+ |
SRC | up-regulates
phosphorylation
|
DDR2 |
0.388 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-140728 |
Tyr736 |
FGMSRNLySGDYYRI |
Homo sapiens |
|
pmid |
sentence |
16186108 |
Here, using baculoviral co-expression of the ddr2 cytosolic domain and src, we show that src targets three tyrosine residues (tyr-736, tyr-740, and tyr-741) in the activation loop of ddr2 for phosphorylation. This phosphorylation by src stimulates ddr2 cis-autophosphorylation of additional tyrosine residues. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-140763 |
Tyr740 |
RNLYSGDyYRIQGRA |
Homo sapiens |
|
pmid |
sentence |
16186108 |
Here, using baculoviral co-expression of the ddr2 cytosolic domain and src, we show that src targets three tyrosine residues (tyr-736, tyr-740, and tyr-741) in the activation loop of ddr2 for phosphorylation. This phosphorylation by src stimulates ddr2 cis-autophosphorylation of additional tyrosine residues. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-140767 |
Tyr741 |
NLYSGDYyRIQGRAV |
Homo sapiens |
|
pmid |
sentence |
16186108 |
Here, using baculoviral co-expression of the ddr2 cytosolic domain and src, we show that src targets three tyrosine residues (tyr-736, tyr-740, and tyr-741) in the activation loop of ddr2 for phosphorylation. This phosphorylation by src stimulates ddr2 cis-autophosphorylation of additional tyrosine residues. |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
DDR2 | up-regulates
binding
|
SHC1 |
0.402 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-140724 |
|
|
Homo sapiens |
|
pmid |
sentence |
16186108 |
Collectively, our findings are consistent with the following mechanism for src-dependent ddr2 activation and signaling: 1) ligand binding promotes phosphorylation of tyr-740 in the ddr2 activation loop by src;2) tyr-740 phosphorylation stimulates intramolecular autophosphorylation of ddr2;3) ddr2 autophosphorylation generates cytosolic domain phosphotyrosines that promote the formation of ddr2 cytosolic domain-shc signaling complexes. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
COL1A1 | up-regulates activity
binding
|
DDR2 |
0.434 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272342 |
|
|
Homo sapiens |
HT-1080 Cell |
pmid |
sentence |
17318226 |
The Discoidin Domain Receptors (DDRs) constitute a unique set of receptor tyrosine kinases that signal in response to collagen.|Consistent with this view128, we showed that ectopic expression of DDR1b or DDR2 in HT1080 cells elicited a potent growth inhibitory effect only when the cells were cultured on 2D or 3D COL1 matrices, in agreement with previous studies in melanoma48, breast cancer76,78, and lung cancer cells74,75. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
COL21A1 | up-regulates activity
binding
|
DDR2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272343 |
|
|
Homo sapiens |
HT-1080 Cell |
pmid |
sentence |
17318226 |
The Discoidin Domain Receptors (DDRs) constitute a unique set of receptor tyrosine kinases that signal in response to collagen.|Consistent with this view128, we showed that ectopic expression of DDR1b or DDR2 in HT1080 cells elicited a potent growth inhibitory effect only when the cells were cultured on 2D or 3D COL1 matrices, in agreement with previous studies in melanoma48, breast cancer76,78, and lung cancer cells74,75. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
regorafenib | down-regulates activity
chemical inhibition
|
DDR2 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259208 |
|
|
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 |