Analysis of fluoromethyl group chirality establishes a common stereochemical course for the enolpyruvyl transfers catalyzed by EPSP synthase and UDP-GlcNAc enolpyruvyl transferase Article

Kim, DH, TuckerKellogg, GW, Lees, WJ et al. (1996). Analysis of fluoromethyl group chirality establishes a common stereochemical course for the enolpyruvyl transfers catalyzed by EPSP synthase and UDP-GlcNAc enolpyruvyl transferase . BIOCHEMISTRY, 35(17), 5435-5440. 10.1021/bi952978s

cited authors

  • Kim, DH; TuckerKellogg, GW; Lees, WJ; Walsh, CT

sustainable development goals

authors

publication date

  • April 30, 1996

published in

keywords

  • 3-PHOSPHATE SYNTHASE
  • 5-ENOLPYRUVYLSHIKIMATE-3-PHOSPHATE SYNTHASE
  • AMINO-ACID-SEQUENCE
  • Biochemistry & Molecular Biology
  • ENZYME
  • GENE-PRODUCT
  • HERBICIDE GLYPHOSATE
  • Life Sciences & Biomedicine
  • NMR-SPECTRA
  • PYRUVATE-KINASE
  • STERIC COURSE
  • SYNTHETASE
  • Science & Technology

Digital Object Identifier (DOI)

publisher

  • AMER CHEMICAL SOC

start page

  • 5435

end page

  • 5440

volume

  • 35

issue

  • 17