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chenodeoxycholoyl-CoA + glycine
CoA + glycochenodeoxycholate
chenodeoxycholoyl-CoA + taurine
CoA + taurochenodeoxycholate
choloyl-CoA + 2-fluoro-beta-alanine
?
-
-
-
?
choloyl-CoA + 2-fluoro-beta-alanine
CoA + 2-fluoro-beta-alanylcholate
-
2-fluoro-beta-alanine is an excellent substrate like taurine
-
-
?
choloyl-CoA + aminomethanesulfonic acid
?
-
-
-
?
choloyl-CoA + beta-alanine
CoA + beta-alanylcholate
choloyl-CoA + D-alpha-alanine
CoA + D-alpha-alanylcholate
-
about 10% of the rate with glycine
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
choloyl-CoA + taurine
CoA + taurocholate
deoxycholoyl-CoA + aminomethanesulfonate
CoA + aminomethanesulfonyldeoxycholate
-
-
-
-
?
deoxycholoyl-CoA + glycine
CoA + glycodeoxycholate
deoxycholoyl-CoA + taurine
CoA + taurodeoxycholate
lithocholoyl-CoA + glycine
CoA + glycolithocholate
lithocholoyl-CoA + taurine
CoA + taurolithocholate
trihydroxycholestanoyl-CoA + glycine
CoA + ?
-
very low activity
-
-
?
ursodeoxycholoyl-CoA + glycine
CoA + glycoursodeoxycholate
-
24.8% of activity with choloyl-CoA
-
-
?
ursodeoxycholoyl-CoA + taurine
CoA + tauroursodeoxycholate
-
35.3% of activity with choloyl-CoA
-
-
?
additional information
?
-
chenodeoxycholoyl-CoA + glycine
CoA + glycochenodeoxycholate
-
rate of conjugation in decreasing order: deoxycholyl-CoA, cholyl-CoA, lithocholyl-CoA, chenodeoxycholyl-CoA
-
-
?
chenodeoxycholoyl-CoA + glycine
CoA + glycochenodeoxycholate
-
91.4% of activity with choloyl-CoA
-
-
?
chenodeoxycholoyl-CoA + glycine
CoA + glycochenodeoxycholate
-
glycine is a slightly better substrate than taurine, thioesterase activity in absence of glycine is about 20% of the conjugation activity
-
-
?
chenodeoxycholoyl-CoA + glycine
CoA + glycochenodeoxycholate
-
-
-
-
?
chenodeoxycholoyl-CoA + taurine
CoA + taurochenodeoxycholate
-
-
-
-
?
chenodeoxycholoyl-CoA + taurine
CoA + taurochenodeoxycholate
-
101.4% of activity with choloyl-CoA
-
-
?
chenodeoxycholoyl-CoA + taurine
CoA + taurochenodeoxycholate
-
-
-
-
?
choloyl-CoA + beta-alanine
CoA + beta-alanylcholate
-
beta-alanine is a poor substrate
-
-
?
choloyl-CoA + beta-alanine
CoA + beta-alanylcholate
-
about 10% of the rate with glycine
-
-
?
choloyl-CoA + beta-alanine
CoA + beta-alanylcholate
-
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
rate of conjugation in decreasing order: deoxycholyl-CoA, cholyl-CoA, lithocholyl-CoA, chenodeoxycholyl-CoA
-
ir
choloyl-CoA + glycine
CoA + glycocholate
-
conjugation of bile acids in the liver with glycine or taurine prior to being secreted into the bile duct
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
taurine can replace glycine, involved in conjugation of bile acids
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
ratio of glycine-/taurine-dependent activity is 1.0-1.4
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
conjugation of bile acids with glycine or taurine favors their excretion into bile and uptake from portal blood into the liver, it promotes absorption of fat and fat-soluble vitamins in the acidic environment of the small intestine by lowering the pKa of the bile acids and hence maintaining its solubility
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
taurine can replace glycine, involved in conjugation of bile acids
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
cholesterol degradation, glycine conjugates of bile acids occur in adult
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
glycine is a slightly better substrate than taurine, thioesterase activity in absence of glycine is about 20% of the conjugation activity
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
produces taurine- but little glycine-conjugated bile acid at physiological concentrations of glycine and taurine, dietary manipulations modify the glycine:taurine ratio
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
-
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
conjugation of bile acids in the liver with glycine or taurine prior to being secreted into the bile duct
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
taurine can replace glycine, involved in conjugation of bile acids
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
synthesizes only taurine but no gylcine conjugates
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
conjugation of the CoA adducts of bile acids with taurine
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
-
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
ratio of glycine-/taurine-dependent activity is 1.0-1.4
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
taurine is an excellent substrate
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
conjugation of bile acids with glycine or taurine favors their excretion into bile and uptake from portal blood into the liver, it promotes absorption of fat and fat-soluble vitamins in the acidic environment of the small intestine by lowering the pKa of the bile acids and hence maintaining its solubility
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
taurine can replace glycine, involved in conjugation of bile acids
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
cholesterol degradation, bile acids are secreted as taurine conjugates in fetus and neonatus
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
taurine-specific enzyme, no use of glycine or fluoro-beta-alanine as substrates
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
taurine-specific enzyme, gallbladder bile contains only taurine conjugates of bile acids, bile acid conjugates increases their detergent properties, prevents their precipitation in the acidic milieu of the upper small intestine, in intestines they are responsible for the solubilization and absorption of fats, vitamins and fat-soluble compounds
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
-
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
preferred substrate
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
produces taurine- but little glycine-conjugated bile acid at physiological concentrations of glycine and taurine, dietary manipulations modify the hepatic taurine concentration and glycine:taurine ratio
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
taurine conjugates predominate in rat bile at normal hepatocellular concentrations of glycine and taurine
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
bile acid conjugation
-
-
?
deoxycholoyl-CoA + glycine
CoA + glycodeoxycholate
-
rate of conjugation in decreasing order: deoxycholyl-CoA, cholyl-CoA, lithocholyl-CoA, chenodeoxycholyl-CoA
-
-
?
deoxycholoyl-CoA + glycine
CoA + glycodeoxycholate
-
92.4% of activity with choloyl-CoA
-
-
?
deoxycholoyl-CoA + glycine
CoA + glycodeoxycholate
-
-
-
?
deoxycholoyl-CoA + taurine
CoA + taurodeoxycholate
-
81.7% of activity with choloyl-CoA
-
-
?
deoxycholoyl-CoA + taurine
CoA + taurodeoxycholate
-
-
-
?
lithocholoyl-CoA + glycine
CoA + glycolithocholate
-
rate of conjugation in decreasing order: deoxycholyl-CoA, cholyl-CoA, lithocholyl-CoA, chenodeoxycholyl-CoA
-
-
?
lithocholoyl-CoA + glycine
CoA + glycolithocholate
-
58.4% of activity with choloyl-CoA
-
-
?
lithocholoyl-CoA + glycine
CoA + glycolithocholate
-
-
-
-
?
lithocholoyl-CoA + taurine
CoA + taurolithocholate
-
43% of activity with choloyl-CoA
-
-
?
lithocholoyl-CoA + taurine
CoA + taurolithocholate
-
-
-
-
?
additional information
?
-
-
not: L-serine, beta-alanine
-
-
?
additional information
?
-
-
not as acyl-CoA donors: acetyl-CoA, phenylacetyl-CoA and benzoyl-CoA
-
-
?
additional information
?
-
-
in absence of amino acid substrate choloyl-CoA is cleaved with the release of CoA and formation of a covalent cholate-enzyme complex
-
-
?
additional information
?
-
-
not: L-alpha-alanine, L-glutamine, L-ornithine
-
-
?
additional information
?
-
-
not: choloyl-CoA + glycine
-
-
?
additional information
?
-
-
not: L-alpha-alanine, DL-cysteic acid, 4-aminobutyric acid, cysteine, sulfanilic acid
-
-
?
additional information
?
-
-
essential catalytic triad consisting of Cys-235, His-362 and Asp-328 with Cys-235 serving as the probable nucleophile and thus the site of covalent attachment of the bile acid molecule
-
-
?
additional information
?
-
-
may play important roles in protection against toxicity by accumulation of unconjugated bile acids and non-esterified very long-chain fatty acids
-
-
?
additional information
?
-
-
in addition to its bile acid conjugating activity, the enzyme also possesses thioesterase and glycine conjugating activities with long- and very long-chain acyl-CoAs, at least in vitro. The enzyme can also hydrolyze long- and very-long-chain saturated acyl-CoAs (mainly C16:0-C26:0), the enzyme also conjugates fatty acids to glycine
-
-
?
additional information
?
-
-
bile acidcoenzyme A:amino acid N-acyltransferase is the sole enzyme responsible for conjugation of primary and secondary bile acids to taurine and glycine
-
-
?
additional information
?
-
-
identification of three novel single nucleotide polymorphisms, 147C>T in exon 2 (silent), 602G>C in exon 3 (Arg201Pro), and 1134C>T in exon 4 (silent), in the gene of bile acid CoA: amino acid N-acyltransferase. The allelic frequencies are 0.005 for 147C>T, 0.095 for 602G>C, and 0.015 for 1134C>T. The two known SNPs, 59G>A (Arg20Gln, rs1572983) and UTR1513G>A (rs2229594), are detected at a frequency of 0.500 and 0.425, respectively. In the haplotype analysis for the 59G>A and 602G>C polymorphisms, the allelic frequency of 59G-602G, 59G-602C, 59A-602G and 59A-602C is 0.405, 0.095, 0.500 and 0.000, respectively. The allelic frequency of the nonsynonymous SNP 602G>C is 0.194 in a Caucasian population
-
-
?
additional information
?
-
-
not: glycine, fluoro-beta-alanine
-
-
?
additional information
?
-
-
Cys-234 may be involved in the formation of a bile acid thioester at the active site
-
-
?
additional information
?
-
-
may play important roles in protection against toxicity by accumulation of unconjugated bile acids and non-esterified very long-chain fatty acids
-
-
?
additional information
?
-
-
not: D-alanine, L-arginine, L-lysine, 2-hydroxyethanesulfonate, 2-aminoethanesulfonate, 1-aminoethanephosphonate and 2-aminoethanephosphonate, 3-aminopropanesulfonate
-
-
?
additional information
?
-
-
not as acyl-CoA donors: acetyl-CoA, phenylacetyl-CoA and benzoyl-CoA
-
-
?
additional information
?
-
-
not as acyl-CoA donors: succinoyl-CoA, palmitoyl-CoA
-
-
?
additional information
?
-
-
not: L-alpha-alanine, L-glutamine, L-ornithine
-
-
?
additional information
?
-
-
bile acid-coenzyme A:amino acid N-acyltransferase is the sole enzyme responsible for conjugation of primary and secondary bile acids to taurine and glycine
-
-
?
additional information
?
-
-
suppression of rBAT occurs at the transcriptional level, and the decrease in retinoid-X receptorY-alpha by septic insult may play a critical role in rBAT suppression at the early stage of polymicrobial sepsis
-
-
?
additional information
?
-
-
the enzyme improves the survival rate of rats and increases the bile acid concentrations in in septic livers
-
-
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
choloyl-CoA + glycine
CoA + glycocholate
choloyl-CoA + taurine
CoA + taurocholate
additional information
?
-
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
conjugation of bile acids in the liver with glycine or taurine prior to being secreted into the bile duct
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
taurine can replace glycine, involved in conjugation of bile acids
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
conjugation of bile acids with glycine or taurine favors their excretion into bile and uptake from portal blood into the liver, it promotes absorption of fat and fat-soluble vitamins in the acidic environment of the small intestine by lowering the pKa of the bile acids and hence maintaining its solubility
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
taurine can replace glycine, involved in conjugation of bile acids
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
cholesterol degradation, glycine conjugates of bile acids occur in adult
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
-
?
choloyl-CoA + glycine
CoA + glycocholate
-
-
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
conjugation of bile acids in the liver with glycine or taurine prior to being secreted into the bile duct
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
taurine can replace glycine, involved in conjugation of bile acids
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
conjugation of the CoA adducts of bile acids with taurine
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
-
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
conjugation of bile acids with glycine or taurine favors their excretion into bile and uptake from portal blood into the liver, it promotes absorption of fat and fat-soluble vitamins in the acidic environment of the small intestine by lowering the pKa of the bile acids and hence maintaining its solubility
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
taurine can replace glycine, involved in conjugation of bile acids
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
cholesterol degradation, bile acids are secreted as taurine conjugates in fetus and neonatus
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
taurine-specific enzyme, gallbladder bile contains only taurine conjugates of bile acids, bile acid conjugates increases their detergent properties, prevents their precipitation in the acidic milieu of the upper small intestine, in intestines they are responsible for the solubilization and absorption of fats, vitamins and fat-soluble compounds
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
taurine conjugates predominate in rat bile at normal hepatocellular concentrations of glycine and taurine
-
-
?
choloyl-CoA + taurine
CoA + taurocholate
-
bile acid conjugation
-
-
?
additional information
?
-
-
may play important roles in protection against toxicity by accumulation of unconjugated bile acids and non-esterified very long-chain fatty acids
-
-
?
additional information
?
-
-
bile acidcoenzyme A:amino acid N-acyltransferase is the sole enzyme responsible for conjugation of primary and secondary bile acids to taurine and glycine
-
-
?
additional information
?
-
-
identification of three novel single nucleotide polymorphisms, 147C>T in exon 2 (silent), 602G>C in exon 3 (Arg201Pro), and 1134C>T in exon 4 (silent), in the gene of bile acid CoA: amino acid N-acyltransferase. The allelic frequencies are 0.005 for 147C>T, 0.095 for 602G>C, and 0.015 for 1134C>T. The two known SNPs, 59G>A (Arg20Gln, rs1572983) and UTR1513G>A (rs2229594), are detected at a frequency of 0.500 and 0.425, respectively. In the haplotype analysis for the 59G>A and 602G>C polymorphisms, the allelic frequency of 59G-602G, 59G-602C, 59A-602G and 59A-602C is 0.405, 0.095, 0.500 and 0.000, respectively. The allelic frequency of the nonsynonymous SNP 602G>C is 0.194 in a Caucasian population
-
-
?
additional information
?
-
-
may play important roles in protection against toxicity by accumulation of unconjugated bile acids and non-esterified very long-chain fatty acids
-
-
?
additional information
?
-
-
bile acid-coenzyme A:amino acid N-acyltransferase is the sole enzyme responsible for conjugation of primary and secondary bile acids to taurine and glycine
-
-
?
additional information
?
-
-
suppression of rBAT occurs at the transcriptional level, and the decrease in retinoid-X receptorY-alpha by septic insult may play a critical role in rBAT suppression at the early stage of polymicrobial sepsis
-
-
?
additional information
?
-
-
the enzyme improves the survival rate of rats and increases the bile acid concentrations in in septic livers
-
-
?
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Vessey, D.A.
The co-purification and common identity of cholyl CoA:glycine- and cholyl CoA: taurine-N-acyltransferase activities from bovine liver
J. Biol. Chem.
254
2059-2063
1979
Bos taurus
brenda
Czuba, B.; Vessey, D.A.
Kinetic characterization of cholyl-CoA glycine-taurine N-acyltransferase from bovine liver
J. Biol. Chem.
255
5296-5299
1980
Bos taurus
brenda
Czuba, B.; Vessey, D.A.
Structural characterization of cholylcoenzyme A: glycine-taurine N-acyltransferase and a covalent substrate intermediate
J. Biol. Chem.
261
6260-6263
1986
Bos taurus
brenda
Kimura, M.; Okuno, E.; Inada, J.; Ohyama, H.; Kido, R.
Purification and characterization of amino-acid N-choloyltransferase from human liver
Hoppe-Seyler's Z. Physiol. Chem.
364
637-645
1983
Homo sapiens
brenda
Killenberg, P.G.; Jordan, J.T.
Purification and characterization of bile acid-CoA:amino acid N-acyltransferase from rat liver
J. Biol. Chem.
253
1005-1010
1978
Rattus norvegicus
brenda
Czuba, B.; Vessey, D.A.
Identification of a unique mammalian species of cholyl-CoA: amino acid N-acyltransferase
Biochim. Biophys. Acta
665
612-614
1981
Canis lupus familiaris
brenda
Poley, J.R.; Dower, J.C.; Owen, J.R.; Owen C.A.; Stickler, G.B.
Bile acids in infants and children
J. Lab. Clin. Med.
63
838-846
1964
Gallus gallus
brenda
Ide, T.; Kano, S.; Murata, M.; Yanagita, T.; Sugano, M.
Dietary modifications of the biliary bile acid glycine:taurine ratio and activity of hepatic bile acid-CoA:amino acid N-acyltransferase (EC 2.3.1) in the rat
Br. J. Nutr.
72
93-100
1994
Rattus norvegicus
brenda
Sfakianos, M.K.; Wilson, L.; Sakalian, M.; Falany, C.N.; Barnes, S.
Conserved residues in the putative catalytic triad of human bile acid coenzyme A:amino acid N-acyltransferase
J. Biol. Chem.
277
47270-47275
2002
Homo sapiens
brenda
Falany, C.N.; Fortinberry, H.; Leiter, E.H.; Barnes, S.
Cloning, expression, and chromosomal localization of mouse liver bile acid CoA:amino acid N-acyltransferase
J. Lipid Res.
38
1139-1148
1997
Mus musculus
brenda
O'Byrne, J.; Hunt, M.C.; Rai, D.K.; Saeki, M.; Alexson, S.E.H.
The Human bile acid-CoA:amino acid N-acyltransferase functions in the conjugation of fatty acids to glycine
J. Biol. Chem.
278
34237-34244
2003
Homo sapiens, Mus musculus
brenda
He, D.; Barnes, S.; Falany, C.N.
Rat liver: Expression, characterization, and peroxisomal localization
J. Lipid Res.
44
2242-2249
2003
Rattus norvegicus
brenda
Pellicoro, A.; van den Heuvel, F.A.; Geuken, M.; Moshage, H.; Jansen, P.L.; Faber, K.N.
Human and rat bile acid-CoA:amino acid N-acyltransferase are liver-specific peroxisomal enzymes: implications for intracellular bile salt transport
Hepatology
45
340-348
2007
Homo sapiens, Rattus norvegicus
brenda
Shonsey, E.M.; Sfakianos, M.; Johnson, M.; He, D.; Falany, C.N.; Falany, J.; Merkler, D.J.; Barnes, S.
Bile acid coenzyme A: amino acid N-acyltransferase in the amino acid conjugation of bile acids
Methods Enzymol.
400
374-394
2005
Homo sapiens (Q14032), Rattus norvegicus
brenda
Tougou, K.; Fukuda, T.; Ito, T.; Yamazaki, H.; Fujio, Y.; Azuma, J.
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Homo sapiens
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Shonsey, E.M.; Eliuk, S.M.; Johnson, M.S.; Barnes, S.; Falany, C.N.; Darley-Usmar, V.M.; Renfrow, M.B.
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Homo sapiens
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Chen, Y.H.; Hong, I.C.; Kuo, K.K.; Hsu, H.K.; Hsu, C.
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Shock
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Rattus norvegicus
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Homo sapiens
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Rattus norvegicus
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Homo sapiens
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