Proteinaceous alpha-amylase inhibitors

Biochim Biophys Acta. 2004 Feb 12;1696(2):145-56. doi: 10.1016/j.bbapap.2003.07.004.

Abstract

Proteins that inhibit alpha-amylases have been isolated from plants and microorganisms. These inhibitors can have natural roles in the control of endogenous alpha-amylase activity or in defence against pathogens and pests; certain inhibitors are reported to be antinutritional factors. The alpha-amylase inhibitors belong to seven different protein structural families, most of which also contain evolutionary related proteins without inhibitory activity. Two families include bifunctional inhibitors acting both on alpha-amylases and proteases. High-resolution structures are available of target alpha-amylases in complex with inhibitors from five families. These structures indicate major diversity but also some similarity in the structural basis of alpha-amylase inhibition. Mutational analysis of the mechanism of inhibition was performed in a few cases and various protein engineering and biotechnological approaches have been outlined for exploitation of the inhibitory function.

Publication types

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

MeSH terms

  • Binding Sites / drug effects
  • Drug Design
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / classification*
  • Enzyme Inhibitors / metabolism
  • Fungal Proteins / chemistry
  • Peptides / chemistry
  • Phytohemagglutinins / chemistry
  • Plant Proteins / chemistry
  • Structure-Activity Relationship
  • alpha-Amylases / antagonists & inhibitors*

Substances

  • Enzyme Inhibitors
  • Fungal Proteins
  • Peptides
  • Phytohemagglutinins
  • Plant Proteins
  • zeamatin protein, Zea mays
  • alpha-Amylases
  • tendamistate