XPNPEP2

Xaa-Pro aminopeptidase 2 · O43895 · XPNPEP2 on Sugi Atlas →

206 patent compounds predicted against XPNPEP2, 87 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL17339957 SCHEMBL17339957 1.00 2/20
SCHEMBL17339958 SCHEMBL17339958 1.00 2/20
SCHEMBL17339960 SCHEMBL17339960 0.75 2/20
SCHEMBL17339961 SCHEMBL17339961 0.74 2/20
SCHEMBL17339959 SCHEMBL17339959 0.61 2/20
SCHEMBL6679094 SCHEMBL6679094 0.55 2/20
SCHEMBL6679097 SCHEMBL6679097 0.55 2/20
SCHEMBL20375838 SCHEMBL20375838 0.51 2/20
SCHEMBL30069057 SCHEMBL30069057 0.48 2/20
SCHEMBL14355658 SCHEMBL14355658 0.45 2/20
SCHEMBL3283616 SCHEMBL3283616 0.45 2/20
SCHEMBL12233572 SCHEMBL12233572 0.45 2/20
SCHEMBL6954392 SCHEMBL6954392 0.43 2/20
SCHEMBL6954395 SCHEMBL6954395 0.43 2/20
SCHEMBL7068510 SCHEMBL7068510 0.43 2/20
SCHEMBL12308700 SCHEMBL12308700 0.40 2/20
SCHEMBL12308668 SCHEMBL12308668 0.40 2/20
SCHEMBL12308734 SCHEMBL12308734 0.39 2/20
SCHEMBL31448343 SCHEMBL31448343 0.48 1/20
SCHEMBL4422194 SCHEMBL4422194 0.48 1/20

Clinical trials — most relevant to XPNPEP2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
ALL SCTped FORUM - Pharmacogenomic Study (add-on Study) PHASE4UNKNOWN
A Study of KRN23 in Pediatric Patients With X-linked Hypophosphatemic Rickets/Osteomalacia PHASE3COMPLETED
Improving Outcomes in Neonatal Abstinence Syndrome PHASE3COMPLETED
A Study to Evaluate the Safety and Efficacy of Afamelanotide in Patients With Xeroderma Pigmentosum (XP) PHASE2UNKNOWN
A Study to Evaluate the Safety, Tolerability and Efficacy of BMN 110 in Subjects With Mucopolysaccharidosis IVA PHASE1/PHASE2COMPLETED
Pappalysin 2 (PAPP-A2) Enzyme Replacement PHASE1COMPLETED
Calcitonin for Treating X-linked Hypophosphatemia nanCOMPLETED
The Effect of Monoallelic Variants in the ALPL Gene on the Natural Course of Hypophosphatasia in Russia nanRECRUITING
Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected By Hypohidrotic Ectodermal Dysplasia (ECP-012) nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Genetic Studies of Lysosomal Storage Disorders nanENROLLING_BY_INVITATION
Cancer Risk in Carriers of the Gene for Xeroderma Pigmentosum nanCOMPLETED
Williams Syndrome (WS) and Supravalvar Aortic Stenosis (SVAS) DNA and Tissue Bank nanCOMPLETED
Genetic Response to Warfarin in Healthy Subjects nanCOMPLETED
Study of Longitudinal Observation for Patient With X-linked Hypophosphatemic Rickets/Osteomalacia in Collaboration With Asian Partners nanACTIVE_NOT_RECRUITING
X-chromosome Inactivation, Epigenetics and the Transcriptome nanCOMPLETED
Molecular Associations With Reproductive Failure nanCOMPLETED
Genome Environment Microbiome and Metabolome in Autism Study nanCOMPLETED
Developing a Management Approach for Patients With Late-Onset Pompe Disease nanACTIVE_NOT_RECRUITING
Observational Study of Adults and Adolescents With Erythropoietic Protoporphyria (EPP) and X-linked Porphyria (XLP) nanRECRUITING
Genetic Investigations in Children With Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam nanUNKNOWN
Genetics of Ehlers-Danlos Syndrome nanCOMPLETED
Genetic Basis of Abdominal Aortic Aneurysm nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Impact of Elastin Mediated Vascular Stiffness on End Organs nanCOMPLETED
Immune Signature of Palmoplantar Pustulosis nanCOMPLETED
Role of ADA SNPs in Subjects With Relapsing Multiple Sclerosis (RMS) nanUNKNOWN
Modeling DNA Diversity in Reverse Cholesterol Transport nanCOMPLETED
The Contribution of Optical Mapping to the Characterization of Chromosomal Rearrangements in Patients With Neurodevelopmental Disorders nanRECRUITING
InsightRP2 Registry nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a XPNPEP2 binder may also engage these)

ProteinNameSimilarity
B1AVD1 1.000 B1AVD1 →
Q95333 0.998 Q95333 →
Q99MA2 0.998 Q99MA2 →
E9EUE6 0.982 E9EUE6 →
B0DZL3 0.981 B0DZL3 →
E9E9B2 0.981 E9E9B2 →
O44750 0.980 O44750 →
Q55E60 0.979 Q55E60 →
B2AWV6 0.979 B2AWV6 →
E3QCU0 0.979 E3QCU0 →
Q58DH9 0.979 Q58DH9 →
Q2VQV9 0.979 Q2VQV9 →
C0NDZ7 0.979 C0NDZ7 →
Q08CS6 0.978 Q08CS6 →
C6HSY3 0.978 C6HSY3 →
MGAM Maltase-glucoamylase 0.978 landscape →
P28843 0.978 P28843 →
C5FHR9 0.978 C5FHR9 →
F4JQH3 0.978 F4JQH3 →
B8M9W2 0.978 B8M9W2 →
A0A2Z5GDY5 0.978 A0A2Z5GDY5 →
P51569 0.978 P51569 →
A2QGR5 0.978 A2QGR5 →
Q5R7P4 0.978 Q5R7P4 →
Q9VJG0 0.978 Q9VJG0 →
Q8RY11 0.977 Q8RY11 →
A1CAQ1 0.977 A1CAQ1 →
Q5EA41 0.977 Q5EA41 →
E9CTR7 0.977 E9CTR7 →
MGAM2 Probable maltase-glucoamylase 2 (Maltase-gluc 0.977 landscape →