+ |
PRKCA | down-regulates quantity
phosphorylation
|
UNC5A |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268180 |
Ser352 |
TSGFQPVsIKPSKAD |
Rattus norvegicus |
Hippocampal Cell Line |
pmid |
sentence |
16554470 |
We show that protein interacting with C-kinase 1 (PICK1) recruits activated protein kinase Cα (PKCα) to MycUNC5A at the plasma membrane, stimulating its endocytosis. We identify two PKCα phosphorylation sites at serines 408 and 587, as well as dileucine internalization motifs, which are required for this endocytosis. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268179 |
Ser532 |
EPSPDSWsLRLKKQS |
Rattus norvegicus |
Hippocampal Cell Line |
pmid |
sentence |
16554470 |
We show that protein interacting with C-kinase 1 (PICK1) recruits activated protein kinase Cα (PKCα) to MycUNC5A at the plasma membrane, stimulating its endocytosis. We identify two PKCα phosphorylation sites at serines 408 and 587, as well as dileucine internalization motifs, which are required for this endocytosis. |
|
Publications: |
2 |
Organism: |
Rattus Norvegicus |
Pathways: | Axon guidance |
+ |
UNC5A | up-regulates activity
binding
|
PICK1 |
0.293 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268181 |
|
|
Rattus norvegicus |
Hippocampal Cell Line |
pmid |
sentence |
16554470 |
Recently, our laboratory showed that UNC5A is coimmunoprecipitated with PICK1 and PKCα. Moreover, we demonstrated that the association of PKCα with UNC5A depends on the activation of PKCα and the ability of UNC5A to bind PICK1 |
|
Publications: |
1 |
Organism: |
Rattus Norvegicus |
Pathways: | Axon guidance |
+ |
UNC5A | down-regulates activity
binding
|
DCC |
0.648 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268164 |
|
|
Homo sapiens |
|
pmid |
sentence |
25881791 |
In the presence of netrin-1, UNC5 co-immuno-precipitates with DCC, suggesting the formation of a ternary complex of netrin-1 with ecto-domains of DCC and UNC5. DCC binding to netrin-1 alone leads to axon attraction. Importantly, DCC has the ability to switch the netrin-1-mediated responses from attraction to repulsion when another receptor UNC5 co-exists. DCC binding to netrin-1 alone leads to axon attraction. Importantly, DCC has the ability to switch the netrin-1-mediated responses from attraction to repulsion when another receptor UNC5 co-exists. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Tissue: |
Nervous System |
Pathways: | Axon guidance |
+ |
NTN4 | up-regulates
binding
|
UNC5A |
0.595 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-98483 |
|
|
Homo sapiens |
|
pmid |
sentence |
12598531 |
The unc5hs are axon guidance receptors that mediate netrin-1-dependent chemorepulsion, and dependence receptors that mediate netrin-1-independent apoptosis. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
UNC5A | up-regulates
|
Chemorepulsion_of_axon |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268182 |
|
|
Homo sapiens |
|
pmid |
sentence |
30108487 |
Netrin binding to the receptor deleted in colorectal cancer (DCC) results in attractive responses, viahomodimerization of DCC (covered in detail in later sections), whereas heterodimerization between DCC and receptor uncoordinated locomotion 5 (UNC5) converts this attractive response into repulsion |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Axon guidance |