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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Dihydroxyacetone phosphate acyltransferase
Summary
- UniProt ID
- O15228
- Gene Symbol
-
- GNPAT
- DAPAT
- DHAPAT
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- O15228
- PubChem
- O15228
- SwissLipids
- The Human Metabolome Database
- HMDBP01543
- The O-GlcNAc Database
- O15228
Annotation
- Keyword
-
- Acetylation
- Acyltransferase
- Alternative splicing
- Cataract
- Direct protein sequencing
- Disease variant
- Dwarfism
- Membrane
- Peroxisome
- Phosphoprotein
- Reference proteome
- Rhizomelic chondrodysplasia punctata
- Gene Ontology (GO)
| GO Term |
|---|
| plasma membrane |
| membrane |
| peroxisome |
| cytosol |
| mitochondrial membrane |
| peroxisomal membrane |
| peroxisomal matrix |
| GO Term |
|---|
| glycerone-phosphate O-acyltransferase activity |
| glycerol-3-phosphate O-acyltransferase activity |
Sequence
MESSSSSNSYFSVGPTSPSAVVLLYSKELKKWDEFEDILEERRHVSDLKFAMKCYTPLVYKGITPCKPIDIKCSVLNSEEIHYVIKQLSKESLQSVDVLREEVSEILDEMSHKLRLGAIRFCAFTLSKVFKQIFSKVCVNEEGIQKLQRAIQEHPVVLLPSHRSYIDFLMLSFLLYNYDLPVPVIAAGMDFLGMKMVGELLRMSGAFFMRRTFGGNKLYWAVFSEYVKTMLRNGYAPVEFFLEGTRSRSAKTLTPKFGLLNIVMEPFFKREVFDTYLVPISISYDKILEETLYVYELLGVPKPKESTTGLLKARKILSENFGSIHVYFGDPVSLRSLAAGRMSRSSYNLVPRYIPQKQSEDMHAFVTEVAYKMELLQIENMVLSPWTLIVAVLLQNRPSMDFDALVEKTLWLKGLTQAFGGFLIWPDNKPAEEVVPASILLHSNIASLVKDQVILKVDSGDSEVVDGLMLQHITLLMCSAYRNQLLNIFVRPSLVAVALQMTPGFRKEDVYSCFRFLRDVFADEFIFLPGNTLKDFEEGCYLLCKSEAIQVTTKDILVTEKGNTVLEFLVGLFKPFVESYQIICKYLLSEEEDHFSEEQYLAAVRKFTSQLLDQGTSQCYDVLSSDVQKNALAACVRLGVVEKKKINNNCIFNVNEPATTKLEEMLGCKTPIGKPATAKL
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
|
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Peroxisomal protein import | Homo sapiens |
| Plasmalogen biosynthesis | Homo sapiens |
| Synthesis of PA | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0111029 | hemochromatosis type 1 | |
| DOID:1059 | intellectual disability | |
| DOID:10652 | Alzheimer's disease | |
| DOID:10907 | microcephaly | |
| DOID:1094 | attention deficit hyperactivity disorder | |
| DOID:11870 | Pick's disease | |
| DOID:12849 | autistic disorder | |
| DOID:1443 | cerebral degeneration | |
| DOID:14525 | Reye syndrome | |
| DOID:162 | cancer |
