ADCK5

Uncharacterized aarF domain-containing protein kinase 5 · Q3MIX3 · ADCK5 on Sugi Atlas →

889 patent compounds predicted against ADCK5, 814 high-confidence (nearest known ligand ≥ 0.5)

Top predicted compounds (top 20 by supporting neighbours, then confidence)

CompoundConfidenceSupporting neighbours
Linsitinib Linsitinib (SCHEMBL400369) 1.00 1/20
Linsitinib Linsitinib (SCHEMBL400734) 1.00 1/20
Linsitinib Linsitinib (SCHEMBL400735) 1.00 1/20
Linsitinib Linsitinib (SCHEMBL10255925) 1.00 1/20
Linsitinib Linsitinib (SCHEMBL528637) 0.98 1/20
Linsitinib Linsitinib (SCHEMBL528638) 0.98 1/20
Linsitinib Linsitinib (SCHEMBL1758871) 0.92 1/20
Linsitinib Linsitinib (SCHEMBL1758866) 0.87 1/20
Linsitinib Linsitinib (SCHEMBL1758701) 0.84 1/20
SCHEMBL13447913 SCHEMBL13447913 0.84 1/20
SCHEMBL13448066 SCHEMBL13448066 0.82 1/20
SCHEMBL397576 SCHEMBL397576 0.81 1/20
SCHEMBL13812511 SCHEMBL13812511 0.81 1/20
SCHEMBL399357 SCHEMBL399357 0.81 1/20
SCHEMBL399670 SCHEMBL399670 0.81 1/20
SCHEMBL401531 SCHEMBL401531 0.81 1/20
Linsitinib Linsitinib (SCHEMBL1758705) 0.80 1/20
SCHEMBL10225384 SCHEMBL10225384 0.79 1/20
SCHEMBL13447908 SCHEMBL13447908 0.79 1/20
SCHEMBL13447930 SCHEMBL13447930 0.79 1/20

Clinical trials — most relevant to ADCK5 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Pharmacogenomic Evaluation of Antihypertensive Responses PHASE4COMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Validation of the RADIAL Algorithm for Diagnosis of Autosomal Recessive Cerebellar Ataxia nanRECRUITING
Assessment of ADCY5-related Movement Disorders With Motion SENSors nanCOMPLETED
Pilot Study on Caffeine Efficiency in ADCY5-related Dyskinesia nanCOMPLETED
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing nanUNKNOWN
Identification of New FTLD Genes nanUNKNOWN
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Study of the Genetic Factors Involved in Autism and Related Disorders nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Genetic Studies of Lysosomal Storage Disorders nanENROLLING_BY_INVITATION
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS nanRECRUITING
Recurrent Acute Myocarditis Registry nanUNKNOWN
Identification of Genetic Basis of Atrioventricular Conduction Defects: From Congenital Forms to Degenerative Forms nanUNKNOWN
Characteristics of Episodic Ataxia Syndrome nanCOMPLETED
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Genome Environment Microbiome and Metabolome in Autism Study nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING

Related proteins — ESM-2 sequence neighbours (a ADCK5 binder may also engage these)

ProteinNameSimilarity
Q80V03 1.000 Q80V03 →
Q6AY19 0.983 Q6AY19 →
Q8Y275 0.978 Q8Y275 →
A0A172M468 0.978 A0A172M468 →
Q9W133 0.977 Q9W133 →
Q5BJQ0 0.977 Q5BJQ0 →
A0A179HKZ8 0.977 A0A179HKZ8 →
B2SX38 0.976 B2SX38 →
Q566J8 0.976 Q566J8 →
Q3BZ34 0.976 Q3BZ34 →
Q06567 0.975 Q06567 →
Q87UZ0 0.975 Q87UZ0 →
Q8PQT0 0.975 Q8PQT0 →
C3K8U2 0.975 C3K8U2 →
B2ST34 0.975 B2ST34 →
Q48PJ6 0.975 Q48PJ6 →
B0U2R2 0.974 B0U2R2 →
COQ8B Atypical kinase COQ8B, mitochondrial 0.974 landscape →
Q8K370 0.974 Q8K370 →
Q3U3Q1 0.974 Q3U3Q1 →
Q9PCE8 0.974 Q9PCE8 →
Q145N7 0.974 Q145N7 →
A2Z1F5 0.974 A2Z1F5 →
B9ME24 0.974 B9ME24 →
A3QJU3 0.974 A3QJU3 →
A1JIF4 0.974 A1JIF4 →
A9BP42 0.973 A9BP42 →
Q1CNB2 0.973 Q1CNB2 →
Q8ZAM1 0.973 Q8ZAM1 →
Q66FS8 0.973 Q66FS8 →