Id: | acc3105 |
Group: | 2sens |
Protein: | ERK1 |
Gene Symbol: | Mapk3 |
Protein Id: | Q63844 |
Protein Name: | MK03_MOUSE |
PTM: | phosphorylation |
Site: | Thr202 |
Site Sequence: | DPEHDHTGFLTEYVATRWYRA |
Disease Category: | Cardiovascular and circulatory system diseases |
Disease: | Ischemia |
Disease Subtype: | Ischemia-Reperfusion Injury |
Disease Cellline: | |
Disease Info: | |
Drug: | FR167653 |
Drug Info: | "FR167653 is a drug. However, specific details about its properties and uses are not provided in the given data." |
Effect: | modulate |
Effect Info: | "Hyperoxia → ↑NO → ↑ERK1/2 & p38 MAPK phosphorylation → Cardioprotective effect (anti-IRI), L-NAME or MAPK inhibitors → ↓ERK1/2 & p38 activation → Blockade of cardioprotection" |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 17268885 |
Sentence Index: | 17268885_11-12 |
Sentence: | "The hyperoxia-induced phosphorylation of ERK1/2 and p38 was reduced by L-NAME and both MAPK inhibitors. CONCLUSION: Nitric oxide triggers hyperoxic protection, and ERK1/2 and p38 MAPK are involved in signaling of protection against ischemia-reperfusion injury." |
Sequence & Structure:
MAAAAAAPGGGGGEPRGTAGVVPVVPGEVEVVKGQPFDVGPRYTQLQYIGEGAYGMVSSAYDHVRKTRVAIKKISPFEHQTYCQRTLREIQILLRFRHENVIGIRDILRAPTLEAMRDVYIVQDLMETDLYKLLKSQQLSNDHICYFLYQILRGLKYIHSANVLHRDLKPSNLLINTTCDLKICDFGLARIADPEHDHTGFLTEYVATRWYRAPEIMLNSKGYTKSIDIWSVGCILAEMLSNRPIFPGKHYLDQLNHILGILGSPSQEDLNCIINMKARNYLQSLPSKTKVAWAKLFPKSDSKALDLLDRMLTFNPNKRITVEEALAHPYLEQYYDPTDEPVAEEPFTFDMELDDLPKERLKELIFQETARFQPGAPEGP
No data.
No data.
Protein Tractability:
source: Open TargetsNo data.
PTM Intensity:
source: CPTACNo data.
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
T | 203 | U | Squamous cell carcinoma | Phosphorylation | 19934324 |
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.