+ |
MTOR | down-regulates activity
phosphorylation
|
AKT1S1 |
0.901 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-178120 |
Ser183 |
PTQQYAKsLPVSVPV |
in vitro |
|
pmid |
sentence |
18372248 |
Pras40 functions as a negative regulator when bound to mtorc1, and it dissociates from mtorc1 in response to insulin. Pras40 has been demonstrated to be a substrate of mtorc1, and one phosphorylation site, ser-183, has been identified. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-154956 |
Ser183 |
PTQQYAKsLPVSVPV |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
17517883 |
The proline-rich Akt substrate of 40 kilodaltons (PRAS40) was identified as a raptor-binding protein that is phosphorylated directly by mammalian target of rapamycin (mTOR) complex 1 (mTORC1) but not mTORC2 in vitro, predominantly at PRAS40 (Ser(183)).PRAS40 binding to raptor was also abolished by mutation of the major mTORC1 phosphorylation site, Ser(183), to Asp. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-178124 |
Ser212 |
EENGPPSsPDLDRIA |
in vitro |
|
pmid |
sentence |
18372248 |
In this study, we used two-dimensional phosphopeptide mapping in conjunction with mutational analysis to show that in addition to ser-183, mtorc1 also phosphorylates ser-212 and ser-221 in pras40 when assayed in vitro. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-178128 |
Ser221 |
DLDRIAAsMRALVLR |
in vitro |
|
pmid |
sentence |
18372248 |
We propose that after mtorc1 kinase activation by upstream regulators, pras40 is phosphorylated directly by mtor, thus contributing to the relief of pras40-mediated substrate competitionwe also find that mutation of ser-221 to ala increases the inhibitory activity of pras40 toward mtorc1. |
|
Publications: |
4 |
Organism: |
In Vitro, Homo Sapiens |
Pathways: | MTOR Signaling |
+ |
AKT1 | down-regulates activity
phosphorylation
|
AKT1S1 |
0.775 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252544 |
Thr246 |
LPRPRLNtSDFQKLK |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
12524439 |
Treatment of these cells with 4-hydroxytamoxifen stimulated the phosphorylation of wt PRAS40 but not the mutant PRAS40 in which Thr-246 was mutated. These results demonstrate that activation of Akt alone is sufficient to induce phosphorylation of PRAS40 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AKT2 | down-regulates activity
phosphorylation
|
AKT1S1 |
0.66 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-248046 |
Thr246 |
LPRPRLNtSDFQKLK |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
12524439 |
1) PRAS40 was phosphorylated in vitro by purified Akt on the same site that was phosphorylated in insulin-treated cells; 2) activation of an inducible Akt was alone sufficient to stimulate the phosphorylation of PRAS40; and 3) cells lacking Akt1 and Akt2 exhibit a diminished ability to phosphorylate this protein |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AKT | down-regulates activity
phosphorylation
|
AKT1S1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-236929 |
Thr246 |
LPRPRLNtSDFQKLK |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
12524439 |
Treatment of these cells with 4-hydroxytamoxifen stimulated the phosphorylation of wt PRAS40 but not the mutant PRAS40 in which Thr-246 was mutated. These results demonstrate that activation of Akt alone is sufficient to induce phosphorylation of PRAS40 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | MTOR Signaling |
+ |
DYRK3 | down-regulates
phosphorylation
|
AKT1S1 |
0.348 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-201002 |
|
|
Homo sapiens |
|
pmid |
sentence |
23415227 |
When dyrk3 is active, it allows stress granule dissolution, releasing mtorc1 for signaling and promoting its activity by directly phosphorylating the mtorc1 inhibitor pras40 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AKT2 | down-regulates
phosphorylation
|
AKT1S1 |
0.66 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-152936 |
|
|
Homo sapiens |
|
pmid |
sentence |
17277771 |
Furthermore, pras40 phosphorylation by akt and association with 14-3-3, a cytosolic anchor protein, are crucial for insulin to stimulate mtor. These findings identify pras40 as an important regulator of insulin sensitivity of the akt-mtor pathway and a potential target for the treatment of cancers, insulin resistance and hamartoma syndromes. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-153931 |
|
|
Homo sapiens |
|
pmid |
sentence |
17386266 |
Insulin-stimulated phosphorylation of pras40 by akt/pkb suppresses its mtorc1 inhibitory activity. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
AKT1S1 | form complex
binding
|
mTORC1 |
0.795 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-205597 |
|
|
Homo sapiens |
|
pmid |
sentence |
25628925 |
Depending on their binding partners and sensitivities to rapamycin, mtor resides in at least two distinct complexes, termed mtor complex 1 (mtorc1, containing raptor, fkbp12, pras40 and mlst8) and mtor complex 2 (mtorc2, containing rictor, sin1, protor and mlst8) |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
14-3-3 | down-regulates
binding
|
AKT1S1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-162003 |
|
|
Homo sapiens |
|
pmid |
sentence |
20006481 |
Akt can phosphorylate pras40, a raptor binding protein that also acts as an inhibitor of torc1. Akt-mediated phosphorylation of pras40 again promotes 14-3-3 binding, in this case leading to relief from pras40-mediated inhibition. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |