PLP2

Proteolipid protein 2 · Q04941 · PLP2 on Sugi Atlas →

0 patent compounds predicted against PLP2, 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 PLP2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Neuroprotective Effect of Vitamin B12 and Vitamin B6 Against Vincristine Induced Peripheral Neuropathy PHASE4COMPLETED
AntiCoagulants and COGnition PHASE4UNKNOWN
D-Cycloserine for Serine Palmitoyltransferase Inhibition PHASE4COMPLETED
Intravenous Immunoglobulin Therapy in Optic Neuritis PHASE3COMPLETED
T Cell Vaccination in Patients With Progressive Multiple Sclerosis PHASE1/PHASE2COMPLETED
Cytotron® Delivered Rotational Field Quantum Nuclear Magnetic Resonance Therapy for Multiple Sclerosis PHASE2UNKNOWN
Study to Identify the Genetic Variations Associated With Phantom Limb Pain nanCOMPLETED
Comparison Between Clinical and MRI Multiple Sclerosis Activity and Expression of Human Endogenous Retrovirus Type W and Herpesvirus nanUNKNOWN
Genetics and Phantom Limb Pain nanWITHDRAWN
The Classification and Cause of Leukodystrophies of Unknown Cause nanCOMPLETED
LeukoSEQ: Whole Genome Sequencing as a First-Line Diagnostic Tool for Leukodystrophies nanCOMPLETED
Natural History of the Leukodystrophies nanCOMPLETED
Rocket Study: A Study to Characterize Biomarkers and Disease Progression in Participants With Pelizaeus-Merzbacher Disease nanRECRUITING
Genetic Studies of Lysosomal Storage Disorders nanENROLLING_BY_INVITATION
Consequences of Mutations in the SPG7 Gene at the Heterozygous State nanCOMPLETED
The Myelin Disorders Biorepository Project nanRECRUITING
Unraveling Genetics of HypoPhosPhatasia (HPP Genetics) nanCOMPLETED
SNAP: Measurement of the Subjective Perception of the Symptom in Hereditary Spastic Paraparesis (HSP) nanCOMPLETED
The Nosology and Etiology of Leukodystrophies of Unknown Causes nanCOMPLETED
Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others nanRECRUITING
Toward Molecular Profiling of Parkinson's Disease in Easily Accessible Biological Matrices nanACTIVE_NOT_RECRUITING
Characterisation of Adult-Onset Hypophosphatasia nanCOMPLETED
Protein Synthesis in the Brain of Patients With Fragile X Syndrome nanCOMPLETED
Registry Gangliosidoses nanUNKNOWN
Initial Clinical Presentation of Inflammatory Optic Neuritis Associated or Not With Autoantibodies Anti-Myelin-oligodendrocyte-glycoprotein nanCOMPLETED
Identification of a New Gene Involved in Hereditary Lipodystrophy nanCOMPLETED
Natural History Study of Patients With Hypophosphatasia (HPP) nanRECRUITING
Volumetrics and Proteomics in Shunted Normal Pressure Hydrocephalus nanUNKNOWN
Using Next-generation Sequencing in the Diagnosis of Epilepsy and/or Intellectual Disability in a Pediatric Cohorte nanCOMPLETED
Clinical Diagnosis of Acute Porphyria nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a PLP2 binder may also engage these)

ProteinNameSimilarity
Q6Y1E2 0.993 Q6Y1E2 →
Q95MN6 0.991 Q95MN6 →
Q9D6G9 0.978 Q9D6G9 →
Q9CZR4 0.968 Q9CZR4 →
Q96FZ5 0.963 Q96FZ5 →
Q6P742 0.962 Q6P742 →
A2VE13 0.959 A2VE13 →
MAL2 Protein MAL2 0.957 landscape →
O09198 0.956 O09198 →
Q28296 0.955 Q28296 →
Q5RAI2 0.954 Q5RAI2 →
Q99LJ5 0.954 Q99LJ5 →
Q64349 0.950 Q64349 →
Q1RMP9 0.949 Q1RMP9 →
P21145 0.947 P21145 →
MYADM Myeloid-associated differentiation marker 0.945 landscape →
Q8BI08 0.945 Q8BI08 →
Q5R6H1 0.940 Q5R6H1 →
Q8CJ61 0.940 Q8CJ61 →
Q3ZBY0 0.939 Q3ZBY0 →
Q9R1Q7 0.939 Q9R1Q7 →
Q96MX0 0.938 Q96MX0 →
P20274 0.933 P20274 →
Q9ESD6 0.932 Q9ESD6 →
Q8IZV2 0.932 Q8IZV2 →
P56563 0.930 P56563 →
D4A9I3 0.929 D4A9I3 →
P54825 0.928 P54825 →
Q9Y5I7 0.928 Q9Y5I7 →
SLC44A1 Choline transporter-like protein 1 0.928 landscape →