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Bile acid-CoA:amino acid N-acyltransferase

Below are the list of possible Bile acid-CoA:amino acid N-acyltransferase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.

Bile acid-CoA:amino acid N-acyltransferase

 Bile acid-CoA:amino acid N-acyltransferase ELISA Kit
 Bile acid-CoA:amino acid N-acyltransferase Recombinant
 Bile acid-CoA:amino acid N-acyltransferase Antibody
Also known as Bile acid-CoA:amino acid N-acyltransferase (BACAT) (BAT) (Glycine N-choloyltransferase) (Kan-1) (Long-chain fatty-acyl-CoA hydrolase).
BAAT: Involved in bile acid metabolism. In liver hepatocytes catalyzes the second step in the conjugation of C24 bile acids (choloneates) to glycine and taurine before excretion into bile canaliculi. The major components of bile are cholic acid and
chenodeoxycholic acid. In a first step the bile acids are converted to an acyl-CoA thioester, either in peroxisomes (primary bile acids deriving from the cholesterol pathway), or cytoplasmic at the endoplasmic reticulum (secondary bile acids). May catalyze the conjugation of primary or secondary bile acids, or both. The conjugation increases the detergent properties of bile acids in the intestine, which facilitates lipid and fat-soluble vitamin absorption. In turn, bile acids are deconjugated by bacteria in the intestine and are recycled back to the liver for reconjugation (secondary bile acids). May also act as an acyl-CoA thioesterase that regulates intracellular levels of free fatty acids. In vitro, catalyzes the hydrolysis of long- and very long-chain saturated acyl-CoAs to the free fatty acid and coenzyme A (CoASH), and conjugates glycine to these acyl-CoAs. Defects in BAAT are involved in familial hypercholanemia (FHCA). FHCA is a disorder characterized by elevated serum bile acid concentrations, itching, and fat malabsorption. Belongs to the C/M/P thioester hydrolase family.

Protein type: EC; EC; Hydrolase; Lipid Metabolism - primary bile acid biosynthesis; Lipid Metabolism - unsaturated fatty acid biosynthesis; Other Amino Acids Metabolism - taurine and hypotaurine; Transferase

Cellular Component: cytosol; peroxisome

Molecular Function: glycine N-choloyltransferase activity; N-acyltransferase activity; receptor binding

Biological Process: acyl-CoA metabolic process; bile acid biosynthetic process; bile acid metabolic process; glycine metabolic process; liver development; organ regeneration; taurine metabolic process
 Baat ELISA Kit
 Baat Recombinant
 Baat Antibody
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