Role of the conserved aspartate and phenylalanine residues in prokaryotic and mitochondrial elongation factor Ts in guanine nucleotide exchange

FEBS Lett. 1996 Aug 12;391(3):330-2. doi: 10.1016/0014-5793(96)00789-2.

Abstract

The guanine nucleotide exchange reaction catalyzed by elongation factor Ts is proposed to arise from the intrusion of the side chains of D80 and F81 near the Mg2+ binding site in EF-Tu. D80A and F81A mutants of E. coli EF-Ts were 2-3-fold less active in promoting GDP exchange with E. coli EF-Tu while the D80AF81A mutant was nearly 10-fold less active. The D84 and F85 mutants of EF-Tsmt were 5-10-fold less active in stimulating the activity of EF-Tumt. The double mutation completely abolished the activity of EF-Tsmt.

MeSH terms

  • Aspartic Acid / metabolism*
  • Electrophoresis, Polyacrylamide Gel
  • Escherichia coli
  • Guanine Nucleotides / metabolism*
  • Guanosine Diphosphate / metabolism
  • Peptide Elongation Factors / metabolism*
  • Phenylalanine / metabolism*
  • Poly U / metabolism
  • Structure-Activity Relationship

Substances

  • Guanine Nucleotides
  • Peptide Elongation Factors
  • elongation factor Ts
  • Guanosine Diphosphate
  • Poly U
  • Aspartic Acid
  • Phenylalanine