+ |
NGLY1 | up-regulates activity
binding
|
RAD23B |
0.814 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261061 |
|
|
Homo sapiens |
|
pmid |
sentence |
16401726 |
The XPCB domain of Rad23 binds Png1, which in turn facilitates the substrate recognition of Rad23. Through interactions with Ub chains and the proteasome mediated by the UBA and UBL domains in Rad23, Rad23 facilitates substrate transfer to the proteasome. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
VCP | up-regulates activity
binding
|
NGLY1 |
0.683 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261058 |
|
|
Homo sapiens |
|
pmid |
sentence |
15362974 |
PNGase is directed to polyubiquitinated MGPs via VCP and the adaptor protein SAKS1, allowing PNGase to deglycosylate MGPs, which can then be degraded by the proteasome. PNGase itself is reported to bind to the S4 component of the 19 S proteasome. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
UBXN1 | up-regulates activity
binding
|
NGLY1 |
0.466 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261060 |
|
|
Homo sapiens |
|
pmid |
sentence |
15362974 |
PNGase is directed to polyubiquitinated MGPs via VCP and the adaptor protein SAKS1, allowing PNGase to deglycosylate MGPs, which can then be degraded by the proteasome. PNGase itself is reported to bind to the S4 component of the 19 S proteasome. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |