Autocatalytic processing of procathepsin E to cathepsin E and their structural differences

Biochem Biophys Res Commun. 1991 Feb 28;175(1):152-8. doi: 10.1016/s0006-291x(05)81213-6.

Abstract

The processing of human gastric procathepsin E to its mature form, cathepsin E, was studied at pH 3.5. The results revealed the autocatalytic and apparently one-step conversion of procathepsin E to cathepsin E within 10 min of incubation at 14 degrees C under the conditions used. Analyses of the amino acid sequences of both procathepsin E and cathepsin E showed that cleavage occurred at the Met36-Ile37 bond to produce the mature form, cathepsin E. The NH2-terminal amino acid sequence of procathepsin E thus determined was identical with that predicted from the cDNA sequence by Azuma et al. except that the NH2-terminal glutamine residue in the latter was converted into a pyroglutamic acid residue in the former and that the glycine residue at position 2 in the latter sequence was deleted in the former. On the other hand, the NH2-terminal amino acid sequence of cathepsin E was identical with that reported previously by us.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cathepsin E
  • Cathepsins / genetics*
  • Cathepsins / metabolism
  • DNA / genetics
  • Enzyme Activation
  • Enzyme Precursors / genetics*
  • Enzyme Precursors / metabolism
  • Gastric Mucosa / enzymology
  • Humans
  • Kinetics
  • Molecular Sequence Data
  • Protein Processing, Post-Translational*
  • Sequence Homology, Nucleic Acid

Substances

  • Enzyme Precursors
  • DNA
  • Cathepsins
  • procathepsin E
  • Cathepsin E