Id: | acc3484 |
Group: | 2sens |
Protein: | MEK1 |
Gene Symbol: | MAP2K1 |
Protein Id: | Q02750 |
Protein Name: | MP2K1_HUMAN |
PTM: | phosphorylation |
Site: | Ser218 |
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:
MPKKKPTPIQLNPAPDGSAVNGTSSAETNLEALQKKLEELELDEQQRKRLEAFLTQKQKVGELKDDDFEKISELGAGNGGVVFKVSHKPSGLVMARKLIHLEIKPAIRNQIIRELQVLHECNSPYIVGFYGAFYSDGEISICMEHMDGGSLDQVLKKAGRIPEQILGKVSIAVIKGLTYLREKHKIMHRDVKPSNILVNSRGEIKLCDFGVSGQLIDSMANSFVGTRSYMSPERLQGTHYSVQSDIWSMGLSLVEMAVGRYPIPPPDAKELELMFGCQVEGDAAETPPRPRTPGRPLSSYGMDSRPPMAIFELLDYIVNEPPPKLPSGVFSLEFQDFVNKCLIKNPAERADLKQLMVHAFIKRSDAEEVDFAGWLCSTIGLNQPSTPTHAAGV
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
MAP2K1 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 4 | - | neoplasm | ATC |
MAP2K1 | SELUMETINIB | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 4 | - | neoplasm | ATC |
MAP2K1 | COBIMETINIB | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 4 | - | neoplasm | ATC |
MAP2K1 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 4 | Recruiting | neoplasm | ClinicalTrials |
MAP2K1 | COBIMETINIB FUMARATE | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 4 | - | melanoma | EMA |
MAP2K1 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 4 | - | melanoma | DailyMed EMA |
MAP2K1 | COBIMETINIB FUMARATE | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 4 | - | metastatic melanoma | DailyMed |
MAP2K1 | TRAMETINIB DIMETHYL SULFOXIDE | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 4 | - | metastatic melanoma | FDA |
MAP2K1 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 4 | - | metastatic melanoma | FDA |
MAP2K1 | SELUMETINIB SULFATE | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 4 | - | neurofibromatosis | DailyMed |
MAP2K1 | TRAMETINIB DIMETHYL SULFOXIDE | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 4 | - | thyroid cancer | DailyMed |
MAP2K1 | TRAMETINIB DIMETHYL SULFOXIDE | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 4 | - | lung cancer | DailyMed |
MAP2K1 | SELUMETINIB SULFATE | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 4 | - | neurofibromatosis type 1 | EMA FDA |
MAP2K1 | SELUMETINIB SULFATE | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 3 | Recruiting | astrocytoma | ClinicalTrials |
MAP2K1 | SELUMETINIB | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 3 | Recruiting | astrocytoma | ClinicalTrials |
MAP2K1 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 3 | Completed | cutaneous melanoma | ClinicalTrials |
MAP2K1 | COBIMETINIB | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 3 | Withdrawn | melanoma | ClinicalTrials |
MAP2K1 | TRAMETINIB | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 3 | Recruiting | melanoma | ClinicalTrials ClinicalTrials |
MAP2K1 | COBIMETINIB | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 3 | Active, not recruiting | melanoma | ClinicalTrials |
MAP2K1 | COBIMETINIB | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 3 | Completed | melanoma | ClinicalTrials |
MAP2K1 | COBIMETINIB | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 3 | Terminated | melanoma | ClinicalTrials |
MAP2K1 | BINIMETINIB | Dual specificity mitogen-activated protein kinase kinase 1 inhibitor | 3 | Active, not recruiting | melanoma | ClinicalTrials ClinicalTrials ClinicalTrials |
MAP2K1 | TRAMETINIB | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 3 | Active, not recruiting | melanoma | ClinicalTrials |
MAP2K1 | TRAMETINIB | Dual specificity mitogen-activated protein kinase kinase; MEK1/2 inhibitor | 3 | Completed | melanoma | ClinicalTrials ClinicalTrials ClinicalTrials ClinicalTrials ClinicalTrials |
MAP2K1 | 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: CPTACMAP2K1-Ser218 | |
---|---|
Cancer | Intensity |
BRCA | 1.025 |
COAD | 0.17 |
HGSC | -2.102 |
ccRCC | |
GBM | -0.726 |
HNSC | 1.253 |
LUAD | 0.502 |
LUSC | 0.141 |
non_ccRCC | -0.26 |
PDAC | -0.732 |
UCEC | 0.729 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
S | 218 | U | Head and neck squamous cell carcinoma | Phosphorylation | 21281788 |
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.