Id: | acc0666 |
Group: | 1sens |
Protein: | PI3K |
Gene Symbol: | PIK3CA |
Protein Id: | P42336 |
Protein Name: | PK3CA_HUMAN |
PTM: | phosphorylation |
Site: | Tyr199 |
Site Sequence: | IIVVIWVIVSPNNDKQKYTLK |
Disease Category: | Cancer |
Disease: | Ovarian Cancer |
Disease Subtype: | |
Disease Cellline: | CAOV3 |
Disease Info: | |
Drug: | sh-TRAF4 |
Drug Info: | - |
Effect: | modulate |
Effect Info: | LY294002 can inhibit the phosphorylation of Akt and PI3K and suppress ovarian cancer cells. |
Note: | Non-conventional drugs |
Score: | 3.0 |
Pubmed(PMID): | 36625999 |
Sentence Index: | 36625999_14 |
Sentence: | "Furthermore, sh-TRAF4 as well as treatment with LY294002, the PI3K/Akt inhibitor, inhibited the phosphorylation of Akt and PI3K, thus repressing the activation of PI3K/AKT signaling pathway in ovarian cancer cell lines." |
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.