Target intelligence / Profile preview

Lactase-phlorizin hydrolase (None)

Target
None
Molecular classification
Enzyme, Glycoprotein, Hydrolase, Membrane-bound protein
01

Overview

Lactase-phlorizin hydrolase (LPH) is a membrane-bound glycoprotein enzyme primarily found in the brush border of enterocytes in the small intestine. It plays a crucial role in carbohydrate digestion, particularly lactose, and also hydrolyzes certain glycosides such as phlorizin. Deficiency or malfunction results in primary or secondary lactose intolerance due to inability to digest dietary lactose. Polymorphisms leading to persistent expression allow continued milk digestion into adulthood—a trait selected for in some populations. Congenital mutations cause rare but severe forms of neonatal-onset malabsorption syndromes.

Other names
LactaseLPHLPH1Lactase-glycosylceramidase
02

Mechanism of action

LPH hydrolyzes lactose into D-glucose and D-galactose, and also hydrolyzes phlorizin and other β-glycosides.

03

Biological functions

Hydrolysis of lactoseHydrolysis of phlorizinCarbohydrate digestion
04

Disease associations

Lactose intoleranceCongenital lactase deficiencyMalabsorption syndromes
05

Safety considerations

Lactose intolerance due to deficiency or malfunction of LPH

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