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Lecithin-cholesterol acyltransferase

LCAT
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases LCAT, entrez:3931, lecithin-cholesterol acyltransferase
External IDs OMIM: 606967 MGI: 96755 HomoloGene: 68042 GeneCards: LCAT
Gene location (Human)
Chromosome 16 (human)
Chr. Chromosome 16 (human)
Chromosome 16 (human)
Genomic location for LCAT
Genomic location for LCAT
Band 16q22.1 Start 67,939,750 bp
End 67,944,131 bp
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000229

NM_008490

RefSeq (protein)

NP_000220

NP_032516

Location (UCSC) Chr 16: 67.94 – 67.94 Mb Chr 8: 105.94 – 105.94 Mb
PubMed search

4X96, 4XWG, 4XX1, 5BV7

NM_000229

NM_008490

NP_000220

NP_032516

Lecithin–cholesterol acyltransferase (LCAT, also called phosphatidylcholine–sterol O-acyltransferase) is an enzyme that converts free cholesterol into cholesteryl ester (a more hydrophobic form of cholesterol), which is then sequestered 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.


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Wikipedia

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