Lysosomal lipase

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lipase A, lysosomal acid, cholesterol esterase (Wolman disease)
Identifiers
Symbol	LIPA
Entrez	3988
HUGO	6617
OMIM	278000
RefSeq	NM_000235
UniProt	P38571
Other data
EC number	3.1.1.3
Locus	Chr. 10 q23.2-23.3

Lysosomal lipase is a form of lipase which functions intracellularly, in the lysosomes.

[edit] Clinical significance

A deficiency is associated with Wolman disease.

Chlorpromazine is an inhibitor of lysosomal lipase.^[1]

[edit] References

1. ^ Sauro VS, Klamut HJ, Lin CH, Strickland KP (1985). "Lysosomal triacylglycerol lipase activity in L6 myoblasts and its changes on differentiation". Biochem. J. 227 (2): 583–9. PMID 4004781. 

[edit] External links

• MeSH lysosomal+acid+lipase,+human

v • d • e Hydrolase: esterases (EC 3.1) 3.1.1: Carboxylic ester hydrolases Cholinesterase - Pectinesterase - 6-phosphogluconolactonase - PAF acetylhydrolase Lipase (Gastric/Lingual, Pancreatic, Lysosomal, Hormone-sensitive, Endothelial, Hepatic, Lipoprotein, Monoacylglycerol, Diacylglycerol) Phospholipase (A1, A2, B) 3.1.2: Thioesterase Palmitoyl thioesterase - Ubiquitin carboxy-terminal hydrolase L1 3.1.3: Phosphatase Alkaline phosphatase - Acid phosphatase (Prostatic)/Tartrate resistant acid phosphatase/Purple acid phosphatases - Nucleotidase - Glucose 6-phosphatase - Fructose 1,6-bisphosphatase - Calcineurin - Phosphoprotein phosphatase (PP2A) - OCRL - Pyruvate dehydrogenase phosphatase - Fructose 2,6-bisphosphatase - Protein tyrosine phosphatase - PTEN 3.1.4: Phosphodiesterase Autotaxin - Phospholipase (C, D) - Sphingomyelin phosphodiesterase - PDE1 - PDE2 - PDE3 - PDE5 3.1.6: Sulfatase Arylsulfatase B - Steroid sulfatase - Galactosamine-6 sulfatase - Arylsulfatase A - Iduronate-2-sulfatase - N-acetylglucosamine-6-sulfatase other Nuclease