MANBA

Beta-mannosidase · O00462 · MANBA on Sugi Atlas →

909 patent compounds predicted against MANBA, 492 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
Gluconolactone Gluconolactone (SCHEMBL10823227) 0.39 3/20
Gluconolactone Gluconolactone (SCHEMBL11053856) 0.39 3/20
SCHEMBL8588768 SCHEMBL8588768 0.34 3/20
SCHEMBL8198571 SCHEMBL8198571 0.34 3/20
SCHEMBL20788789 SCHEMBL20788789 1.00 2/20
Gluconolactone Gluconolactone (SCHEMBL15320) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL221828) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL333412) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL2214579) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL2461264) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL2464302) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL2466355) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL2466472) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL2468364) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL7148519) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL7152056) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL10173017) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL10221981) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL12377168) 0.47 2/20
Gluconolactone Gluconolactone (SCHEMBL13176828) 0.47 2/20

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

TrialPhaseStatus
Pharmacokinetics of Alglucosidase Alfa in Patients With Pompe Disease PHASE4COMPLETED
High Dose or High Dose Frequency Study of Alglucosidase Alfa PHASE4COMPLETED
Interventional Study to Assess Efficacy and Safety of Velmanase Alfa in Patients With Alpha Mannosidosis PHASE3WITHDRAWN
A Study of Gene-Activated® Human Glucocerebrosidase (GA-GCB) Enzyme Replacement Therapy in Gaucher Disease PHASE3COMPLETED
Study of Gene-Activated® Human Glucocerebrosidase (GA-GCB) ERT Compared With Imiglucerase in Type I Gaucher Disease PHASE3COMPLETED
Study of GA-GCB Enzyme Replacement Therapy in Type 1 Gaucher Disease Patients Previously Treated With Imiglucerase PHASE2/PHASE3COMPLETED
A Placebo-Controlled Phase 3 Trial of Repeated Lamazym Treatment of Subjects With Alpha-Mannosidosis PHASE3COMPLETED
An Open-Label Extension Study of GA-GCB ERT in Patients With Type 1 Gaucher Disease PHASE3COMPLETED
Dose Finding Study of Recombinant Human Alpha-mannosidase for the Treatment of Patients With Alpha-mannosidosis PHASE2UNKNOWN
Study of Safety, Tolerability and Efficacy of PBGM01 in Pediatric Participants With GM1 Gangliosidosis PHASE1/PHASE2ACTIVE_NOT_RECRUITING
Trial on Safety and Efficacy of Velmanase Alfa Treatment in Pediatric Patients With Alpha-Mannosidosis PHASE2COMPLETED
Long-term Efficacy and Safety of Lamazym for the Treatment of Patients With Alpha-Mannosidosis PHASE2COMPLETED
Recombinant Human Mannose-Binding Lectin (MBL) in Treating Young Patients With MBL Deficiency and Fever and Neutropenia PHASE1WITHDRAWN
A Study of Safety, Tolerability, and Pk of rhMBL in Pediatric Hematology/Oncology Pts With Fever and Neutropenia PHASE1WITHDRAWN
Biomarker for Mannosidosis Disease (BioMannosidosis) nanWITHDRAWN
The Natural History of Alpha-Mannosidosis nanCOMPLETED
Lyso-Gb1 as a Long-term Prognostic Biomarker in Gaucher Disease nanCOMPLETED
Registry Gangliosidoses nanUNKNOWN
Analysis of Velmanase Alfa (Lamzede®)'s Effects in the Body of Children With Alpha-Mannosidosis Under the Age 3 nanRECRUITING
Biomarker for Mucolipidosis Disorder Type I, II, III, IV (BioML) nanWITHDRAWN
Effect of Migalastat on Cardiac Involvement in Fabry Disease nanCOMPLETED
A Study to Evaluate and Characterize the Effect of Pharmacological Chemicals on Blood From Patients With Gaucher Disease nanCOMPLETED
Study to Collect Data on Fabry Disease Patients With Enhanceable Alpha-Galactosidase A Activity nanCOMPLETED
Treatment Protocol of Velaglucerase Alfa for Patients With Type 1 Gaucher Disease nanAPPROVED_FOR_MARKETING
Biomarker for Gangliosidosis: BioGM1/BioGM2 (BioGM1/GM2) nanWITHDRAWN
Expanded Access Use of Myozyme (Alglucosidase Alfa) in Patients With Infantile-onset Pompe Disease nanAPPROVED_FOR_MARKETING
BMN 110 US Expanded Access Program nanAPPROVED_FOR_MARKETING
Characterization of the Patient Population With Galactosialidosis nanCOMPLETED
Screening of Fabry Disease in Patients With GI Symptoms nanUNKNOWN
Clinical Biomarkers in Alpha-mannosidosis nanCOMPLETED

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

ProteinNameSimilarity
Q29444 1.000 Q29444 →
Q8K2I4 1.000 Q8K2I4 →
Q95327 1.000 Q95327 →
Q4FZV0 0.994 Q4FZV0 →
Q5R5N6 0.984 Q5R5N6 →
O77695 0.984 O77695 →
O97524 0.982 O97524 →
GUSB Beta-glucuronidase 0.981 landscape →
Q4FAT7 0.981 Q4FAT7 →
O18835 0.979 O18835 →
P12265 0.978 P12265 →
FUCA2 Plasma alpha-L-fucosidase 0.976 landscape →
P06760 0.976 P06760 →
Q99KR8 0.975 Q99KR8 →
Q9FNA3 0.974 Q9FNA3 →
Q5RFI5 0.974 Q5RFI5 →
HEXA Beta-hexosaminidase subunit alpha 0.972 landscape →
Q6DYE8 0.971 Q6DYE8 →
W8E7D1 0.971 W8E7D1 →
P70665 0.971 P70665 →
Q2M3T9 0.970 Q2M3T9 →
Q6AYS4 0.970 Q6AYS4 →
P97675 0.970 P97675 →
Q5RFU0 0.970 Q5RFU0 →
Q10RB4 0.970 Q10RB4 →
O95498 0.970 O95498 →
Q8BHN3 0.969 Q8BHN3 →
Q6AXR4 0.969 Q6AXR4 →
Q641Z7 0.969 Q641Z7 →
Q8GX69 0.969 Q8GX69 →