+ |
GSK3B | up-regulates activity
phosphorylation
|
ARHGAP31 |
0.307 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262879 |
Thr789 |
PPAPPPPtPLEESTP |
Mus musculus |
NIH-3T3 Cell |
pmid |
sentence |
17158447 |
We show that GSK-3alpha and -beta interact with CdGAP in mammalian cells. We also demonstrate that GSK-3 phosphorylates CdGAP both in vitro and in vivo on Thr-776, which we have previously shown to be an ERK 1/2 phosphorylation site involved in CdGAP regulation. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
ERK1/2 | up-regulates activity
phosphorylation
|
ARHGAP31 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-263057 |
Thr789 |
PPAPPPPtPLEESTP |
Chlorocebus aethiops |
COS-7 Cell |
pmid |
sentence |
16024771 |
CdGAP interacts with and is phosphorylated by ERK-1 and RSK-1 in vitro. A putative DEF (docking for ERK FXFP) domain located in the proline-rich region of CdGAP is required for efficient binding and phosphorylation by ERK1/2. We identify Thr776 as an in vivo target site of ERK1/2 and as an important regulatory site of CdGAP activity. Together, these data suggest that CdGAP is a novel substrate of ERK1/2 and mediates cross talk between the Ras/mitogen-activated protein kinase pathway and regulation of Rac1 activity. |
|
Publications: |
1 |
Organism: |
Chlorocebus Aethiops |
+ |
GSK3A | up-regulates activity
phosphorylation
|
ARHGAP31 |
0.344 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262878 |
Thr789 |
PPAPPPPtPLEESTP |
Mus musculus |
NIH-3T3 Cell |
pmid |
sentence |
17158447 |
We show that GSK-3alpha and -beta interact with CdGAP in mammalian cells. We also demonstrate that GSK-3 phosphorylates CdGAP both in vitro and in vivo on Thr-776, which we have previously shown to be an ERK 1/2 phosphorylation site involved in CdGAP regulation. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
ARHGAP31 | down-regulates activity
gtpase-activating protein
|
RAC1 |
0.546 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260489 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
32203420 |
We therefore developed a screening-compatible live-cell imaging assay, using FRET-based biosensors for the prototype GTPases RHOA, RAC1 and CDC4215,19,20 (Extended Data Fig. 2 and Supplementary Note 1)|We found catalytic activities for 45/75 RhoGEFs and 48/63 RhoGAPs| Our data thus not only reveal extensive promiscuity among regulators, but also that the inactivating RhoGAPs are less selective than the activating RhoGEFs (p-value=0.02)(Supplementary Table 2). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ARHGAP31 | down-regulates activity
gtpase-activating protein
|
CDC42 |
0.66 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260490 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
32203420 |
We therefore developed a screening-compatible live-cell imaging assay, using FRET-based biosensors for the prototype GTPases RHOA, RAC1 and CDC4215,19,20 (Extended Data Fig. 2 and Supplementary Note 1)|We found catalytic activities for 45/75 RhoGEFs and 48/63 RhoGAPs| Our data thus not only reveal extensive promiscuity among regulators, but also that the inactivating RhoGAPs are less selective than the activating RhoGEFs (p-value=0.02)(Supplementary Table 2). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ARHGAP31 | down-regulates activity
gtpase-activating protein
|
RHOA |
0.509 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260488 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
32203420 |
We therefore developed a screening-compatible live-cell imaging assay, using FRET-based biosensors for the prototype GTPases RHOA, RAC1 and CDC4215,19,20 (Extended Data Fig. 2 and Supplementary Note 1)|We found catalytic activities for 45/75 RhoGEFs and 48/63 RhoGAPs| Our data thus not only reveal extensive promiscuity among regulators, but also that the inactivating RhoGAPs are less selective than the activating RhoGEFs (p-value=0.02)(Supplementary Table 2). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |