+ |
APH1A | form complex
binding
|
gamma-secretase |
0.958 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-209714 |
|
|
Homo sapiens |
|
pmid |
sentence |
25610395 |
-Secretase is a four subunit, 19-pass transmembrane enzymeBiochemical studies indicated that -secretase activity is catalyzed by the presenilin (PS)-containing macromolecular complex (Li et al., 2000a). The search for other components of the complex revealed three additional proteins: nicastrin (Nct), anterior pharynx-defective-1 (Aph-1), and presenilin enhancer-2 (Pen-2) |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
gamma-secretase | down-regulates quantity
cleavage
|
DSCAM |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264271 |
|
|
Homo sapiens |
Neuron |
pmid |
sentence |
30745319 |
γ‐secretase‐mediated intra‐membrane cleavage of DSCAM receptors results in the release of the DSCAM ICD, which is likely proceeded by shedding of the DSCAM ectodomain. Interaction of IPO5 with the NLS of DSCAM then leads to importin‐mediated nuclear import of the DSCAM ICD. In the nucleus, the DSCAM ICD may regulate the transcription of genes involved in neuronal development and function, thereby regulating processes such as neurite outgrowth, branching, and repulsion, as well as synapse formation, axon guidance, and neuronal cell death and survival. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
gamma-secretase | up-regulates activity
cleavage
|
NOTCH3 |
0.558 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-209726 |
|
|
Homo sapiens |
|
pmid |
sentence |
25610395 |
The membrane-bound Notch segment that results from this cleavage, known as Notch Intracellular Truncation domain (NEXT), is a -secretase substrate (Kopan and Ilagan, 2009). -Secretase performs the subsequent cleavage at S3 (De Strooper et al., 1999), releasing Notch intracellular domain (NICD) from the membrane and allowing for signal transduction through binding with the CBL-1, Su(H), Lag-1 (CSL; Schroeter et al., 1998; Struhl and Adachi, 1998) family of DNA binding proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
gamma-secretase | up-regulates activity
cleavage
|
APP |
0.597 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251576 |
|
|
Homo sapiens |
Alzheimer Disease Specific Cell Type |
pmid |
sentence |
19958215 |
The production and accumulation of the beta amyloid protein (Abeta) is a key event in the cascade of oxidative and inflammatory processes that characterizes Alzheimer's disease (AD). A multi-subunit enzyme complex, referred to as gamma (gamma) secretase, plays a pivotal role in the generation of Abeta from its parent molecule, the amyloid precursor protein (APP). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Alzheimer |
+ |
gamma-secretase | up-regulates activity
cleavage
|
NOTCH1 |
0.665 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-209717 |
|
|
Homo sapiens |
|
pmid |
sentence |
25610395 |
The membrane-bound Notch segment that results from this cleavage, known as Notch Intracellular Truncation domain (NEXT), is a γ-secretase substrate. γ-Secretase performs the subsequent cleavage at S3, releasing Notch intracellular domain (NICD) from the membrane and allowing for signal transduction through binding with the CBL-1, Su(H), Lag-1 family of DNA binding proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | NOTCH Signaling, NOTCH Signaling and Myogenesis |
+ |
NCSTN | form complex
binding
|
gamma-secretase |
0.964 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-209711 |
|
|
Homo sapiens |
|
pmid |
sentence |
25610395 |
-Secretase is a four subunit, 19-pass transmembrane enzymeBiochemical studies indicated that -secretase activity is catalyzed by the presenilin (PS)-containing macromolecular complex (Li et al., 2000a). The search for other components of the complex revealed three additional proteins: nicastrin (Nct), anterior pharynx-defective-1 (Aph-1), and presenilin enhancer-2 (Pen-2) |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Alzheimer |
+ |
PSEN1 | up-regulates
cleavage
|
gamma-secretase |
0.956 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-217743 |
|
|
Homo sapiens |
|
pmid |
sentence |
10593990 |
Presenilin-1 (ps1), a polytopic membrane protein primarily localized to the endoplasmic reticulum, is required for efficient proteolysis of both notch and beta-amyloid precursor protein (app) within their trans- membrane domains. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-217746 |
|
|
Homo sapiens |
|
pmid |
sentence |
10497236 |
Presenilin-1 (ps1), a polytopic membrane protein primarily localized to the endoplasmic reticulum, is required for efficient proteolysis of both notch and beta-amyloid precursor protein (app) within their trans- membrane domains. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
Pathways: | Alzheimer |
+ |
IFITM3 | up-regulates activity
binding
|
gamma-secretase |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266303 |
|
|
Mus musculus |
|
pmid |
sentence |
32879487 |
IFITM3 directly binds to γ-secretase. IFITM3 KO reduced γ-secretase activity for both Aβ40 and Aβ42 cleavages as compared to the EV (empty vector guide RNA) cell line by 36% and 27%, respectively (Fig. 2d, bar 1 and 3). |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
gamma-secretase | up-regulates activity
cleavage
|
NOTCH2 |
0.572 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-209723 |
|
|
Homo sapiens |
|
pmid |
sentence |
25610395 |
The membrane-bound Notch segment that results from this cleavage, known as Notch Intracellular Truncation domain (NEXT), is a -secretase substrate (Kopan and Ilagan, 2009). -Secretase performs the subsequent cleavage at S3 (De Strooper et al., 1999), releasing Notch intracellular domain (NICD) from the membrane and allowing for signal transduction through binding with the CBL-1, Su(H), Lag-1 (CSL; Schroeter et al., 1998; Struhl and Adachi, 1998) family of DNA binding proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
gamma-secretase | up-regulates activity
cleavage
|
NOTCH |
0.666 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254328 |
|
|
Homo sapiens |
|
pmid |
sentence |
25610395 |
The membrane-bound Notch segment that results from this cleavage, known as Notch Intracellular Truncation domain (NEXT), is a -secretase substrate (Kopan and Ilagan, 2009). -Secretase performs the subsequent cleavage at S3 (De Strooper et al., 1999), releasing Notch intracellular domain (NICD) from the membrane and allowing for signal transduction through binding with the CBL-1, Su(H), Lag-1 (CSL; Schroeter et al., 1998; Struhl and Adachi, 1998) family of DNA binding proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
gamma-secretase | up-regulates
cleavage
|
NOTCH |
0.666 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255372 |
|
|
|
|
pmid |
sentence |
23729744 |
Receptor–ligand engagement triggers a second NECD cleavage (S2 cleavage) by a metalloproteinase ADAM (known as Kuzbanian in Drosophila melanogaster), which in turn facilitates a further crucial signaling cleavage within the Notch transmembrane domain by a γ-secretase complex that contains Presenilin (S3 cleavage) |
|
Publications: |
1 |
+ |
PSEN1 | form complex
binding
|
gamma-secretase |
0.956 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-209705 |
|
|
Homo sapiens |
|
pmid |
sentence |
25610395 |
-Secretase is a four subunit, 19-pass transmembrane enzymeBiochemical studies indicated that -secretase activity is catalyzed by the presenilin (PS)-containing macromolecular complex (Li et al., 2000a). The search for other components of the complex revealed three additional proteins: nicastrin (Nct), anterior pharynx-defective-1 (Aph-1), and presenilin enhancer-2 (Pen-2) |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Alzheimer |
+ |
gamma-secretase | up-regulates activity
cleavage
|
NOTCH4 |
0.515 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-209729 |
|
|
Homo sapiens |
|
pmid |
sentence |
25610395 |
The membrane-bound Notch segment that results from this cleavage, known as Notch Intracellular Truncation domain (NEXT), is a -secretase substrate (Kopan and Ilagan, 2009). -Secretase performs the subsequent cleavage at S3 (De Strooper et al., 1999), releasing Notch intracellular domain (NICD) from the membrane and allowing for signal transduction through binding with the CBL-1, Su(H), Lag-1 (CSL; Schroeter et al., 1998; Struhl and Adachi, 1998) family of DNA binding proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PSENEN | form complex
binding
|
gamma-secretase |
0.96 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-209708 |
|
|
Homo sapiens |
|
pmid |
sentence |
25610395 |
-Secretase is a four subunit, 19-pass transmembrane enzymeBiochemical studies indicated that -secretase activity is catalyzed by the presenilin (PS)-containing macromolecular complex (Li et al., 2000a). The search for other components of the complex revealed three additional proteins: nicastrin (Nct), anterior pharynx-defective-1 (Aph-1), and presenilin enhancer-2 (Pen-2) |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
gamma-secretase | down-regulates quantity
cleavage
|
DSCAML1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264272 |
|
|
Homo sapiens |
Neuron |
pmid |
sentence |
30745319 |
γ‐secretase‐mediated intra‐membrane cleavage of DSCAM receptors results in the release of the DSCAM ICD, which is likely proceeded by shedding of the DSCAM ectodomain. Interaction of IPO5 with the NLS of DSCAM then leads to importin‐mediated nuclear import of the DSCAM ICD. In the nucleus, the DSCAM ICD may regulate the transcription of genes involved in neuronal development and function, thereby regulating processes such as neurite outgrowth, branching, and repulsion, as well as synapse formation, axon guidance, and neuronal cell death and survival. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |