Serine peptidases: classification, structure and function

Cell Mol Life Sci. 2008 Apr;65(7-8):1220-36. doi: 10.1007/s00018-008-7565-9.

Abstract

Serine peptidases play key roles in human health and disease and their biochemical properties shaped the molecular evolution of these processes. Of known proteolytic enzymes, the serine peptidase family is the major cornerstone of the vertebrate degradome. We describe the known diversity of serine peptidases with respect to structure and function. Particular emphasis is placed on the S1 peptidase family, the trypsins, which underwent the most predominant genetic expansion yielding the enzymes responsible for vital processes in man such as digestion, blood coagulation, fibrinolysis, development, fertilization, apoptosis and immunity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Allosteric Regulation
  • Amino Acids / metabolism
  • Humans
  • Protein Structure, Secondary
  • Serine Endopeptidases / chemistry*
  • Serine Endopeptidases / classification
  • Serine Endopeptidases / metabolism*
  • Sodium / metabolism
  • Thrombin / chemistry
  • Thrombin / metabolism

Substances

  • Amino Acids
  • Sodium
  • Serine Endopeptidases
  • Thrombin