S-deoxo-Abu1,Ile3-amaninamide, an inactive amatoxin analogue

Int J Pept Protein Res. 1990 Mar;35(3):263-70. doi: 10.1111/j.1399-3011.1990.tb00947.x.

Abstract

The title compound 3, an amatoxin analogue containing L-alpha-aminobutyric acid instead of L-asparagine in position 1, as in natural toad stool peptides, has been synthesized. It does not inhibit the eukaryotic DNA-dependent RNA polymerase form II (or B) in concentrations up to 10(-4)M, whereas 50% inhibition is exerted in 10(-6)M solution by the corresponding Asn-analogue S-deoxo-Ile3-amaninamide 2. The striking difference seems to be due to a relatively small variation of the conformation recognized by sensitive NMR spectroscopic methods.

Publication types

  • Comparative Study

MeSH terms

  • Amanitins* / chemical synthesis*
  • Amanitins* / pharmacology
  • Amino Acid Sequence
  • Circular Dichroism
  • Magnetic Resonance Spectroscopy
  • Molecular Sequence Data
  • Molecular Structure
  • Protein Conformation
  • RNA Polymerase II / antagonists & inhibitors
  • Temperature

Substances

  • Amanitins
  • amaninamide, S-deoxo-Abu(1)-Ile(3)-
  • amatoxin
  • RNA Polymerase II