Cbl-b acts as a negative regulator for signaling activities requiring PAK activation.
- Subjects :
- Cell Cycle Proteins
Plasma protein binding
Biochemistry
environment and public health
SH3 domain
0302 clinical medicine
Structural Biology
hemic and lymphatic diseases
Tumor Cells, Cultured
Guanine Nucleotide Exchange Factors
Proto-Oncogene Proteins c-cbl
Cdc42
p21-activated kinases
0303 health sciences
3. Good health
Cell biology
Pleckstrin homology domain
030220 oncology & carcinogenesis
COS Cells
Female
Guanine nucleotide exchange factor
biological phenomena, cell phenomena, and immunity
Protein Binding
Cbl
Protein family
Ubiquitin-Protein Ligases
Molecular Sequence Data
Biophysics
Breast Neoplasms
macromolecular substances
Protein Serine-Threonine Kinases
Biology
p21-activated kinase
Binding, Competitive
src Homology Domains
03 medical and health sciences
Proto-Oncogene Proteins
Two-Hybrid System Techniques
Genetics
Animals
Humans
Amino Acid Sequence
Molecular Biology
Adaptor Proteins, Signal Transducing
030304 developmental biology
Breast cancer cell
Cell Biology
Phosphoproteins
Molecular biology
enzymes and coenzymes (carbohydrates)
p21-Activated Kinases
Kinase binding
Carrier Proteins
Rho Guanine Nucleotide Exchange Factors
Subjects
Details
- Language :
- English
- ISSN :
- 00145793
- Issue :
- 1-3
- Database :
- OpenAIRE
- Journal :
- FEBS Letters
- Accession number :
- edsair.doi.dedup.....eb836a4513bd57958bf039248f273362
- Full Text :
- https://doi.org/10.1016/S0014-5793(03)00853-6