OLA1

Obg-like ATPase 1 · Q9NTK5 · OLA1 on Sugi Atlas →

0 patent compounds predicted against OLA1, 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 OLA1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Applying Proton Pump Inhibitor to Prevent and Treat Acute Fluctuating Hearing Loss in Patients With SLC26A4 Mutation PHASE2/PHASE3UNKNOWN
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
Rare Kidney Stone Consortium Biobank nanRECRUITING
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts nanCOMPLETED
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Prospective Genetic Study in Patients With Ovarian Insufficiency nanUNKNOWN
Clinical, Cellular, and Molecular Investigation Into Oculocutaneous Albinism nanCOMPLETED
Investigation of Copy Number Variations and Genetic Variants in POI nanRECRUITING
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS nanRECRUITING
Family Studies in Primary Biliary Cirrhosis (PBC) nanUNKNOWN
Genetic Evaluation of AAAS Gene in Early-Onset Achalasia and Alacrima Patients nanCOMPLETED
Study to Investigate Genetic Causes of Severe Early Childhood Onset Obesity. nanRECRUITING
Stone Disease in Children and Their Families nanCOMPLETED
Pilot Study to Evaluate the Contribution of Gene Variants to Idiopathic Urolithiasis nanENROLLING_BY_INVITATION
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Genetic Variations That Increase the Risk for Calcium Kidney Stones: a Family-based Study nanCOMPLETED
A Multicenter Observational Study on the Development and Health Effects of Premature Ovarian Insufficiency nanRECRUITING
Epidemiology of Atherosclerosis nanCOMPLETED
Proteomics of Primary Hyperoxaluria Type 1 nanCOMPLETED
Amyotrophic Lateral Sclerosis (ALS) Families Project nanRECRUITING
Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation nanRECRUITING
Primary Hyperoxaluria Mutation Genotyping/Phenotyping nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
The LD Lync Study - Natural History Study of Lipodystrophy Syndromes nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a OLA1 binder may also engage these)

ProteinNameSimilarity
Q9CZ30 1.000 Q9CZ30 →
A0JPJ7 1.000 A0JPJ7 →
Q5R821 1.000 Q5R821 →
Q5ZM25 1.000 Q5ZM25 →
Q7ZU42 1.000 Q7ZU42 →
Q2HJ33 1.000 Q2HJ33 →
Q6Z1J6 1.000 Q6Z1J6 →
Q7ZWM6 1.000 Q7ZWM6 →
Q9SA73 1.000 Q9SA73 →
P91917 1.000 P91917 →
Q66JG0 1.000 Q66JG0 →
B8BBN7 1.000 B8BBN7 →
Q8SWU7 1.000 Q8SWU7 →
O13998 1.000 O13998 →
P38219 0.999 P38219 →
P38746 0.997 P38746 →
P43690 0.994 P43690 →
Q7VMI2 0.994 Q7VMI2 →
Q54HP3 0.993 Q54HP3 →
Q9CP90 0.993 Q9CP90 →
P09604 0.993 P09604 →
P32234 0.993 P32234 →
Q9SVA6 0.992 Q9SVA6 →
A9A9U4 0.992 A9A9U4 →
Q6L200 0.992 Q6L200 →
P44681 0.992 P44681 →
A4FWF0 0.992 A4FWF0 →
P0ABU2 0.992 P0ABU2 →
Q979T3 0.992 Q979T3 →
A6UV44 0.992 A6UV44 →