Gene Ontology annotation through association of InterPro records with GO terms
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Combined Automated Annotation using Multiple IEA Methods
Isolation of human glycogen branching enzyme cDNAs by screening complementation in yeast.
Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy.
Novel missense mutations in the glycogen-branching enzyme gene in adult polyglucosan body disease.
Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV).
Complete sequencing and characterization of 21,243 full-length human cDNAs.
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Immunoaffinity profiling of tyrosine phosphorylation in cancer cells.
The DNA sequence, annotation and analysis of human chromosome 3.
Initial characterization of the human central proteome.
Comparative large scale characterization of plant versus mammal proteins reveals similar and idiosyncratic N-α-acetylation features.
An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
Large-scale proteomics and phosphoproteomics of urinary exosomes.
In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.
The carbohydrate-binding domain of overexpressed STBD1 is important for its stability and protein-protein interactions.
Structural basis of glycogen branching enzyme deficiency and pharmacologic rescue by rational peptide design.
A proteome-scale map of the SARS-CoV-2-human contactome.
GBE1 catalyzes branch formation in polyGlc-GYG1 complexed with GYS1-a
GBE1 catalyzes branch formation in polyGlc-GYG2 complexed with GYS2-a
GBE1 catalyzes branch formation in polyGlc-GYG1 complexed with GYS1-b
Defective GBE1 does not catalyze branch formation in growing glycogen chains (liver)
Glycogen storage disease type IV (GBE1)
1,4-alpha-glucan-branching enzyme
Starch-binding domain-containing protein 1
Replicase polyprotein 1ab
Alpha-amylase/branching enzyme, C-terminal all beta