Gene Ontology annotation through association of InterPro records with GO terms

Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara

Combined Automated Annotation using Multiple IEA Methods

UniProtKB entry P16278 (BGAL_HUMAN), Beta-galactosidase

Endothelial cell senescence in human atherosclerosis: role of telomere in endothelial dysfunction.

Role of a novel EGF-like domain-containing gene NGX6 in cell adhesion modulation in nasopharyngeal carcinoma cells.

Role of beta-galactosidase and elastin binding protein in lysosomal and nonlysosomal complexes of patients with GM1-gangliosidosis.

Large-scale proteomics and phosphoproteomics of urinary exosomes.

GM1 gangliosidosis and Morquio B disease: expression analysis of missense mutations affecting the catalytic site of acid beta-galactosidase.

Crystal structure of human β-galactosidase: structural basis of Gm1 gangliosidosis and morquio B diseases.

In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.

Structural basis of pharmacological chaperoning for human β-galactosidase.

Alternative splicing of beta-galactosidase mRNA generates the classic lysosomal enzyme and a beta-galactosidase-related protein.

Recurrent and novel GLB1 mutations in India.

Immunoelectron microscopical localization of lysosomal beta-galactosidase and its precursor forms in normal and mutant human fibroblasts.

Cloning, sequencing, and expression of cDNA for human beta-galactosidase.

Characterization of glycan substrates accumulating in GM1 Gangliosidosis.

A reference map of the human binary protein interactome.

Intracellular processing and maturation of mutant gene products in hereditary beta-galactosidase deficiency (beta-galactosidosis).

Hydrolysis of lactosylceramide by human galactosylceramidase and GM1-beta-galactosidase in a detergent-free system and its stimulation by sphingolipid activator proteins, sap-B and sap-C. Activator proteins stimulate lactosylceramide hydrolysis.

Beta-galactosidases hydrolyse mobilized GM1 to mobilized GM2

NEU1,4 hydrolyze PSAP(195-273):GM3:PE

GLB1 hydrolyzes SapB/C:LacCer

GLB1 hydrolyses a glycosaminoglycan

GLB1 hydrolyses linker chain(2)

Defective GLB1 does not hydrolyse a glycosaminoglycan

NEU1 hydrolyses Neu5Ac from glycoconjugates

Defective NEU1 does not hydrolyse Neu5Ac from glycoconjugates

Exocytosis of azurophil granule lumen proteins

Exocytosis of ficolin-rich granule lumen proteins

Defective GLB1 does not hydrolyse linker chain(2)

NEU4 hydrolyses Neu5Ac from glycoconjugates

Beta-galactosidases hydrolyze GM2A:GA1 to GM2A:GA2