Id: | acc2254 |
Group: | 2sens |
Protein: | RelA |
Gene Symbol: | RELA |
Protein Id: | Q04206 |
Protein Name: | TF65_HUMAN |
PTM: | phosphorylation |
Site: | Ser276 |
Site Sequence: | RVSMQLRRPSDRELSEPMEFQ |
Disease Category: | Cancer |
Disease: | Colorectal Cancer |
Disease Subtype: | |
Disease Cellline: | HCT116? |
Disease Info: | |
Drug: | RITA |
Drug Info: | "RITA (NSC 652287): A small molecule p53 activator that induces DNA-protein and DNA-DNA cross-links, inhibits MDM2-p53 interaction, and is used in experimental cancer therapy, such as glioblastoma research. Temozolomide (TMZ): A chemotherapeutic alkylating agent used primarily in the treatment of glioblastoma multiforme and other malignant gliomas." |
Effect: | resist |
Effect Info: | "In the parental MCF7 and HCT116 cells with a large number of apoptosis induced by RITA, the phosphorylation of RelA/p65 at Ser536 increases, but that at Ser276 and Ser468 decreases." |
Note: | |
Score: | 5.0 |
Pubmed(PMID): | 27721021 |
Sentence Index: | 27721021_4-5 |
Sentence: | "This study found that the site-differential phosphorylation of nuclear factor-kappaB (NF-kappaB) RelA/p65 creates a barcode for RITA chemosensitivity in cancer cells. In naive MCF7 and HCT116 cells where RITA triggered vast apoptosis, phosphorylation of RelA/p65 increased at Ser536, but decreased at Ser276 and Ser468; oppositely, in RITA-resistant cells, RelA/p65 phosphorylation decreased at Ser536, but increased at Ser276 and Ser468." |
Sequence & Structure:
MDELFPLIFPAEPAQASGPYVEIIEQPKQRGMRFRYKCEGRSAGSIPGERSTDTTKTHPTIKINGYTGPGTVRISLVTKDPPHRPHPHELVGKDCRDGFYEAELCPDRCIHSFQNLGIQCVKKRDLEQAISQRIQTNNNPFQVPIEEQRGDYDLNAVRLCFQVTVRDPSGRPLRLPPVLSHPIFDNRAPNTAELKICRVNRNSGSCLGGDEIFLLCDKVQKEDIEVYFTGPGWEARGSFSQADVHRQVAIVFRTPPYADPSLQAPVRVSMQLRRPSDRELSEPMEFQYLPDTDDRHRIEEKRKRTYETFKSIMKKSPFSGPTDPRPPPRRIAVPSRSSASVPKPAPQPYPFTSSLSTINYDEFPTMVFPSGQISQASALAPAPPQVLPQAPAPAPAPAMVSALAQAPAPVPVLAPGPPQAVAPPAPKPTQAGEGTLSEALLQLQFDDEDLGALLGNSTDPAVFTDLASVDNSEFQQLLNQGIPVAPHTTEPMLMEYPEAITRLVTGAQRPPDPAPAPLGAPGLPNGLLSGDEDFSSIADMDFSALLSQISS
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
RELA | EDASALONEXENT | Nuclear factor NF-kappa-B complex inhibitor | 3 | Terminated | Duchenne muscular dystrophy | ClinicalTrials |
RELA | EDASALONEXENT | Nuclear factor NF-kappa-B complex inhibitor | 3 | Completed | Duchenne muscular dystrophy | ClinicalTrials |
RELA | EDASALONEXENT | Nuclear factor NF-kappa-B complex inhibitor | 1 | Completed | type 2 diabetes mellitus | ClinicalTrials |
RELA | EDASALONEXENT | Nuclear factor NF-kappa-B complex inhibitor | 1 | Completed | Duchenne muscular dystrophy | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACNo intensity data of this site,
show all other sites!
RELA-Ser112 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | 0.367 | ||||
GBM | |||||
HNSC | |||||
LUAD | |||||
LUSC | 0.765 | ||||
non_ccRCC | |||||
PDAC | |||||
UCEC | -1.132 |
RELA-Ser177 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | 0.675 | ||||
GBM | -0.474 | ||||
HNSC | |||||
LUAD | -0.6 | ||||
LUSC | -0.083 | ||||
non_ccRCC | 1.626 | ||||
PDAC | |||||
UCEC | -1.143 |
RELA-Ser200 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | 0.131 | ||||
HGSC | -2.56 | ||||
ccRCC | 0.526 | ||||
GBM | 0.516 | ||||
HNSC | 0.416 | ||||
LUAD | |||||
LUSC | 0.737 | ||||
non_ccRCC | -0.008 | ||||
PDAC | 0.386 | ||||
UCEC | -0.143 |
RELA-Ser202 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | |||||
GBM | 1.142 | ||||
HNSC | -0.719 | ||||
LUAD | -0.423 | ||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
RELA-Ser235 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -0.452 | ||||
COAD | -0.397 | ||||
HGSC | 2.387 | ||||
ccRCC | -0.206 | ||||
GBM | -0.643 | ||||
HNSC | 0.08 | ||||
LUAD | -0.689 | ||||
LUSC | 0.666 | ||||
non_ccRCC | |||||
PDAC | |||||
UCEC | -0.747 |
RELA-Ser42 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | 0.381 | ||||
GBM | -1.76 | ||||
HNSC | 0.615 | ||||
LUAD | 0.173 | ||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC | 0.591 |
RELA-Ser45 | |
---|---|
Cancer | Intensity |
BRCA | |
COAD | |
HGSC | -0.868 |
ccRCC | -0.94 |
GBM | |
HNSC | 1.524 |
LUAD | |
LUSC | |
non_ccRCC | |
PDAC | 0.148 |
UCEC | 0.137 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
S | 276 | U | Colon cancer/carcinoma | Phosphorylation | 23784084 |
State Note: Based on the distinct PTM states in diseases, PTMD classified all disease-associated PTMs into six classes, including whether the up-regulation (U) or down-regulation (D) of PTM levels, the absence (A) or presence (P) of PTMs, and the creation (C) or disruption (N) of PTM sites are associated with diseases.
PTM-Drug Perturbation Response:
source: DecryptMNo data.
Function score:
source: funscoRNo data.