ARPC5

Actin-related protein 2/3 complex subunit 5 · O15511 · ARPC5 on Sugi Atlas →

1 patent compounds predicted against ARPC5, 1 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL24532060 SCHEMBL24532060 0.77 2/20

Clinical trials — most relevant to ARPC5 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Family Blood Pressure Program - SAPPHIRe Network nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Family Blood Pressure Program - GenNet Network nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Family Blood Pressure Program - HyperGEN nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Genetic Basis of Mitral Valve Prolapse nanUNKNOWN
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Nuclear Myosin VI - a Therapeutic Target in Breast Cancer nanUNKNOWN
The Genetics of Cardiomyopathy and Heart Failure nanWITHDRAWN
Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF) nanUNKNOWN
Family Blood Pressure Program - GENOA nanCOMPLETED
Autophagy Bladder Cancer nanUNKNOWN
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease nanCOMPLETED
Genetic Analysis of Familial Hypertrophic Cardiomyopathy nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Pediatric Cardiomyopathy Mutation Analysis nanRECRUITING
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Mayo AVC Registry and Biobank nanRECRUITING
Molecular Genetics of Retinal Degenerations nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a ARPC5 binder may also engage these)

ProteinNameSimilarity
Q4KLF8 1.000 Q4KLF8 →
Q5R516 1.000 Q5R516 →
Q9CPW4 1.000 Q9CPW4 →
Q3SYX9 1.000 Q3SYX9 →
A1L108 1.000 A1L108 →
Q5E963 1.000 Q5E963 →
Q5R4M1 1.000 Q5R4M1 →
Q68FI4 1.000 Q68FI4 →
Q9D898 1.000 Q9D898 →
ARPC5L Actin-related protein 2/3 complex subunit 5-like protein 1.000 landscape →
Q641B9 0.999 Q641B9 →
Q10316 0.995 Q10316 →
O96626 0.994 O96626 →
P40518 0.994 P40518 →
Q6DE18 0.993 Q6DE18 →
Q9VN19 0.991 Q9VN19 →
P91167 0.990 P91167 →
Q19555 0.987 Q19555 →
C4YCB9 0.987 C4YCB9 →
Q9U2Y2 0.987 Q9U2Y2 →
A8WN14 0.987 A8WN14 →
Q751P7 0.987 Q751P7 →
Q9M117 0.987 Q9M117 →
O14164 0.987 O14164 →
Q6C855 0.987 Q6C855 →
O02328 0.987 O02328 →
Q4WDK4 0.986 Q4WDK4 →
P35848 0.986 P35848 →
G5EES6 0.986 G5EES6 →
Q9Y3A3 0.986 Q9Y3A3 →