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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alkyldihydroxyacetonephosphate synthase, peroxisomal
Summary
- UniProt ID
- O00116
- Gene Symbol
-
- AGPS
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- O00116
- PubChem
- O00116
- SwissLipids
- The Human Metabolome Database
- HMDBP01542
- The O-GlcNAc Database
- O00116
- RaftProt
- O00116
Annotation
- Keyword
-
- Acetylation
- Cataract
- Disease variant
- Dwarfism
- FAD
- Lipid biosynthesis
- Membrane
- Peroxisome
- Phosphoprotein
- Reference proteome
- Rhizomelic chondrodysplasia punctata
- Transferase
- Transit peptide
- Gene Ontology (GO)
| GO Term |
|---|
| lipid biosynthetic process |
| ether lipid biosynthetic process |
| GO Term |
|---|
| peroxisomal membrane |
| peroxisomal matrix |
| membrane |
| mitochondrion |
| peroxisome |
| cytosol |
| GO Term |
|---|
| alkylglycerone-phosphate synthase activity |
| FAD binding |
Sequence
MAEAAAAAGGTGLGAGASYGSAADRDRDPDPDRAGRRLRVLSGHLLGRPREALSTNECKARRAASAATAAPTATPAAQESGTIPKKRQEVMKWNGWGYNDSKFIFNKKGQIELTGKRYPLSGMGLPTFKEWIQNTLGVNVEHKTTSKASLNPSDTPPSVVNEDFLHDLKETNISYSQEADDRVFRAHGHCLHEIFLLREGMFERIPDIVLWPTCHDDVVKIVNLACKYNLCIIPIGGGTSVSYGLMCPADETRTIISLDTSQMNRILWVDENNLTAHVEAGITGQELERQLKESGYCTGHEPDSLEFSTVGGWVSTRASGMKKNIYGNIEDLVVHIKMVTPRGIIEKSCQGPRMSTGPDIHHFIMGSEGTLGVITEATIKIRPVPEYQKYGSVAFPNFEQGVACLREIAKQRCAPASIRLMDNKQFQFGHALKPQVSSIFTSFLDGLKKFYITKFKGFDPNQLSVATLLFEGDREKVLQHEKQVYDIAAKFGGLAAGEDNGQRGYLLTYVIAYIRDLALEYYVLGESFETSAPWDRVVDLCRNVKERITRECKEKGVQFAPFSTCRVTQTYDAGACIYFYFAFNYRGISDPLTVFEQTEAAAREEILANGGSLSHHHGVGKLRKQWLKESISDVGFGMLKSVKEYVDPNNIFGNRNLL
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 348 |
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Peroxisomal protein import | Homo sapiens |
| Plasmalogen biosynthesis | Homo sapiens |
| TYSND1 cleaves peroxisomal proteins | 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:0050585 | congenital generalized lipodystrophy | |
| DOID:0060292 | X-linked chondrodysplasia punctata 1 | |
| DOID:0060293 | autosomal dominant chondrodysplasia punctata | |
| DOID:0080348 | Alzheimer's disease 1 | |
| DOID:0080476 | peroxisome biogenesis disorder 1A | |
| DOID:0110035 | Alzheimer's disease 2 | |
| DOID:0110037 | Alzheimer's disease 5 | |
| DOID:0110038 | Alzheimer's disease 6 | |
| DOID:0110039 | Alzheimer's disease 7 | |
| DOID:0110041 | Alzheimer's disease 8 |
