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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Phosphatidylcholine-sterol acyltransferase
Summary
- UniProt ID
- P04180
- Gene Symbol
-
- LCAT
- Organism
- Homo sapiens (human)
External Links
- GlycoProtDB
- GPDB0011357
- GlyConnect
- GlyGen
- P04180
- PubChem
- P04180
- SwissLipids
- The Human Metabolome Database
- HMDBP00069
Annotation
- Keyword
-
- 3D-structure
- Acyltransferase
- Cholesterol metabolism
- Corneal dystrophy
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Glycoprotein
- Hydrolase
- Reference proteome
- Secreted
- Signal
- Gene Ontology (GO)
| GO Term |
|---|
| extracellular region |
| extracellular space |
| extracellular exosome |
| high-density lipoprotein particle |
Sequence
MGPPGSPWQWVTLLLGLLLPPAAPFWLLNVLFPPHTTPKAELSNHTRPVILVPGCLGNQLEAKLDKPDVVNWMCYRKTEDFFTIWLDLNMFLPLGVDCWIDNTRVVYNRSSGLVSNAPGVQIRVPGFGKTYSVEYLDSSKLAGYLHTLVQNLVNNGYVRDETVRAAPYDWRLEPGQQEEYYRKLAGLVEEMHAAYGKPVFLIGHSLGCLHLLYFLLRQPQAWKDRFIDGFISLGAPWGGSIKPMLVLASGDNQGIPIMSSIKLKEEQRITTTSPWMFPSRMAWPEDHVFISTPSFNYTGRDFQRFFADLHFEEGWYMWLQSRDLLAGLPAPGVEVYCLYGVGLPTPRTYIYDHGFPYTDPVGVLYEDGDDTVATRSTELCGLWQGRQPQPVHLLPLHGIQHLNMVFSNLTLEHINAILLGAYRQGPPASPTASPEPPPPE
Glycosylation Sites
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| HDL remodeling | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110205 | Charcot-Marie-Tooth disease dominant intermediate E | |
| DOID:0110206 | Charcot-Marie-Tooth disease dominant intermediate F | |
| DOID:0110207 | Charcot-Marie-Tooth disease X-linked dominant 6 | |
| DOID:0110208 | Charcot-Marie-Tooth disease X-linked recessive 2 | |
| DOID:0110209 | Charcot-Marie-Tooth disease X-linked dominant 1 | |
| DOID:0110210 | Charcot-Marie-Tooth disease X-linked recessive 5 | |
| DOID:0110211 | Charcot-Marie-Tooth disease X-linked recessive 3 | |
| DOID:0110212 | Charcot-Marie-Tooth disease X-linked recessive 4 | |
| DOID:0111368 | cholesterol-ester transfer protein deficiency | |
| DOID:0111369 | hyperalphalipoproteinemia 1 |
