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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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Guidelines
MIRAGE
Apolipoprotein A-I
Summary
- UniProt ID
- P02647
- Gene Symbol
-
- APOA1
- Gene ID
- 335
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P02647
- PubChem
- P02647
- The Human Metabolome Database
- HMDBP01620
- RaftProt
- P02647
- Re-Glyco
- P02647
Annotation
- Keyword
-
- 3D-structure
- Amyloid
- Amyloidosis
- Atherosclerosis
- Cholesterol metabolism
- Direct protein sequencing
- Disease variant
- Glycation
- HDL
- Lipid transport
- Neuropathy
- Oxidation
- Palmitate
- Phosphoprotein
- Reference proteome
- Repeat
- Secreted
- Signal
- Gene Ontology (GO)
| GO Term |
|---|
| endocytic vesicle lumen |
| spherical high-density lipoprotein particle |
| extracellular vesicle |
| extracellular region |
| extracellular space |
| plasma membrane |
| cytoplasmic vesicle |
| chylomicron |
| collagen-containing extracellular matrix |
| endocytic vesicle |
Sequence
MKAAVLTLAVLFLTGSQARHFWQQDEPPQSPWDRVKDLATVYVDVLKDSGRDYVSQFEGSALGKQLNLKLLDNWDSVTSTFSKLREQLGPVTQEFWDNLEKETEGLRQEMSKDLEEVKAKVQPYLDDFQKKWQEEMELYRQKVEPLRAELQEGARQKLHELQEKLSPLGEEMRDRARAHVDALRTHLAPYSDELRQRLAARLEALKENGGARLAEYHAKATEHLSTLSEKAKPALEDLRQGLLPVLESFKVSFLSALEEYTKKLNTQ
Glycosylation Sites
G57321FI
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| ABC transporters in lipid homeostasis | Homo sapiens |
| Amyloid fiber formation | Homo sapiens |
| Chylomicron assembly | Homo sapiens |
| Chylomicron remodeling | Homo sapiens |
| Defective ABCA1 causes TGD | Homo sapiens |
| HDL assembly | Homo sapiens |
| HDL clearance | Homo sapiens |
| HDL remodeling | Homo sapiens |
| Heme signaling | Homo sapiens |
| PPARA activates gene expression | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | |
| DOID:0080958 | primary hypoalphalipoproteinemia 2 | |
| DOID:10652 | Alzheimer's disease | |
| DOID:13810 | familial hypercholesterolemia | |
| DOID:1387 | hypolipoproteinemia | |
| DOID:1936 | atherosclerosis | |
| DOID:5844 | myocardial infarction | |
| DOID:9074 | systemic lupus erythematosus |
