Id: | acc3485 |
Group: | 2sens |
Protein: | MEK2 |
Gene Symbol: | MAP2K2 |
Protein Id: | P36507 |
Protein Name: | MP2K2_HUMAN |
PTM: | phosphorylation |
Site: | Ser222 |
Site Sequence: | FGVSGQLIDSMANSFVGTRSY |
Disease Category: | Cancer |
Disease: | Sarcoma |
Disease Subtype: | Ewing's sarcoma |
Disease Cellline: | SK-ES-1 |
Disease Info: | |
Drug: | Magnolol |
Drug Info: | "Magnolol is a bioactive compound found in Magnolia officinalis. It has various potential health benefits, such as anti - inflammatory and antioxidant properties. " |
Effect: | modulate |
Effect Info: | "The drug induces apoptosis and inhibits the proliferation of human Ewing's sarcoma SK–ES–1 cells through the mitochondrial and death receptor pathways, and is involved in the MAPK/ERK and JAK/STAT3 signaling pathways." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 32509168 |
Sentence Index: | 32509168_4-5 |
Sentence: | "The results demonstrated that magnolol inhibited the proliferation of ES and induced ES cell apoptosis through the mitochondrial and death receptor pathways. Magnolol reduced MEK1/2, ERK1/2, and STAT3 phosphorylation in ES cells, suggesting that the MAPK/ERK and JAK/STAT3 signal transduction pathways are involved in the inhibition of ES cell growth by magnolol." |
Sequence & Structure:
MLARRKPVLPALTINPTIAEGPSPTSEGASEANLVDLQKKLEELELDEQQKKRLEAFLTQKAKVGELKDDDFERISELGAGNGGVVTKVQHRPSGLIMARKLIHLEIKPAIRNQIIRELQVLHECNSPYIVGFYGAFYSDGEISICMEHMDGGSLDQVLKEAKRIPEEILGKVSIAVLRGLAYLREKHQIMHRDVKPSNILVNSRGEIKLCDFGVSGQLIDSMANSFVGTRSYMAPERLQGTHYSVQSDIWSMGLSLVELAVGRYPIPPPDAKELEAIFGRPVVDGEEGEPHSISPRPRPPGRPVSGHGMDSRPAMAIFELLDYIVNEPPPKLPNGVFTPDFQEFVNKCLIKNPAERADLKMLTNHTFIKRSEVEEVDFAGWLCKTLRLNQPGTPTRTAV
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
MAP2K2 | COBIMETINIB | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 4 | - | neoplasm | ATC |
MAP2K2 | SELUMETINIB | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 4 | - | neoplasm | ATC |
MAP2K2 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 4 | - | neoplasm | ATC |
MAP2K2 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 4 | Recruiting | neoplasm | ClinicalTrials |
MAP2K2 | COBIMETINIB FUMARATE | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 4 | - | melanoma | EMA |
MAP2K2 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 4 | - | melanoma | DailyMed EMA |
MAP2K2 | COBIMETINIB FUMARATE | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 4 | - | metastatic melanoma | DailyMed |
MAP2K2 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 4 | - | metastatic melanoma | FDA |
MAP2K2 | TRAMETINIB DIMETHYL SULFOXIDE | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 4 | - | metastatic melanoma | FDA |
MAP2K2 | SELUMETINIB SULFATE | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 4 | - | neurofibromatosis | DailyMed |
MAP2K2 | TRAMETINIB DIMETHYL SULFOXIDE | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 4 | - | thyroid cancer | DailyMed |
MAP2K2 | TRAMETINIB DIMETHYL SULFOXIDE | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 4 | - | lung cancer | DailyMed |
MAP2K2 | SELUMETINIB SULFATE | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 4 | - | neurofibromatosis type 1 | FDA EMA |
MAP2K2 | SELUMETINIB | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 3 | Recruiting | astrocytoma | ClinicalTrials |
MAP2K2 | SELUMETINIB SULFATE | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 3 | Recruiting | astrocytoma | ClinicalTrials |
MAP2K2 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 3 | Completed | cutaneous melanoma | ClinicalTrials |
MAP2K2 | COBIMETINIB | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 3 | Active, not recruiting | melanoma | ClinicalTrials |
MAP2K2 | COBIMETINIB | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 3 | Completed | melanoma | ClinicalTrials |
MAP2K2 | COBIMETINIB | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 3 | Terminated | melanoma | ClinicalTrials |
MAP2K2 | COBIMETINIB | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 3 | Withdrawn | melanoma | ClinicalTrials |
MAP2K2 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 2 inhibitor | 3 | Active, not recruiting | melanoma | ClinicalTrials ClinicalTrials ClinicalTrials |
MAP2K2 | TRAMETINIB | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 3 | Recruiting | melanoma | ClinicalTrials ClinicalTrials |
MAP2K2 | TRAMETINIB | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 3 | Active, not recruiting | melanoma | ClinicalTrials |
MAP2K2 | TRAMETINIB | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 3 | Completed | melanoma | ClinicalTrials ClinicalTrials ClinicalTrials ClinicalTrials ClinicalTrials |
MAP2K2 | SELUMETINIB | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 3 | Active, not recruiting | non-small cell lung carcinoma | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACMAP2K2-Ser222 | |
---|---|
Cancer | Intensity |
BRCA | 1.103 |
COAD | 0.207 |
HGSC | -2.178 |
ccRCC | -0.277 |
GBM | -0.734 |
HNSC | 1.342 |
LUAD | 0.555 |
LUSC | 0.176 |
non_ccRCC | -0.246 |
PDAC | -0.741 |
UCEC | 0.793 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
T | 394 | U | Breast cancer | Phosphorylation | 33226073 |
- | - | U | Breast cancer | Phosphorylation | 15193230 |
K | 48 | U | Hepatocellular carcinoma | Ubiquitination | 29706623 |
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.