The primary structure of porcine liver acylamino acid-releasing enzyme deduced from cDNA sequences

J Biochem. 1989 Oct;106(4):548-51. doi: 10.1093/oxfordjournals.jbchem.a122891.

Abstract

Two overlapping cloned cDNAs encoding the entire amino acid sequences of the subunits of acylamino acid-releasing enzyme (AARE) [EC 3.4.19.1] have been isolated from porcine liver cDNA lambda gt10 cDNA libraries and sequenced. Sequence analyses of the cDNA and several Achromobacter protease I-digested peptides of the purified protein revealed that porcine liver AARE consists of four identical subunits, and each comprising a single chain of 732 amino acids with acetylmethionine at the N-terminus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • DNA / genetics*
  • Liver / enzymology*
  • Molecular Sequence Data
  • Peptide Hydrolases / genetics*
  • Restriction Mapping
  • Swine

Substances

  • DNA
  • Peptide Hydrolases
  • acylaminoacyl-peptidase