Id: | acc0317 |
Group: | 1sens |
Protein: | AKT |
Gene Symbol: | AKT1 |
Protein Id: | P31749 |
Protein Name: | AKT1_HUMAN |
PTM: | phosphorylation |
Site: | Ser473 |
Site Sequence: | ERRPHFPQFSYSASGTA---- |
Disease Category: | Cancer |
Disease: | Colorectal Cancer |
Disease Subtype: | colon cancer stem cells (CCSC) |
Disease Cellline: | |
Disease Info: | |
Drug: | 3-deazaneplanocin A (DZNep) |
Drug Info: | "3-Deazaneplanocin A (DZNep) is a potent dual inhibitor of histone methyltransferase EZH2 and S-adenosylhomocysteine hydrolase (AHCY), known for its antipoxidative and antifibrotic activities. It induces proteasomal degradation of its targets, reducing toxicity and inhibiting fibrosis in organs such as the liver, kidneys, and airways in animal models. DZNep also exhibits anticancer properties by depleting EZH2, reducing histone H3 lysine 27 trimethylation (H3K27me3), and inducing cell cycle arrest and apoptosis in various cancer cell lines, including non-small cell lung cancer (NSCLC) and acute myeloid leukemia (AML)." |
Effect: | modulate |
Effect Info: | "The use of DZNep (an EZH2 inhibitor) leads to an increase in the apoptosis level in colorectal cancer stem cells (CCSCs), accompanied by a decrease in Akt phosphorylation." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 23588203 |
Sentence Index: | 23588203_3 |
Sentence: | "Using colon cancer stem cells (CCSC) isolated from human primary colorectal tumors, we demonstrate that SUZ12 knockdown and treatment with DZNep, one of the most potent EZH2 inhibitors, increase apoptosis levels, marked by decreased Akt phosphorylation, in CCSCs, while embryonic stem (ES) cell survival is not affected." |
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.