DTD1

D-aminoacyl-tRNA deacylase 1 · Q8TEA8 · DTD1 on Sugi Atlas →

0 patent compounds predicted against DTD1, 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 DTD1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
A Study of the Efficacy and Safety of MT1621 in Thymidine Kinase 2 (TK2) Deficiency (Treatment naïve) PHASE3WITHDRAWN
Peptide Vaccine Focusing on Prevention of the Recurrence for Bladder Cancer PHASE2UNKNOWN
Nucleoside Therapy in Patients With Telomere Biology Disorders PHASE1RECRUITING
Effect of Gemfibrozil on Serum Glycosylphosphatidylinositol (GPI) Phospholipase D and Triglycerides PHASE1COMPLETED
Biomarker Research in Inherited Movement Disorders nanRECRUITING
New Signaling Pathway Targeting Systemic Lupus Erythematosus nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Characterization of Angelman Syndrome nanCOMPLETED
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Thymidylate Synthase Polymorphisms as a Predictor of Toxicity to 5-Fluorouracil Based Chemotherapy in Stage III Colon Cancer nanUNKNOWN
Imaging Genetics of Laryngeal Dystonia nanRECRUITING
Erythropoietic Protoporphyrias: Studies of the Natural History, Genotype-Phenotype Correlations, and Psychosocial Impact nanCOMPLETED
Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia nanRECRUITING
Consortium On Risk for Early-onset Parkinson's Disease (CORE PD) nanCOMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
EXtremely Early-onset Type 1 Diabetes EXtremely Early-onset Type 1 Diabetes (A Musketeers' Memorandum Study) nanRECRUITING
Gait in Rare Diseases nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Speech and Short-term Memory Functions in Dyslexia: a Combined MEG and EEG Study nanUNKNOWN
Identification of New FTLD Genes nanUNKNOWN
Genetic Studies of Lysosomal Storage Disorders nanENROLLING_BY_INVITATION
Result Of Karyotyping in Pediatric Patients With Congenital Anomalies and Developmental Delay nanNOT_YET_RECRUITING
Genetics of Recurrent Early Onset Major Depression nanCOMPLETED
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Thalamic Deep Brain Stimulation for Secondary Dystonia in Children and Young Adults nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DTD1 binder may also engage these)

ProteinNameSimilarity
F1QGC8 1.000 F1QGC8 →
Q2T9V8 1.000 Q2T9V8 →
Q9DD18 1.000 Q9DD18 →
Q9D992 1.000 Q9D992 →
Q20PL8 1.000 Q20PL8 →
P69278 1.000 P69278 →
Q5VKP5 1.000 Q5VKP5 →
Q3YPY9 1.000 Q3YPY9 →
P06747 1.000 P06747 →
P11806 1.000 P11806 →
P69279 1.000 P69279 →
P13778 1.000 P13778 →
P24741 1.000 P24741 →
P0DJV7 1.000 P0DJV7 →
A4K149 1.000 A4K149 →
P0DJU0 1.000 P0DJU0 →
P17042 1.000 P17042 →
A0A2B4SJZ1 1.000 A0A2B4SJZ1 →
Q8QPI8 1.000 Q8QPI8 →
A4GBY3 1.000 A4GBY3 →
A4GCJ2 1.000 A4GCJ2 →
P0CK89 1.000 P0CK89 →
P0DJV8 1.000 P0DJV8 →
Q63073 1.000 Q63073 →
P08274 1.000 P08274 →
O59835 1.000 O59835 →
Q00686 1.000 Q00686 →
Q9LV40 1.000 Q9LV40 →
A4U6V8 1.000 A4U6V8 →
B2JG54 1.000 B2JG54 →