+ |
ATM | up-regulates
phosphorylation
|
RASSF1 |
0.566 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-161934 |
Ser135 |
EWETPDLsQAEIEQK |
Homo sapiens |
|
pmid |
sentence |
19962312 |
We show that, upon dna damage, rassf1a is phosphorylated by atm on ser131 and is involved in the activation of both mst2 and lats1, leading to the stabilization of p73. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CHEK1 |
phosphorylation
|
RASSF1 |
0.36 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-203144 |
Ser188 |
PSSKKPPsLQDARRG |
Homo sapiens |
|
pmid |
sentence |
24197116 |
This study reveals that chk1-mediated phosphorylation of rassf1a, at serine 184, plays an important role in cell-cycle regulation |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CyclinD/CDK4 | down-regulates
phosphorylation
|
RASSF1 |
0.489 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-216976 |
Ser207 |
TSVRRRTsFYLPKDA |
Homo sapiens |
|
pmid |
sentence |
18071316 |
This skp2-dependent destruction of rassf1a requires phosphorylation of the latter on serine-203 by cyclin d-cyclin-dependent kinase 4. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CDK4 | down-regulates
phosphorylation
|
RASSF1 |
0.419 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-159849 |
Ser207 |
TSVRRRTsFYLPKDA |
Homo sapiens |
|
pmid |
sentence |
18071316 |
This skp2-dependent destruction of rassf1a requires phosphorylation of the latter on serine-203 by cyclin d-cyclin-dependent kinase 4. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AURKA | down-regulates
phosphorylation
|
RASSF1 |
0.46 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-155815 |
Ser207 |
TSVRRRTsFYLPKDA |
Homo sapiens |
|
pmid |
sentence |
17563743 |
Aurora-a appears to phosphorylate rassf1a at threonine202 and/or serine203 that reside within the known microtubule-binding domain of rassf1a. Substitutions of these residues with glutamic acid at both positions, mimicking constitutive phosphorylation of rassf1a, disrupt rassf1a interactions with microtubules and abolish its ability to induce m-phase cell cycle arrest. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-155819 |
Thr206 |
GTSVRRRtSFYLPKD |
Homo sapiens |
|
pmid |
sentence |
17563743 |
AuroraT-a appears to phosphorylate rassf1a at threonine202 and/or serine203 that reside within the known microtubule-binding domain of rassf1a. Substitutions of these residues with glutamic acid at both positions, mimicking constitutive phosphorylation of rassf1a, disrupt rassf1a interactions with microtubules and abolish its ability to induce m-phase cell cycle arrest. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
AURKB | down-regulates
phosphorylation
|
RASSF1 |
0.45 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-184561 |
Ser207 |
TSVRRRTsFYLPKDA |
Homo sapiens |
|
pmid |
sentence |
19276349 |
Here, we show that aurora a and b associate with and phosphorylate rassf1a on serine 203 aurora a regulates prometaphase progression by inhibiting the ability of rassf1a to suppress apc-cdc20 activity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
FAS | up-regulates
|
RASSF1 |
0.26 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-198435 |
|
|
Homo sapiens |
|
pmid |
sentence |
22830020 |
It was also shown that the fas active receptor induces rassf1a to compete with raf1 in binding to mst2, thus promoting the formation of a lats1 complex. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CNKSR1 | up-regulates
binding
|
RASSF1 |
0.412 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-198432 |
|
|
Homo sapiens |
|
pmid |
sentence |
22830020 |
Cnk1 binds to rassf1a and promotes apoptosis through a pathway that requires rassf1a and mst kinases. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RASSF1 | up-regulates activity
binding
|
STK3 |
0.687 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-249588 |
|
|
Homo sapiens |
|
pmid |
sentence |
22195963 |
Mutant K-Ras promotes MST2 activation in two ways (i.e., by direct disruption of the inhibitory Raf-1-MST2 complex (Matallanas et al., 2008) and by forming an activating K-Ras-RASSF1AMST2 complex, as reported here. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Hippo Signaling |
+ |
RASSF5 | up-regulates activity
binding
|
RASSF1 |
0.526 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-249587 |
|
|
Homo sapiens |
|
pmid |
sentence |
22195963 |
NORE1A can heterodimerize with RASSF1A and, thus, mediate K-Ras regulation of RASSF1A |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RASSF1 | up-regulates
binding
|
STK3/4 |
0.801 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269950 |
|
|
Homo sapiens |
|
pmid |
sentence |
21808241 |
Mst1/2 is also activated by binding to Ras association domain family (RASSF) proteins, possibly owing to alteration of Mst1/2 subcellular localization. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Hippo Signaling |
+ |
RASSF1 | up-regulates
binding
|
STK3 |
0.687 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-175790 |
|
|
Homo sapiens |
|
pmid |
sentence |
21808241 |
Mst1/2 is also activated by binding to Ras association domain family (RASSF) proteins, possibly owing to alteration of Mst1/2 subcellular localization. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Hippo Signaling |
+ |
MOAP1 | up-regulates activity
binding
|
RASSF1 |
0.591 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272914 |
|
|
Homo sapiens |
|
pmid |
sentence |
26269600 |
Modulator of apoptosis 1 (MOAP-1) is a BH3-like protein that plays key roles in cell death or apoptosis. It is an integral partner to the tumor suppressor protein, Ras association domain family 1A (RASSF1A), and functions to activate the Bcl-2 family pro-apoptotic protein Bax. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
KRAS | up-regulates activity
binding
|
RASSF1 |
0.638 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-249585 |
|
|
Homo sapiens |
|
pmid |
sentence |
22195963 |
Mutant K-Ras promotes MST2 activation in two ways (i.e., by direct disruption of the inhibitory Raf-1-MST2 complex (Matallanas et al., 2008) and by forming an activating (i.e., by direct disruption of the inhibitory Raf-1-MST2 complex K-Ras-RASSF1AMST2 complex, as reported here |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Non-small-cell lung cancer (NSCLC) |
+ |
14-3-3 | down-regulates
binding
|
RASSF1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-175121 |
|
|
Homo sapiens |
|
pmid |
sentence |
21776416 |
Basal inactivation of rassf1a is achieved by rassf1a self association and via 14-3-3 interactions (to isoforms s and e) at serine 175/178/179 of rassf1a. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Hippo Signaling |
+ |
RASSF1 | down-regulates quantity by repression
post transcriptional regulation
|
CCND1 |
0.56 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259455 |
|
|
Homo sapiens |
NCI-H1299 Cell |
pmid |
sentence |
12024041 |
RASSF1A expression dramatically inhibits native cyclin D1 accumulation | Regulation of cyclin D1 accumulation by RASSF1A is independent of the cyclin D1 promoter and likely occurs through inhibition of mRNA translation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RASSF1 | up-regulates
binding
|
STK4 |
0.801 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-197744 |
|
|
Homo sapiens |
|
pmid |
sentence |
22683405 |
Rassf1a and mst1 co-exist as a complex localizing at microtubules throughout the cell cycle, of which the rassf1a mst1 interaction is stimulatory to the mst1 kinase activity. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-175793 |
|
|
Homo sapiens |
|
pmid |
sentence |
21808241 |
Mst1/2 is also activated by binding to Ras association domain family (RASSF) proteins, possibly owing to alteration of Mst1/2 subcellular localization. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
Pathways: | Hippo Signaling |