Id: | acc3273 |
Group: | 2sens |
Protein: | Tau |
Gene Symbol: | MAPT |
Protein Id: | P10636 |
Protein Name: | TAU_HUMAN |
PTM: | acetylation |
Site: | Lys174 |
Site Sequence: | EATRQPSGTGPEDTEGGRHAP |
Disease Category: | Nervous system diseases |
Disease: | Alzheimer's Disease |
Disease Subtype: | |
Disease Cellline: | N2aSwe? |
Disease Info: | |
Drug: | Cilostazol + resveratrol |
Drug Info: | "Cilostazol is a medication used to treat intermittent claudication by improving blood flow. | Resveratrol is a natural compound with potential health benefits, including antioxidant and anti - inflammatory properties. " |
Effect: | modulate |
Effect Info: | "Cilostazol inhibits Aβ-induced tau acetylation. By activating the CK2α/SIRT1 pathway, it suppresses P300, activates SIRT1, and alleviates tauopathy." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 24254769 |
Sentence Index: | 24254769_1-2 |
Sentence: | "beta-Amyloid (Abeta) deposits and hyperphosphorylated tau aggregates are the chief hallmarks in the Alzheimer's disease (AD) brains, but the strategies for controlling these pathological events remain elusive. We hypothesized that CK2-coupled SIRT1 activation stimulated by cilostazol suppresses tau acetylation (Ac-tau) and tau phosphorylation (P-tau) by inhibiting activation of P300 and GSK3beta." |
Sequence & Structure:
MAEPRQEFEVMEDHAGTYGLGDRKDQGGYTMHQDQEGDTDAGLKESPLQTPTEDGSEEPGSETSDAKSTPTAEDVTAPLVDEGAPGKQAAAQPHTEIPEGTTAEEAGIGDTPSLEDEAAGHVTQEPESGKVVQEGFLREPGPPGLSHQLMSGMPGAPLLPEGPREATRQPSGTGPEDTEGGRHAPELLKHQLLGDLHQEGPPLKGAGGKERPGSKEEVDEDRDVDESSPQDSPPSKASPAQDGRPPQTAAREATSIPGFPAEGAIPLPVDFLSKVSTEIPASEPDGPSVGRAKGQDAPLEFTFHVEITPNVQKEQAHSEEHLGRAAFPGAPGEGPEARGPSLGEDTKEADLPEPSEKQPAAAPRGKPVSRVPQLKARMVSKSKDGTGSDDKKAKTSTRSSAKTLKNRPCLSPKHPTPGSSDPLIQPSSPAVCPEPPSSPKYVSSVTSRTGSSGAKEMKLKGADGKTKIATPRGAAPPGQKGQANATRIPAKTPPAPKTPPSSGEPPKSGDRSGYSSPGSPGTPGSRSRTPSLPTPPTREPKKVAVVRTPPKSPSSAKSRLQTAPVPMPDLKNVKSKIGSTENLKHQPGGGKVQIINKKLDLSNVQSKCGSKDNIKHVPGGGSVQIVYKPVDLSKVTSKCGSLGNIHHKPGGGQVEVKSEKLDFKDRVQSKIGSLDNITHVPGGGNKKIETHKLTFRENAKAKTDHGAEIVYKSPVVSGDTSPRHLSNVSSTGSIDMVDSPQLATLADEVSASLAKQGL
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
MAPT | TILAVONEMAB | Microtubule-associated protein tau inhibitor | 2 | Terminated | Alzheimer disease | ClinicalTrials |
MAPT | ZAGOTENEMAB | Microtubule-associated protein tau inhibitor | 2 | Completed | Alzheimer disease | ClinicalTrials |
MAPT | SEMORINEMAB | Microtubule-associated protein tau inhibitor | 2 | Completed | Alzheimer disease | ClinicalTrials |
MAPT | BEPRANEMAB | Microtubule-associated protein tau inhibitor | 2 | Active, not recruiting | Alzheimer disease | ClinicalTrials |
MAPT | GOSURANEMAB | Microtubule-associated protein tau inhibitor | 2 | Terminated | Alzheimer disease | ClinicalTrials |
MAPT | TILAVONEMAB | Microtubule-associated protein tau inhibitor | 2 | Completed | Alzheimer disease | ClinicalTrials |
MAPT | SEMORINEMAB | Microtubule-associated protein tau inhibitor | 2 | Terminated | Alzheimer disease | ClinicalTrials |
MAPT | TILAVONEMAB | Microtubule-associated protein tau inhibitor | 2 | Terminated | progressive supranuclear palsy | ClinicalTrials ClinicalTrials |
MAPT | GOSURANEMAB | Microtubule-associated protein tau inhibitor | 2 | Terminated | Classical progressive supranuclear palsy | ClinicalTrials |
MAPT | SEMORINEMAB | Microtubule-associated protein tau inhibitor | 1 | Completed | Alzheimer disease | ClinicalTrials |
MAPT | POSDINEMAB | Microtubule-associated protein tau inhibitor | 1 | Completed | Alzheimer disease | ClinicalTrials |
MAPT | ZAGOTENEMAB | Microtubule-associated protein tau inhibitor | 1 | Completed | Alzheimer disease | ClinicalTrials ClinicalTrials |
MAPT | GOSURANEMAB | Microtubule-associated protein tau inhibitor | 1 | Completed | progressive supranuclear palsy | ClinicalTrials |
MAPT | TILAVONEMAB | Microtubule-associated protein tau inhibitor | 1 | Completed | progressive supranuclear palsy | ClinicalTrials |
MAPT | BEPRANEMAB | Microtubule-associated protein tau inhibitor | 1 | Active, not recruiting | progressive supranuclear palsy | ClinicalTrials |
MAPT | BEPRANEMAB | Microtubule-associated protein tau inhibitor | 1 | Completed | progressive supranuclear palsy | ClinicalTrials |
MAPT | GOSURANEMAB | Microtubule-associated protein tau inhibitor | 1 | Terminated | Classical progressive supranuclear palsy | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACMAPT-Lys24 | |
---|---|
Cancer | Intensity |
BRCA | -0.707 |
COAD | |
HGSC | |
ccRCC | |
GBM | 0.707 |
HNSC | |
LUAD | |
LUSC | |
non_ccRCC | |
PDAC | |
UCEC |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
K | 174 | D | Alzheimer's disease | Acetylation | 33910019 |
K | 174 | P | Tauopathies | Acetylation | 35269542 |
K | 174 | P | Alzheimer's disease | Methylation | 22033876 |
K | 174 | U | Alzheimer's disease | Acetylation | 26390242 |
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.