" /> lipoprotein lipase - CISMeF





Preferred Label : lipoprotein lipase;

MeSH definition : An enzyme of the hydrolase class that catalyzes the reaction of triacylglycerol and water to yield diacylglycerol and a fatty acid anion. The enzyme hydrolyzes triacylglycerols in chylomicrons, very-low-density lipoproteins, low-density lipoproteins, and diacylglycerols. It occurs on capillary endothelial surfaces, especially in mammary, muscle, and adipose tissue. Genetic deficiency of the enzyme causes familial hyperlipoproteinemia Type I. (Dorland, 27th ed) EC 3.1.1.34.;

MeSH synonym : lipase, postheparin lipoprotein; lipase, postheparin; factor, heparin-clearing; lipoprotein lipase, postheparin; post-heparin lipase; heparin-clearing factor; postheparin lipase; lipase, diacylglycerol; postheparin lipoprotein lipase; diacylglycerol lipase; lipemia-clearing factor; lipase, lipoprotein; diglyceride lipase; lipase, diglyceride; heparin clearing factor; lipase, post-heparin; post heparin lipase; factor, lipemia-clearing; lipemia clearing factor;

MeSH CAS label : triacylglycero-protein acylhydrolase;

Registry Number MeSH : EC 3.1.1.34;

MeSH annotation : /defic: consider also HYPERLIPOPROTEINEMIA TYPE I;

Wikipedia link : https://en.wikipedia.org/wiki/Lipoprotein lipase;

Is substance : O;

UNII : EC 3.1.1.34;

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An enzyme of the hydrolase class that catalyzes the reaction of triacylglycerol and water to yield diacylglycerol and a fatty acid anion. The enzyme hydrolyzes triacylglycerols in chylomicrons, very-low-density lipoproteins, low-density lipoproteins, and diacylglycerols. It occurs on capillary endothelial surfaces, especially in mammary, muscle, and adipose tissue. Genetic deficiency of the enzyme causes familial hyperlipoproteinemia Type I. (Dorland, 27th ed) EC 3.1.1.34.

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26/04/2025


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