Title : Synthesis and biological evaluation of a MraY selective analogue of tunicamycins.

Pub. Date : 2020

PMID : 31566068






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Tunicamycins, which are nucleoside natural products, inhibit both bacterial phospho-N-acetylmuraminic acid (MurNAc)-pentapeptide translocase (MraY) and human UDP-N-acetylglucosamine (GlcNAc): polyprenol phosphate translocase (GPT). Tunicamycin glutamic--pyruvic transaminase Homo sapiens