+ |
A5/b1 integrin | up-regulates quantity by expression
|
DLL1 |
0.27 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253286 |
|
|
Mus musculus |
|
pmid |
sentence |
25786978 |
First, EPCs incorporated into the neovascular region recognize the TGFBIp secreted by cells in the environment via binding to integrins a4 and a5. Second, binding of TGFBIp to integrins in EPCs induces phosphorylation of intracellular signaling molecules in a pathway necessary for TGFBIp-mediated angiogenic activity of EPCs. In addition, binding of TGFBIp to integrins activates the NF-kappaB signaling pathway that induces expression of DLL1 and JAG1 in EPCs. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
DLL1 | up-regulates
binding
|
NOTCH3 |
0.614 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-82398 |
|
|
Homo sapiens |
|
pmid |
sentence |
11006133 |
These results suggest that delta1, jagged1, and jagged2 are ligands for notch1 and notch3 receptors. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DLL1 | up-regulates activity
binding
|
PP2B |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-209741 |
|
|
Homo sapiens |
B-lymphocyte |
pmid |
sentence |
16140393 |
Notch signaling is a highly conserved pathway involved in cell fate choice during development with Delta and Jagged constituting the two evolutionary conserved families of Notch ligands. These ligands are transmembrane proteins with conserved biochemical structure that share their receptors and signal through a common mechanism. Upon ligand binding Notch receptors are proteoliticaly cleaved, the intracellular domain of Notch (NICD) is released and translocated to the nucleus, where it activates target genes. In mammals, four receptors and five ligands have been described. Delta-1, Delta-3 and Delta-4 are homologues to Drosophila Delta and Jagged-1 and Jagged-2 to Drosophila Serrate. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DLL1 | up-regulates
binding
|
NOTCH |
0.625 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255368 |
|
|
|
|
pmid |
sentence |
12361602 |
When activated by its ligands (Delta and Jagged in vertebrates and Serrate in invertebrates), the intracellular portion of Notch is cleaved and translocates to the nucleus |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255369 |
|
|
|
|
pmid |
sentence |
23729744 |
The NECD undergoes O-linked glycosylation during Notch synthesis and secretion, which is crucial for proper folding of the Notch receptor and the interaction with its ligand DSL (Delta, Serrate, Lag-2)(Rana and Haltiwanger, 2011). The Notch receptor on the signal-receiving cell binds directly to ligands located on the apposing signal-sending cell |
|
Publications: |
2 |
Tissue: |
Skeletal Muscle |
+ |
DLL1 | up-regulates
binding
|
NOTCH2 |
0.62 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-199320 |
|
|
Homo sapiens |
|
pmid |
sentence |
23111325 |
In this study, we demonstrate that dll1 can activate notch signaling mostly through notch2 receptor and can contribute to drug resistance to bortezomib, both in murine and human mm cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DLL1 | up-regulates activity
binding
|
NOTCH |
0.625 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254315 |
|
|
Homo sapiens |
B-lymphocyte |
pmid |
sentence |
16140393 |
Notch signaling is a highly conserved pathway involved in cell fate choice during development with Delta and Jagged constituting the two evolutionary conserved families of Notch ligands. These ligands are transmembrane proteins with conserved biochemical structure that share their receptors and signal through a common mechanism. Upon ligand binding Notch receptors are proteoliticaly cleaved, the intracellular domain of Notch (NICD) is released and translocated to the nucleus, where it activates target genes. In mammals, four receptors and five ligands have been described. Delta-1, Delta-3 and Delta-4 are homologues to Drosophila Delta and Jagged-1 and Jagged-2 to Drosophila Serrate. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
A4/b1 integrin | up-regulates quantity by expression
|
DLL1 |
0.27 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253285 |
|
|
Mus musculus |
|
pmid |
sentence |
25786978 |
First, EPCs incorporated into the neovascular region recognize the TGFBIp secreted by cells in the environment via binding to integrins a4 and a5. Second, binding of TGFBIp to integrins in EPCs induces phosphorylation of intracellular signaling molecules in a pathway necessary for TGFBIp-mediated angiogenic activity of EPCs. In addition, binding of TGFBIp to integrins activates the NF-kappaB signaling pathway that induces expression of DLL1 and JAG1 in EPCs. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
LFNG | up-regulates
binding
|
DLL1 |
0.46 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-107699 |
|
|
Homo sapiens |
|
pmid |
sentence |
11346656 |
The modification of notch by fringe would influence binding between the notch receptor and its ligand. It was reported previously that mfng and lfng inhibited notch1-mediated signaling triggered by jagged1 and enhanced that triggered by delta1, and either jagged1- or delta1-triggered notch2 signaling was enhanced by lfng |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DLL1 | up-regulates activity
binding
|
NOTCH1 |
0.61 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-209732 |
|
|
Homo sapiens |
B-lymphocyte |
pmid |
sentence |
16140393 |
Notch signaling is a highly conserved pathway involved in cell fate choice during development with Delta and Jagged constituting the two evolutionary conserved families of Notch ligands. These ligands are transmembrane proteins with conserved biochemical structure that share their receptors and signal through a common mechanism. Upon ligand binding Notch receptors are proteoliticaly cleaved, the intracellular domain of Notch (NICD) is released and translocated to the nucleus, where it activates target genes. In mammals, four receptors and five ligands have been described. Delta-1, Delta-3 and Delta-4 are homologues to Drosophila Delta and Jagged-1 and Jagged-2 to Drosophila Serrate. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | NOTCH Signaling, NOTCH Signaling and Myogenesis, Rett syndrome |
+ |
MECP2 | down-regulates quantity by repression
transcriptional regulation
|
DLL1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264674 |
|
|
Mus musculus |
|
pmid |
sentence |
25420914 |
As the first step to reveal how MeCP2 phosphorylation may regulate Notch signaling, we conducted chromatin immunoprecipitation (ChIP) experiment to determine whether the phosphor-mutant MeCP2 protein has altered promoter occupancy at the promoters of Dll1 and Notch1. We found increased binding of the phosphor-mutant protein at the promoters of both Dll1 and Notch1 |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | Rett syndrome |
+ |
MIB1 | up-regulates activity
ubiquitination
|
DLL1 |
0.731 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-209750 |
|
|
Homo sapiens |
|
pmid |
sentence |
16140393 |
Mib physically interacts with Delta and promotes its ubiquitination and internalization [66], which have been shown to up-regulate Notch activity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | NOTCH Signaling |