Id: | acc1255 |
Group: | 2sens |
Protein: | beta-catenin |
Gene Symbol: | CTNNB1 |
Protein Id: | P35222 |
Protein Name: | CTNB1_HUMAN |
PTM: | phosphorylation |
Site: | Ser675 |
Site Sequence: | KPQDYKKRLSVELTSSLFRTE |
Disease Category: | Cancer |
Disease: | Colorectal Cancer |
Disease Subtype: | Colon Cancer |
Disease Cellline: | HCT116 |
Disease Info: | |
Drug: | Rp-8-Br-cAMPS |
Drug Info: | - |
Effect: | modulate |
Effect Info: | PKA antagonists block the phosphorylation of beta-catenin at Ser552 and Ser675 and the downstream regulation of c-Myc in human colon cancer cell lines. |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 22168384 |
Sentence Index: | 22168384_3-4 |
Sentence: | "Recent reports show that PGE(2)-induced phosphorylation of beta-catenin by protein kinase A (PKA) increases nuclear translocation indicating two mechanisms of action of PGE(2) on beta-catenin homeostasis. FINDINGS: Treatment of Apc(Min/+) mice that spontaneously develop intestinal adenomas with a PKA antagonist (Rp-8-Br-cAMPS) selectively targeting only the latter pathway reduced tumor load, but not the number of adenomas." |
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CTNNB1 | PRI-724 | CBP/beta catenin inhibitor | 2 | Withdrawn | colorectal adenocarcinoma | ClinicalTrials |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-Ser675 | |
---|---|
Cancer | Intensity |
BRCA | -0.341 |
COAD | -0.152 |
HGSC | 2.444 |
ccRCC | -0.185 |
GBM | 0.26 |
HNSC | 0.094 |
LUAD | -0.329 |
LUSC | 0.129 |
non_ccRCC | -0.617 |
PDAC | -1.752 |
UCEC | 0.448 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
S | 675 | U | Lung cancer | Phosphorylation | 36000549 |
S | 675 | U | Hepatocellular carcinoma | Phosphorylation | 36000549 |
S | 675 | U | Cholangiocarcinoma | Phosphorylation | 34799729 |
S | 675 | U | Glioblastoma | Phosphorylation | 32102932 |
S | 675 | U | Intrahepatic cholangiocarcinoma | Phosphorylation | 29415992 |
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.