Β-Mannosidase

Protein-coding gene in humans From Wikipedia, the free encyclopedia

β-Mannosidase (EC 3.2.1.25}, mannanase, mannase, β-D-mannosidase, β-mannoside mannohydrolase, exo-β-D-mannanase, lysosomal β A mannosidase) is an enzyme with systematic name β-D-mannoside mannohydrolase, which is in humans encoded by the MANBA gene.[5][6][7][8][9][10] This enzyme catalyses the following chemical reaction

Hydrolysis of terminal, non-reducing β-D-mannose residues in β-D-mannosides
Quick facts MANBA, Identifiers ...
MANBA
Identifiers
AliasesMANBA, MANB1, mannosidase beta
External IDsOMIM: 609489; MGI: 88175; HomoloGene: 4317; GeneCards: MANBA; OMA:MANBA - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005908

NM_027288

RefSeq (protein)

NP_005899

NP_081564

Location (UCSC)Chr 4: 102.63 – 102.76 MbChr 3: 135.19 – 135.28 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Close

This gene encodes a member of the glycosyl hydrolase 2 family. The encoded protein localizes to the lysosome where it is the final exoglycosidase in the pathway for N-linked glycoprotein oligosaccharide catabolism. Mutations in this gene are associated with β-mannosidosis, a lysosomal storage disease that has a wide spectrum of neurological involvement.[5]

References

Further reading

Related Articles

Wikiwand AI