ALG1

Chitobiosyldiphosphodolichol beta-mannosyltransferase · Q9BT22 · ALG1 on Sugi Atlas →

0 patent compounds predicted against ALG1, 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 ALG1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
High Dose or High Dose Frequency Study of Alglucosidase Alfa PHASE4COMPLETED
China Post-approval Commitment (PAC) Study of Avalglucosidase Alfa in Participants With IOPD PHASE4RECRUITING
Study of Safety, Tolerability and Efficacy of PBGM01 in Pediatric Participants With GM1 Gangliosidosis PHASE1/PHASE2ACTIVE_NOT_RECRUITING
A Study of GlcNAc on Tear Production in NGLY1-CDDG PHASE2ACTIVE_NOT_RECRUITING
A Phase 1/2 Study of Intravenous Gene Transfer With an AAV9 Vector Expressing Human Beta-galactosidase in Type I and Type II GM1 Gangliosidosis PHASE1/PHASE2RECRUITING
An Open Label Phase 2 Study of ManNAc in Subjects With GNE Myopathy PHASE2COMPLETED
Open-Label Extension Study to Assess GLM101 in PMM2-CDG Patients PHASE2ENROLLING_BY_INVITATION
24-Week Study to Assess the PD, Safety, Tolerability, and PK of GLM101 in Participants With PMM2-CDG PHASE2COMPLETED
Long-term Efficacy and Safety of Lamazym for the Treatment of Patients With Alpha-Mannosidosis PHASE2COMPLETED
A Phase 1 Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ManNAc in Subjects With Primary Podocyte Diseases PHASE1COMPLETED
A Study of the Tolerance, Safety, and Pharmacokinetics of GNR-055 in Healthy Volunteers PHASE1COMPLETED
Biomarker for Mucolipidosis Disorder Type I, II, III, IV (BioML) nanWITHDRAWN
Biomarker for Mannosidosis Disease (BioMannosidosis) nanWITHDRAWN
The Natural History of Alpha-Mannosidosis nanCOMPLETED
Glycosylation in Patients With Galactosaemia nanCOMPLETED
Registry Gangliosidoses nanUNKNOWN
Efficacy of Intravaginal Carboxymethyl-β-glucan and Polycarbophil on Low-grade Cervical Lesions (GLUCANCIN) nanUNKNOWN
Biomarker for Metachromatic Leukodystrophy (BioMeta) Disease nanWITHDRAWN
Longitudinal Studies of the Glycoproteinoses nanCOMPLETED
Natural History of Glycosphingolipid Storage Disorders and Glycoprotein Disorders nanRECRUITING
Using D-Galactose as a Food Supplement in Congenital Disorders of Glycosylation nanCOMPLETED
Lyso-Gb1 as a Long-term Prognostic Biomarker in Gaucher Disease nanCOMPLETED
A Natural History Study of the Gangliosidoses nanRECRUITING
The Classification and Cause of Leukodystrophies of Unknown Cause nanCOMPLETED
Expanded Access Use of Myozyme (Alglucosidase Alfa) in Patients With Infantile-onset Pompe Disease nanAPPROVED_FOR_MARKETING
Diagnostic Accuracy of Pleural Effusion Aspergillosis Biomarker Testing nanUNKNOWN
Characterization of the Patient Population With Galactosialidosis nanCOMPLETED
Expanded Access Trial of Plant Expressed Recombinant Glucocerebrosidase (prGCD) in Patients With Gaucher Disease nanNO_LONGER_AVAILABLE
The Natural History of Sialidosis Type I nanRECRUITING
Efficacy of an Intravaginal Treatment With Carboxymethyl-β-glucan and Polycarbophil in HR-HPV Clearance nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a ALG1 binder may also engage these)

ProteinNameSimilarity
Q5R7A2 1.000 Q5R7A2 →
Q921Q3 1.000 Q921Q3 →
Q8L7M0 0.979 Q8L7M0 →
Q9D0Z3 0.975 Q9D0Z3 →
Q7ZW24 0.973 Q7ZW24 →
LPCAT1 Lysophosphatidylcholine acyltransferase 1 0.972 landscape →
Q4V9J0 0.971 Q4V9J0 →
Q2TAA5 0.971 Q2TAA5 →
Q1HAQ0 0.970 Q1HAQ0 →
Q5R7Z6 0.969 Q5R7Z6 →
Q3TFD2 0.969 Q3TFD2 →
Q5NVK5 0.969 Q5NVK5 →
Q2TBP5 0.968 Q2TBP5 →
Q64323 0.968 Q64323 →
A5PK19 0.968 A5PK19 →
Q3TZM9 0.967 Q3TZM9 →
Q08B22 0.967 Q08B22 →
Q5EA80 0.966 Q5EA80 →
Q148G5 0.966 Q148G5 →
Q9XEE9 0.966 Q9XEE9 →
F4ZGF2 0.965 F4ZGF2 →
A5A779 0.965 A5A779 →
Q14CH1 0.965 Q14CH1 →
Q9JLV6 0.965 Q9JLV6 →
Q8N6R0 0.965 Q8N6R0 →
P22734 0.965 P22734 →
Q922Z0 0.965 Q922Z0 →
Q91YR5 0.965 Q91YR5 →
O43272 0.964 O43272 →
Q5I0L3 0.964 Q5I0L3 →