Id: | acc5072 |
Group: | 1sens |
Protein: | NF-kappaB p65 |
Gene Symbol: | RELA |
Protein Id: | Q04206 |
Protein Name: | TF65_HUMAN |
PTM: | phosphorylation |
Site: | Ser536 |
Site Sequence: | LLSGDEDFSSIADMDFSALLS |
Disease Category: | Immune system diseases |
Disease: | Rheumatoid Arthritis |
Disease Subtype: | |
Disease Cellline: | |
Disease Info: | |
Drug: | Resveratrol |
Drug Info: | "Resveratrol is a polyphenolic compound found in various plants, such as grapes and peanuts. It has antioxidant and anti - inflammatory properties and is being researched for potential health benefits including cardiovascular protection and anti - aging effects." |
Effect: | modulate |
Effect Info: | "Resveratrol exerts an anti - inflammatory effect by upregulating Sirt1 and inhibiting the phosphorylation and acetylation of p65 (a subunit of NF - kappaB), c - Jun, and c - Fos (subunits of AP - 1) induced by BK. It has emerged as a potential drug for the treatment of inflammatory arthritis." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 28288820 |
Sentence Index: | 28288820_0 |
Sentence: | Resveratrol inhibits BK-induced COX-2 transcription by suppressing acetylation of AP-1 and NF-kappaB in human rheumatoid arthritis synovial fibroblasts. |
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 | 536 | P | Hepatocellular carcinoma | Phosphorylation | 34380537 |
S | 536 | P | Glioblastoma | Phosphorylation | 36116131 |
S | 536 | U | Pancreatic ductal adenocarcinoma | Phosphorylation | 29363544 |
S | 536 | U | Colonic inflammation | Phosphorylation | 34803708 |
S | 536 | U | Hepatocellular carcinoma/hepatocarcinoma/hepatoma | Phosphorylation | 20224721 |
S | 536 | U | Oral squamous cell carcinoma | Phosphorylation | 24063540 |
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.