Id: | acc4732 |
Group: | 1sens |
Protein: | JNK |
Gene Symbol: | MAPK8 |
Protein Id: | P45983 |
Protein Name: | MK08_HUMAN |
PTM: | phosphorylation |
Site: | Tyr185 |
Site Sequence: | AGTSFMMTPYVVTRYYRAPEV |
Disease Category: | Cancer |
Disease: | Cervical Cancer |
Disease Subtype: | |
Disease Cellline: | HeLa |
Disease Info: | |
Drug: | SP-FA |
Drug Info: | "SP - FA is a drug with specific pharmacological effects and applications, though detailed information isn't provided here. " |
Effect: | modulate |
Effect Info: | "Treatment with SP and SP-FA enhances the cytotoxicity of NK cells against HeLa cells by upregulating IFN-γ, TNF-α, perforin, and granzyme-B, and stimulates NK cell activation through the NF–κB and MAPK pathways." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 33357846 |
Sentence Index: | 33357846_4 |
Sentence: | "However, the treatment of SP and SP-FA enhance the NK cells cytotoxicity against HeLa cells by the upregulation of IFN-gamma, TNF-alpha, perforin, and Granzyme-B." |
Sequence & Structure:
MSRSKRDNNFYSVEIGDSTFTVLKRYQNLKPIGSGAQGIVCAAYDAILERNVAIKKLSRPFQNQTHAKRAYRELVLMKCVNHKNIIGLLNVFTPQKSLEEFQDVYIVMELMDANLCQVIQMELDHERMSYLLYQMLCGIKHLHSAGIIHRDLKPSNIVVKSDCTLKILDFGLARTAGTSFMMTPYVVTRYYRAPEVILGMGYKENVDLWSVGCIMGEMVCHKILFPGRDYIDQWNKVIEQLGTPCPEFMKKLQPTVRTYVENRPKYAGYSFEKLFPDVLFPADSEHNKLKASQARDLLSKMLVIDASKRISVDEALQHPYINVWYDPSEAEAPPPKIPDKQLDEREHTIEEWKELIYKEVMDLEERTKNGVIRGQPSPLGAAVINGSQHPSSSSSVNDVSSMSTDPTLASDTDSSLEAAAGPLGCCR
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
MAPK8 | BENTAMAPIMOD | c-Jun N-terminal kinase, JNK inhibitor | 2 | Completed | endometriosis | ClinicalTrials |
MAPK8 | TANZISERTIB | c-Jun N-terminal kinase 1 inhibitor | 2 | Terminated | idiopathic pulmonary fibrosis | ClinicalTrials |
MAPK8 | TANZISERTIB | c-Jun N-terminal kinase 1 inhibitor | 2 | Terminated | lupus erythematosus | ClinicalTrials |
MAPK8 | CC-401 | c-Jun N-terminal kinase 1 inhibitor | 1 | Terminated | myeloid leukemia | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACMAPK8-Tyr185 | |
---|---|
Cancer | Intensity |
BRCA | |
COAD | -0.707 |
HGSC | 0.707 |
ccRCC | |
GBM | |
HNSC | |
LUAD | |
LUSC | |
non_ccRCC | |
PDAC | |
UCEC |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
Y | 185 | U | Pancreatic cancer | Phosphorylation | 37016317 |
Y | 185 | U | Type 2 diabetes | Phosphorylation | 21931634 |
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.