NDUFAF2

NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2 · Q8N183 · NDUFAF2 on Sugi Atlas →

1,318 patent compounds predicted against NDUFAF2, 818 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL15258558 SCHEMBL15258558 0.76 8/20
SCHEMBL12362713 SCHEMBL12362713 0.77 7/20
SCHEMBL15080621 SCHEMBL15080621 0.77 7/20
SCHEMBL12362702 SCHEMBL12362702 0.73 7/20
SCHEMBL14351066 SCHEMBL14351066 0.69 7/20
SCHEMBL12226742 SCHEMBL12226742 0.61 7/20
SCHEMBL12362734 SCHEMBL12362734 0.60 6/20
SCHEMBL12362700 SCHEMBL12362700 0.57 6/20
SCHEMBL13973668 SCHEMBL13973668 0.47 6/20
SCHEMBL16316892 SCHEMBL16316892 0.47 6/20
Auraptene Auraptene (SCHEMBL2535029) 1.00 5/20
Auraptene Auraptene (SCHEMBL2535034) 1.00 5/20
Umbelliprenin Umbelliprenin (SCHEMBL18265478) 0.98 5/20
SCHEMBL12362712 SCHEMBL12362712 0.80 5/20
SCHEMBL14437596 SCHEMBL14437596 0.57 5/20
SCHEMBL14437626 SCHEMBL14437626 0.57 5/20
SCHEMBL14515244 SCHEMBL14515244 0.57 5/20
SCHEMBL13743063 SCHEMBL13743063 0.43 5/20
SCHEMBL18197750 SCHEMBL18197750 0.41 5/20
SCHEMBL18265492 SCHEMBL18265492 0.74 4/20

Clinical trials — most relevant to NDUFAF2 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
Trial of Nicotinamide Riboside and Co-enzyme Q10 in Chronic Kidney Disease PHASE2COMPLETED
Parkinson's Disease Treatment With Coenzyme Q10 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
Tissue Sample Study for Mitochondrial Disorders nanENROLLING_BY_INVITATION
North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC) nanRECRUITING
Nicotinamide Riboside and Mitochondrial Biogenesis nanCOMPLETED
MITOMICS : a Multi-OMICS Approach for the Diagnosis of Mitochondrial Diseases nanRECRUITING
Diagnostic Odyssey Survey 2 nanCOMPLETED
Effect of Subtle Energy Transmission and Tao Calligraphy Mindfulness Practice on Mitochondrial DNA in Peripheral Blood Leukocytes nanNOT_YET_RECRUITING
Natural History in Primary Mitochondrial Myopathies nanRECRUITING
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
Identification of Large-Scale Mutations of POLG Gene by QMPSF in Patients With Mitochondrial DNA Instability. nanUNKNOWN
Ccf mtDNA as a Neurodegenerative Biomarker nanUNKNOWN
Abnormalities in the Effects of Insulin and Exercise on Glucose- and Lipid Metabolism in Obesity and Type 2 Diabetes nanCOMPLETED
GDF-15 as a Biomarker for Mitochondrial Disease nanCOMPLETED
Gastrointestinal Dysfunction in Children Affected With Mitochondrial Disorders nanCOMPLETED
Nicotinamide Riboside in Ulcerative Colitis nanRECRUITING
Cardiac Mitochondrial Function in Explanted Human Hearts nanUNKNOWN
Q10 Ubiquinol in Autism Spectrum Disorder and in Phelan-McDermid Syndrome. nanUNKNOWN
Exercise-mediated Rescue of Mitochondrial Dysfunctions Driving Insulin Resistance nanCOMPLETED
A Study Into the Underlying Biochemical Pathways Involved in Parkinson's Disease, Such as Mitochondrial (Cellular Powerhouse) Dysfunction nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a NDUFAF2 binder may also engage these)

ProteinNameSimilarity
Q32P65 1.000 Q32P65 →
Q59J78 0.997 Q59J78 →
Q3KQD1 0.978 Q3KQD1 →
O48713 0.978 O48713 →
Q9NQ50 0.978 Q9NQ50 →
P58501 0.978 P58501 →
Q8VCE1 0.977 Q8VCE1 →
Q9M9M9 0.977 Q9M9M9 →
Q5EAW4 0.977 Q5EAW4 →
A1XD94 0.977 A1XD94 →
Q9ERA6 0.977 Q9ERA6 →
A1XD95 0.976 A1XD95 →
Q5R5K8 0.976 Q5R5K8 →
SMARCC2 SWI/SNF complex subunit SMARCC2 0.976 landscape →
P82925 0.976 P82925 →
Q9W1X9 0.976 Q9W1X9 →
Q5U2Y6 0.976 Q5U2Y6 →
Q96G28 0.975 Q96G28 →
Q61733 0.975 Q61733 →
Q1L987 0.975 Q1L987 →
P83565 0.975 P83565 →
Q28E45 0.975 Q28E45 →
Q66JD1 0.975 Q66JD1 →
Q9D5W4 0.975 Q9D5W4 →
Q0VFC7 0.975 Q0VFC7 →
Q9VH39 0.975 Q9VH39 →
Q7T0S7 0.975 Q7T0S7 →
Q0MQ85 0.974 Q0MQ85 →
P31399 0.974 P31399 →
Q92665 0.974 Q92665 →