Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Tissue alpha-L-fucosidase
Summary
- UniProt ID
- P04066
- Gene Symbol
-
- FUCA1
- Organism
- Homo sapiens (human)
External Links
- GlycoProtDB
- GPDB0011351
- GlyConnect
- GlyGen
- P04066
- PubChem
- P04066
- SwissLipids
- The Human Metabolome Database
- HMDBP00875
- The O-GlcNAc Database
- P04066
- O-GlcNAcAtlas
- P04066
Annotation
- Keyword
-
- 3D-structure
- Disease variant
- Glycoprotein
- Glycosidase
- Lipid metabolism
- Lysosome
- Phosphoprotein
- Reference proteome
- Signal
- Gene Ontology (GO)
| GO Term |
|---|
| glycosaminoglycan catabolic process |
| fucose metabolic process |
| glycolipid catabolic process |
| glycoside catabolic process |
| GO Term |
|---|
| extracellular exosome |
| azurophil granule lumen |
| lysosomal lumen |
| extracellular region |
| cytoplasm |
| lysosome |
| intracellular membrane-bounded organelle |
| GO Term |
|---|
| alpha-L-fucosidase activity |
Sequence
MRAPGMRSRPAGPALLLLLLFLGAAESVRRAQPPRRYTPDWPSLDSRPLPAWFDEAKFGVFIHWGVFSVPAWGSEWFWWHWQGEGRPQYQRFMRDNYPPGFSYADFGPQFTARFFHPEEWADLFQAAGAKYVVLTTKHHEGFTNWPSPVSWNWNSKDVGPHRDLVGELGTALRKRNIRYGLYHSLLEWFHPLYLLDKKNGFKTQHFVSAKTMPELYDLVNSYKPDLIWSDGEWECPDTYWNSTNFLSWLYNDSPVKDEVVVNDRWGQNCSCHHGGYYNCEDKFKPQSLPDHKWEMCTSIDKFSWGYRRDMALSDVTEESEIISELVQTVSLGGNYLLNIGPTKDGLIVPIFQERLLAVGKWLSINGEAIYASKPWRVQWEKNTTSVWYTSKGSAVYAIFLHWPENGVLNLESPITTSTTKITMLGIQGDLKWSTDPDKGLFISLPQLPPSAVPAEFAWTIKLTGVK
Glycosylation Sites
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Neutrophil degranulation | Homo sapiens |
| Reactions specific to the complex N-glycan synthesis pathway | 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:4766 | embryoma | |
| DOID:479 | angiokeratoma | |
| DOID:526 | human immunodeficiency virus infectious disease | |
| DOID:5672 | large intestine cancer | |
| DOID:574 | peripheral nervous system disease | |
| DOID:635 | acquired immunodeficiency syndrome | |
| DOID:6688 | autoimmune lymphoproliferative syndrome | |
| DOID:811 | lipodystrophy | |
| DOID:870 | neuropathy | |
| DOID:8927 | learning disability |
