1242450-41-4Relevant academic research and scientific papers
Decoding the logic of the tRNA regiospecificity of nonribosomal femX Wv aminoacyl transferase www.angewandte.org
Fonvielle, Matthieu,Chemama, Maryline,Lecerf, Maxime,Villet, Regis,Busca, Patricia,Bouhss, Ahmed,Etheve-Quelquejeu, Melanie,Arthur, Michel
supporting information; experimental part, p. 5115 - 5119 (2010/11/04)
Natural selection: Replacement of the 3′-OH group of Ala-tRNA Ala with 3′-H affected FemXWv-catalyzed aminoacyl transfer from the 2 -position, but not substrate binding. The ability of FemXWv to bind and transacylate the 3′-O-Ala isomer initially formed by alanyl-tRNA synthetase (AlaRS) may be crucial for efficient competition with the ribosome (see scheme). (Figure Presented).
The synthesis of diverse adenosine 5'-phosphonate analogues as chain terminators against hepatitis C virus (HCV)
Kim, Bo-Seung,Kim, Beom-Tae,Hwang, Ki-Jun
experimental part, p. 1643 - 1648 (2010/10/19)
Adenosine 5'-phosphonates have been reported as potential chain terminators against Hepatitis C virus (HCV); therefore, we developed convenient sequences for synthesis of modified adenosine 5'-phosphonates in which the hydroxyl group at 2' or 3'-position of the sugar moiety is substituted with the azido or amino group and the oxymethyl group at the 4'-position is modified by the ethylene or vinyl group. This synthetic sequence can provide six adenosine 5'-phosphonates via one protocol, and is considered to be very efficient and a convenient route of synthesis. An assay of adenosine 5'-phosphonate analogues (1, 2, 3, 4, 5, and 6) against HCV infection is now in progress.
