QARS1

Glutamine--tRNA ligase · P47897 · QARS1 on Sugi Atlas →

169 patent compounds predicted against QARS1, 143 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL1893417 SCHEMBL1893417 0.54 3/20
SCHEMBL5063172 SCHEMBL5063172 0.69 2/20
Adenosine Phosphate Adenosine Phosphate (SCHEMBL7225652) 0.67 2/20
Adenosine Phosphate Adenosine Phosphate (SCHEMBL15670721) 0.67 2/20
Adenosine Phosphate Adenosine Phosphate (SCHEMBL15670863) 0.59 2/20
SCHEMBL10886080 SCHEMBL10886080 0.58 2/20
SCHEMBL4750533 SCHEMBL4750533 0.57 2/20
SCHEMBL3898255 SCHEMBL3898255 0.56 2/20
SCHEMBL1893409 SCHEMBL1893409 0.54 2/20
SCHEMBL10883635 SCHEMBL10883635 0.51 2/20
SCHEMBL5063184 SCHEMBL5063184 0.78 1/20
SCHEMBL5063189 SCHEMBL5063189 0.78 1/20
SCHEMBL5067246 SCHEMBL5067246 0.75 1/20
Adenosine Phosphate Adenosine Phosphate (SCHEMBL15670584) 0.74 1/20
Adenosine Triphosphate Adenosine Triphosphate (SCHEMBL27831091) 0.71 1/20
Adenosine Triphosphate Adenosine Triphosphate (SCHEMBL28794921) 0.69 1/20
Adenosine Triphosphate Adenosine Triphosphate (SCHEMBL4419692) 0.68 1/20
Adenosine Triphosphate Adenosine Triphosphate (SCHEMBL27722788) 0.68 1/20
Adenosine Phosphate Adenosine Phosphate (SCHEMBL1331852) 0.67 1/20
SCHEMBL18423487 SCHEMBL18423487 0.67 1/20

Clinical trials — most relevant to QARS1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Impact of tdrd9 Gene Mutations in the Therapeutic Response to L-carnitine in Oligoasthenozoospermic Men PHASE3ACTIVE_NOT_RECRUITING
Therapeutic Efficacy of L-Ornithine L-Aspartate Infusion in Patients With Acute Liver Failure PHASE2UNKNOWN
Allogeneic Hematopoietic Stem Cell Transplant for GATA2 Mutations PHASE2RECRUITING
Testing the Combination of MLN4924 (Pevonedistat), Carboplatin, and Paclitaxel in Patients With Advanced Non-small Cell Lung Cancer (NSCLC) Who Have Previously Been Treated With Immunotherapy PHASE2ACTIVE_NOT_RECRUITING
Glutamine Supplementation in People With Immune Dysregulation EARLY_PHASE1WITHDRAWN
Transcriptomic Profile of Patients Treated With Different Modalities of Spinal Cord Stimulation nanUNKNOWN
Genetic Contribution to the Pathophysiology of the Charcot Foot in Qatari Patients With Diabetes nanCOMPLETED
Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others nanRECRUITING
Biomarker for Mucolipidosis Disorder Type I, II, III, IV (BioML) nanWITHDRAWN
The Genetic and the Functional Study of DNA Repair System and the Susceptibility to Rheumatoid Arthritis nanCOMPLETED
Study to Identify the Genetic Variations Associated With Phantom Limb Pain nanCOMPLETED
Genetic Analysis of Immune Disorders nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Differential Gene Expression of Liver Tissue and Blood From Individuals With Chronic Viral Hepatitis nanUNKNOWN
Core Stability Exercises and Hereditary Ataxia nanCOMPLETED
Advancing Neurogenetic Diagnoses Through Long-Read Sequencing nanNOT_YET_RECRUITING
Congenital Hemolytic and Dyserythropoietic Anemias nanRECRUITING
Thymidylate Synthase Polymorphisms as a Predictor of Toxicity to 5-Fluorouracil Based Chemotherapy in Stage III Colon Cancer nanUNKNOWN
Whole Genome Sequencing in the Neonatal Intensive Care Unit nanCOMPLETED
Genomic of CONgenital Sideroblastic Anemias nanRECRUITING
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Genetic Studies Spermatogenic Failure nanCOMPLETED
Impact of Mutations in Aminoacyl tRNA Synthetases on Protein Translation and Cellular Stress nanWITHDRAWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Gene Modifiers of Cystic Fibrosis Lung Disease nanACTIVE_NOT_RECRUITING
The Molecular Pathogenesis Study of Cataract nanUNKNOWN
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Gene Analysis of Parkinson's Disease nanCOMPLETED
Phenotype/Genotype Correlations in Neuromuscular Disorders nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a QARS1 binder may also engage these)

ProteinNameSimilarity
Q8BML9 1.000 Q8BML9 →
Q66H61 1.000 Q66H61 →
Q3MHH4 1.000 Q3MHH4 →
Q8W4F3 0.979 Q8W4F3 →
P52780 0.979 P52780 →
F4I116 0.973 F4I116 →
A3KMV5 0.971 A3KMV5 →
Q5RGJ5 0.971 Q5RGJ5 →
Q9Y105 0.971 Q9Y105 →
Q9YH58 0.970 Q9YH58 →
P31254 0.969 P31254 →
Q5I598 0.969 Q5I598 →
Q6YXZ7 0.969 Q6YXZ7 →
Q02053 0.969 Q02053 →
Q9ER88 0.969 Q9ER88 →
Q5U300 0.969 Q5U300 →
Q641Y5 0.969 Q641Y5 →
Q5I0L3 0.969 Q5I0L3 →
Q60HE5 0.968 Q60HE5 →
Q7ZY60 0.967 Q7ZY60 →
Q9WU20 0.967 Q9WU20 →
PRMT5 Protein arginine N-methyltransferase 5 0.967 landscape →
P42898 0.966 P42898 →
PC Pyruvate carboxylase, mitochondrial 0.966 landscape →
Q8BYL4 0.966 Q8BYL4 →
A2X0Q3 0.966 A2X0Q3 →
NAT10 RNA cytidine acetyltransferase 0.966 landscape →
Q57RP8 0.966 Q57RP8 →
ATG7 Ubiquitin-like modifier-activating enzyme ATG7 0.966 landscape →
C5BGA4 0.966 C5BGA4 →