The structural basis for catalysis and specificity of the X-prolyl dipeptidyl aminopeptidase from Lactococcus lactis

Structure. 2002 Oct;10(10):1383-94. doi: 10.1016/s0969-2126(02)00851-1.

Abstract

The X-prolyl dipeptidyl aminopeptidase (X-PDAP) from Lactococcus lactis is a dimeric enzyme catalyzing the removal of Xaa-Pro dipeptides from the N terminus of peptides. The structure of the enzyme was solved at 2.2 A resolution and provides a model for the peptidase family S15. Each monomer is composed of four domains. The larger one presents an alpha/beta hydrolase fold and comprises the active site serine. The specificity pocket is mainly built by residues from a small helical domain which is, together with the N-terminal domain, essential for dimerization. A C-terminal moiety probably plays a role in the tropism of X-PDAP toward the cellular membrane. These results give new insights for further exploration of the role of the enzymes of the SC clan.

MeSH terms

  • Amino Acid Sequence
  • Catalysis
  • Dimerization
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases / chemistry
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases / metabolism*
  • Lactococcus lactis / enzymology*
  • Models, Molecular
  • Molecular Sequence Data
  • Protein Conformation
  • Protein Folding
  • Sequence Homology, Amino Acid
  • Substrate Specificity

Substances

  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases
  • PepX dipeptidyl aminopeptidase

Associated data

  • PDB/1LNS