Lecithin–cholesterol acyltransferase

LCAT
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesLCAT, entrez:3931, lecithin-cholesterol acyltransferase
External IDsOMIM: 606967; MGI: 96755; HomoloGene: 68042; GeneCards: LCAT; OMA:LCAT - orthologs
Orthologs
SpeciesHumanMouse
Entrez

3931

16816

Ensembl

ENSG00000213398

ENSMUSG00000035237

UniProt

P04180

P16301

RefSeq (mRNA)

NM_000229

NM_008490

RefSeq (protein)

NP_000220

NP_032516

Location (UCSC)Chr 16: 67.94 – 67.94 MbChr 8: 106.67 – 106.67 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Lecithin–cholesterol acyltransferase (LCAT, also called phosphatidylcholine–sterol O-acyltransferase) is an enzyme found in many animals, including humans. It converts free cholesterol into cholesteryl ester, a more hydrophobic form of cholesterol. This process sequesters cholesterol ester into the core of a lipoprotein particle, eventually making the newly synthesized HDL spherical and forcing the reaction to become unidirectional since the particles are removed from the surface. The enzyme is bound to high-density lipoproteins (HDLs) (alpha-LCAT) and LDLs (beta-LCAT) in the blood plasma. LCAT deficiency can cause impaired vision due to cholesterol corneal opacities, anemia, and kidney damage. It belongs to the family of phospholipid:diacylglycerol acyltransferases.