D-amino acids in the brain: structure and function of pyridoxal phosphate-dependent amino acid racemases

FEBS J. 2008 Jul;275(14):3527-37. doi: 10.1111/j.1742-4658.2008.06516.x.

Abstract

D-serine serves as a co-agonist of the N-methyl D-aspartate receptor in mammalian brains, and its behavior is probably related to neurological disorders such as schizophrenia, Alzheimer's disease and amyotrophic lateral sclerosis. D-Serine is synthesized by a pyridoxal 5'-phosphate (PLP)-dependent serine racemase. In this minireview, we provide a detailed discussion on the reaction mechanism of the PLP-dependent amino acid racemase on the basis of its 3D structure. We compared the eukaryotic serine racemase with bacterial alanine racemase, the best-studied enzyme among the PLP-dependent amino acid racemases, and thus suggested a putative reaction mechanism for mammalian D-serine synthesis.

Publication types

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

MeSH terms

  • Alanine Racemase / chemistry*
  • Amino Acid Isomerases / chemistry
  • Animals
  • Bacteria / enzymology
  • Brain / enzymology
  • Isomerism
  • Pyridoxal Phosphate / chemistry*
  • Racemases and Epimerases / chemistry*
  • Serine / biosynthesis*
  • Serine / chemistry

Substances

  • Serine
  • Pyridoxal Phosphate
  • Racemases and Epimerases
  • Amino Acid Isomerases
  • Alanine Racemase
  • aspartate racemase
  • serine racemase