ATAD5

ATPase family AAA domain-containing protein 5 · Q96QE3 · ATAD5 on Sugi Atlas →

0 patent compounds predicted against ATAD5, 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 ATAD5 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Compared the Efficacy and Safety of CDOP Combined With Chidamide and CDOP in de Novo Peripheral T Cell Lymphoma Patients PHASE3UNKNOWN
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
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Genetic Basis of Abdominal Aortic Aneurysm nanCOMPLETED
Genetic Evaluation of AAAS Gene in Early-Onset Achalasia and Alacrima Patients nanCOMPLETED
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Amyotrophic Lateral Sclerosis (ALS) Families Project nanRECRUITING
Familial Intracranial Aneurysm Study II nanCOMPLETED
Autophagy Bladder Cancer nanUNKNOWN
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Study on Genetically Affected Sporadic Thoracic Aortic Aneurysm and Dissection nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Stone Disease in Children and Their Families nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Collection of Blood Samples for DNA in Motor Neuron Disease nanCOMPLETED
Gene Analysis of Parkinson's Disease nanCOMPLETED
Genetic and Functional Analysis of Aplasia Cutis Congenital (ACC) nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders nanCOMPLETED
Genetics of Recurrent Early Onset Major Depression nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a ATAD5 binder may also engage these)

ProteinNameSimilarity
CDCA2 Cell division cycle-associated protein 2 0.997 landscape →
MKI67 Proliferation marker protein Ki-67 0.996 landscape →
Q5FBB7 0.994 Q5FBB7 →
Q28DZ0 0.994 Q28DZ0 →
ASH1L Histone-lysine N-methyltransferase ASH1L 0.994 landscape →
Q9UKL3 0.993 Q9UKL3 →
A0A087WXM9 0.993 A0A087WXM9 →
Q6P0N0 0.993 Q6P0N0 →
E1BC15 0.993 E1BC15 →
A2AEY4 0.992 A2AEY4 →
Q4QY64 0.992 Q4QY64 →
A4IGL8 0.992 A4IGL8 →
Q3ZBP0 0.992 Q3ZBP0 →
Q8N7Z5 0.992 Q8N7Z5 →
Q7Z570 0.992 Q7Z570 →
O60673 0.992 O60673 →
B4QIJ9 0.992 B4QIJ9 →
B4IH30 0.992 B4IH30 →
Q5VWN6 0.992 Q5VWN6 →
Q9VIF5 0.991 Q9VIF5 →
F6ULY3 0.991 F6ULY3 →
Q9D4V4 0.991 Q9D4V4 →
Q90ZS6 0.991 Q90ZS6 →
Q5DTW7 0.991 Q5DTW7 →
A1L2H3 0.991 A1L2H3 →
Q0P5H2 0.991 Q0P5H2 →
Q9W1R4 0.991 Q9W1R4 →
Q9WUF3 0.991 Q9WUF3 →
Q3TNU4 0.991 Q3TNU4 →
Q9ULD2 0.991 Q9ULD2 →