Jansson Anna M, Jakobsson Emma, Johansson Patrik, Lantez Violaine, Coutard Bruno, de Lamballerie Xavier, Unge Torsten, Jones T Alwyn
Department of Cell and Molecular Biology, Uppsala University, Biomedical Center, SE 751 24 Uppsala, Sweden.
Acta Crystallogr D Biol Crystallogr. 2009 Aug;65(Pt 8):796-803. doi: 10.1107/S0907444909017260. Epub 2009 Jul 10.
The Modoc virus (MODV) is a flavivirus with no known vector (NKV). Evolutionary studies have shown that the viruses in the MODV group have evolved in association with mammals (bats, rodents) without transmission by an arthropod vector. MODV methyltransferase is the first enzyme from this evolutionary branch to be structurally characterized. The high-resolution structure of the methyltransferase domain of the MODV NS5 protein (MTase(MODV)) was determined. The protein structure was solved in the apo form and in complex with its cofactor S-adenosyl-L-methionine (SAM). Although it belongs to a separate evolutionary branch, MTase(MODV) shares structural characteristics with flaviviral MTases from the other branches. Its capping machinery is a relatively new target in flaviviral drug development and the observed structural conservation between the three flaviviral branches indicates that it may be possible to identify a drug that targets a range of flaviviruses. The structural conservation also supports the choice of MODV as a possible model for flavivirus studies.
莫多克病毒(MODV)是一种无已知传播媒介的黄病毒(NKV)。进化研究表明,MODV组中的病毒是与哺乳动物(蝙蝠、啮齿动物)共同进化的,没有通过节肢动物媒介传播。MODV甲基转移酶是该进化分支中首个进行结构表征的酶。确定了MODV NS5蛋白甲基转移酶结构域(MTase(MODV))的高分辨率结构。该蛋白质结构以无辅因子形式及其与辅因子S-腺苷-L-甲硫氨酸(SAM)的复合物形式解析得到。尽管MTase(MODV)属于一个独立的进化分支,但它与其他分支的黄病毒甲基转移酶具有结构特征。其封端机制是黄病毒药物开发中一个相对较新的靶点,并且观察到的三个黄病毒分支之间的结构保守性表明,有可能鉴定出一种针对多种黄病毒的药物。这种结构保守性也支持选择MODV作为黄病毒研究的一种可能模型。