Id: | acc3368 |
Group: | 2sens |
Protein: | PI3K |
Gene Symbol: | PIK3CA |
Protein Id: | P42336 |
Protein Name: | PK3CA_HUMAN |
PTM: | phosphorylation |
Site: | Tyr199 |
Site Sequence: | IIVVIWVIVSPNNDKQKYTLK |
Disease Category: | Nervous system diseases |
Disease: | Alzheimer's Disease |
Disease Subtype: | |
Disease Cellline: | |
Disease Info: | |
Drug: | cannabidiol (CBD) + Mesenchymal stem cells (MSCs) |
Drug Info: | Cannabidiol (CBD) is a non - psychoactive compound derived from cannabis plants. | Mesenchymal stem cells (MSCs) are multipotent stromal cells that can differentiate into a variety of cell types. |
Effect: | modulate |
Effect Info: | "CBD pretreatment can inhibit the expression of proteins in GMSCs that may be involved in tau phosphorylation and Aβ production, which is more beneficial for the treatment of AD. p-PI3K, PI3K, p-Akt, and Akt are significantly expressed. " |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 28025562 |
Sentence Index: | 28025562_5-6 |
Sentence: | "By comparing the expression profiles between GMSCs treated with CBD (CBD-GMSCs) and control GMSCs (CTR-GMSCs), we found that CBD led to the downregulation of genes linked to AD, including genes coding for the kinases responsible of tau phosphorylation and for the secretases involved in Abeta generation. In parallel, immunocytochemistry analysis has shown that CBD inhibited the expression of GSK3beta, a central player in AD pathogenesis, by promoting PI3K/Akt signalling." |
Sequence & Structure:
MPPRPSSGELWGIHLMPPRILVECLLPNGMIVTLECLREATLITIKHELFKEARKYPLHQLLQDESSYIFVSVTQEAEREEFFDETRRLCDLRLFQPFLKVIEPVGNREEKILNREIGFAIGMPVCEFDMVKDPEVQDFRRNILNVCKEAVDLRDLNSPHSRAMYVYPPNVESSPELPKHIYNKLDKGQIIVVIWVIVSPNNDKQKYTLKINHDCVPEQVIAEAIRKKTRSMLLSSEQLKLCVLEYQGKYILKVCGCDEYFLEKYPLSQYKYIRSCIMLGRMPNLMLMAKESLYSQLPMDCFTMPSYSRRISTATPYMNGETSTKSLWVINSALRIKILCATYVNVNIRDIDKIYVRTGIYHGGEPLCDNVNTQRVPCSNPRWNEWLNYDIYIPDLPRAARLCLSICSVKGRKGAKEEHCPLAWGNINLFDYTDTLVSGKMALNLWPVPHGLEDLLNPIGVTGSNPNKETPCLELEFDWFSSVVKFPDMSVIEEHANWSVSREAGFSYSHAGLSNRLARDNELRENDKEQLKAISTRDPLSEITEQEKDFLWSHRHYCVTIPEILPKLLLSVKWNSRDEVAQMYCLVKDWPPIKPEQAMELLDCNYPDPMVRGFAVRCLEKYLTDDKLSQYLIQLVQVLKYEQYLDNLLVRFLLKKALTNQRIGHFFFWHLKSEMHNKTVSQRFGLLLESYCRACGMYLKHLNRQVEAMEKLINLTDILKQEKKDETQKVQMKFLVEQMRRPDFMDALQGFLSPLNPAHQLGNLRLEECRIMSSAKRPLWLNWENPDIMSELLFQNNEIIFKNGDDLRQDMLTLQIIRIMENIWQNQGLDLRMLPYGCLSIGDCVGLIEVVRNSHTIMQIQCKGGLKGALQFNSHTLHQWLKDKNKGEIYDAAIDLFTRSCAGYCVATFILGIGDRHNSNIMVKDDGQLFHIDFGHFLDHKKKKFGYKRERVPFVLTQDFLIVISKGAQECTKTREFERFQEMCYKAYLAIRQHANLFINLFSMMLGSGMPELQSFDDIAYIRKTLALDKTEQEALEYFMKQMNDAHHGGWTTKMDWIFHTIKQHALN
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
PIK3CA | COPANLISIB HYDROCHLORIDE | PI3-kinase p110-alpha subunit inhibitor | 4 | - | neoplasm of mature B-cells | FDA |
PIK3CA | ALPELISIB | PI3-kinase p110-alpha subunit inhibitor | 4 | - | breast carcinoma | FDA |
PIK3CA | ALPELISIB | PI3-kinase p110-alpha subunit inhibitor | 4 | - | neoplasm | ATC |
PIK3CA | COPANLISIB | PI3-kinase p110-alpha subunit inhibitor | 4 | - | neoplasm | ATC |
PIK3CA | ALPELISIB | PI3-kinase p110-alpha subunit inhibitor | 4 | - | breast neoplasm | EMA FDA |
PIK3CA | ALPELISIB | PI3-kinase p110-alpha subunit inhibitor | 4 | - | breast cancer | DailyMed |
PIK3CA | ALPELISIB | PI3-kinase p110-alpha subunit inhibitor | 4 | Recruiting | breast cancer | ClinicalTrials |
PIK3CA | COPANLISIB HYDROCHLORIDE | PI3-kinase p110-alpha subunit inhibitor | 4 | - | follicular lymphoma | DailyMed |
PIK3CA | DACTOLISIB | PI3-kinase class I inhibitor | 3 | Completed | infection | ClinicalTrials |
PIK3CA | ALPELISIB | PI3-kinase p110-alpha subunit inhibitor | 3 | Active, not recruiting | breast neoplasm | ClinicalTrials |
PIK3CA | COPANLISIB | PI3-kinase p110-alpha subunit inhibitor | 3 | Active, not recruiting | non-Hodgkins lymphoma | ClinicalTrials |
PIK3CA | COPANLISIB | PI3-kinase p110-alpha subunit inhibitor | 3 | Completed | non-Hodgkins lymphoma | ClinicalTrials |
PIK3CA | COPANLISIB | PI3-kinase p110-alpha subunit inhibitor | 3 | Terminated | non-Hodgkins lymphoma | ClinicalTrials |
PIK3CA | BUPARLISIB | PI3-kinase class I inhibitor | 3 | Active, not recruiting | head and neck malignant neoplasia | ClinicalTrials |
PIK3CA | BUPARLISIB | PI3-kinase class I inhibitor | 3 | Completed | breast cancer | ClinicalTrials |
PIK3CA | BUPARLISIB | PI3-kinase class I inhibitor | 3 | Terminated | breast cancer | ClinicalTrials |
PIK3CA | TASELISIB | PI3-kinase class I inhibitor | 3 | Terminated | breast cancer | ClinicalTrials |
PIK3CA | ALPELISIB | PI3-kinase p110-alpha subunit inhibitor | 3 | Active, not recruiting | breast cancer | ClinicalTrials ClinicalTrials |
PIK3CA | ALPELISIB | PI3-kinase p110-alpha subunit inhibitor | 3 | Completed | breast cancer | ClinicalTrials ClinicalTrials |
PIK3CA | ALPELISIB | PI3-kinase p110-alpha subunit inhibitor | 3 | Recruiting | breast cancer | ClinicalTrials ClinicalTrials ClinicalTrials |
PIK3CA | GEDATOLISIB | PI3-kinase class I inhibitor | 3 | Recruiting | breast cancer | ClinicalTrials |
PIK3CA | INAVOLISIB | PI3-kinase p110-alpha subunit inhibitor | 3 | Recruiting | breast cancer | ClinicalTrials ClinicalTrials |
PIK3CA | BUPARLISIB | PI3-kinase class I inhibitor | 2 | Terminated | head and neck squamous cell carcinoma | ClinicalTrials |
PIK3CA | ALPELISIB | PI3-kinase p110-alpha subunit inhibitor | 2 | Unknown status | head and neck squamous cell carcinoma | ClinicalTrials |
PIK3CA | BUPARLISIB | PI3-kinase class I inhibitor | 2 | Unknown status | head and neck squamous cell carcinoma | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACNo data.
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
Y | 508 | P | Colorectal cancer | Phosphorylation | 37689735 |
Y | 317 | P | Colorectal cancer | Phosphorylation | 37689735 |
- | - | U | Gastric cancer | Methylation | 24513424 |
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.