+ |
MAPK1 | up-regulates
phosphorylation
|
ERF |
0.578 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-67520 |
Ser161 |
SPTEDPRsPPACSSS |
Homo sapiens |
|
pmid |
sentence |
10330152 |
The experiments presented here indicate that erf is regulated during nuclear import and/or export and that this process depends on its phosphorylation by erks our analysis indicates that in addition to t526 (position 7), s161 (position 2), s246 (position 3), and s251 (position 4) are also phosphorylated in vitro by erk2 and in vivo after mitogenic stimulation (fig. 3a). |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-67524 |
Ser246 |
RGGPEPLsPFPVSPL |
Homo sapiens |
|
pmid |
sentence |
10330152 |
The experiments presented here indicate that erf is regulated during nuclear import and/or export and that this process depends on its phosphorylation by erks our analysis indicates that in addition to t526 (position 7), s161 (position 2), s246 (position 3), and s251 (position 4) are also phosphorylated in vitro by erk2 and in vivo after mitogenic stimulation (fig. 3a). |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-67528 |
Ser251 |
PLSPFPVsPLAGPGS |
Homo sapiens |
|
pmid |
sentence |
10330152 |
The experiments presented here indicate that erf is regulated during nuclear import and/or export and that this process depends on its phosphorylation by erks our analysis indicates that in addition to t526 (position 7), s161 (position 2), s246 (position 3), and s251 (position 4) are also phosphorylated in vitro by erk2 and in vivo after mitogenic stimulation (fig. 3a). |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
MAPK1 | down-regulates
phosphorylation
|
ERF |
0.578 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-29505 |
Thr526 |
GEAGGPLtPRRVSSD |
Homo sapiens |
|
pmid |
sentence |
7588608 |
Consistent with the in vivo phosphorylation and inactivation by ras, erf is efficiently phosphorylated in vitro by erk2 and cdc2/cyclin b kinases, at sites similar to those detected in vivo. Furthermore, a single mutation at position 526 results in the loss of a specific phosphopeptide both in in vivo and in vitro (by erk2) labeling. Substitution of thr526 for glutamic acid also decreases the repression ability of erf |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CDK1 | down-regulates
phosphorylation
|
ERF |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-29501 |
|
|
Homo sapiens |
|
pmid |
sentence |
7588608 |
Consistent with the in vivo phosphorylation and inactivation by ras, erf is efficiently phosphorylated in vitro by erk2 and cdc2/cyclin b kinases, at sites similar to those detected in vivo. Furthermore, a single mutation at position 526 results in the loss of a specific phosphopeptide both in in vivo and in vitro (by erk2) labeling. Substitution of thr526 for glutamic acid also decreases the repression ability of erf |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CyclinB/CDK1 | down-regulates
phosphorylation
|
ERF |
0.375 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-216852 |
|
|
Homo sapiens |
|
pmid |
sentence |
7588608 |
Consistent with the in vivo phosphorylation and inactivation by ras, erf is efficiently phosphorylated in vitro by erk2 and cdc2/cyclin b kinases, at sites similar to those detected in vivo. Furthermore, a single mutation at position 526 results in the loss of a specific phosphopeptide both in in vivo and in vitro (by erk2) labeling. Substitution of thr526 for glutamic acid also decreases the repression ability of erf |
|
Publications: |
1 |
Organism: |
Homo Sapiens |