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- Table of Contents
6 Q&As
Facts about Bile acyl-CoA synthetase.
Seems to trigger secondary bile acids entering the liver in the enterohepatic circulation. In vitro, also activates 3-alpha,7- alpha,12-alpha-trihydroxy-5-beta-cholestanate (THCA), the C27 precursor of cholic acid deriving in the de novo synthesis from cholesterol.
Human | |
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Gene Name: | SLC27A5 |
Uniprot: | Q9Y2P5 |
Entrez: | 10998 |
Belongs to: |
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ATP-dependent AMP-binding enzyme family |
ACSB; ACSBBACS; ACSVL6; ACSVL6BAL; BA-CoA ligase; Bile acid-CoA ligase; bile acyl-CoA synthetase; Cholate--CoA ligase; EC 6.2.1.7; FACVL3; FACVL3FATP-5; FATP5; FATP5Solute carrier family 27 member 5; Fatty acid transport protein 5; Fatty-acid-coenzyme A ligase, very long-chain 3; FLJ22987; SLC27A5; solute carrier family 27 (fatty acid transporter), member 5; VLACSR; VLACSRVery long-chain acyl-CoA synthetase homolog 2; VLCSH2; VLCSH2Very long-chain acyl-CoA synthetase-related protein; VLCS-H2VLACS-related
Mass (kDA):
75.385 kDA
Human | |
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Location: | 19q13.43 |
Sequence: | 19; NC_000019.10 (58498333..58512065, complement) |
Predominantly expressed in liver.
Endoplasmic reticulum membrane; Multi-pass membrane protein. Microsome. Cell membrane; Multi-pass membrane protein.
PMID: 10479480 by Steinberg S.J., et al. Human liver-specific very-long-chain acyl-coenzyme A synthetase: cDNA cloning and characterization of a second enzymatically active protein.
PMID: 10749848 by Steinberg S.J., et al. The human liver-specific homolog of very long-chain acyl-CoA synthetase is cholate:CoA ligase.