Gene Ontology annotation through association of InterPro records with GO terms
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on curation of immunofluorescence data
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Combined Automated Annotation using Multiple IEA Methods
Molecular cloning and nucleotide sequence of cDNA encoding human muscle glycogen debranching enzyme.
A role for AGL ubiquitination in the glycogen storage disorders of Lafora and Cori's disease.
The carbohydrate-binding domain of overexpressed STBD1 is important for its stability and protein-protein interactions.
Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage disease.
Exocytosis of secretory granule lumen proteins
Exocytosis of ficolin-rich granule lumen proteins
Glycogen breakdown (glycogenolysis)
limit dextrin-glycogenin => ((1,6)-alpha-glucosyl)poly((1,4)-alpha-glucosyl) glycogenin
((1,6)-alpha-glucosyl)poly((1,4)-alpha-glucosyl)glycogenin => poly{(1,4)-alpha-glucosyl} glycogenin + alpha-D-glucose
UniProt record for human AGL (P35573)
Molecular architecture and catalytic mechanism of human glycogen debranching enzyme.
Glycogen debranching enzyme is associated with rat skeletal muscle sarcoplasmic reticulum.
[Development and control of liver amylo-1,6-glucosidase activity in the fetal rat].
[Effect of biogenic amines on glycogen degradation in isolated rat hepatocytes].
Glycogen-binding protein components of rat tissues.
Proteome profiling of human neutrophil granule subsets, secretory vesicles, and cell membrane: correlation with transcriptome profiling of neutrophil precursors.