NDUFA2

NADH dehydrogenase [ubiquinone] 1 alpha subco · O43678 · NDUFA2 on Sugi Atlas →

3,245 patent compounds predicted against NDUFA2, 2,019 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
Auraptene Auraptene (SCHEMBL2535029) 1.00 5/20
Auraptene Auraptene (SCHEMBL2535034) 1.00 5/20
SCHEMBL8491443 SCHEMBL8491443 0.56 4/20
SCHEMBL8489900 SCHEMBL8489900 0.52 4/20
SCHEMBL8489907 SCHEMBL8489907 0.52 4/20
SCHEMBL8489902 SCHEMBL8489902 0.51 4/20
SCHEMBL8489908 SCHEMBL8489908 0.51 4/20
SCHEMBL8491154 SCHEMBL8491154 0.51 4/20
SCHEMBL8491160 SCHEMBL8491160 0.51 4/20
SCHEMBL8491619 SCHEMBL8491619 0.50 4/20
SCHEMBL8491624 SCHEMBL8491624 0.50 4/20
SCHEMBL8491634 SCHEMBL8491634 0.50 4/20
7-Prenyloxycoumarin 7-Prenyloxycoumarin (SCHEMBL4898255) 0.79 3/20
SCHEMBL712741 SCHEMBL712741 0.57 3/20
Geiparvarin Geiparvarin (SCHEMBL2532495) 0.56 3/20
SCHEMBL6267768 SCHEMBL6267768 0.55 3/20
SCHEMBL1095981 SCHEMBL1095981 0.55 3/20
SCHEMBL4293165 SCHEMBL4293165 0.55 3/20
SCHEMBL8490928 SCHEMBL8490928 0.53 3/20
SCHEMBL8490937 SCHEMBL8490937 0.53 3/20

Clinical trials — most relevant to NDUFA2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Phase III Trial of Coenzyme Q10 in Mitochondrial Disease PHASE3COMPLETED
Coenzyme Q10 as a Symptomatic Treatment in Parkinson's Disease PHASE3COMPLETED
A Study of the Efficacy and Safety of MT1621 in Thymidine Kinase 2 (TK2) Deficiency (Treatment naïve) PHASE3WITHDRAWN
Mitochondrial Dysfunction in the Pathophysiology and Treatment of Bipolar Disorder PHASE2WITHDRAWN
A Study of Bezafibrate in Mitochondrial Myopathy PHASE2COMPLETED
Parkinson's Disease Treatment With Coenzyme Q10 PHASE2COMPLETED
Trial of Nicotinamide Riboside and Co-enzyme Q10 in Chronic Kidney Disease PHASE2COMPLETED
A Study to Evaluate Vitamin B3 Derivative to Treat Mitochondrial Myopathy PHASE2ACTIVE_NOT_RECRUITING
Does Clinical Treatment of Mitochondrial Dysfunction Impact Autism Spectrum Disorder (ASD)? PHASE1UNKNOWN
Genomic Profiling of Mitochondrial Disease - Imaging Analysis for Precise Mitochondrial Medicine nanCOMPLETED
The Natural History of Mitochondrial Diseases nanRECRUITING
North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC) nanRECRUITING
Tissue Sample Study for Mitochondrial Disorders nanENROLLING_BY_INVITATION
Effect of Subtle Energy Transmission and Tao Calligraphy Mindfulness Practice on Mitochondrial DNA in Peripheral Blood Leukocytes nanNOT_YET_RECRUITING
Nicotinamide Riboside and Mitochondrial Biogenesis nanCOMPLETED
Natural History in Primary Mitochondrial Myopathies nanRECRUITING
MITOMICS : a Multi-OMICS Approach for the Diagnosis of Mitochondrial Diseases nanRECRUITING
Identification of Large-Scale Mutations of POLG Gene by QMPSF in Patients With Mitochondrial DNA Instability. nanUNKNOWN
Gastrointestinal Dysfunction in Children Affected With Mitochondrial Disorders nanCOMPLETED
Diagnostic Odyssey Survey 2 nanCOMPLETED
Identification of New Candidate Genes in Patients With Mitochondrial Disease by High Resolution Chromosome Analysis on DNA Chip nanCOMPLETED
Evaluation of Impact of Disease and Visual Disability on Quality of Life and Loss of Independence of Patients Living in France With Leber's Hereditary Optic Neuropathy (LHON) Through Qualitative and Quantitative Data Collection nanCOMPLETED
Ccf mtDNA as a Neurodegenerative Biomarker nanUNKNOWN
A Study Into the Underlying Biochemical Pathways Involved in Parkinson's Disease, Such as Mitochondrial (Cellular Powerhouse) Dysfunction nanCOMPLETED
Nicotinamide Riboside in Ulcerative Colitis nanRECRUITING
Mitochondrial Dysfunctions Driving Insulin Resistance nanCOMPLETED
GDF-15 as a Biomarker for Mitochondrial Disease nanCOMPLETED
Abnormalities in the Effects of Insulin and Exercise on Glucose- and Lipid Metabolism in Obesity and Type 2 Diabetes nanCOMPLETED
Genetic Diagnosis in Inborn Errors of Metabolism nanENROLLING_BY_INVITATION
Coenzyme Q10 Plus NADH Supplementation in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a NDUFA2 binder may also engage these)

ProteinNameSimilarity
P0CB80 1.000 P0CB80 →
Q4R5E2 1.000 Q4R5E2 →
Q9CQ75 0.999 Q9CQ75 →
P0CB79 0.996 P0CB79 →
Q02370 0.996 Q02370 →
Q0MQ92 0.995 Q0MQ92 →
Q9FIJ2 0.987 Q9FIJ2 →
Q07842 0.968 Q07842 →
Q95KE5 0.956 Q95KE5 →
P63301 0.953 P63301 →
P63300 0.952 P63300 →
O19097 0.951 O19097 →
Q80Y14 0.950 Q80Y14 →
Q5NVB2 0.948 Q5NVB2 →
P63303 0.948 P63303 →
P63302 0.948 P63302 →
ATP5PO ATP synthase peripheral stalk subunit OSCP, mitochondrial 0.948 landscape →
Q4R5Y4 0.948 Q4R5Y4 →
B0VXH3 0.948 B0VXH3 →
Q95KL4 0.948 Q95KL4 →
Q24439 0.948 Q24439 →
P13621 0.947 P13621 →
D0EYG3 0.947 D0EYG3 →
Q5RBT4 0.946 Q5RBT4 →
NAT10 RNA cytidine acetyltransferase 0.946 landscape →
Q3UQA7 0.945 Q3UQA7 →
Q2TBG7 0.945 Q2TBG7 →
Q9DB20 0.945 Q9DB20 →
Q68FX0 0.945 Q68FX0 →
Q6ZJS7 0.945 Q6ZJS7 →