+ |
TEK | up-regulates activity
phosphorylation
|
TEK |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-109786 |
Tyr1048 |
GMTCAELyEKLPQGY |
in vitro |
|
pmid |
sentence |
11513602 |
Isoelectric focusing electrophoresis and mass spectrometric analysis of a tie2 autophosphorylation time course showed that tyr992 on the putative activation loop was phosphorylated first followed by tyr1108 in the c-terminal tail autophosphorylation of tie2 to produce ptie2 resulted in a 100-fold increase in kcat and a 460-fold increase in kcat/km. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259834 |
Tyr1102 |
MLEERKTyVNTTLYE |
Homo sapiens |
Endothelial Cell |
pmid |
sentence |
20973951 |
This phosphorylation requires a kinase competent Tie2 as well as intact tyrosines 1100 and 1106 (Y1100 and Y1106) on the receptor. This suggests that Y1100 and Y1106 on Tie2 play a role in Grb14 mediated signal transduction downstream of this receptor. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-246657 |
Tyr1102 |
MLEERKTyVNTTLYE |
Mus musculus |
NIH-3T3 Cell |
pmid |
sentence |
12082108 |
Recently, insights into Tie2 activation were provided by a solution of the Tie2 crystal structure (12). This structural analysis revealed several novel features, including two potential autoinhibitory mechanismsIn the unphosphorylated state, the hydroxyl groups of two important tyrosine residues, Tyr1101 and Tyr1112 (murine residue numbers), are hydrogen-bonded to surrounding residues, which may stabilize the C tail in this inhibitory conformationDeletion of the Tie2 C Tail Enhances Autophosphorylation and Kinase Activity in VitroDeletion of the C tail dramatically enhanced Tie2 autophosphorylation, despite the removal of Tyr1112, which was previously shown to be an important autophosphorylation site |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259833 |
Tyr1108 |
TYVNTTLyEKFTYAG |
Homo sapiens |
Endothelial Cell |
pmid |
sentence |
20973951 |
This phosphorylation requires a kinase competent Tie2 as well as intact tyrosines 1100 and 1106 (Y1100 and Y1106) on the receptor. This suggests that Y1100 and Y1106 on Tie2 play a role in Grb14 mediated signal transduction downstream of this receptor. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-109790 |
Tyr992 |
LSRGQEVyVKKTMGR |
in vitro |
|
pmid |
sentence |
11513602 |
Isoelectric focusing electrophoresis and mass spectrometric analysis of a tie2 autophosphorylation time course showed that tyr992 on the putative activation loop was phosphorylated first followed by tyr1108 in the c-terminal tail autophosphorylation of tie2 to produce ptie2 resulted in a 100-fold increase in kcat and a 460-fold increase in kcat/km. |
|
Publications: |
5 |
Organism: |
In Vitro, Homo Sapiens, Mus Musculus |
+ |
TEK | down-regulates activity
phosphorylation
|
TEK |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-246662 |
Tyr897 |
GACEHRGyLYLAIEY |
in vitro |
|
pmid |
sentence |
11080633 |
The Tie2 nucleotide binding loop is in an inhibitory conformation, which is not seen in other kinase structures, while its activation loop adopts an activated-like conformation in the absence of phosphorylation. Tyr-897, located in the N-terminal domain, may negatively regulate the activity of Tie2 by preventing dimerization of the kinase domains or by recruiting phosphatases when it is phosphorylated. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
N-[[3-fluoro-4-[[2-(1-methyl-4-imidazolyl)-7-thieno[3,2-b]pyridinyl]oxy]anilino]-sulfanylidenemethyl]-2-phenylacetamide | down-regulates
chemical inhibition
|
TEK |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-194349 |
|
|
Homo sapiens |
|
pmid |
sentence |
Other |
|
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TEK | up-regulates activity
binding
|
PIK3R1 |
0.517 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-242634 |
|
|
Chlorocebus aethiops |
|
pmid |
sentence |
14665640 |
Signal transduction pathways triggered by Tie2 have been extensively examined. Tyr-1101of Tie2 directly associates in a phosphotyrosine (pTyr)-dependent manner with the p85 regulatory subunit of phosphatidylinositol (PI) 3-kinase, which in turn activate PI 3-kinase, leading to cell motility and survival |
|
Publications: |
1 |
Organism: |
Chlorocebus Aethiops |
+ |
TEK | up-regulates quantity by expression
transcriptional regulation
|
MYOD1 |
0.276 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-241532 |
|
|
Mus musculus |
Myoblast |
pmid |
sentence |
26042050 |
the effects of the angiopoietins are not specific for vascular endothelial cells, as their receptors (Tie1, Tie2) are known to be expressed in hematopoietic cells and they have also recently been shown to be expressed in skeletal muscle cellsExogenous Ang-1 enhanced myogenic (MyoD and Myogenin) mRNA in differentiating myoblasts and increased myosin heavy chain protein. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
TEK | up-regulates quantity by expression
transcriptional regulation
|
MYH2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-241538 |
|
|
Mus musculus |
Myoblast |
pmid |
sentence |
26042050 |
the effects of the angiopoietins are not specific for vascular endothelial cells, as their receptors (Tie1, Tie2) are known to be expressed in hematopoietic cells and they have also recently been shown to be expressed in skeletal muscle cellsExogenous Ang-1 enhanced myogenic (MyoD and Myogenin) mRNA in differentiating myoblasts and increased myosin heavy chain protein. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
TEK | up-regulates activity
binding
|
SHC1 |
0.562 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-242573 |
|
|
Homo sapiens |
|
pmid |
sentence |
14665640 |
Our results identified a novel interaction between Tie2 with the adapter molecule ShcA and suggested that this interaction may play a role in the regulation of migration and three-dimensional organization of endothelial cells induced by angiopoietin-1. Furthermore, Tyr-1101 of Tie2 was identified as the primary binding site for the SH2 domain of ShcA. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TEK | up-regulates quantity by expression
transcriptional regulation
|
MYOG |
0.248 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-241535 |
|
|
Mus musculus |
Myoblast |
pmid |
sentence |
26042050 |
the effects of the angiopoietins are not specific for vascular endothelial cells, as their receptors (Tie1, Tie2) are known to be expressed in hematopoietic cells and they have also recently been shown to be expressed in skeletal muscle cellsExogenous Ang-1 enhanced myogenic (MyoD and Myogenin) mRNA in differentiating myoblasts and increased myosin heavy chain protein. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
ANGPTL1 | up-regulates
binding
|
TEK |
0.521 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-127354 |
|
|
Homo sapiens |
|
pmid |
sentence |
15284220 |
In experiments with human endothelial cell lines, ang3 was identified as an antagonist of tie2 and ang4 was identified as an agonist of tie2. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-65110 |
|
|
Homo sapiens |
|
pmid |
sentence |
10051567 |
Ang3 and ang4 are agonists of tie2, but mouse ang3 has strong activity only on endothelial cells of its own species. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
TEK | up-regulates activity
binding
|
PI3K |
0.483 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252728 |
|
|
Chlorocebus aethiops |
COS Cell |
pmid |
sentence |
14665640 |
Signal transduction pathways triggered by Tie2 have been extensively examined. Tyr-1101of Tie2 directly associates in a phosphotyrosine (pTyr)-dependent manner with the p85 regulatory subunit of phosphatidylinositol (PI) 3-kinase, which in turn activate PI 3-kinase, leading to cell motility and survival |
|
Publications: |
1 |
Organism: |
Chlorocebus Aethiops |
+ |
regorafenib | down-regulates activity
chemical inhibition
|
TEK |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259213 |
|
|
Homo sapiens |
|
pmid |
sentence |
24756792 |
In biochemical in vitro or cell-based assays, Regorafenib or its major human active metabolites M-2 and M-5 inhibited the activity of RET,VEGFR 1-3, KIT, PDGFR-alpha, PDGFR-beta, FGFR1, FGFR2, TIE2, DDR2, TrkA, Eph2A, RAF-1, BRAF, BRAFV600E, SAPK2, PTK5, and Abl at concentrations that can be achieved clinically. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ANGPT4 | up-regulates
binding
|
TEK |
0.688 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-127351 |
|
|
Homo sapiens |
Uveal Melanoma Cell |
pmid |
sentence |
15284220 |
In experiments with human endothelial cell lines, ang3 was identified as an antagonist of tie2 and ang4 was identified as an agonist of tie2. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Tissue: |
Lung |
+ |
ANGPT2 | up-regulates
binding
|
TEK |
0.923 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-59808 |
|
|
Homo sapiens |
|
pmid |
sentence |
9723709 |
Angiopoietin-1 and -2, bound to tek with similar affinities, and angiopoietin-1 effectively induced tek phosphorylation in hematopoietic cells. Angiopoietin-2 also induced a low level of tek phosphorylation and weakened the phosphorylation induced by angiopoietin-1 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ANGPT1 | up-regulates
binding
|
TEK |
0.79 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-49355 |
|
|
Homo sapiens |
|
pmid |
sentence |
9204896 |
Angiopoietin-1 (ang1) is an angiogenic factor that signals through the endothelial cell-specific tie2 receptor tyrosine kinase. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
4-[4-(6-methoxy-2-naphthalenyl)-2-(4-methylsulfinylphenyl)-1H-imidazol-5-yl]pyridine | down-regulates
chemical inhibition
|
TEK |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-207287 |
|
|
Homo sapiens |
|
pmid |
sentence |
Other |
|
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PTPRB | down-regulates activity
dephosphorylation
|
TEK |
0.572 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277059 |
|
|
Homo sapiens |
|
pmid |
sentence |
34417472 |
Simultaneous inhibition of Tie2 cleavage and VE-PTP synergistically enhances Tie2 activation by up to 10-fold (Fig. 7A).|Tie2 activation is also importantly regulated by vascular endothelial protein tyrosine phosphatase (VE-PTP), which dephosphorylates Tie2 to inhibit its vascular stabilizing effects .|Tie2 activation is also importantly regulated by vascular endothelial protein tyrosine phosphatase (VE-PTP), which dephosphorylates Tie2 to inhibit its vascular stabilizing effects. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TEK | up-regulates quantity by expression
transcriptional regulation
|
MYH1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-241541 |
|
|
Mus musculus |
Myoblast |
pmid |
sentence |
26042050 |
the effects of the angiopoietins are not specific for vascular endothelial cells, as their receptors (Tie1, Tie2) are known to be expressed in hematopoietic cells and they have also recently been shown to be expressed in skeletal muscle cellsExogenous Ang-1 enhanced myogenic (MyoD and Myogenin) mRNA in differentiating myoblasts and increased myosin heavy chain protein. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
MECOM | up-regulates quantity by expression
transcriptional regulation
|
TEK |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266063 |
|
|
Mus musculus |
Embryonic Cell Line |
pmid |
sentence |
15889140 |
We finally observed that the forced expression of Evi1 induced GATA-2 expression in a hematopoietic cell line, EML C1, along with GATA-1, Ang-1, Ang-2 and Tie2 |
|
Publications: |
1 |
Organism: |
Mus Musculus |