+ |
FRK | up-regulates quantity by stabilization
phosphorylation
|
BRCA1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275454 |
Tyr1552 |
HDLTETSyLPRQDLE |
Homo sapiens |
HCC-1937 Cell |
pmid |
sentence |
29156836 |
Herein, we demonstrate that Fyn-related kinase (Frk)/Rak plays an important role in maintaining genomic stability, possibly in part through positively regulating BRCA1 protein stability and function via tyrosine phosphorylation on BRCA1 Tyr1552. Rak-mediated tyrosine phosphorylation of BRCA1 is essential for its stability and function |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
FRK | up-regulates quantity by stabilization
phosphorylation
|
PTEN |
0.581 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275458 |
Tyr336 |
NKDKANRyFSPNFKV |
Homo sapiens |
MCF-7 Cell |
pmid |
sentence |
19345329 |
Rak phosphorylates PTEN on Tyr 336 to prevent its protein degradation. In this study, we demonstrate that the Rak tyrosine kinase physically interacts with PTEN and phosphorylates PTEN on Tyr336. Knockdown of Rak enhanced the binding of PTEN to its E3 ligase NEDD4-1 and promoted PTEN polyubiquitination, leading to PTEN protein degradation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
FRK | down-regulates quantity by destabilization
phosphorylation
|
YAP1 |
0.278 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275455 |
Tyr391 |
PFLNSGTyHSRDEST |
Homo sapiens |
U-251MG Cell |
pmid |
sentence |
35723276 |
Mechanistically, FRK interacted with and phosphorylated YAP on Tyr391/407/444, which recruited the classical E3 ubiquitin ligase Siah1 to catalyze ubiquitination and eventually degradation of YAP. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275456 |
Tyr407 |
SGLSMSSySVPRTPD |
Homo sapiens |
U-251MG Cell |
pmid |
sentence |
35723276 |
Mechanistically, FRK interacted with and phosphorylated YAP on Tyr391/407/444, which recruited the classical E3 ubiquitin ligase Siah1 to catalyze ubiquitination and eventually degradation of YAP. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275457 |
Tyr444 |
QQNRFPDyLEAIPGT |
Homo sapiens |
U-251MG Cell |
pmid |
sentence |
35723276 |
Mechanistically, FRK interacted with and phosphorylated YAP on Tyr391/407/444, which recruited the classical E3 ubiquitin ligase Siah1 to catalyze ubiquitination and eventually degradation of YAP. |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
regorafenib | down-regulates activity
chemical inhibition
|
FRK |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259207 |
|
|
Homo sapiens |
|
pmid |
sentence |
24756792 |
In biochemical in vitro or cell-based assays, Regorafenib or its major human active metabolites M-2 and M-5 inhibited the activity of RET,VEGFR 1-3, KIT, PDGFR-alpha, PDGFR-beta, FGFR1, FGFR2, TIE2, DDR2, TrkA, Eph2A, RAF-1, BRAF, BRAFV600E, SAPK2, PTK5, and Abl at concentrations that can be achieved clinically. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |