Hodel A E, Gershon P D, Shi X, Quiocho F A
Howard Hughes Medical Institute, Baylor College of Medicine, Houston, Texas 77030, USA.
Cell. 1996 Apr 19;85(2):247-56. doi: 10.1016/s0092-8674(00)81101-0.
VP39 is a bifunctional vaccinia virus protein that acts as both an mRNA cap-specific RNA 2'-O-methyltransferase and a poly(A) polymerase processivity factor. Here, we report the 1.85 A crystal structure of a VP39 variant complexed with its AdoMet cofactor. VP39 comprises a single core domain with structural similarity to the catalytic domains of other methyltransferases. Surface features and mutagenesis data suggest two possible RNA-binding sites with novel underlying architecture, one of which forms a cleft spanning the region adjacent to the methyltransferase active site. This report provides a prototypic structure for an RNA methyltransferase, a protein that interacts with the mRNA 5' cap, and an intact poxvirus protein.
VP39是一种双功能痘苗病毒蛋白,它既是一种mRNA帽特异性RNA 2'-O-甲基转移酶,也是一种聚腺苷酸聚合酶持续合成因子。在此,我们报告了与AdoMet辅因子复合的VP39变体的1.85埃晶体结构。VP39由一个单一的核心结构域组成,其结构与其他甲基转移酶的催化结构域相似。表面特征和诱变数据表明存在两个具有新型潜在结构的可能RNA结合位点,其中一个形成了一个跨越甲基转移酶活性位点相邻区域的裂缝。本报告提供了一种RNA甲基转移酶、一种与mRNA 5'帽相互作用的蛋白质以及一种完整痘病毒蛋白的原型结构。