作者
Immacolata Speciale, Maria Elena Laugieri, Eric Noel, Sicheng Lin, Todd L Lowary, Antonio Molinaro, Garry A Duncan, Irina V Agarkova, Domenico Garozzo, Michela G Tonetti, James L Van Etten, Cristina De Castro
发表日期
2020/11/17
期刊
Proceedings of the National Academy of Sciences
卷号
117
期号
46
页码范围
28735-28742
出版商
National Academy of Sciences
简介
Paramecium bursaria chlorella virus-1 (PBCV-1) is a large double-stranded DNA (dsDNA) virus that infects the unicellular green alga Chlorella variabilis NC64A. Unlike many other viruses, PBCV-1 encodes most, if not all, of the enzymes involved in the synthesis of the glycans attached to its major capsid protein. Importantly, these glycans differ from those reported from the three domains of life in terms of structure and asparagine location in the sequon of the protein. Previous data collected from 20 PBCV-1 spontaneous mutants (or antigenic variants) suggested that the a064r gene encodes a glycosyltransferase (GT) with three domains, each with a different function. Here, we demonstrate that: domain 1 is a β-l-rhamnosyltransferase; domain 2 is an α-l-rhamnosyltransferase resembling only bacterial proteins of unknown function, and domain 3 is a methyltransferase that methylates the C-2 hydroxyl group of the …
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