VPS51

Vacuolar protein sorting-associated protein 51 homolog · Q9UID3 · VPS51 on Sugi Atlas →

0 patent compounds predicted against VPS51, 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 VPS51 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Treatment of Wolfram Syndrome Type 2 With the Chelator Deferiprone and Incretin Based Therapy PHASE2/PHASE3UNKNOWN
Safety and Efficacy of AAV9/AP4B1 (BFB-101) For Patients With AP4B1-related Hereditary Spastic Paraplegia Type 47 (SPG47) PHASE1/PHASE2NOT_YET_RECRUITING
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Effects of Cannabidiol (CBD) on the Activation of Autophagy and Inflammation Genes, Functional Consequences in Virologically Controlled HIV-infected Patients PHASE2COMPLETED
Reverse Transcriptase Inhibitors in AGS PHASE2COMPLETED
Nilotinib in Huntington's Disease PHASE1UNKNOWN
MERC Proteins in Saliva and GCF in Periodontal Disease (ELISA Study) nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Natural History Study of Patients With VCP-related Disease nanCOMPLETED
Autophagy Bladder Cancer nanUNKNOWN
A Natural History Study of Neuronal Ceroid Lipofuscinosis Type 5 (CLN5) nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
The Role of DNA and RNA in NGS Analyses for Advaced Stage NSCLC Patients nanRECRUITING
Nuclear Myosin VI - a Therapeutic Target in Breast Cancer nanUNKNOWN
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Parkinson's Foundation PD GENEration Genetic Registry nanRECRUITING
Association of Autophagy-related Genes ,LncRNA and SNPs With Colorectal Cancer in Egyptian Population nanCOMPLETED
The Natural History of Alpha-Mannosidosis nanCOMPLETED
Study of Chediak-Higashi Syndrome nanRECRUITING
Genetic Analysis of Gray Platelet Syndrome nanCOMPLETED
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Genetic Basis of Mitral Valve Prolapse nanUNKNOWN
Evaluation of Serum Gasdermin D Level As a Potential Biomarker of Disease Activity in Vitiligo Patients nanUNKNOWN
Structural Validity and Inter-rater Reliabitiliy of the Ataxia Trunk, Lower And Upper Extremity Scale (ATLAS) nanNOT_YET_RECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Identification of New FTLD Genes nanUNKNOWN
Consortium On Risk for Early-onset Parkinson's Disease (CORE PD) nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a VPS51 binder may also engage these)

ProteinNameSimilarity
A6QQ47 1.000 A6QQ47 →
Q3UVL4 1.000 Q3UVL4 →
Q5ZJ25 0.987 Q5ZJ25 →
Q4V9Y0 0.987 Q4V9Y0 →
Q155U0 0.986 Q155U0 →
Q505L3 0.984 Q505L3 →
Q9UJX6 0.971 Q9UJX6 →
O55166 0.968 O55166 →
Q8N1B4 0.967 Q8N1B4 →
Q5TJF0 0.966 Q5TJF0 →
Q8BZQ7 0.964 Q8BZQ7 →
PKN1 Serine/threonine-protein kinase N1 0.963 landscape →
Q96JH8 0.961 Q96JH8 →
O75146 0.961 O75146 →
A1A4I4 0.961 A1A4I4 →
Q8C754 0.961 Q8C754 →
Q8R1U1 0.960 Q8R1U1 →
Q29RB1 0.960 Q29RB1 →
A2SXS5 0.960 A2SXS5 →
P70268 0.960 P70268 →
Q9Y2B5 0.960 Q9Y2B5 →
Q6ZT62 0.959 Q6ZT62 →
Q3MII6 0.959 Q3MII6 →
Q8TBN0 0.959 Q8TBN0 →
Q8C190 0.959 Q8C190 →
P23726 0.959 P23726 →
Q9JKY5 0.958 Q9JKY5 →
B2DCZ9 0.958 B2DCZ9 →
Q2KJ58 0.958 Q2KJ58 →
Q69Z89 0.957 Q69Z89 →