Unexpected effects of FERM domain mutations on catalytic activity of Jak3: structural implication for Janus kinases.
Janus kinases comprise carboxyterminal kinase, pseudokinase, SH2-like, and N-terminal FERM domains. We identified three patient-derived mutations in the FERM domain of Jak3 and investigated the functional consequences of these mutations. These mutations inhibited receptor binding and also abrogated kinase activity, suggesting interactions between the FERM and kinase domains. In fact, the domains were found to physically associate, and coexpression of the FERM domain enhanced activity of the isolated kinase domain. Conversely, staurosporine, which alters kinase domain structure, disrupted receptor binding, even though the catalytic activity of Jak3 is dispensable for receptor binding. Thus, the Jak FERM domain appears to have two critical functions: receptor interaction and maintenance of kinase integrity.
Duke Scholars
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- src-Family Kinases
- Staurosporine
- Sequence Alignment
- Recombinant Fusion Proteins
- Receptors, Interleukin-7
- Pyrimidines
- Protein-Tyrosine Kinases
- Protein Structure, Tertiary
- Mutation
- Mutagenesis, Site-Directed
Citation
Published In
DOI
ISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- src-Family Kinases
- Staurosporine
- Sequence Alignment
- Recombinant Fusion Proteins
- Receptors, Interleukin-7
- Pyrimidines
- Protein-Tyrosine Kinases
- Protein Structure, Tertiary
- Mutation
- Mutagenesis, Site-Directed