+ |
MAPK1 | up-regulates quantity by stabilization
phosphorylation
|
METTL3 |
0.276 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265950 |
Ser43 |
RNPEAALsPTFRSDS |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
33217317 |
Mass spectrometry analysis showed that ERK phosphorylates METTL3 at three highly conserved residues: S43, S50, and S525 (Figures 2D and 2E). Mutational analysis further confirmed these three sites as main ERK phosphorylation sites (Figure 2F). Phosphorylation of METTL3 increases interaction with USP5, decreasing ubiquitination to stabilize the m6 A methyltransferase complex. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265946 |
Ser50 |
SPTFRSDsPVPTAPT |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
33217317 |
Mass spectrometry analysis showed that ERK phosphorylates METTL3 at three highly conserved residues: S43, S50, and S525 (Figures 2D and 2E). Mutational analysis further confirmed these three sites as main ERK phosphorylation sites (Figure 2F). Phosphorylation of METTL3 increases interaction with USP5, decreasing ubiquitination to stabilize the m6 A methyltransferase complex. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265948 |
Ser525 |
YGMIERLsPGTRKIE |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
33217317 |
Mass spectrometry analysis showed that ERK phosphorylates METTL3 at three highly conserved residues: S43, S50, and S525 (Figures 2D and 2E). Mutational analysis further confirmed these three sites as main ERK phosphorylation sites (Figure 2F). Phosphorylation of METTL3 increases interaction with USP5, decreasing ubiquitination to stabilize the m6 A methyltransferase complex. |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
ERK1/2 | up-regulates quantity by stabilization
phosphorylation
|
METTL3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265953 |
Ser43 |
RNPEAALsPTFRSDS |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
33217317 |
Mass spectrometry analysis showed that ERK phosphorylates METTL3 at three highly conserved residues: S43, S50, and S525 (Figures 2D and 2E). Mutational analysis further confirmed these three sites as main ERK phosphorylation sites (Figure 2F). Phosphorylation of METTL3 increases interaction with USP5, decreasing ubiquitination to stabilize the m6 A methyltransferase complex. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265951 |
Ser50 |
SPTFRSDsPVPTAPT |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
33217317 |
Mass spectrometry analysis showed that ERK phosphorylates METTL3 at three highly conserved residues: S43, S50, and S525 (Figures 2D and 2E). Mutational analysis further confirmed these three sites as main ERK phosphorylation sites (Figure 2F). Phosphorylation of METTL3 increases interaction with USP5, decreasing ubiquitination to stabilize the m6 A methyltransferase complex. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265952 |
Ser525 |
YGMIERLsPGTRKIE |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
33217317 |
Mass spectrometry analysis showed that ERK phosphorylates METTL3 at three highly conserved residues: S43, S50, and S525 (Figures 2D and 2E). Mutational analysis further confirmed these three sites as main ERK phosphorylation sites (Figure 2F). Phosphorylation of METTL3 increases interaction with USP5, decreasing ubiquitination to stabilize the m6 A methyltransferase complex. |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
MAPK3 | up-regulates quantity by stabilization
phosphorylation
|
METTL3 |
0.274 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265949 |
Ser43 |
RNPEAALsPTFRSDS |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
33217317 |
Mass spectrometry analysis showed that ERK phosphorylates METTL3 at three highly conserved residues: S43, S50, and S525 (Figures 2D and 2E). Mutational analysis further confirmed these three sites as main ERK phosphorylation sites (Figure 2F). Phosphorylation of METTL3 increases interaction with USP5, decreasing ubiquitination to stabilize the m6 A methyltransferase complex. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265945 |
Ser50 |
SPTFRSDsPVPTAPT |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
33217317 |
Mass spectrometry analysis showed that ERK phosphorylates METTL3 at three highly conserved residues: S43, S50, and S525 (Figures 2D and 2E). Mutational analysis further confirmed these three sites as main ERK phosphorylation sites (Figure 2F). Phosphorylation of METTL3 increases interaction with USP5, decreasing ubiquitination to stabilize the m6 A methyltransferase complex. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265947 |
Ser525 |
YGMIERLsPGTRKIE |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
33217317 |
Mass spectrometry analysis showed that ERK phosphorylates METTL3 at three highly conserved residues: S43, S50, and S525 (Figures 2D and 2E). Mutational analysis further confirmed these three sites as main ERK phosphorylation sites (Figure 2F). Phosphorylation of METTL3 increases interaction with USP5, decreasing ubiquitination to stabilize the m6 A methyltransferase complex. |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
ATM | up-regulates activity
phosphorylation
|
METTL3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265969 |
Ser43 |
RNPEAALsPTFRSDS |
|
|
pmid |
sentence |
32615088 |
Here, we report that, in response to DSBs, the RNA methyltransferase METTL3 is activated by ATM-mediated phosphorylation at S43. |
|
Publications: |
1 |
+ |
METTL3 | up-regulates quantity by stabilization
post transcriptional regulation
|
UCK2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275862 |
|
|
|
|
pmid |
sentence |
34430596 |
Furthermore, the m6A modification regulated by METTL3 led to UCK2 increased messenger RNA (mRNA) stability in melanoma cancer. Functional and mechanistic experiments indicated that UCK2 enhanced the metastasis of melanoma cancer cells through the WNT/β-catenin pathway. |
|
Publications: |
1 |
+ |
Gbeta | up-regulates quantity by stabilization
phosphorylation
|
METTL3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270035 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
33217317 |
Mass spectrometry analysis showed that ERK phosphorylates METTL3 at three highly conserved residues: S43, S50, and S525 (Figures 2D and 2E). Mutational analysis further confirmed these three sites as main ERK phosphorylation sites (Figure 2F). Phosphorylation of METTL3 increases interaction with USP5, decreasing ubiquitination to stabilize the m6 A methyltransferase complex. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
METTL3 | up-regulates quantity by expression
transcriptional regulation
|
EGFR |
0.339 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265954 |
|
|
Homo sapiens |
HEK-293 Cell, HeLa Cell |
pmid |
sentence |
27117702 |
Here we find that METTL3 promotes translation of certain mRNAs including epidermal growth factor receptor (EGFR) and the Hippo pathway effector TAZ in human cancer cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
METTL3 | up-regulates quantity by expression
transcriptional regulation
|
WWTR1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265955 |
|
|
Homo sapiens |
HEK-293 Cell, HeLa Cell |
pmid |
sentence |
27117702 |
Here we find that METTL3 promotes translation of certain mRNAs including epidermal growth factor receptor (EGFR) and the Hippo pathway effector TAZ in human cancer cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
METTL3 | up-regulates quantity by stabilization
post transcriptional regulation
|
USP13 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275839 |
|
|
|
|
pmid |
sentence |
36528756 |
Furthermore, N6-methyladenosine methyltransferase-like 3 (METTL3) mediated stabilization of USP13 mRNA that required the m6A reader IGF2BP2. |
|
Publications: |
1 |