Id: | acc0518 |
Group: | 1sens |
Protein: | beta-catenin |
Gene Symbol: | CTNNB1 |
Protein Id: | P35222 |
Protein Name: | CTNB1_HUMAN |
PTM: | phosphorylation |
Site: | Ser45 |
Site Sequence: | HSGATTTAPSLSGKGNPEEED |
Disease Category: | Cancer |
Disease: | Thyroid Cancer |
Disease Subtype: | anaplastic thyroid carcinoma |
Disease Cellline: | SW1736 |
Disease Info: | |
Drug: | I131 |
Drug Info: | "Iodine-131 (I-131) is a radioactive isotope used as a therapeutic agent for hyperthyroidism and thyroid cancer, functioning by emitting beta radiation to selectively destroy overactive thyroid cells or malignant thyroid tissue, with a physical half-life of approximately 8 days and administered orally or intravenously as a radiopharmaceutical. " |
Effect: | inhibit |
Effect Info: | "ATRA treatment reduced the phosphorylation of beta - catenin (Ser45 and Y654) and GSK - 3beta (Ser9), thereby enhancing the sensitivity of undifferentiated thyroid cancer to isotopic therapy." |
Note: | Non-conventional drugs |
Score: | 4.5 |
Pubmed(PMID): | 29344218 |
Sentence Index: | 29344218_0 |
Sentence: | ATRA increases iodine uptake and inhibits the proliferation and invasiveness of human anaplastic thyroid carcinoma SW1736 cells: Involvement of beta-catenin phosphorylation inhibition. |
Sequence & Structure:
MATQADLMELDMAMEPDRKAAVSHWQQQSYLDSGIHSGATTTAPSLSGKGNPEEEDVDTSQVLYEWEQGFSQSFTQEQVADIDGQYAMTRAQRVRAAMFPETLDEGMQIPSTQFDAAHPTNVQRLAEPSQMLKHAVVNLINYQDDAELATRAIPELTKLLNDEDQVVVNKAAVMVHQLSKKEASRHAIMRSPQMVSAIVRTMQNTNDVETARCTAGTLHNLSHHREGLLAIFKSGGIPALVKMLGSPVDSVLFYAITTLHNLLLHQEGAKMAVRLAGGLQKMVALLNKTNVKFLAITTDCLQILAYGNQESKLIILASGGPQALVNIMRTYTYEKLLWTTSRVLKVLSVCSSNKPAIVEAGGMQALGLHLTDPSQRLVQNCLWTLRNLSDAATKQEGMEGLLGTLVQLLGSDDINVVTCAAGILSNLTCNNYKNKMMVCQVGGIEALVRTVLRAGDREDITEPAICALRHLTSRHQEAEMAQNAVRLHYGLPVVVKLLHPPSHWPLIKATVGLIRNLALCPANHAPLREQGAIPRLVQLLVRAHQDTQRRTSMGGTQQQFVEGVRMEEIVEGCTGALHILARDVHNRIVIRGLNTIPLFVQLLYSPIENIQRVAAGVLCELAQDKEAAEAIEAEGATAPLTELLHSRNEGVATYAAAVLFRMSEDKPQDYKKRLSVELTSSLFRTEPMAWNETADLGLDIGAQGEPLGYRQDDPSYRSFHSGGYGQDALGMDPMMEHEMGGHHPGADYPVDGLPDLGHAQDLMDGLPPGDSNQLAWFDTDL
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
CTNNB1 | PRI-724 | CBP/beta catenin inhibitor | 2 | Withdrawn | colorectal adenocarcinoma | ClinicalTrials |
CTNNB1 | PRI-724 | CBP/beta catenin inhibitor | 2 | Recruiting | cirrhosis of liver | ClinicalTrials |
CTNNB1 | PRI-724 | CBP/beta catenin inhibitor | 1 | Completed | acute myeloid leukemia | ClinicalTrials |
CTNNB1 | PRI-724 | CBP/beta catenin inhibitor | 1 | Completed | chronic myelogenous leukemia | ClinicalTrials |
CTNNB1 | PRI-724 | CBP/beta catenin inhibitor | 1 | Terminated | neoplasm | ClinicalTrials |
CTNNB1 | PRI-724 | CBP/beta catenin inhibitor | 1 | Completed | pancreatic carcinoma | ClinicalTrials |
CTNNB1 | PRI-724 | CBP/beta catenin inhibitor | 1 | Completed | pancreatic adenocarcinoma | ClinicalTrials |
CTNNB1 | PRI-724 | CBP/beta catenin inhibitor | 1 | Completed | Malignant Pancreatic Neoplasm | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACCTNNB1-Ser45 | |
---|---|
Cancer | Intensity |
BRCA | |
COAD | -0.184 |
HGSC | -1.332 |
ccRCC | |
GBM | 0.613 |
HNSC | |
LUAD | |
LUSC | |
non_ccRCC | |
PDAC | |
UCEC | 0.904 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
S | 45 | A | Wilms tumor | Phosphorylation | 12239584 |
S | 45 | D | Esophageal carcinoma | Phosphorylation | 31933784 |
S | 45 | D | Head and neck squamous cell carcinoma | Phosphorylation | 21281788 |
S | 45 | D | Non-small cell lung cancer | Phosphorylation | 35277183 |
S | 45 | D | Colon cancer | Phosphorylation | 32041324 |
S | 45 | N | Cutaneous melanoma | Phosphorylation | 11351304 |
S | 45 | N | Nephroblastoma | Phosphorylation | 12239584 |
S | 45 | N | Wilms tumor | Phosphorylation | 12239584 |
S | 45 | N | Colorectal cancer | Phosphorylation | 11955436 |
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.