+ |
Cullin 1-RBX1-Skp1 | down-regulates quantity by destabilization
polyubiquitination
|
BIRC5 |
0.326 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272438 |
Lys90 |
GCAFLSVkKQFEELT |
Mus musculus |
MLE-12 Cell |
pmid |
sentence |
25778398 |
Fbxl7 targets survivin for polyubiquitylation and proteasomal degradation.these data suggest that the Skp1·Cul1·F-box protein complex subunit Fbxl7 modulates mitochondrial function by controlling the cellular abundance of survivin. These results suggest that both Lys-90 and Lys-91 are critical for Fbxl7-mediated polyubiquitylation. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272439 |
Lys91 |
CAFLSVKkQFEELTL |
Mus musculus |
MLE-12 Cell |
pmid |
sentence |
25778398 |
Fbxl7 targets survivin for polyubiquitylation and proteasomal degradation.these data suggest that the Skp1·Cul1·F-box protein complex subunit Fbxl7 modulates mitochondrial function by controlling the cellular abundance of survivin. These results suggest that both Lys-90 and Lys-91 are critical for Fbxl7-mediated polyubiquitylation. |
|
Publications: |
2 |
Organism: |
Mus Musculus |
+ |
PLK1 | up-regulates
phosphorylation
|
BIRC5 |
0.566 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-170460 |
Ser20 |
FLKDHRIsTFKNWPF |
Homo sapiens |
|
pmid |
sentence |
21148584 |
Thus, we conclude that plk1-mediated phosphorylation of sur at ser20 is critical for accurate chromosome segregation|SUR (survivin) |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
AURKB | down-regulates
phosphorylation
|
BIRC5 |
0.786 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-154569 |
Thr117 |
KNKIAKEtNNKKKEF |
Homo sapiens |
|
pmid |
sentence |
17457057 |
Phosphorylation by aurora-b negatively regulates survivin function . hat survivin is phosphorylated at t117 during mitosis, and once phosphorylated, dephosphorylation is crucial for chromosome congression and progression into anaphaseduring mitosis |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CDK1 | up-regulates
phosphorylation
|
BIRC5 |
0.672 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-115129 |
Thr34 |
FLEGCACtPERMAEA |
Homo sapiens |
|
pmid |
sentence |
11861764 |
Survivin is a member of the inhibitor of apoptosis gene family that has been implicated in both apoptosis inhibition and regulation of mitosisin synchronized cultures, cytosolic survivin abruptly increased at mitosis, physically associated with p34(cdc2), and was phosphorylated by p34(cdc2) on thr(34), in vivo |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
BIRC5 | down-regulates
binding
|
CASP3 |
0.502 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-62484 |
|
|
Homo sapiens |
|
pmid |
sentence |
9850056 |
Survivin binds specifically to caspase-3. Survivin protected from apoptosis induced by overexpression of procaspase-3 and inhibited the processing of these zymogens into active caspases. Survivin, which is commonly expressed in human tumor cell lines, can bind the effector cell death proteases caspase-3 in vitro and inhibits caspase activity |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-72882 |
|
|
Homo sapiens |
|
pmid |
sentence |
10587640 |
Use of a dominant-negative survivin mutant or antisense survivin complementary dna disrupts a supramolecular assembly of survivin, caspase-3 and the cyclin-dependent-kinase inhibitor p21waf1/cip1 within centrosomes, and results in caspase-dependent cleavage of p21. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
BIRC5 | up-regulates
binding
|
XIAP |
0.509 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-126367 |
|
|
Homo sapiens |
|
pmid |
sentence |
15218035 |
Formation of a survivin-xiap complex promotes increased xiap stability against ubiquitination/proteasomal destruction and synergistic apoptosis |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
BIRC5 | down-regulates
binding
|
CASP9 |
0.518 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-84065 |
|
|
Homo sapiens |
|
pmid |
sentence |
11069302 |
Survivin (an inhibitor of apoptosis) phosphorylation on thr34 may regulate apoptosis at cell division via an interaction with caspase-9. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
E2F4 | down-regulates quantity by repression
transcriptional regulation
|
BIRC5 |
0.341 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271678 |
|
|
|
|
pmid |
sentence |
18504435 |
This TGF-beta response is triggered through a Smad2/3-dependent hypophosphorylation of Rb and the subsequent association of the Rb/E2F4 repressive complex to CDE/CHR elements in the proximal region of the survivin promoter. |
|
Publications: |
1 |
+ |
DIABLO | down-regulates
binding
|
BIRC5 |
0.586 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-80212 |
|
|
Homo sapiens |
|
pmid |
sentence |
10929711 |
Diablo seem to function as a general iaps neutralizer by binding to these protein. Diablo promotes casp9 activation by binding to inhibitor of apoptosis proteins, iaps, and removing their inhibitory activity. mitochondrial survivin associated with smac/diablo, delaying its release. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-155364 |
|
|
Homo sapiens |
|
pmid |
sentence |
17546047 |
Diablo seem to function as a general iaps neutralizer by binding to these protein. Diablo promotes casp9 activation by binding to inhibitor of apoptosis proteins, iaps, and removing their inhibitory activity. mitochondrial survivin associated with smac/diablo, delaying its release. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
BIRC5 | down-regulates
binding
|
DIABLO |
0.586 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-155361 |
|
|
Homo sapiens |
|
pmid |
sentence |
17546047 |
Mitochondrial survivin associated with smac/diablo, delaying its release. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
sepantronium bromide | down-regulates activity
chemical inhibition
|
BIRC5 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262245 |
|
|
Homo sapiens |
|
pmid |
sentence |
25659731 |
The survivin suppressant YM155 (Sepantronium Bromide) has pre-clinical activity against a range of solid cancers and leukemias, although data in AML is limited. These data suggest that YM155-mediated inhibition of survivin is a potentially beneficial therapeutic strategy for AML, particularly paediatric disease, and warrants further evaluation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TP53 | down-regulates quantity by repression
transcriptional regulation
|
BIRC5 |
0.544 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-117328 |
|
|
Homo sapiens |
|
pmid |
sentence |
11965534 |
Further analyses suggested that the modification of chromatin within the survivin promoter could be a molecular explanation for silencing of survivin gene transcription by p53. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
STAT3 | up-regulates quantity by expression
transcriptional regulation
|
BIRC5 |
0.61 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254762 |
|
|
Homo sapiens |
|
pmid |
sentence |
26512963 |
DAB2IP could interact with the signal transducer and activator of transcription 3 (STAT3) via its unique PR domain and suppress STAT3 phosphorylation and transactivation, leading to the inhibition of survivin expression in PCa cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TP53 | down-regulates
binding
|
BIRC5 |
0.544 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-111971 |
|
|
Homo sapiens |
|
pmid |
sentence |
11714700 |
This study identifies the anti-apoptotic survivin gene as a p53-repressed gene;notably, survivin repression by p53 is shown to be distinct from p53-dependent growth arrest. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
FBXL7 | down-regulates quantity by destabilization
binding
|
BIRC5 |
0.311 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272436 |
|
|
Mus musculus |
MLE-12 Cell |
pmid |
sentence |
25778398 |
Fbxl7 targets survivin for polyubiquitylation and proteasomal degradation.these data suggest that the Skp1·Cul1·F-box protein complex subunit Fbxl7 modulates mitochondrial function by controlling the cellular abundance of survivin. These results suggest that both Lys-90 and Lys-91 are critical for Fbxl7-mediated polyubiquitylation. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
FHIT | down-regulates quantity by repression
transcriptional regulation
|
BIRC5 |
0.273 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-159870 |
|
|
Homo sapiens |
|
pmid |
sentence |
18077326 |
In binding to the beta-catenin c-terminal domain, fhit represses transcription of target genes such as cyclin d1, axin2, mmp-14, and survivin. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
BIRC5 | form complex
binding
|
CPC |
0.793 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275424 |
|
|
Homo sapiens |
|
pmid |
sentence |
23175282 |
It is now known that the chromosomal passenger complex (CPC) is composed of four subunits: the enzymatic component Aurora B and the three regulatory and targeting components INCENP, Survivin and Borealin (also known as Dasra)5–7 (Figure 1A). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |