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Alpha-N-acetylgalactosaminidase

Summary

UniProt ID

P17050

Gene Symbol

NAGA

Organism

Homo sapiens (human)

External Links

GlyConnect

GlyGen

P17050

PubChem

P17050

SwissLipids

SLP:000001402

The Human Metabolome Database

HMDBP00433

The O-GlcNAc Database

P17050

Annotation

Keyword

3D-structure
Direct protein sequencing
Disease variant
Disulfide bond
Epilepsy
Glycoprotein
Glycosidase
Lipid metabolism
Lysosome
Phosphoprotein
Reference proteome
Signal

Gene Ontology (GO)

Displaying **all 4** entries
GO Term
oligosaccharide metabolic process
carbohydrate catabolic process
glycolipid catabolic process
glycoside catabolic process

Displaying **all 3** entries
GO Term
cytoplasm
lysosome
extracellular exosome

Displaying **all 3** entries
GO Term
protein homodimerization activity
alpha-galactosidase activity
alpha-N-acetylgalactosaminidase activity

Annotation information from UniProt.

Sequence

MLLKTVLLLGHVAQVLMLDNGLLQTPPMGWLAWERFRCNINCDEDPKNCISEQLFMEMADRMAQDGWRDMGYTYLNIDDCWIGGRDASGRLMPDPKRFPHGIPFLADYVHSLGLKLGIYADMGNFTCMGYPGTTLDKVVQDAQTFAEWKVDMLKLDGCFSTPEERAQGYPKMAAALNATGRPIAFSCSWPAYEGGLPPRVNYSLLADICNLWRNYDDIQDSWWSVLSILNWFVEHQDILQPVAGPGHWNDPDMLLIGNFGLSLEQSRAQMALWTVLAAPLLMSTDLRTISAQNMDILQNPLMIKINQDPLGIQGRRIHKEKSLIEVYMRPLSNKASALVFFSCRTDMPYRYHSSLGQLNFTGSVIYEAQDVYSGDIISGLRDETNFTVIINPSGVVMWYLYPIKNLEMSQQ

N : N-glycosylation Site
___ : Potential Sequon

Glycosylation Sites

Displaying **all 6** entries
Position	Description	PubMed ID	GlyTouCan ID	Source
124	N-linked (GlcNAc...) asparagine	19683538	G91413ZX G63889NK G17689DH G77252PU G45359RY G86357DX G44444MB G23984SE G29857RC G79809MM G93284HQ G66129DI G78059CC G03275SD G10486CT G36191CD G16828VN G71470CO G72735IY G97720QM G05724UK G31852PQ G83161QT G90575OW G61334IA G39188ZX G41247ZX G80966KZ G25637MV G50282JC G02815KT G06110VR G07617FP G00406II G84349RE G92050GC G74724QE G82348BZ G92275SC G14669DU	UniProt GlyGen GlyConnect
177	N-linked (GlcNAc...) asparagine	19159218 19683538	G91413ZX G63889NK G17689DH G77252PU G45359RY G86357DX G44444MB G29857RC G79809MM G93284HQ G66129DI G20210JR G78059CC G03275SD G12313PD G82463GQ G36191CD G16828VN G71470CO G72291OX G97720QM G83161QT G61334IA G39188ZX G80966KZ G02815KT G07617FP G82348BZ	UniProt GlyGen GlyConnect
201	N-linked (GlcNAc...) asparagine	19159218	G91413ZX G63889NK G17689DH G77252PU G45359RY G86357DX G44444MB G83460ZZ G29857RC G79809MM G93284HQ G66129DI G78059CC G03275SD G36191CD G16828VN G71470CO G97720QM G31852PQ G83161QT G61334IA G41247ZX G80966KZ G02815KT G07617FP G82348BZ	UniProt GlyGen
359	N-linked (GlcNAc...) asparagine		G91413ZX G63889NK G17689DH G77252PU G45359RY G86357DX G44444MB G29857RC G79809MM G93284HQ G66129DI G78059CC G03275SD G36191CD G16828VN G71470CO G97720QM G83161QT G61334IA G80966KZ G07617FP G82348BZ G92275SC	UniProt GlyGen
385	N-linked (GlcNAc...) asparagine	19683538	G91413ZX G63889NK G17689DH G77252PU G45359RY G86357DX G44444MB G29857RC G79809MM G93284HQ G66129DI G78059CC G03275SD G36191CD G16828VN G71470CO G97720QM G83161QT G61334IA G80966KZ G07617FP G82348BZ	UniProt GlyGen
			G14389GM G39595FH G57789QC G64394MX G15169WU G45209NR G91413ZX G34617SM G45546UR G01543ZX G11629QQ G74239ZQ G63889NK G90093AU G00155YT G53280MT G81263BG G17689DH G22310AV G61962FK G48414YA G77252PU G78790NZ G81349OI G45359RY G72797UR G86357DX G61138BO G44444MB G84452RH G51640FO G55521GY G20425TQ G29857RC G79809MM G60723SV G59575FI G06356OH G93284HQ G03842KQ G66129DI G33282QL G03382KH G75594YZ G90717TP G05808PZ G23863VK G78059CC G03275SD G12849CJ G97183VL G20512LK G36191CD G50045TK G14889BN G03005MJ G16828VN G71470CO G72735IY G72291OX G97720QM G05724UK G83161QT G93180LE G06885ZB G29880MM G61334IA G39188ZX G80966KZ G90448RI G82350PP G06110VR G07617FP G55220VL G74724QE G82348BZ G14669DU G22768VO G49108TO	GlyGen The O-GlcNAc Database GlyConnect

Feature

: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt

Human Protein Atlas

ENSG00000198951

Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.

Data available from v23.0.proteinatlas.org. Image credit: Human Protein Atlas

Disease

Displaying entries **1 - 10** of 50 in total

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DO ID	Disease Name	Source
DOID:1826	epilepsy	DisGeNET
DOID:0050635	alternating hemiplegia of childhood	DisGeNET
DOID:0050700	cardiomyopathy	DisGeNET DisGeNET
DOID:0050841	focal hand dystonia	DisGeNET
DOID:0060262	gallbladder disease	DisGeNET
DOID:0060357	chylomicron retention disease	DisGeNET
DOID:0060823	syndromic X-linked intellectual disability 94	DisGeNET
DOID:0080326	familial hypertrophic cardiomyopathy	DisGeNET
DOID:0110735	neurodegeneration with brain iron accumulation 2a	DisGeNET
DOID:0112318	Schindler disease type 1	Glyco-Disease Genes Database

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

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