+ |
AXL | up-regulates quantity by stabilization
phosphorylation
|
MLKL |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-274119 |
Tyr376 |
DRVKSTAyLSPQELE |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
31230815 |
TAM kinases phosphorylate MLKL to promote necroptosis. MLKL is then recruited to the plasma membrane, where TAM kinases phosphorylate MLKL at Tyr376 (Figure 5G, step 5), promoting its oligomerization and formation of membrane-rupturing pores that result in necrotic cell death (Figure 5G, step 6). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AXL | up-regulates activity
phosphorylation
|
YES1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277555 |
Tyr426 |
RLIEDNEyTARQGAK |
Homo sapiens |
AGS Cell |
pmid |
sentence |
33941853 |
Here, we show that EphA2, YES1, and ANXA2 form a signal axis, in which YES1 activated by EphA2 phosphorylates ANXA2 at Tyr24 site, leading to ANXA2 activation and increased ANXA2 nuclear distribution in gastric cancer (GC) cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AXL | up-regulates activity
phosphorylation
|
AXL |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-250591 |
Tyr779 |
ADCLDGLyALMSRCW |
in vitro |
|
pmid |
sentence |
9178760 |
Our data showed that various receptor substrates are at least associated with the C-terminal tyrosine pY821. Two additional potential autophosphorylation sites (pY866 and pY779) may play a minor role in binding of eector proteins |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-250592 |
Tyr821 |
QEPDEILyVNMDEGG |
in vitro |
|
pmid |
sentence |
9178760 |
Our data showed that various receptor substrates are at least associated with the C-terminal tyrosine pY821. Two additional potential autophosphorylation sites (pY866 and pY779) may play a minor role in binding of eector proteins |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-250593 |
Tyr866 |
EVHPAGRyVLCPSTT |
in vitro |
|
pmid |
sentence |
9178760 |
Our data showed that various receptor substrates are at least associated with the C-terminal tyrosine pY821. Two additional potential autophosphorylation sites (pY866 and pY779) may play a minor role in binding of eector proteins |
|
Publications: |
3 |
Organism: |
In Vitro |
+ |
GAS6 | up-regulates
binding
|
AXL |
0.906 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-34339 |
|
|
Homo sapiens |
|
pmid |
sentence |
7867073 |
Receptor tyrosine kinases of the axl family are activated by the vitamin k-dependent protein gas6. We report the identification of ligands for tyro 3 (alternatively called sky, rse, brt, or tif) and axl (alternatively, ark or ufo), members of a previously orphan family of receptor-like tyrosine kinases. These ligands correspond to protein s, a protease regulator that is a potent anticoagulant, and gas6, a protein related to protein s but lacking any known function. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-143109 |
|
|
Homo sapiens |
|
pmid |
sentence |
16362042 |
Receptor tyrosine kinases of the axl family are activated by the vitamin k-dependent protein gas6. We report the identification of ligands for tyro 3 (alternatively called sky, rse, brt, or tif) and axl (alternatively, ark or ufo), members of a previously orphan family of receptor-like tyrosine kinases. These ligands correspond to protein s, a protease regulator that is a potent anticoagulant, and gas6, a protein related to protein s but lacking any known function. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
N1'-[3-fluoro-4-[[6-methoxy-7-[3-(4-morpholinyl)propoxy]-4-quinolinyl]oxy]phenyl]-N1-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide | down-regulates activity
chemical inhibition
|
AXL |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-258109 |
|
|
in vitro |
|
pmid |
sentence |
22037378 |
Our data set represents the most detailed comprehensive assessment of the reactivity of known and clinical kinase inhibitors across the kinome published to date. | The data also show that for at least 15 of the 27 kinases that are the primary, intended targets for the compounds tested and that are represented in the assay panel, selective inhibitors, as assessed by both absolute selectivity across the kinome and selectivity relative to the primary target, are among the 72 tested here. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
PROS1 | up-regulates
binding
|
AXL |
0.479 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-34483 |
|
|
Homo sapiens |
|
pmid |
sentence |
7867073 |
We report the identification of ligands for tyro 3 (alternatively called sky, rse, brt, or tif) and axl (alternatively, ark or ufo), members of a previously orphan family of receptor-like tyrosine kinases. These ligands correspond to protein s, a protease regulator that is a potent anticoagulant, and gas6, a protein related to protein s but lacking any known function. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
cabozantinib | down-regulates activity
chemical inhibition
|
AXL |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262241 |
|
|
Homo sapiens |
Medullary Thyroid Carcinoma Cell |
pmid |
sentence |
26536165 |
Cabozantinib (XL184) is a small-molecule kinase inhibitor with potent activity toward MET and VEGF receptor 2 (VEGFR2), as well as a number of other receptor tyrosine kinases that have also been implicated in tumor pathobiology, including RET, KIT, AXL, and FLT3. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
N-[4-[(2-amino-3-chloro-4-pyridinyl)oxy]-3-fluorophenyl]-4-ethoxy-1-(4-fluorophenyl)-2-oxo-3-pyridinecarboxamide | down-regulates
chemical inhibition
|
AXL |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-190401 |
|
|
Homo sapiens |
|
pmid |
sentence |
Other |
|
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
GAS6 | up-regulates activity
binding
|
AXL |
0.906 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277720 |
|
|
Homo sapiens |
Neutrophil |
pmid |
sentence |
35022267 |
Chemotherapy-induced infiltration of neutrophils promotes pancreatic cancer metastasis via Gas6/AXL signalling axis. neutrophils are recruited to the metastatic liver via CXCL1 and 2 secretion by metastatic tumour cells. These neutrophils express growth arrest specific 6 (Gas6) which leads to AXL receptor activation on tumour cells enabling their regrowth.Taken together, these results show that the neutrophil attracting cytokines Cxcl1 and 2 are highly expressed in metastatic livers in response to gemcitabine withdrawal and this favours CXCR2-dependent recruitment of neutrophils at the hepatic metastatic site. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AXL | up-regulates activity
binding
|
Epithelial-mesenchymal_transition |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277723 |
|
|
Homo sapiens |
Neutrophil |
pmid |
sentence |
35022267 |
Gas6 and its main receptor AXL are overexpressed in pancreatic cancer and their expression correlates with poor prognosis.Gas6/AXL signalling in cancer cells is associated with tumour cell proliferation, epithelial mesenchymal transition and metastases. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AXL | up-regulates
|
Metastasis |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277725 |
|
|
Homo sapiens |
|
pmid |
sentence |
35022267 |
Gas6 and its main receptor AXL are overexpressed in pancreatic cancer and their expression correlates with poor prognosis.Gas6/AXL signalling in cancer cells is associated with tumour cell proliferation, epithelial mesenchymal transition and metastases. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |