How nature deals with stereoisomers

Curr Opin Struct Biol. 1995 Dec;5(6):830-6. doi: 10.1016/0959-440x(95)80018-2.

Abstract

All natural proteins are composed of L-amino acids and are inherently chiral. The properties of both L- and chemically synthesized D-amino acids are identical except in optically asymmetric interactions. Structural studies of D-I racemic mixtures of crystallographic interest are discussed. The review also gives some recent examples of stereospecificity: how L-proteins deal with L- or D-substrates and how enzymes can function as racemases. Two particular examples of stereoselectivity are then discussed.

Publication types

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

MeSH terms

  • Amino Acids / chemistry
  • Carbohydrate Conformation
  • Glycoside Hydrolases / metabolism
  • Lipase / metabolism
  • Molecular Structure
  • Oxidoreductases / metabolism
  • Peptides / chemistry
  • Proteins / chemistry*
  • Proteins / metabolism
  • Racemases and Epimerases / metabolism
  • Stereoisomerism*

Substances

  • Amino Acids
  • Peptides
  • Proteins
  • Oxidoreductases
  • Lipase
  • Glycoside Hydrolases
  • Racemases and Epimerases