+ |
MARK4 | down-regulates activity
phosphorylation
|
MAPT (isoform 5) |
0.429 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273933 |
Ser262 |
NVKSKIGsTENLKHQ |
in vitro |
|
pmid |
sentence |
21204788 |
AMPK phosphorylation inhibits tau binding of microtubules. In order to study further the phosphorylation of tau by AMPK, we compared phosphorylation of tau by MARK4 or AMPK using a panel of phospho-tau antibodies (Figure 2A). Five phosphorylation sites common to both kinases were identified (Thr231, Ser262, Ser356, Ser396 and Ser422). In addition, AMPK, but not MARK4, was capable of phosphorylating Ser214 (Figure 2A). |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273932 |
Thr231 |
KKVAVVRtPPKSPSS |
in vitro |
|
pmid |
sentence |
21204788 |
AMPK phosphorylation inhibits tau binding of microtubules. In order to study further the phosphorylation of tau by AMPK, we compared phosphorylation of tau by MARK4 or AMPK using a panel of phospho-tau antibodies (Figure 2A). Five phosphorylation sites common to both kinases were identified (Thr231, Ser262, Ser356, Ser396 and Ser422). In addition, AMPK, but not MARK4, was capable of phosphorylating Ser214 (Figure 2A). |
|
Publications: |
2 |
Organism: |
In Vitro |
+ |
MARK4 | down-regulates activity
phosphorylation
|
MAPT (isoform 4) |
0.429 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273934 |
Ser353 |
RHLSNVSsTGSIDMV |
in vitro |
|
pmid |
sentence |
21204788 |
AMPK phosphorylation inhibits tau binding of microtubules. In order to study further the phosphorylation of tau by AMPK, we compared phosphorylation of tau by MARK4 or AMPK using a panel of phospho-tau antibodies (Figure 2A). Five phosphorylation sites common to both kinases were identified (Thr231, Ser262, Ser356, Ser396 and Ser422). In addition, AMPK, but not MARK4, was capable of phosphorylating Ser214 (Figure 2A). |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
MARK4 | down-regulates activity
phosphorylation
|
MAPT |
0.429 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273935 |
Ser396 |
DDKKAKTsTRSSAKT |
in vitro |
|
pmid |
sentence |
21204788 |
AMPK phosphorylation inhibits tau binding of microtubules. In order to study further the phosphorylation of tau by AMPK, we compared phosphorylation of tau by MARK4 or AMPK using a panel of phospho-tau antibodies (Figure 2A). Five phosphorylation sites common to both kinases were identified (Thr231, Ser262, Ser356, Ser396 and Ser422). In addition, AMPK, but not MARK4, was capable of phosphorylating Ser214 (Figure 2A). |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273936 |
Ser420 |
KHPTPGSsDPLIQPS |
in vitro |
|
pmid |
sentence |
21204788 |
AMPK phosphorylation inhibits tau binding of microtubules. In order to study further the phosphorylation of tau by AMPK, we compared phosphorylation of tau by MARK4 or AMPK using a panel of phospho-tau antibodies (Figure 2A). Five phosphorylation sites common to both kinases were identified (Thr231, Ser262, Ser356, Ser396 and Ser422). In addition, AMPK, but not MARK4, was capable of phosphorylating Ser214 (Figure 2A). |
|
Publications: |
2 |
Organism: |
In Vitro |
+ |
MARK4 | down-regulates activity
phosphorylation
|
TNK1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273865 |
Ser502 |
RMKGISRsLESVLSL |
Homo sapiens |
A-549 Cell |
pmid |
sentence |
34504101 |
We also discover a MARK-mediated phosphorylation on TNK1 at S502 that promotes an interaction between TNK1 and 14-3-3, which sequesters TNK1 and inhibits its kinase activity.Phosphorylation of TNK1 at S502 within the proline rich domain is required for TNK1 binding to 14-3-3.MARKs mediate phosphorylation at S502 and 14-3-3 binding to TNK1, which restrains the movement of TNK1 into heavy membrane-associated clusters. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
STK11 | up-regulates
phosphorylation
|
MARK4 |
0.515 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-122682 |
Thr214 |
TLGSKLDtFCGSPPY |
Homo sapiens |
|
pmid |
sentence |
14976552 |
Lkb1 is a master kinase that activates 13 kinases of the ampk subfamily, including mark/par-1we recently demonstrated that the lkb1 tumour suppressor kinase, in complex with the pseudokinase strad and the scaffolding protein mo25, phosphorylates and activates amp-activated protein kinase (ampk). A total of 12 human kinases (nuak1, nuak2, brsk1, brsk2, qik, qsk, sik, mark1, mark2, mark3, mark4 and melk) are related to ampk. Here we demonstrate that lkb1 can phosphorylate the t-loop of all the members of this subfamily, apart from melk, increasing their activity >50-fold |
|
Publications: |
1 |
Organism: |
Homo Sapiens |