+ |
PRKACA | down-regulates activity
phosphorylation
|
RARA |
0.378 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276281 |
Ser219 |
NSSEQRVsLDIDLWD |
Homo sapiens |
|
pmid |
sentence |
20215566 |
Mutagenesis of serine 219 (S219) and S369 at the PKA sites on RARA to either double alanines or double glutamic acids showed that both PKA sites are important for RARA activity. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276282 |
Ser369 |
YVRKRRPsRPHMFPK |
Homo sapiens |
|
pmid |
sentence |
20215566 |
Mutagenesis of serine 219 (S219) and S369 at the PKA sites on RARA to either double alanines or double glutamic acids showed that both PKA sites are important for RARA activity. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
CDK7 | up-regulates
phosphorylation
|
RARA |
0.526 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-49693 |
Ser77 |
EIVPSPPsPPPLPRI |
Homo sapiens |
HeLa Cell |
pmid |
sentence |
9230306 |
However, only the coexpression of cdk7 stimulated ser-77 phosphorylation in vivo and enhanced transactivation by rar alpha, but not by a s77a rar mutant. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CDK7 |
phosphorylation
|
RARA |
0.526 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-116582 |
Ser77 |
EIVPSPPsPPPLPRI |
Homo sapiens |
|
pmid |
sentence |
11955452 |
Thus, we demonstrate that the cdk7 kinase of tfiih phosphorylates the nuclear receptor, then allowing ligand-dependent control of the activation of the hormone-responsive genes. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TFIIH |
phosphorylation
|
RARA |
0.272 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269332 |
Ser77 |
EIVPSPPsPPPLPRI |
Homo sapiens |
|
pmid |
sentence |
11955452 |
Thus, we demonstrate that the cdk7 kinase of tfiih phosphorylates the nuclear receptor, then allowing ligand-dependent control of the activation of the hormone-responsive genes. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AKT | down-regulates
phosphorylation
|
RARA |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-143721 |
Ser96 |
FVCQDKSsGYHYGVS |
Homo sapiens |
Lung Cancer Cell |
pmid |
sentence |
16417524 |
We report that akt, which is constitutively activated in nsclc cells, phosphorylates raralpha and inhibits its transactivation. / mutation of ser96 to alanine abrogated the suppressive effect of akt. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Acute Myeloid Leukemia, ASXL1 in AML |
+ |
AKT1 | down-regulates
phosphorylation
|
RARA |
0.584 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252489 |
Ser96 |
FVCQDKSsGYHYGVS |
Homo sapiens |
Lung Cancer Cell |
pmid |
sentence |
16417524 |
We report that akt, which is constitutively activated in nsclc cells, phosphorylates raralpha and inhibits its transactivation. / mutation of ser96 to alanine abrogated the suppressive effect of akt. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RARA | down-regulates quantity by repression
transcriptional regulation
|
CCNA1 |
0.246 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-249636 |
|
|
Homo sapiens |
NB-4 Cell |
pmid |
sentence |
11090075 |
RARα is involved in the regulation of cyclin A1. Further studies using ligands selective for various retinoic acid receptors suggested that cyclin A1 expression is negatively regulated by activated RARα. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Acute Myeloid Leukemia, ASXL1 in AML |
+ |
THR | up-regulates
binding
|
RARA |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270313 |
|
|
Homo sapiens |
|
pmid |
sentence |
15650024 |
We report that the retinoic acid receptors (rars), a distinct class of nuclear receptors, are also efficient heterodimer partners for trs. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
NCOA2 | up-regulates
binding
|
RARA |
0.615 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-96827 |
|
|
Homo sapiens |
|
pmid |
sentence |
12503607 |
Transcriptional coactivator for steroid receptors and nuclear receptors.nteracts with casp8ap2 and ttll5/stamp. Interacts with esr1, rara and rxra. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RARA | up-regulates
binding
|
RXRA |
0.711 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-16433 |
|
|
Homo sapiens |
|
pmid |
sentence |
1310351 |
Here we report that the transcriptional activity of rar and rxr can be reciprocally modulated by direct interactions between the two proteins |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Acute Myeloid Leukemia, ASXL1 in AML, Retinoic acid Signaling |
+ |
RXRB | up-regulates
binding
|
RARA |
0.708 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-16674 |
|
|
Homo sapiens |
|
pmid |
sentence |
1310351 |
Here we report that the transcriptional activity of rar and rxr can be reciprocally modulated by direct interactions between the two proteins |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
THRA | up-regulates
binding
|
RARA |
0.407 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-133240 |
|
|
Homo sapiens |
|
pmid |
sentence |
15650024 |
We report that the retinoic acid receptors (rars), a distinct class of nuclear receptors, are also efficient heterodimer partners for trs. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Oxytocin signaling |
+ |
all-trans-retinoic acid | up-regulates activity
chemical activation
|
RARA |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256194 |
|
|
Homo sapiens |
|
pmid |
sentence |
17132853 |
The physiological effects of retinoic acids (RAs) are mediated by members of two families of nuclear receptors, the retinoic acid receptors (RARs) and the retinoid X receptors (RXRs), which are encoded by three distinct human genes, RXRalpha, RXRbeta, and RXRgamma. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-258138 |
|
|
Chlorocebus aethiops |
COS-7 Cell |
pmid |
sentence |
19058965 |
Tazarotene and its analogue 8 are RAR-β,γ selective acetylenic retinoids, whereas analogue 9 is very active on the three subtypes. |
|
Publications: |
2 |
Organism: |
Homo Sapiens, Chlorocebus Aethiops |
Pathways: | Acute Myeloid Leukemia, Retinoic acid Signaling |
+ |
RARA | down-regulates quantity by repression
transcriptional regulation
|
NR4A1 |
0.296 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-76980 |
|
|
Homo sapiens |
|
pmid |
sentence |
10772826 |
Retinoic acid and its receptors repress the expression and transactivation functions of nur77 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RARA | up-regulates
binding
|
THR |
0.516 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270293 |
|
|
Homo sapiens |
|
pmid |
sentence |
15650024 |
We report that the retinoic acid receptors (rars), a distinct class of nuclear receptors, are also efficient heterodimer partners for trs. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RARA | up-regulates
binding
|
THRA |
0.407 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-133231 |
|
|
Homo sapiens |
|
pmid |
sentence |
15650024 |
We report that the retinoic acid receptors (rars), a distinct class of nuclear receptors, are also efficient heterodimer partners for trs. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Oxytocin signaling |
+ |
ASXL1 | up-regulates activity
binding
|
RARA |
0.456 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255910 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
16606617 |
Therefore, ASXL1, a vertebrate PcG/TrxG protein, may mediate RA-regulated cell growth by modulating RAR activity.Finally, the ASXL1-induced accumulation of acetylated H3 may enhance the RAR-mediated transcriptional activity. In this study, we demonstrate that mammalian ASXL1 interacts with the AF-2 AD core of RAR (and RXR) through a novel, promiscuous NR box (LVMQLL) and enhances transcriptional activity of the receptors in certain cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Acute Myeloid Leukemia, ASXL1 in AML |
+ |
RARA | down-regulates quantity by repression
transcriptional regulation
|
EGFR |
0.405 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-114087 |
|
|
Homo sapiens |
|
pmid |
sentence |
11788593 |
We show that retinoic acid receptor (rar)-selective ligands reduce egfr level and the magnitude and duration of egfr activation in egf-stimulated cells |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Acute Myeloid Leukemia |
+ |
ASXL1 | up-regulates quantity by expression
transcriptional regulation
|
RARA |
0.456 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255933 |
|
|
Homo sapiens |
|
pmid |
sentence |
16606617 |
We also show that ASXL1 associates specifically with SRC-1 and cooperates synergistically in the transcriptional activation. Further data indicated that the transactivation domain (AD; amino acids 300–655) of ASXL1, newly defined in this study, interacts with the C-terminal AD2 (amino acids 1217–1441) of SRC-1, suggesting that one AD cooperates with the other AD in transcriptional activation by RAR. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Acute Myeloid Leukemia, ASXL1 in AML |
+ |
KMT2E | up-regulates activity
binding
|
RARA |
0.341 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260041 |
|
|
Homo sapiens |
|
pmid |
sentence |
21205756 |
MLL5 binds to retinoic acid receptor α (RARα) and induces transcriptional activation of RARα target genes by methylation of lysine residues of histone H3. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RARA | down-regulates
|
CTNNB1 |
0.383 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-73274 |
|
|
Homo sapiens |
|
pmid |
sentence |
10607566 |
We shown that retinoic acid (ra) decreases the activity of the beta-catenin-lef/tcf signaling pathway |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Acute Myeloid Leukemia, Retinoic acid Signaling |
+ |
RARA | up-regulates quantity by expression
transcriptional regulation
|
SLCO1B3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268989 |
|
|
|
|
pmid |
sentence |
15322262 |
Taken together, these findings suggest that the LPS-induced down-regulation of Oatp4 is likely due to reduction in the binding of HNF1alpha, C/EBP, HNF3, and RXR:RAR to the Oatp4 promoter. |
|
Publications: |
1 |
+ |
RXRA | up-regulates
binding
|
RARA |
0.711 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-16665 |
|
|
Homo sapiens |
|
pmid |
sentence |
1310351 |
Here we report that the transcriptional activity of rar and rxr can be reciprocally modulated by direct interactions between the two proteins |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Acute Myeloid Leukemia, ASXL1 in AML, Retinoic acid Signaling |
+ |
RARA | up-regulates activity
binding
|
THR |
0.516 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267801 |
|
|
Homo sapiens |
|
pmid |
sentence |
15650024 |
We report that the retinoic acid receptors (rars), a distinct class of nuclear receptors, are also efficient heterodimer partners for trs. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RARA | up-regulates
binding
|
RXRG |
0.653 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-16466 |
|
|
Homo sapiens |
|
pmid |
sentence |
1310351 |
Here we report that the transcriptional activity of rar and rxr can be reciprocally modulated by direct interactions between the two proteins |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RARA | up-regulates quantity by expression
transcriptional regulation
|
RXRG |
0.653 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-16469 |
|
|
Homo sapiens |
|
pmid |
sentence |
1310351 |
Here we report that the transcriptional activity of rar and rxr can be reciprocally modulated by direct interactions between the two proteins |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
9-cis-retinoic acid | up-regulates activity
chemical activation
|
RARA |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259234 |
|
|
Homo sapiens |
|
pmid |
sentence |
18321241 |
Alitretinoin (9-cis-retinoic acid) is a unique panagonist retinoid, capable of binding to all six known retinoid receptors (RAR-alpha, -beta, -gamma, and RXR-alpha, -beta, -gamma). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
THR | up-regulates activity
binding
|
RARA |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267779 |
|
|
Homo sapiens |
|
pmid |
sentence |
15650024 |
We report that the retinoic acid receptors (rars), a distinct class of nuclear receptors, are also efficient heterodimer partners for trs. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RARA | up-regulates quantity by expression
transcriptional regulation
|
OXT |
0.256 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268548 |
|
|
Homo sapiens |
|
pmid |
sentence |
6153132 |
The human and rat OT promoters could be stimulated by the ligand-activated estrogen receptors ERalpha and ERbeta, the thyroid hormone receptor THRapha, and the retinoic acid receptors RARalpha and RARbeta in a variety of cells (3, 477, 478). However, it is important to note that these results were obtained from cotransfection experiments in cell lines, i.e., under nonphysiological circumstances. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Oxytocin signaling |
+ |
NCOA1 | up-regulates quantity by expression
transcriptional regulation
|
RARA |
0.696 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255932 |
|
|
Homo sapiens |
|
pmid |
sentence |
16606617 |
We also show that ASXL1 associates specifically with SRC-1 and cooperates synergistically in the transcriptional activation. Further data indicated that the transactivation domain (AD; amino acids 300–655) of ASXL1, newly defined in this study, interacts with the C-terminal AD2 (amino acids 1217–1441) of SRC-1, suggesting that one AD cooperates with the other AD in transcriptional activation by RAR. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Acute Myeloid Leukemia, ASXL1 in AML |