Id: | acc3365 |
Group: | 2sens |
Protein: | AKT |
Gene Symbol: | AKT1 |
Protein Id: | P31749 |
Protein Name: | AKT1_HUMAN |
PTM: | phosphorylation |
Site: | Ser473 |
Site Sequence: | ERRPHFPQFSYSASGTA---- |
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:
MSDVAIVKEGWLHKRGEYIKTWRPRYFLLKNDGTFIGYKERPQDVDQREAPLNNFSVAQCQLMKTERPRPNTFIIRCLQWTTVIERTFHVETPEEREEWTTAIQTVADGLKKQEEEEMDFRSGSPSDNSGAEEMEVSLAKPKHRVTMNEFEYLKLLGKGTFGKVILVKEKATGRYYAMKILKKEVIVAKDEVAHTLTENRVLQNSRHPFLTALKYSFQTHDRLCFVMEYANGGELFFHLSRERVFSEDRARFYGAEIVSALDYLHSEKNVVYRDLKLENLMLDKDGHIKITDFGLCKEGIKDGATMKTFCGTPEYLAPEVLEDNDYGRAVDWWGLGVVMYEMMCGRLPFYNQDHEKLFELILMEEIRFPRTLGPEAKSLLSGLLKKDPKQRLGGGSEDAKEIMQHRFFAGIVWQHVYEKKLSPPFKPQVTSETDTRYFDEEFTAQMITITPPDQDDSMECVDSERRPHFPQFSYSASGTA
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
AKT1 | IPATASERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Completed | metastatic prostate cancer | ClinicalTrials |
AKT1 | CAPIVASERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Active, not recruiting | breast neoplasm | ClinicalTrials |
AKT1 | IPATASERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Completed | triple-negative breast cancer | ClinicalTrials |
AKT1 | IPATASERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Recruiting | cancer | ClinicalTrials |
AKT1 | IPATASERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Active, not recruiting | breast cancer | ClinicalTrials |
AKT1 | IPATASERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Completed | breast cancer | ClinicalTrials |
AKT1 | IPATASERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Terminated | breast cancer | ClinicalTrials |
AKT1 | AFURESERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Recruiting | breast cancer | ClinicalTrials |
AKT1 | CAPIVASERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Active, not recruiting | breast cancer | ClinicalTrials |
AKT1 | CAPIVASERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Recruiting | breast cancer | ClinicalTrials |
AKT1 | CAPIVASERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Recruiting | prostate cancer | ClinicalTrials |
AKT1 | CAPIVASERTIB | Serine/threonine-protein kinase AKT inhibitor | 3 | Active, not recruiting | prostate cancer | ClinicalTrials |
AKT1 | MK-2206 | Serine/threonine-protein kinase AKT inhibitor | 2 | Completed | hepatocellular carcinoma | ClinicalTrials |
AKT1 | MK-2206 | Serine/threonine-protein kinase AKT inhibitor | 2 | Completed | head and neck squamous cell carcinoma | ClinicalTrials |
AKT1 | CAPIVASERTIB | Serine/threonine-protein kinase AKT inhibitor | 2 | Active, not recruiting | neoplasm of mature B-cells | ClinicalTrials |
AKT1 | UPROSERTIB | Serine/threonine-protein kinase AKT inhibitor | 2 | Terminated | acute myeloid leukemia | ClinicalTrials |
AKT1 | CAPIVASERTIB | Serine/threonine-protein kinase AKT inhibitor | 2 | Active, not recruiting | adenocarcinoma | ClinicalTrials |
AKT1 | MK-2206 | Serine/threonine-protein kinase AKT inhibitor | 2 | Completed | breast carcinoma | ClinicalTrials |
AKT1 | MK-2206 | Serine/threonine-protein kinase AKT inhibitor | 2 | Terminated | breast carcinoma | ClinicalTrials |
AKT1 | MK-2206 | Serine/threonine-protein kinase AKT inhibitor | 2 | Completed | adenosquamous lung carcinoma | ClinicalTrials |
AKT1 | UPROSERTIB | Serine/threonine-protein kinase AKT inhibitor | 2 | Completed | breast carcinoma | ClinicalTrials |
AKT1 | MK-2206 | Serine/threonine-protein kinase AKT inhibitor | 2 | Completed | bronchoalveolar adenocarcinoma | ClinicalTrials |
AKT1 | MK-2206 | Serine/threonine-protein kinase AKT inhibitor | 2 | Completed | diffuse large B-cell lymphoma | ClinicalTrials |
AKT1 | MK-2206 | Serine/threonine-protein kinase AKT inhibitor | 2 | Terminated | diffuse large B-cell lymphoma | ClinicalTrials |
AKT1 | CAPIVASERTIB | Serine/threonine-protein kinase AKT inhibitor | 2 | Terminated | gastric adenocarcinoma | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACNo intensity data of this site,
show all other sites!
AKT1-Ser124 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | -0.707 | ||||
HGSC | 0.707 | ||||
ccRCC | |||||
GBM | |||||
HNSC | |||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
AKT1-Ser126 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | -0.707 | ||||
HGSC | 0.707 | ||||
ccRCC | |||||
GBM | |||||
HNSC | |||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
AKT1-Ser129 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | -0.707 | ||||
HGSC | 0.707 | ||||
ccRCC | |||||
GBM | |||||
HNSC | |||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
AKT1-Thr448 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | -0.707 | ||||
ccRCC | |||||
GBM | |||||
HNSC | |||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC | 0.707 |
AKT1-Thr450 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | -0.936 | ||||
HGSC | -1.526 | ||||
ccRCC | 0.252 | ||||
GBM | 0.594 | ||||
HNSC | |||||
LUAD | 0.617 | ||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC | 0.999 |
AKT1-Tyr315 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | 0.788 | ||||
COAD | |||||
HGSC | |||||
ccRCC | |||||
GBM | |||||
HNSC | |||||
LUAD | -1.125 | ||||
LUSC | 0.336 | ||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
AKT1S1-Ser183 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | 1.667 | ||||
COAD | 0.891 | ||||
HGSC | 0.725 | ||||
ccRCC | -1.189 | ||||
GBM | 0.792 | ||||
HNSC | 0.064 | ||||
LUAD | -0.194 | ||||
LUSC | -0.266 | ||||
non_ccRCC | -1.722 | ||||
PDAC | -0.879 | ||||
UCEC | 0.11 |
AKT1S1-Ser202 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -0.344 | ||||
COAD | -0.013 | ||||
HGSC | -2.725 | ||||
ccRCC | -0.093 | ||||
GBM | -0.249 | ||||
HNSC | 0.707 | ||||
LUAD | 0.324 | ||||
LUSC | 0.615 | ||||
non_ccRCC | 0.322 | ||||
PDAC | 0.379 | ||||
UCEC | 1.076 |
AKT1S1-Ser203 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -0.189 | ||||
COAD | 0.095 | ||||
HGSC | -2.902 | ||||
ccRCC | 0.277 | ||||
GBM | 0.142 | ||||
HNSC | 0.479 | ||||
LUAD | 0.265 | ||||
LUSC | 0.603 | ||||
non_ccRCC | 0.04 | ||||
PDAC | 0.419 | ||||
UCEC | 0.771 |
AKT1S1-Ser211 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -1.13 | ||||
COAD | 0.333 | ||||
HGSC | -2.178 | ||||
ccRCC | 0.627 | ||||
GBM | 0.09 | ||||
HNSC | 1.177 | ||||
LUAD | -0.47 | ||||
LUSC | 0.383 | ||||
non_ccRCC | |||||
PDAC | 0.715 | ||||
UCEC | 0.451 |
AKT1S1-Ser212 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -1.05 | ||||
COAD | 0.546 | ||||
HGSC | -2.08 | ||||
ccRCC | -0.197 | ||||
GBM | 0.641 | ||||
HNSC | 1.003 | ||||
LUAD | -0.628 | ||||
LUSC | 0.311 | ||||
non_ccRCC | |||||
PDAC | 0.36 | ||||
UCEC | 1.094 |
AKT1S1-Ser247 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | -1.124 | ||||
HGSC | |||||
ccRCC | |||||
GBM | 0.791 | ||||
HNSC | 0.334 | ||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
AKT1S1-Ser88 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -1.265 | ||||
COAD | -0.583 | ||||
HGSC | |||||
ccRCC | -0.267 | ||||
GBM | 0.344 | ||||
HNSC | 2.36 | ||||
LUAD | -0.052 | ||||
LUSC | 0.649 | ||||
non_ccRCC | -0.088 | ||||
PDAC | -0.187 | ||||
UCEC | -0.912 |
AKT1S1-Ser92 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -1.122 | ||||
COAD | -0.689 | ||||
HGSC | |||||
ccRCC | 0.068 | ||||
GBM | -0.037 | ||||
HNSC | 2.235 | ||||
LUAD | 0.28 | ||||
LUSC | 0.221 | ||||
non_ccRCC | -0.997 | ||||
PDAC | 0.777 | ||||
UCEC | -0.735 |
AKT1S1-Thr198 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | -0.647 | ||||
GBM | |||||
HNSC | |||||
LUAD | -0.505 | ||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC | 1.152 |
AKT1S1-Thr246 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | -0.468 | ||||
HGSC | 0.953 | ||||
ccRCC | |||||
GBM | -1.179 | ||||
HNSC | |||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC | 0.694 |
AKT1S1-Thr90 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | 0.347 | ||||
HGSC | -1.784 | ||||
ccRCC | 0.431 | ||||
GBM | |||||
HNSC | 0.542 | ||||
LUAD | 0.465 | ||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
AKT1S1-Thr97 | |
---|---|
Cancer | Intensity |
BRCA | 1.061 |
COAD | -1.872 |
HGSC | |
ccRCC | 0.814 |
GBM | -0.592 |
HNSC | 0.541 |
LUAD | 0.201 |
LUSC | |
non_ccRCC | |
PDAC | |
UCEC | -0.152 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
S | 473 | D | Oral squamous cell carcinoma | Phosphorylation | 31889370 |
S | 473 | D | Triple-negative breast cancer | Phosphorylation | 34077419 |
S | 473 | D | Bladder cancer | Phosphorylation | 23799035 |
S | 473 | D | Pancreatic cancer | Phosphorylation | 28363942 ;  15467756 |
S | 473 | D | Colon cancer | Phosphorylation | 35190555 |
S | 473 | D | Head and neck squamous cell carcinoma | Phosphorylation | 21281788 |
S | 473 | P | Acute myeloid leukemia/acute myelogenous leukemia | Phosphorylation | 18056483 |
S | 473 | P | Gastric cancer | Phosphorylation | 23969493 ;  23440515 |
S | 473 | P | Ovarian cancer/carcinoma | Phosphorylation | 23877012 |
S | 473 | P | Breast cancer | Phosphorylation | 36632451 |
S | 473 | P | Anaplastic astrocytoma | Phosphorylation | 23596468 |
S | 473 | P | Esophageal squamous cell carcinoma | Phosphorylation | 23510069 |
S | 473 | P | Non-small cell lung cancer/carcinoma | Phosphorylation | 23091605 |
S | 473 | P | Prostate cancer/carcinoma/adenocarcinoma | Phosphorylation | 23732709 |
S | 473 | U | Pancreatic cancer | Phosphorylation | 15467756 ;  28363942 |
S | 473 | U | Uveal melanoma | Phosphorylation | 34918581 |
S | 473 | U | Osteosarcoma | Phosphorylation | 34476004 |
S | 473 | U | Cancer | Phosphorylation | 34767444 |
S | 473 | U | Cervical cancer | Phosphorylation | 32047568 |
S | 473 | U | Acute myeloid leukemia/acute myelogenous leukemia | Phosphorylation | 15289327 |
S | 473 | U | Breast cancer | Phosphorylation | 17545609 ;  12244301 ;  12244301 ;  17545609 ;  21743495 ;  30413706 |
S | 473 | U | Chronic lymphocytic leukemia | Phosphorylation | 16940331 |
S | 473 | U | Esophageal squamous cell carcinoma | Phosphorylation | 31897228 |
S | 473 | U | Gallbladder cancer | Phosphorylation | 33407730 |
S | 473 | U | Hepatocellular carcinoma | Phosphorylation | 37573318 ;  36348350 |
S | 473 | U | Multiple myeloma | Phosphorylation | 37781194 |
S | 473 | U | Pancreatic cancer/carcinoma/adenocarcinoma | Phosphorylation | 15467756 ;  21474066 ;  28363942 |
S | 473 | U | Rhabdomyosarcoma | Phosphorylation | 17848913 |
S | 473 | U | Synovial sarcoma | Phosphorylation | 35556229 |
S | 473 | U | HER2-positive breast cancer | Phosphorylation | 36314765 |
S | 473 | U | Thymic carcinoma | Phosphorylation | 20597130 |
S | 473 | U | Systemic lupus erythematosus | Phosphorylation | 23735868 ;  34522717 ;  23735868 |
S | 473 | U | Squamous cell carcinoma | Phosphorylation | 21795477 ;  37109043 |
S | 473 | U | Sjogren's syndrome | Phosphorylation | 34948236 |
S | 473 | U | Breast cancer/tumor/carcinoma | Phosphorylation | 17545609 ;  12244301 ;  22476852 |
S | 473 | U | Cancer | Phosphorylation | 21795477 |
S | 473 | U | Cholangiocarcinoma | Phosphorylation | 37752233 |
S | 473 | U | Colon cancer/carcinoma | Phosphorylation | 22975685 |
S | 473 | U | Colorectal cancer | Phosphorylation | 37430297 |
S | 473 | U | Diabetes mellitus | Phosphorylation | 35835217 |
S | 473 | U | Glioma | Phosphorylation | 33820494 |
S | 473 | U | Renal cancer/carcinoma | Phosphorylation | 19118035 ;  16247451 ;  12649200 |
S | 473 | U | Kidney cancer | Phosphorylation | 12649200 ;  12649200 ;  22580611 |
S | 473 | U | Liver cancer | Phosphorylation | 15684384 |
S | 473 | U | Lymphocytic leukemia | Phosphorylation | 20576813 |
S | 473 | U | Melanoma | Phosphorylation | 19996208 ;  12499277 ;  12499277 ;  19996208 ;  12499277 |
S | 473 | U | Neuroblastoma | Phosphorylation | 17234785 |
S | 473 | U | Non-small cell squamous cell lung carcinoma | Phosphorylation | 20008839 |
S | 473 | U | Obesity | Phosphorylation | 35413055 |
S | 473 | U | Ovarian cancer | Phosphorylation | 15208673 |
S | 473 | U | Ovarian epithelial carcinoma | Phosphorylation | 32194423 |
S | 473 | U | Urethral cancer | Phosphorylation | 22975685 |
S | 473 | U | Parkinson's disease | Phosphorylation | 19800394 ;  19800394 ;  21658387 |
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.