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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Lipoprotein lipase
Summary
- UniProt ID
- P06858
- Gene Symbol
-
- LPL
- LIPD
- Organism
- Homo sapiens (human)
External Links
- GlyConnect
- GlyGen
- P06858
- PubChem
- P06858
- SwissLipids
- The Human Metabolome Database
- HMDBP00310
- The O-GlcNAc Database
- P06858
Annotation
- Keyword
-
- 3D-structure
- Calcium
- Cell membrane
- Chylomicron
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Extracellular matrix
- Glycoprotein
- Heparin-binding
- Hydrolase
- Hyperlipidemia
- Lipid degradation
- Metal-binding
- Nitration
- Reference proteome
- Signal
- VLDL
- Gene Ontology (GO)
| GO Term |
|---|
| extracellular region |
| extracellular space |
| plasma membrane |
| catalytic complex |
| cell surface |
| very-low-density lipoprotein particle |
| chylomicron |
Sequence
MESKALLVLTLAVWLQSLTASRGGVAAADQRRDFIDIESKFALRTPEDTAEDTCHLIPGVAESVATCHFNHSSKTFMVIHGWTVTGMYESWVPKLVAALYKREPDSNVIVVDWLSRAQEHYPVSAGYTKLVGQDVARFINWMEEEFNYPLDNVHLLGYSLGAHAAGIAGSLTNKKVNRITGLDPAGPNFEYAEAPSRLSPDDADFVDVLHTFTRGSPGRSIGIQKPVGHVDIYPNGGTFQPGCNIGEAIRVIAERGLGDVDQLVKCSHERSIHLFIDSLLNEENPSKAYRCSSKEAFEKGLCLSCRKNRCNNLGYEINKVRAKRSSKMYLKTRSQMPYKVFHYQVKIHFSGTESETHTNQAFEISLYGTVAESENIPFTLPEVSTNKTYSFLIYTEVDIGELLMLKLKWKSDSYFSWSDWWSSPGFAIQKIRVKAGETQKKVIFCSREKVSHLQKGKAPAVFVKCHDKSLNKKSG
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 70 | N-linked (GlcNAc...) asparagine | |||
| 386 | N-linked (GlcNAc...) asparagine |
|
||
| 417 |
|
|
||
|
|
G50427EO
G77582RK
G20312EM
G11629QQ
G86795LJ
G96577RX
G81263BG
G47012YE
G51413EV
G08146BT
G22310AV
G66163OV
G71146HJ
G75983OB
G42358LZ
G48414YA
G72797UR
G25451PN
G45495MK
G84452RH
G06356OH
G37868ZX
G80920RR
G23863VK
G57818FI
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Assembly of active LPL and LIPC lipase complexes | Homo sapiens |
| Chylomicron remodeling | Homo sapiens |
| Retinoid metabolism and transport | Homo sapiens |
| Transcriptional regulation of white adipocyte differentiation | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110759 | type 1 diabetes mellitus 22 | |
| DOID:0110760 | type 1 diabetes mellitus 23 | |
| DOID:0110761 | type 1 diabetes mellitus 24 | |
| DOID:0110892 | inflammatory bowel disease 1 | |
| DOID:0111095 | Fanconi anemia complementation group A | |
| DOID:0111135 | congenital generalized lipodystrophy type 1 | |
| DOID:0111136 | congenital generalized lipodystrophy type 2 | |
| DOID:0111137 | congenital generalized lipodystrophy type 3 | |
| DOID:0111138 | congenital generalized lipodystrophy type 4 | |
| DOID:0111218 | Friedreich ataxia 1 |
