ATP1B3

Sodium/potassium-transporting ATPase subunit beta-3 · P54709 · ATP1B3 on Sugi Atlas →

17,660 patent compounds predicted against ATP1B3, 10,167 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
Metildigoxin Metildigoxin (SCHEMBL43349) 0.89 16/20
Digoxin Digoxin (SCHEMBL20506) 1.00 15/20
Digoxin Digoxin (SCHEMBL126382) 1.00 15/20
Digoxin Digoxin (SCHEMBL428012) 1.00 15/20
Digoxin Digoxin (SCHEMBL597821) 0.94 15/20
Digoxin Digoxin (SCHEMBL1559560) 0.94 15/20
Digoxin Digoxin (SCHEMBL1584137) 0.93 15/20
Digoxin Digoxin (SCHEMBL1461589) 0.58 15/20
SCHEMBL475105 SCHEMBL475105 0.51 15/20
SCHEMBL475107 SCHEMBL475107 0.51 15/20
Digoxin Digoxin (SCHEMBL1830809) 0.91 14/20
SCHEMBL1302063 SCHEMBL1302063 0.85 14/20
SCHEMBL1484406 SCHEMBL1484406 0.65 14/20
Deslanoside Deslanoside (SCHEMBL125311) 0.80 13/20
Deslanoside Deslanoside (SCHEMBL125312) 0.80 13/20
SCHEMBL1483332 SCHEMBL1483332 0.74 13/20
SCHEMBL1483335 SCHEMBL1483335 0.74 13/20
Uzarin Uzarin (SCHEMBL702463) 0.92 12/20
Digitoxigenin Gentiobioside Digitoxigenin Gentiobioside (SCHEMBL702464) 0.92 12/20
Digitoxigenin Gentiobioside Digitoxigenin Gentiobioside (SCHEMBL1652279) 0.92 12/20

Clinical trials — most relevant to ATP1B3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Sulphonylurea Receptor Mutation and Responsiveness to Gliclazide - a Pilot Proof of Concept, Randomised Cross-over Study PHASE4COMPLETED
Long-Term Sulfonylurea Response in ABCC8 Neonatal Diabetes (SuResponsSUR) PHASE4UNKNOWN
Prevention of Post-Cardiac Surgery Acute Kidney Injury by Proton Pump Inhibitor PHASE2COMPLETED
Post-Cardiac Surgery Acute Kidney Injury Prevention by Administration of Proton Pump Inhibitor (P2 Trial) PHASE2RECRUITING
Pilot Study, Comparative, Single-center, Randomized, Crossover, Double-blind, Against Placebo, Testing the Effectiveness of Triheptanoin Oil in Alternating Hemiplegia of Childhood PHASE2COMPLETED
Natural History Study of ATP1A3-related Disease nanUNKNOWN
Sodium Transport: Genetics and Hypertension nanCOMPLETED
Bile Acids Metabolism and Genetic Mutation Profile in the Intrahepatic Cholestasis of Pregnacy in Indian Population nanRECRUITING
Impact of Sulphonylureas on Neurodevelopmental Outcomes in KCNJ11-related Intermediate Developmental Delay, Epilepsy and Neonatal Diabetes (iDEND) Syndrome nanRECRUITING
Sodium Accumulation Study in Haemodialysis: Brain Study nanRECRUITING
Genetic and Environmental Determinants of Hypertension nanCOMPLETED
Hydroxychloroquin (HCQ) in chILD of Genetic Defect nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Coproporphyrine Isomers and Methotrexate Elimination nanCOMPLETED
The Role of Biomarkers in Inherited Cardiac Conditions nanWITHDRAWN
Biomarkers in the Etiology of Idiopathic Intracranial Hypertension nanUNKNOWN
Pediatric Cardiomyopathy Mutation Analysis nanRECRUITING
Heart and Skeletal Muscle Problems in Neuroacanthocytosis nanCOMPLETED
Prevalence and Risk Factors of Nephrocalcinosis in Children at Sohag University Hospital nanUNKNOWN
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED
Double Blind Crossover Comparison of Diuretics in the Young nanUNKNOWN
Genetic Causes and Clinical Features of Childhood Interstitial Lung Diseases in China nanCOMPLETED
Specificities of Atypical Non AutoImmune Diabetes (ANAID) in the French West Indies nanNOT_YET_RECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts nanCOMPLETED
Artificial Intelligence for the Prioritization of Genetic Background in Brugada Syndrome nanCOMPLETED
Multidrug Resistance Genes in Patients With Acute Myeloid Leukemia nanACTIVE_NOT_RECRUITING
Evaluation of the Effects of KCNQ1 Mutation on Insulin Tolerance and Obsessive Compulsive Features in Long QT Romano-Ward Syndrome Patients. nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Genetic Testing in Detection of Late-Onset Hearing Loss nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a ATP1B3 binder may also engage these)

ProteinNameSimilarity
Q63377 1.000 Q63377 →
Q9GLC3 1.000 Q9GLC3 →
Q3T0C6 1.000 Q3T0C6 →
Q60489 1.000 Q60489 →
P97370 1.000 P97370 →
Q202B1 0.998 Q202B1 →
P30715 0.997 P30715 →
P25169 0.996 P25169 →
P30716 0.996 P30716 →
P18597 0.995 P18597 →
P33879 0.995 P33879 →
P05029 0.995 P05029 →
ATP4B Potassium-transporting ATPase subunit beta (G 0.994 landscape →
Q93235 0.993 Q93235 →
P18598 0.992 P18598 →
P43002 0.992 P43002 →
Q9XUY5 0.992 Q9XUY5 →
P21188 0.992 P21188 →
P50992 0.992 P50992 →
P33704 0.991 P33704 →
P18434 0.990 P18434 →
P51165 0.990 P51165 →
A8X4W9 0.989 A8X4W9 →
P2RX3 P2X purinoceptor 3 0.989 landscape →
Q24046 0.988 Q24046 →
Q9BDK6 0.986 Q9BDK6 →
Q99ME6 0.986 Q99ME6 →
Q9I9C3 0.986 Q9I9C3 →
Q9UN42 0.986 Q9UN42 →
Q3UR32 0.985 Q3UR32 →