+ |
XPO1 | down-regulates
relocalization
|
SMAD4 |
0.308 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-84247 |
|
|
Homo sapiens |
|
pmid |
sentence |
11074002 |
We demonstrate that inhibition of crm1-mediated nuclear export by treatment of cells with leptomycin b results in endogenous smad4 accumulating very rapidly in the nucleus. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
XPO1 | down-regulates activity
relocalization
|
TP53 |
0.572 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260067 |
|
|
Homo sapiens |
|
pmid |
sentence |
17891139 |
We identify the major poly(ADP-ribosyl)ated sites of p53 by PARP-1 and find that PARP-1-mediated poly(ADP-ribosyl)ation blocks the interaction between p53 and the nuclear export receptor Crm1, resulting in nuclear accumulation of p53. These findings molecularly link PARP-1 and p53 in the DNA-damage response, providing the mechanism for how p53 accumulates in the nucleus in response to DNA damage.|PARP-1 is super-activated by binding to damaged DNA, and poly(ADP-ribosyl)ates p53. Poly(ADP-ribosyl)ation probably induces a structural change that mask the NES, and thus Crm1 can no longer target p53 to the nuclear export machinery, resulting in accumulation of p53 in the nucleus. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | FLT3-ITD signaling |
+ |
Verdinexor | down-regulates
chemical inhibition
|
XPO1 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261129 |
|
|
Homo sapiens |
|
pmid |
sentence |
30541831 |
We show that KPT-335 inhibits XPO1-mediated nuclear export, leading to nuclear accumulation of RSV M protein and a reduction inRSV titers. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RAN | up-regulates activity
binding
|
XPO1 |
0.925 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275848 |
|
|
|
|
pmid |
sentence |
31075303 |
The nuclear export by CRM1 requires an interaction with the small GTPase Ras-related nuclear antigen (Ran), which cycles between GTP- and GDP-bound states. The binding of Ran GTP to CRM1 in the nucleus increases the affinity of CRM1 for cargo proteins |
|
Publications: |
1 |
+ |
Selinexor | down-regulates activity
chemical inhibition
|
XPO1 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262537 |
|
|
Homo sapiens |
|
pmid |
sentence |
30510142 |
Selinexor (KPT-330) is a first-in-class selective inhibitor of nuclear export (C17H11F6N7O; see ref. 4; for its chemical structure). The drug binds and inhibits exportin XPO-1 that mediates nuclear export of proteins and mRNAs. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | FLT3-ITD signaling |