+ |
TSPAN33 | up-regulates activity
binding
|
ADAM10 |
0.496 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261251 |
|
|
Rattus norvegicus |
|
pmid |
sentence |
30463011 |
Using cell biological and biochemical methods, we now show that ADAM10 is docked to junctions by its transmembrane partner Tspan33, whose cytoplasmic C terminus binds to the WW domain of PLEKHA7 in the presence of PDZD11. |
|
Publications: |
1 |
Organism: |
Rattus Norvegicus |
+ |
ADAM10 | up-regulates activity
cleavage
|
ERBB2 |
0.352 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259845 |
|
|
Homo sapiens |
|
pmid |
sentence |
26284334 |
The ADAM proteases are best known for their role in shedding the extracellular domain of transmembrane proteins. Among the transmembrane proteins shed by ADAM10 are notch, HER2, E-cadherin, CD44, L1 and the EGFR ligands, EGF and betacellulin. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ELAVL1 | up-regulates quantity
post transcriptional regulation
|
ADAM10 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266862 |
|
|
Homo sapiens |
|
pmid |
sentence |
19221430 |
Neuronal ELAV (nELAV) proteins are RNA-binding proteins which play a physiological role in controlling gene expression in memory formation, and their alteration may contribute to cognitive impairment associated with neurodegenerative pathologies such as Alzheimer's disease (AD). The experiments show for the first time that ADAM10mRNA represents a nELAV target and that these RNA-binding proteins can play a role in the post-transcriptional regulation of ADAM10 expression. nELAV proteins specifically bind the ADAM10 mRNA and this binding is disrupted following Aβ exposure |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SP1 | up-regulates quantity by expression
transcriptional regulation
|
ADAM10 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255192 |
|
|
Homo sapiens |
MCF-7 Cell |
pmid |
sentence |
21854868 |
Doxorubixin-evoked β-TrCP up-regulation promoted Sp1 degradation, which subsequently suppressed ADAM10 expression in MCF-7 and MCF-7/Dox cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ADAM10 | up-regulates activity
cleavage
|
CDH1 |
0.529 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259846 |
|
|
Homo sapiens |
|
pmid |
sentence |
26284334 |
The ADAM proteases are best known for their role in shedding the extracellular domain of transmembrane proteins. Among the transmembrane proteins shed by ADAM10 are notch, HER2, E-cadherin, CD44, L1 and the EGFR ligands, EGF and betacellulin. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ADAM10 | up-regulates activity
cleavage
|
NOTCH1 |
0.773 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259838 |
|
|
Homo sapiens |
T-lymphocyte |
pmid |
sentence |
28624438 |
ADAM10-mediated Notch1 cleavage is the rate limiting-step for release of the NICD and subsequent activation of Notch1 signaling. In T cells ADAM10-mediated Notch1 shedding controls T cell development |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ADAM10 | up-regulates activity
cleavage
|
CD44 |
0.354 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259847 |
|
|
Homo sapiens |
|
pmid |
sentence |
26284334 |
The ADAM proteases are best known for their role in shedding the extracellular domain of transmembrane proteins. Among the transmembrane proteins shed by ADAM10 are notch, HER2, E-cadherin, CD44, L1 and the EGFR ligands, EGF and betacellulin. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ELAVL2 | up-regulates quantity
post transcriptional regulation
|
ADAM10 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266863 |
|
|
Homo sapiens |
|
pmid |
sentence |
19221430 |
Neuronal ELAV (nELAV) proteins are RNA-binding proteins which play a physiological role in controlling gene expression in memory formation, and their alteration may contribute to cognitive impairment associated with neurodegenerative pathologies such as Alzheimer's disease (AD). The experiments show for the first time that ADAM10mRNA represents a nELAV target and that these RNA-binding proteins can play a role in the post-transcriptional regulation of ADAM10 expression. nELAV proteins specifically bind the ADAM10 mRNA and this binding is disrupted following Aβ exposure |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ADAM10 | up-regulates activity
cleavage
|
NOTCH |
0.773 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259836 |
|
|
Homo sapiens |
|
pmid |
sentence |
28624438 |
One of the most important and best characterized ADAM10 substrates is the Notch receptor [16]. After ligand binding to the Notch receptor, ADAM10 liberates the ectodomain and the membrane remaining part is processed by the γ-secretase complex, which releases a Notch Intracellular Domain (NICD). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
USF1 | up-regulates quantity by expression
transcriptional regulation
|
ADAM10 |
0.274 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259837 |
|
|
Homo sapiens |
|
pmid |
sentence |
28624438 |
The promoter region of ADAM10 contains several transcription factor binding sites that can stimulate its transcription. These include binding sites for transcription factors SP1 and USF, and the spliced form of the X-box binding protein (XBP)-1 as well as a retinoic acid-responsive element |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ADAM10 | up-regulates activity
cleavage
|
EGF |
0.549 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259840 |
|
|
Homo sapiens |
|
pmid |
sentence |
26284334 |
Like ADAM17, ADAM10 has also been implicated in the activation of specific EGFR ligands, especially EGF and betacellulin |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ADAM10 | up-regulates activity
cleavage
|
BTC |
0.382 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259839 |
|
|
Homo sapiens |
|
pmid |
sentence |
26284334 |
Like ADAM17, ADAM10 has also been implicated in the activation of specific EGFR ligands, especially EGF and betacellulin |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ELAVL3 | up-regulates quantity
post transcriptional regulation
|
ADAM10 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266864 |
|
|
Homo sapiens |
|
pmid |
sentence |
19221430 |
Neuronal ELAV (nELAV) proteins are RNA-binding proteins which play a physiological role in controlling gene expression in memory formation, and their alteration may contribute to cognitive impairment associated with neurodegenerative pathologies such as Alzheimer's disease (AD). The experiments show for the first time that ADAM10mRNA represents a nELAV target and that these RNA-binding proteins can play a role in the post-transcriptional regulation of ADAM10 expression. nELAV proteins specifically bind the ADAM10 mRNA and this binding is disrupted following Aβ exposure |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ELAVL4 | up-regulates quantity
post transcriptional regulation
|
ADAM10 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266865 |
|
|
Homo sapiens |
|
pmid |
sentence |
19221430 |
Neuronal ELAV (nELAV) proteins are RNA-binding proteins which play a physiological role in controlling gene expression in memory formation, and their alteration may contribute to cognitive impairment associated with neurodegenerative pathologies such as Alzheimer's disease (AD). The experiments show for the first time that ADAM10mRNA represents a nELAV target and that these RNA-binding proteins can play a role in the post-transcriptional regulation of ADAM10 expression. nELAV proteins specifically bind the ADAM10 mRNA and this binding is disrupted following Aβ exposure |
|
Publications: |
1 |
Organism: |
Homo Sapiens |