In:
Scientific Reports, Springer Science and Business Media LLC, Vol. 6, No. 1 ( 2016-08-17)
Kurzfassung:
Systematic structural modifications of the muramic acid, peptide and nucleotide moieties of Park’s nucleotide were performed to investigate the substrate specificity of B. subtilis MraY (MraY BS ). It was found that the simplest analogue of Park’s nucleotide only bearing the first two amino acids, l -alanine- iso - d -glutamic acid, could function as a MraY BS substrate. Also, the acid group attached to the C α of iso - d -glutamic acid was found to play an important role for substrate activity. Epimerization of the C 4-hydroxyl group of muramic acid and modification at the 5-position of the uracil in Park’s nucleotide were both found to dramatically impair their substrate activity. Unexpectedly, structural modifications on the uracil moiety changed the parent molecule from a substrate to an inhibitor, blocking the MraY BS translocation. One unoptimized inhibitor was found to have a K i value of 4 ± 1 μM against MraY BS , more potent than tunicamycins.
Materialart:
Online-Ressource
ISSN:
2045-2322
Sprache:
Englisch
Verlag:
Springer Science and Business Media LLC
Publikationsdatum:
2016
ZDB Id:
2615211-3