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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alpha-N-acetylglucosaminidase
Summary
- UniProt ID
- P54802
- Gene Symbol
-
- NAGLU
- UFHSD1
- Organism
- Homo sapiens (human)
External Links
- GlycoProtDB
- GPDB0011738
- GlyConnect
- GlyGen
- P54802
- PubChem
- P54802
- The Human Metabolome Database
- HMDBP01596
- The O-GlcNAc Database
- P54802
Annotation
- Keyword
-
- 3D-structure
- Charcot-Marie-Tooth disease
- Direct protein sequencing
- Disease variant
- Glycoprotein
- Glycosidase
- Lysosome
- Mucopolysaccharidosis
- Neurodegeneration
- Reference proteome
- Signal
- Gene Ontology (GO)
| GO Term |
|---|
| lysosome |
| extracellular exosome |
| lysosomal lumen |
| GO Term |
|---|
| alpha-N-acetylglucosaminidase activity |
Sequence
MEAVAVAAAVGVLLLAGAGGAAGDEAREAAAVRALVARLLGPGPAADFSVSVERALAAKPGLDTYSLGGGGAARVRVRGSTGVAAAAGLHRYLRDFCGCHVAWSGSQLRLPRPLPAVPGELTEATPNRYRYYQNVCTQSYSFVWWDWARWEREIDWMALNGINLALAWSGQEAIWQRVYLALGLTQAEINEFFTGPAFLAWGRMGNLHTWDGPLPPSWHIKQLYLQHRVLDQMRSFGMTPVLPAFAGHVPEAVTRVFPQVNVTKMGSWGHFNCSYSCSFLLAPEDPIFPIIGSLFLRELIKEFGTDHIYGADTFNEMQPPSSEPSYLAAATTAVYEAMTAVDTEAVWLLQGWLFQHQPQFWGPAQIRAVLGAVPRGRLLVLDLFAESQPVYTRTASFQGQPFIWCMLHNFGGNHGLFGALEAVNGGPEAARLFPNSTMVGTGMAPEGISQNEVVYSLMAELGWRKDPVPDLAAWVTSFAARRYGVSHPDAGAAWRLLLRSVYNCSGEACRGHNRSPLVRRPSLQMNTSIWYNRSDVFEAWRLLLTSAPSLATSPAFRYDLLDLTRQAVQELVSLYYEEARSAYLSKELASLLRAGGVLAYELLPALDEVLASDSRFLLGSWLEQARAAAVSEAEADFYEQNSRYQLTLWGPEGNILDYANKQLAGLVANYYTPRWRLFLEALVDSVAQGIPFQQHQFDKNVFQLEQAFVLSKQRYPSQPRGDTVDLAKKIFLKYYPRWVAGSW
Glycosylation Sites
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| HS-GAG degradation | Homo sapiens |
| MPS IIIB - Sanfilippo syndrome B | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070094 | oculocutaneous albinism type IA | |
| DOID:0050572 | cone-rod dystrophy | |
| DOID:0050699 | Dent disease | |
| DOID:0050908 | myelodysplastic syndrome | |
| DOID:0060162 | dentatorubral-pallidoluysian atrophy | |
| DOID:0060823 | syndromic X-linked intellectual disability 94 | |
| DOID:0060891 | Parkinson's disease 19A | |
| DOID:0060895 | Parkinson's disease 4 | |
| DOID:0060896 | Parkinson's disease 23 | |
| DOID:0070226 | progressive familial intrahepatic cholestasis 1 |
