Article
Lipoconjugates: structure-activity studies for pheromone analogues of Ustilago maydis with varied lipophilicity.
International journal of peptide and protein research - 1 Oct 1996
Koppitz M, Spellig T, Kahmann R, Kessler H
Abstract excerpt
The synthesis, biological activities and conformational behaviour of a variety of analogues of the mating pheromones of the basidomycete Ustilago maydis are reported. The pheromone analogues derived from the two allelic forms H-G-R-D-N-G-S-P-I-G-Y-S-S-Xaa-Z (a1) and H-N-R-G-Q-P-G-Y-Y-Xaa-Z (a2), with Xaa-Z being an unidentified lipophilic cysteine derivative, all differ in the C-terminal residue and include...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.