+ |
p38 | down-regulates
phosphorylation
|
NFATC4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-87393 |
Ser168 |
QGGGAFFsPSPGSSS |
Homo sapiens |
|
pmid |
sentence |
11997522 |
Phosphorylation of nfatc4 by p38 mitogen-activated protein kinasesthe p38 map kinase phosphorylates multiple residues, including ser(168) and ser(170), in the nfat homology domain of nfatc4. Replacement of ser(168,170) with ala promotes nuclear localization of nfatc4 and increases nfat-mediated transcription activity. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-87397 |
Ser170 |
GGAFFSPsPGSSSLS |
Homo sapiens |
|
pmid |
sentence |
11997522 |
Phosphorylation of nfatc4 by p38 mitogen-activated protein kinasesthe p38 map kinase phosphorylates multiple residues, including ser(168) and ser(170), in the nfat homology domain of nfatc4. Replacement of ser(168,170) with ala promotes nuclear localization of nfatc4 and increases nfat-mediated transcription activity. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
MAPK14 | down-regulates activity
phosphorylation
|
NFATC4 |
0.411 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-250107 |
Ser168 |
QGGGAFFsPSPGSSS |
Cricetulus griseus |
BHK Cell |
pmid |
sentence |
11997522 |
P38 MAP kinase phosphorylates Ser168 and Ser170 of NFATc4. Mutational replacement of Ser168,170 with Ala promotes NFATc4 nuclear localization and increases NFATc4-mediated transcription activity. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-250108 |
Ser170 |
GGAFFSPsPGSSSLS |
Cricetulus griseus |
BHK Cell |
pmid |
sentence |
11997522 |
P38 MAP kinase phosphorylates Ser168 and Ser170 of NFATc4. Mutational replacement of Ser168,170 with Ala promotes NFATc4 nuclear localization and increases NFATc4-mediated transcription activity. |
|
Publications: |
2 |
Organism: |
Cricetulus Griseus |
+ |
RPS6KA3 | up-regulates
phosphorylation
|
NFATC4 |
0.394 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-234465 |
Ser281 |
SGTPSSAsPALSRRG |
Mus musculus |
|
pmid |
sentence |
17213202 |
Serines 281 and 285 of the nfat3 protein might be target amino acids of rsk2 phosphorylationrsk2 induced nuclear localization of nfat3. Rsk2 phosphorylated nfat3 in vitro (km=3.559 microm), and activation of nfat3 by rsk2 enhanced the promoter activity of nfat3 downstream target genes in vivo. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-234469 |
Ser285 |
SSASPALsRRGSLGE |
Mus musculus |
|
pmid |
sentence |
17213202 |
Serines 281 and 285 of the nfat3 protein might be target amino acids of rsk2 phosphorylationrsk2 induced nuclear localization of nfat3. Rsk2 phosphorylated nfat3 in vitro (km=3.559 microm), and activation of nfat3 by rsk2 enhanced the promoter activity of nfat3 downstream target genes in vivo. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-234473 |
Ser289 |
PALSRRGsLGEEGSE |
Mus musculus |
|
pmid |
sentence |
17213202 |
The results indicated that rsk2 phosphorylated two additional sites at ser289 (peptide 2) and ser344 (peptide 3)rsk2 induced nuclear localization of nfat3. Rsk2 phosphorylated nfat3 in vitro (km=3.559 microm), and activation of nfat3 by rsk2 enhanced the promoter activity of nfat3 downstream target genes in vivo. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-235652 |
Ser344 |
QAVALPRsEEPASCN |
Mus musculus |
C2C12 Cell, Myoblast |
pmid |
sentence |
17213202 |
The results indicated that rsk2 phosphorylated two additional sites at ser289 (peptide 2) and ser344 (peptide 3)rsk2 induced nuclear localization of nfat3. Rsk2 phosphorylated nfat3 in vitro (km=3.559 microm), and activation of nfat3 by rsk2 enhanced the promoter activity of nfat3 downstream target genes in vivo. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-133283 |
Ser676 |
SNGRRKRsPTQSFRF |
Homo sapiens |
|
pmid |
sentence |
15657420 |
We demonstrate that p90 ribosomal s6 kinase (rsk) is recruited to the nfat-dna transcription complex upon activation.Bound Rsk phosphorylates ser(676) and potentiates nfatc4 dna binding. Ser(676) is also targeted by the erk map kinase. |
|
Publications: |
5 |
Organism: |
Mus Musculus, Homo Sapiens |
Tissue: |
Muscle, Skeletal Muscle, Myotube |
+ |
MAPK1 | up-regulates
phosphorylation
|
NFATC4 |
0.287 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-133272 |
Ser676 |
SNGRRKRsPTQSFRF |
Homo sapiens |
|
pmid |
sentence |
15657420 |
We demonstrate that p90 ribosomal s6 kinase (rsk) is recruited to the nfat-dna transcription complex upon activation.Bound Rsk phosphorylates ser(676) and potentiates nfatc4 dna binding. Ser(676) is also targeted by the erk map kinase. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MAPK3 | up-regulates
phosphorylation
|
NFATC4 |
0.294 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-133276 |
Ser676 |
SNGRRKRsPTQSFRF |
Homo sapiens |
|
pmid |
sentence |
15657420 |
The formation of rsk-nfatc4-dna transcription complex is also apparent upon adipogenesis. Bound rsk phosphorylates ser(676) and potentiates nfatc4 dna binding by escalating nfat-dna association. Ser(676) is also targeted by the erk map kinase, which interacts with nfat at a distinct region than rsk. Thus, integration of the erk/rsk signaling pathway provides a mechanism to modulate nfatc4 transcription activity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
Gbeta | up-regulates
phosphorylation
|
NFATC4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270047 |
|
|
Homo sapiens |
|
pmid |
sentence |
15657420 |
The formation of rsk-nfatc4-dna transcription complex is also apparent upon adipogenesis. Bound rsk phosphorylates ser(676) and potentiates nfatc4 dna binding by escalating nfat-dna association. Ser(676) is also targeted by the erk map kinase, which interacts with nfat at a distinct region than rsk. Thus, integration of the erk/rsk signaling pathway provides a mechanism to modulate nfatc4 transcription activity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
NFATC4 | up-regulates quantity by expression
transcriptional regulation
|
PTGS2 |
0.286 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264027 |
|
|
Homo sapiens |
|
pmid |
sentence |
21871017 |
NFAT induces the transcription of the COX2 (cyclo-oxygenase-2) gene incancer cells thereby enhancing invasive migration |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
Calcineurin | up-regulates
dephosphorylation
|
NFATC4 |
0.551 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252322 |
|
|
Homo sapiens |
|
pmid |
sentence |
21880741 |
Calcineurin directly dephosphorylates nfat resulting in the nuclear import of nfat. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERK1/2 | up-regulates
phosphorylation
|
NFATC4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270160 |
|
|
Homo sapiens |
|
pmid |
sentence |
15657420 |
The formation of rsk-nfatc4-dna transcription complex is also apparent upon adipogenesis. Bound rsk phosphorylates ser(676) and potentiates nfatc4 dna binding by escalating nfat-dna association. Ser(676) is also targeted by the erk map kinase, which interacts with nfat at a distinct region than rsk. Thus, integration of the erk/rsk signaling pathway provides a mechanism to modulate nfatc4 transcription activity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PPP3CA | up-regulates
dephosphorylation
|
NFATC4 |
0.56 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-176379 |
|
|
Homo sapiens |
|
pmid |
sentence |
21880741 |
Calcineurin directly dephosphorylates nfat resulting in the nuclear import of nfat. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
NFATC4 | up-regulates quantity by expression
transcriptional regulation
|
GPC6 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264023 |
|
|
Homo sapiens |
Breast Cancer Cell |
pmid |
sentence |
21871017 |
NFAT transcriptionally regulates GPC6 induction in breast cancer cells and binds to three regulatory elements in the GPC6 proximal promoter. Expression of GPC6 in response to NFAT signalling promotes invasive migration, whereas GPC6 silencing with shRNA (small-hairpin RNA) potently blocks this phenotype. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |