Cloning and sequencing of rat liver carboxylesterase ES-3 (egasyn).

Biochem Biophys Res Commun

Laboratoire de Chimie Physiologique, Université de Louvain, Brussels, Belgium.

Published: September 1994

The cDNA of the rat carboxylesterase ES-3 encodes a polypeptide with 561 amino acid residues including a cleavable signal peptide at the N-terminus. The processed polypeptide shows over 90% sequence identity to mouse egasyn (ES-22); its calculated pI (5.5) matches the value determined for purified liver ES-3. The product expressed in COS cells migrates in native gels in the region of ES-3 and is similarly active on acetanilide. It is retained in the cells, as predicted from its C-terminus HTEL, and bears a single endo-H sensitive oligosaccharide chain. The nonglycosylated form expressed in the presence of tunicamycin is also intracellular, but substantially less active.

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http://dx.doi.org/10.1006/bbrc.1994.2341DOI Listing

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Cloning and sequencing of rat liver carboxylesterase ES-3 (egasyn).

Biochem Biophys Res Commun

September 1994

Laboratoire de Chimie Physiologique, Université de Louvain, Brussels, Belgium.

The cDNA of the rat carboxylesterase ES-3 encodes a polypeptide with 561 amino acid residues including a cleavable signal peptide at the N-terminus. The processed polypeptide shows over 90% sequence identity to mouse egasyn (ES-22); its calculated pI (5.5) matches the value determined for purified liver ES-3.

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