+ |
EIF3E | up-regulates quantity
translation regulation
|
PLAU |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259155 |
|
|
Homo sapiens |
MDA-MB-231 Cell, U2-OS Cell |
pmid |
sentence |
20453879 |
Validated mRNA targets regulated positively at the translational level by eIF3e included urokinase-type plasminogen activator and apoptotic regulator BCL-XL, whereas synthesis of proteins including the mitotic checkpoint component MAD2L1 was negatively regulated. Taken together, our study data suggest that eIF3e has a positive role in breast cancer progression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
EIF3E | form complex
binding
|
EIF3_complex |
0.94 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266396 |
|
|
in vitro |
|
pmid |
sentence |
16920360 |
Consistent with its diverse functions, eIF3 is the largest and most complex initiation factor: the mammalian version, for example, contains 13 nonidentical subunits that are designated eIF3a to eIF3m 8, 9, 10, 11, 12, 13 (Table 1). |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
EIF3E | up-regulates quantity by stabilization
binding
|
MCM7 |
0.341 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259154 |
|
|
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
17310990 |
Our data show that INT6 interacts with a C-terminal domain of MCM7. Collectively, our observations suggest that INT6 restrains the increased degradation of MCM7 occurring during DNA replication by protecting its polyubiquitylated derivatives from the proteasome activity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
EIF3E | down-regulates quantity
translation regulation
|
MAD2L1 |
0.266 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259157 |
|
|
Homo sapiens |
MDA-MB-231 Cell, U2-OS Cell |
pmid |
sentence |
20453879 |
Validated mRNA targets regulated positively at the translational level by eIF3e included urokinase-type plasminogen activator and apoptotic regulator BCL-XL, whereas synthesis of proteins including the mitotic checkpoint component MAD2L1 was negatively regulated. Taken together, our study data suggest that eIF3e has a positive role in breast cancer progression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
EIF3E | up-regulates quantity
translation regulation
|
BCL2L1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259156 |
|
|
Homo sapiens |
MDA-MB-231 Cell, U2-OS Cell |
pmid |
sentence |
20453879 |
Validated mRNA targets regulated positively at the translational level by eIF3e included urokinase-type plasminogen activator and apoptotic regulator BCL-XL, whereas synthesis of proteins including the mitotic checkpoint component MAD2L1 was negatively regulated. Taken together, our study data suggest that eIF3e has a positive role in breast cancer progression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |