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Identification of p...
Identification of phosphorylation sites within the SH3 domains of Tec family tyrosine kinases
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Nore, Beston F (author)
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Mattsson, Pekka T (author)
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Antonsson, Per (author)
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Bäckesjö, Carl-Magnus (author)
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Westlund, Anna (author)
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- Lennartsson, Johan (author)
- Uppsala universitet,Ludwiginstitutet för cancerforskning
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Hansson, Henrik (author)
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Löw, Peter (author)
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- Rönnstrand, Lars (author)
- Lund University,Lunds universitet,Uppsala universitet,Ludwiginstitutet för cancerforskning,Institutionen för translationell medicin,Medicinska fakulteten,Department of Translational Medicine,Faculty of Medicine
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Smith, C I Edvard (author)
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(creator_code:org_t)
- 2003
- 2003
- English.
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In: Biochimica et Biophysica Acta. - 0006-3002 .- 1878-2434. ; 1645:2, s. 123-132
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http://www.ncbi.nlm....
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http://dx.doi.org/10...
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Abstract
Subject headings
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- Tec family protein tyrosine kinases (TFKs) play a central role in hematopoietic cellular signaling. Initial activation takes place through specific tyrosine phosphorylation situated in the activation loop. Further activation occurs within the SH3 domain via a transphosphorylation mechanism, which for Bruton's tyrosine kinase (Btk) affects tyrosine 223. We found that TFKs phosphorylate preferentially their own SH3 domains, but differentially phosphorylate other member family SH3 domains, whereas non-related SH3 domains are not phosphorylated. We demonstrate that SH3 domains are good and reliable substrates. We observe that transphosphorylation is selective not only for SH3 domains, but also for dual SH3SH2 domains. However, the dual domain is phosphorylated more effectively. The major phosphorylation sites were identified as conserved tyrosines, for Itk Y180 and for Bmx Y215, both sites being homologous to the Y223 site in Btk. There is, however, one exception because the Tec-SH3 domain is phosphorylated at a non-homologous site, nevertheless a conserved tyrosine, Y206. Consistent with these findings, the 3D structures for SH3 domains point out that these phosphorylated tyrosines are located on the ligand-binding surface. Because a number of Tec family kinases are coexpressed in cells, it is possible that they could regulate the activity of each other through transphosphorylation.
Subject headings
- NATURVETENSKAP -- Biologi (hsv//swe)
- NATURAL SCIENCES -- Biological Sciences (hsv//eng)
Keyword
- Amino Acid Sequence
- Binding Sites/genetics
- Cell Line
- Cloning; Molecular
- Humans
- Molecular Sequence Data
- Phosphorylation
- Protein-Tyrosine Kinases/biosynthesis/*chemistry/metabolism
- Recombinant Proteins/biosynthesis
- Sequence Alignment
- src Homology Domains/genetics/*physiology
- Immunodeficiency
- Tyrosine kinase
- Btk
- Itk
- Tec
- Bmx
- Signal transduction
- X-linked agammaglobulinemia
- XLA
Publication and Content Type
- ref (subject category)
- art (subject category)
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- By the author/editor
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Nore, Beston F
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Mattsson, Pekka ...
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Antonsson, Per
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Bäckesjö, Carl-M ...
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Westlund, Anna
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Lennartsson, Joh ...
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show more...
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Hansson, Henrik
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Löw, Peter
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Rönnstrand, Lars
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Smith, C I Edvar ...
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show less...
- About the subject
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- NATURAL SCIENCES
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NATURAL SCIENCES
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and Biological Scien ...
- Articles in the publication
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Biochimica et Bi ...
- By the university
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Uppsala University
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Lund University