Id: | acc0875 |
Group: | 2sens |
Protein: | PTEN |
Gene Symbol: | PTEN |
Protein Id: | P60484 |
Protein Name: | PTEN_HUMAN |
PTM: | phosphorylation |
Site: | Thr382 |
Site Sequence: | EPDHYRYSDTTDSDPENEPFD |
Disease Category: | Cancer |
Disease: | Melanoma |
Disease Subtype: | |
Disease Cellline: | A375 |
Disease Info: | |
Drug: | chondroitin-4-sulfate(CHSA) |
Drug Info: | Chondroitin-4-sulfate (CHSA) is a sulfated glycosaminoglycan commonly used as a dietary supplement to support joint health and alleviate symptoms of osteoarthritis by promoting cartilage integrity and reducing inflammation. |
Effect: | modulate |
Effect Info: | CHSA treatment increased the phosphorylation levels of AKT and PTEN in A375 and SK-MEL-5 cells and enhanced the cell proliferation rate. |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 29547721 |
Sentence Index: | 29547721_3-4 |
Sentence: | "Here we report that chondroitin-4-sulfate (CHSA), a natural glycosaminoglycan approved as a dietary supplement used for osteoarthritis, selectively promotes the tumor growth potential of BRAF V600E-expressing human melanoma cells in patient- and cell line-derived xenograft mice and confers resistance to BRAF inhibitors. Mechanistically, chondroitin sulfate glucuronyltransferase (CSGlcA-T) signals through its product CHSA to enhance casein kinase 2 (CK2)-PTEN binding and consequent phosphorylation and inhibition of PTEN, which requires CHSA chains and is essential to sustain AKT activation in BRAF V600E-expressing melanoma cells." |
Sequence & Structure:
MTAIIKEIVSRNKRRYQEDGFDLDLTYIYPNIIAMGFPAERLEGVYRNNIDDVVRFLDSKHKNHYKIYNLCAERHYDTAKFNCRVAQYPFEDHNPPQLELIKPFCEDLDQWLSEDDNHVAAIHCKAGKGRTGVMICAYLLHRGKFLKAQEALDFYGEVRTRDKKGVTIPSQRRYVYYYSYLLKNHLDYRPVALLFHKMMFETIPMFSGGTCNPQFVVCQLKVKIYSSNSGPTRREDKFMYFEFPQPLPVCGDIKVEFFHKQNKMLKKDKMFHFWVNTFFIPGPEETSEKVENGSLCDQEIDSICSIERADNDKEYLVLTLTKNDLDKANKDKANRYFSPNFKVKLYFTKTVEEPSNPEASSSTSVTPDVSDNEPDHYRYSDTTDSDPENEPFDEDQHTQITKV
Select PDB:
No data.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACNo intensity data of this site,
show all other sites!
PTEN-Ser294 | |||||||||
---|---|---|---|---|---|---|---|---|---|
Cancer | Intensity | ||||||||
BRCA | |||||||||
COAD | -0.741 | ||||||||
HGSC | |||||||||
ccRCC | -0.738 | ||||||||
GBM | |||||||||
HNSC | 1.65 | ||||||||
LUAD | -0.543 | ||||||||
LUSC | 0.557 | ||||||||
non_ccRCC | -1.263 | ||||||||
PDAC | 0.989 | ||||||||
UCEC | 0.088 |
PTEN-Ser364 | |||||||||
---|---|---|---|---|---|---|---|---|---|
Cancer | Intensity | ||||||||
BRCA | |||||||||
COAD | |||||||||
HGSC | |||||||||
ccRCC | |||||||||
GBM | |||||||||
HNSC | |||||||||
LUAD | 0.707 | ||||||||
LUSC | |||||||||
non_ccRCC | |||||||||
PDAC | |||||||||
UCEC | -0.707 |
PTEN-Ser370 | |||||||||
---|---|---|---|---|---|---|---|---|---|
Cancer | Intensity | ||||||||
BRCA | |||||||||
COAD | -1.229 | ||||||||
HGSC | |||||||||
ccRCC | 0.576 | ||||||||
GBM | |||||||||
HNSC | |||||||||
LUAD | 1.014 | ||||||||
LUSC | |||||||||
non_ccRCC | |||||||||
PDAC | |||||||||
UCEC | -0.361 |
PTEN-Ser467 | |||||||||
---|---|---|---|---|---|---|---|---|---|
Cancer | Intensity | ||||||||
BRCA | 0.471 | ||||||||
COAD | |||||||||
HGSC | -1.149 | ||||||||
ccRCC | |||||||||
GBM | 0.677 | ||||||||
HNSC | |||||||||
LUAD | |||||||||
LUSC | |||||||||
non_ccRCC | |||||||||
PDAC | |||||||||
UCEC |
PTEN-Thr363 | |||||||||
---|---|---|---|---|---|---|---|---|---|
Cancer | Intensity | ||||||||
BRCA | |||||||||
COAD | |||||||||
HGSC | |||||||||
ccRCC | |||||||||
GBM | |||||||||
HNSC | |||||||||
LUAD | 0.707 | ||||||||
LUSC | |||||||||
non_ccRCC | |||||||||
PDAC | |||||||||
UCEC | -0.707 |
PTEN-Thr366 | |
---|---|
Cancer | Intensity |
BRCA | |
COAD | |
HGSC | |
ccRCC | 0.707 |
GBM | |
HNSC | |
LUAD | |
LUSC | |
non_ccRCC | |
PDAC | |
UCEC | -0.707 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
T | 382 | D | Non-small cell lung cancer | Phosphorylation | 35240162 |
T | 382 | U | Lymphocytic leukemia | Phosphorylation | 20576813 |
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: DecryptMProtein | Gene | PTM | Position | Modified sequence | Cell | Drug | pEC50 | Regulation | Experiment |
---|---|---|---|---|---|---|---|---|---|
P60484 | PTEN | P | Thr382 | YSDT(ph)TDSDPENEPFDEDQHTQITK | A549 | Pictilisib | 4.1859 | - |
pEC50 Note: pEC50 is the negative logarithm of EC50 (half-maximal effective concentration, dosage unit Mol), calculated as pEC50 = -log10(EC50), which quantifies the potency of a drug or compound.
Function score:
source: funscoRNo data.