N-acylethanolamine acid amide hydrolase - significado y definición. Qué es N-acylethanolamine acid amide hydrolase
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Qué (quién) es N-acylethanolamine acid amide hydrolase - definición


N-acylethanolamine acid amide hydrolase         
  • This mechanism shows the inhibition of the catalytic cysteine by the most-tested β-lactone, ARN077.
  • This is the speculated mechanism for the hydrolysis of ethanolamides by NAAA, which is very similar to that of acid ceramise.
MEMBER OF THE CHOLOYLGLYCINE HYDROLASE FAMILY
N-acylethanolamine acid amide hydrolase (NAAA) is a member of the choloylglycine hydrolase family, a subset of the N-terminal nucleophile hydrolase superfamily. NAAA has a molecular weight of 31 kDa.
N-Acylethanolamine         
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CLASS OF CHEMICAL COMPOUNDS
N-acylethanolamine; N-acylethanolamines
An N-acylethanolamine (NAE) is a type of fatty acid amide formed when one of several types of acyl group is linked to the nitrogen atom of ethanolamine. These amides conceptually can be formed from a fatty acid and ethanolamine with the release of a molecule of water, but the known biological synthesis uses a specific phospholipase D to cleave the phospholipid unit from N-acylphosphatidylethanolamines.
Fatty acid amide hydrolase         
MAMMALIAN PROTEIN FOUND IN HOMO SAPIENS
Fatty acyl amide hydrolase; FAAH; EC 3.5.1.99; Oleamide hydrolase; Anandamide amidohydrolase; FAAH inhibitor; Fatty acylamide amidohydrolase; FAAH-OUT
Fatty acid amide hydrolase or FAAH (, oleamide hydrolase, anandamide amidohydrolase) is a member of the serine hydrolase family of enzymes. It was first shown to break down anandamide in 1993.