Sugi Predict

Sugi Predict / Targets / ATAD3B

ATAD3B

ATPase family AAA domain-containing protein 3B · Q5T9A4 · ATAD3B on Sugi Atlas →

0 patent compounds predicted against ATAD3B, 0 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours

Clinical trials — most relevant to ATAD3B by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
PhII 5-Azacytidine Plus Valproic Acid and Eventually Atra in Intermediate II and High Risk MDS PHASE2COMPLETED
Trial of the Histone-Deacetylase Inhibitor ITF2357 Followed by Mechlorethamine in Relapsed/Refractory Hodgkin's Lymphoma PHASE1/PHASE2COMPLETED
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED
Genetic Basis of Abdominal Aortic Aneurysm nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Autophagy Bladder Cancer nanUNKNOWN
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS nanRECRUITING
Molecular Studies on the Candidate Genes of Dopaminergic and Noradrenergic Systems in ADHD nanCOMPLETED
Amyotrophic Lateral Sclerosis (ALS) Families Project nanRECRUITING
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Familial Intracranial Aneurysm Study II nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Core Stability Exercises and Hereditary Ataxia nanCOMPLETED
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Collection of Blood Samples for DNA in Motor Neuron Disease nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Genetic Studies of Inflammatory Bowel Disease nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Phenotype/Genotype Correlations in Neuromuscular Disorders nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a ATAD3B binder may also engage these)

ProteinNameSimilarity
A7YWC4 — 1.000 A7YWC4 →
Q3KRE0 — 0.999 Q3KRE0 →
Q925I1 — 0.998 Q925I1 →
Q9VEX6 — 0.996 Q9VEX6 →
ATAD3A ATPase family AAA domain-containing protein 3A 0.995 landscape →
Q58E76 — 0.995 Q58E76 →
Q6NVR9 — 0.995 Q6NVR9 →
Q20748 — 0.994 Q20748 →
Q6PAX2 — 0.993 Q6PAX2 →
Q5T2N8 — 0.989 Q5T2N8 →
Q80KJ8 — 0.988 Q80KJ8 →
Q9UQ90 — 0.988 Q9UQ90 →
B2B1M4 — 0.988 B2B1M4 →
Q149L6 — 0.988 Q149L6 →
Q525S7 — 0.988 Q525S7 →
Q7TNB8 — 0.987 Q7TNB8 →
F4IF36 — 0.987 F4IF36 →
A0A0D1E2P6 — 0.987 A0A0D1E2P6 →
B3M301 — 0.987 B3M301 →
Q920A7 — 0.987 Q920A7 →
Q64332 — 0.987 Q64332 →
B7PXE3 — 0.987 B7PXE3 →
Q925S8 — 0.987 Q925S8 →
Q9D5Z5 — 0.987 Q9D5Z5 →
Q0JLS6 — 0.987 Q0JLS6 →
B2RYN7 — 0.987 B2RYN7 →
P54634 — 0.987 P54634 →
O35066 — 0.987 O35066 →
B4NBP4 — 0.987 B4NBP4 →
P0CR72 — 0.986 P0CR72 →