The nuclear function of the c-Abl tyrosine kinase is not well understood. In order to identify nuclear substrates of Abl, we constructed a constitutively active and nuclear form of the protein. We found that active nuclear Abl efficiently phosphorylate c-Jun, a transcription factor not previously known to be tyrosine phosphorylated. After phosphorylation of c-Jun by Abl on Tyr170, both proteins interacted via the SH2 domain of Abl. Surprisingly, elevated levels of c-Jun activated nuclear Abl, resulting in activation of the JNK serine/threonine kinase. This phosphorylation circuit generates nuclear tyrosine phosphorylation and represents a reversal of previously known signalling models
The kinase activity of c-Abl is known to be tightly regulated. Mechanisms of c-Abl kinase regulation...
YT521-B is a ubiquitously expressed nuclear protein that changes alternative splice site usage in a ...
<p><b>A</b> The c-Abl isoform Ib is characterized by myristoylation (Myr) on Gly-2 of the N-terminal...
The nuclear function of the c-Abl tyrosine kinase is not well understood. In order to identify nucle...
The regulation of c-Jun transcriptional activity by Jun N-terminal kinase (JNK) has become a paradig...
Tyrosine phosphorylation is usually associated with cytoplasmic events. Yet, over the years, many re...
c-Abl is a non-receptor protein-tyrosine kinase lacking a clear physiological role. A clue to its no...
Tyrosine phosphorylation of proteins by protein tyrosine kinases is an important step in initiating ...
Genetic alterations causing constitutive tyrosine kinase activation are observed in a broad spectrum...
Protein tyrosine kinases of the Abl family have diverse roles in normal cellular regulation and driv...
The activity of protein kinases is regulated by multiple molecular mechanisms, and their disruption ...
The c-ABL tyrosine kinase is activated following either the loss or mutation of its Src homology dom...
The ABL1 proto-oncogene encodes a cytoplasmic and nuclear protein tyrosine kinase (c-Abl) that has b...
Many extracellular and intracellular signals promote the c-Abl tyrosine kinase activity. c-Abl in tu...
Using the specific Abl tyrosine kinase inhibitor STI 571, we purified unphosphorylated murine type I...
The kinase activity of c-Abl is known to be tightly regulated. Mechanisms of c-Abl kinase regulation...
YT521-B is a ubiquitously expressed nuclear protein that changes alternative splice site usage in a ...
<p><b>A</b> The c-Abl isoform Ib is characterized by myristoylation (Myr) on Gly-2 of the N-terminal...
The nuclear function of the c-Abl tyrosine kinase is not well understood. In order to identify nucle...
The regulation of c-Jun transcriptional activity by Jun N-terminal kinase (JNK) has become a paradig...
Tyrosine phosphorylation is usually associated with cytoplasmic events. Yet, over the years, many re...
c-Abl is a non-receptor protein-tyrosine kinase lacking a clear physiological role. A clue to its no...
Tyrosine phosphorylation of proteins by protein tyrosine kinases is an important step in initiating ...
Genetic alterations causing constitutive tyrosine kinase activation are observed in a broad spectrum...
Protein tyrosine kinases of the Abl family have diverse roles in normal cellular regulation and driv...
The activity of protein kinases is regulated by multiple molecular mechanisms, and their disruption ...
The c-ABL tyrosine kinase is activated following either the loss or mutation of its Src homology dom...
The ABL1 proto-oncogene encodes a cytoplasmic and nuclear protein tyrosine kinase (c-Abl) that has b...
Many extracellular and intracellular signals promote the c-Abl tyrosine kinase activity. c-Abl in tu...
Using the specific Abl tyrosine kinase inhibitor STI 571, we purified unphosphorylated murine type I...
The kinase activity of c-Abl is known to be tightly regulated. Mechanisms of c-Abl kinase regulation...
YT521-B is a ubiquitously expressed nuclear protein that changes alternative splice site usage in a ...
<p><b>A</b> The c-Abl isoform Ib is characterized by myristoylation (Myr) on Gly-2 of the N-terminal...