NAGA (gene)

N-acetylgalactosaminidase, alpha-
Rendering based on PDB 3H53.
Available structures PDB 3H53, 3H54, 3H55, 3IGU
Identifiers
Symbols	NAGA; D22S674; GALB
External IDs	OMIM: 104170 MGI: 1261422 HomoloGene: 221 GeneCards: NAGA Gene
EC number	3.2.1.49
Gene Ontology Molecular function • hydrolase activity, hydrolyzing O-glycosyl compounds • alpha-galactosidase activity • alpha-N-acetylgalactosaminidase activity • protein homodimerization activity • cation binding Cellular component • cytoplasm • lysosome Biological process • oligosaccharide metabolic process • carbohydrate catabolic process • glycoside catabolic process • glycolipid catabolic process • glycosylceramide catabolic process Sources: Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	4668	17939
Ensembl	ENSG00000198951	ENSMUSG00000022453
UniProt	P17050	Q3U6T2
RefSeq (mRNA)	NM_000262	NM_008669.4
RefSeq (protein)	NP_000253	NP_032695.3
Location (UCSC)	Chr 22: 42.43 – 42.47 Mb	Chr 15: 82.16 – 82.17 Mb
PubMed search	[1]	[2]

Alpha-N-acetylgalactosaminidase is an enzyme that in humans is encoded by the NAGA gene.^[1]

NAGA encodes the lysosomal enzyme alpha-N-acetylgalactosaminidase, which cleaves alpha-N-acetylgalactosaminyl moieties from glycoconjugates. Mutations in NAGA have been identified as the cause of Schindler disease types I and II (type II also known as Kanzaki disease).^[1]

References

1. ^ ^{a b} "Entrez Gene: NAGA N-acetylgalactosaminidase, alpha-". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4668. 

Further reading

• Cantz M, Ulrich-Bott B (1990). "Disorders of glycoprotein degradation.". J. Inherit. Metab. Dis. 13 (4): 523–37. doi:10.1007/BF01799510. PMID 2122119. 
• Wang AM, Desnick RJ (1991). "Structural organization and complete sequence of the human alpha-N-acetylgalactosaminidase gene: homology with the alpha-galactosidase A gene provides evidence for evolution from a common ancestral gene.". Genomics 10 (1): 133–42. doi:10.1016/0888-7543(91)90493-X. PMID 1646157. 
• Wang AM, Bishop DF, Desnick RJ (1991). "Human alpha-N-acetylgalactosaminidase-molecular cloning, nucleotide sequence, and expression of a full-length cDNA. Homology with human alpha-galactosidase A suggests evolution from a common ancestral gene.". J. Biol. Chem. 265 (35): 21859–66. PMID 2174888. 
• Wang AM, Schindler D, Desnick R (1990). "Schindler disease: the molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes an infantile neuroaxonal dystrophy.". J. Clin. Invest. 86 (5): 1752–6. doi:10.1172/JCI114901. PMC 296929. PMID 2243144. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=296929. 
• Warner TG, Louie A, Potier M (1991). "Photolabeling of the alpha-neuraminidase/beta-galactosidase complex from human placenta with a photoreactive neuraminidase inhibitor.". Biochem. Biophys. Res. Commun. 173 (1): 13–9. doi:10.1016/S0006-291X(05)81014-9. PMID 2256909. 
• Yamauchi T, Hiraiwa M, Kobayashi H, et al. (1990). "Molecular cloning of two species of cDNAs for human alpha-N-acetylgalactosaminidase and expression in mammalian cells.". Biochem. Biophys. Res. Commun. 170 (1): 231–7. doi:10.1016/0006-291X(90)91264-S. PMID 2372288. 
• Tsuji S, Yamauchi T, Hiraiwa M, et al. (1989). "Molecular cloning of a full-length cDNA for human alpha-N-acetylgalactosaminidase (alpha-galactosidase B).". Biochem. Biophys. Res. Commun. 163 (3): 1498–504. doi:10.1016/0006-291X(89)91149-2. PMID 2551294. 
• Chabás A, Coll MJ, Aparicio M, Rodriguez Diaz E (1995). "Mild phenotypic expression of alpha-N-acetylgalactosaminidase deficiency in two adult siblings.". J. Inherit. Metab. Dis. 17 (6): 724–31. doi:10.1007/BF00712015. PMID 7707696. 
• Wang AM, Kanzaki T, Desnick RJ (1994). "The molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes angiokeratoma corporis diffusum with glycopeptiduria.". J. Clin. Invest. 94 (2): 839–45. doi:10.1172/JCI117404. PMC 296165. PMID 8040340. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=296165. 
• de Jong J, van den Berg C, Wijburg H, et al. (1994). "alpha-N-acetylgalactosaminidase deficiency with mild clinical manifestations and difficult biochemical diagnosis.". J. Pediatr. 125 (3): 385–91. doi:10.1016/S0022-3476(05)83281-0. PMID 8071745. 
• Keulemans JL, Reuser AJ, Kroos MA, et al. (1996). "Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype.". J. Med. Genet. 33 (6): 458–64. doi:10.1136/jmg.33.6.458. PMC 1050630. PMID 8782044. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1050630. 
• Den Tandt WR, Scharpé S (1997). "Micromethod for the fluorimetric determination of plasma N-acetyl-alpha-D-galactosaminidase and study of some of its characteristics.". Enzyme Protein 49 (5–6): 273–80. PMID 9252785. 
• Gaudet R, Savage JR, McLaughlin JN, et al. (1999). "A molecular mechanism for the phosphorylation-dependent regulation of heterotrimeric G proteins by phosducin". Mol. Cell 3 (5): 649–60. doi:10.1016/S1097-2765(00)80358-5. PMID 10360181. 
• Dunham I, Shimizu N, Roe BA, et al. (1999). "The DNA sequence of human chromosome 22". Nature 402 (6761): 489–95. doi:10.1038/990031. PMID 10591208. 
• Ohta M, Ohnishi T, Ioannou YA, et al. (2000). "Human alpha-N-acetylgalactosaminidase: site occupancy and structure of N-linked oligosaccharides". Glycobiology 10 (3): 251–61. doi:10.1093/glycob/10.3.251. PMID 10704524. 
• Kodama K, Kobayashi H, Abe R, et al. (2001). "A new case of alpha-N-acetylgalactosaminidase deficiency with angiokeratoma corporis diffusum, with Ménière's syndrome and without mental retardation". Br. J. Dermatol. 144 (2): 363–8. doi:10.1046/j.1365-2133.2001.04028.x. PMID 11251574. 
• Mohamad SB, Nagasawa H, Uto Y, Hori H (2003). "Tumor cell alpha-N-acetylgalactosaminidase activity and its involvement in GcMAF-related macrophage activation". Comp. Biochem. Physiol., Part a Mol. Integr. Physiol. 132 (1): 1–8. doi:10.1016/S1095-6433(01)00522-0. PMID 12062184. 
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=139241. 
• Collins JE, Wright CL, Edwards CA, et al. (2005). "A genome annotation-driven approach to cloning the human ORFeome". Genome Biol. 5 (10): R84. doi:10.1186/gb-2004-5-10-r84. PMC 545604. PMID 15461802. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=545604.