+ |
MAPK1 | up-regulates
phosphorylation
|
TPR |
0.382 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-181014 |
Ser2155 |
GFAEAIHsPQVAGVP |
Homo sapiens |
|
pmid |
sentence |
18794356 |
Tpr is phosphorylated by erk2 at four different sites. / because phosphorylation of tpr by activated erk stabilizes their interaction, we hypothesize that this phosphorylation is not part of a signal amplification cascade but rather positions activated erk to perform a continuing function in the nuclear pore. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-181018 |
Thr2116 |
VGRGLQLtPGIGGMQ |
Homo sapiens |
|
pmid |
sentence |
18794356 |
Tpr is phosphorylated by erk2 at four different sites. / because phosphorylation of tpr by activated erk stabilizes their interaction, we hypothesize that this phosphorylation is not part of a signal amplification cascade but rather positions activated erk to perform a continuing function in the nuclear pore. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-181022 |
Thr2137 |
EDRTVPStPTLVVPH |
Homo sapiens |
|
pmid |
sentence |
18794356 |
Tpr is phosphorylated by erk2 at four different sites. / because phosphorylation of tpr by activated erk stabilizes their interaction, we hypothesize that this phosphorylation is not part of a signal amplification cascade but rather positions activated erk to perform a continuing function in the nuclear pore. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-181026 |
Thr2214 |
GGRSVPTtPLQVAAP |
Homo sapiens |
|
pmid |
sentence |
18794356 |
Tpr is phosphorylated by erk2 at four different sites. / because phosphorylation of tpr by activated erk stabilizes their interaction, we hypothesize that this phosphorylation is not part of a signal amplification cascade but rather positions activated erk to perform a continuing function in the nuclear pore. |
|
Publications: |
4 |
Organism: |
Homo Sapiens |
+ |
TPR | up-regulates
binding
|
MAD1L1 |
0.498 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-181918 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
18981471 |
Tpr directly binds to mad1 and mad2. / depletion of tpr decreases the levels of mad1 at kinetochores during prometaphase, correlating with the inability of mad1 to activate mad2, which is required for inhibiting apc(cdc20). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TPR | up-regulates
binding
|
MAD2L1 |
0.315 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-181975 |
|
|
Homo sapiens |
|
pmid |
sentence |
18981471 |
Tpr directly binds to mad1 and mad2. / depletion of tpr decreases the levels of mad1 at kinetochores during prometaphase, correlating with the inability of mad1 to activate mad2, which is required for inhibiting apc(cdc20). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TPR | form complex
binding
|
NPC |
0.592 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262070 |
|
|
|
|
pmid |
sentence |
27016207 |
The protein inventory of the NPC has been studied for a very diverse set of eukaryotes, including trypanosomes, fungi, plants, animals, and humans [4], [5], [6], [7], [8], [9]. In all cases, about 30 different Nups were found (Fig. 2). |
|
Publications: |
1 |