2OXT

Crystal structure of Meaban virus nucleoside-2'-O-methyltransferase

2OXT の概要

• エントリーDOI: 10.2210/pdb2oxt/pdb
• 分子名称: NUCLEOSIDE-2'-O-METHYLTRANSFERASE, S-ADENOSYLMETHIONINE (3 entities in total)
• 機能のキーワード: flavivirus, nucleoside-2'-o-methyltransferase, viral enzyme, rna capping, s-adenosyl-l-methionine, viral protein
• 由来する生物種: Meaban virus
• 細胞内の位置: Envelope protein E: Virion membrane; Multi- pass membrane protein: A0EKU1
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 120186.15

構造登録者

Mastrangelo, E.,Milani, M.,Bollati, M.,Bolognesi, M. (登録日: 2007-02-21, 公開日: 2007-05-15, 最終更新日: 2023-08-30)

主引用文献

Mastrangelo, E.,Bollati, M.,Milani, M.,Selisko, B.,Peyrane, F.,Canard, B.,Grard, G.,de Lamballerie, X.,Bolognesi, M.
Structural bases for substrate recognition and activity in Meaban virus nucleoside-2'-O-methyltransferase
Protein Sci., 16:1133-1145, 2007

PubMed Abstract: Viral methyltransferases are involved in the mRNA capping process, resulting in the transfer of a methyl group from S-adenosyl-L-methionine to capped RNA. Two groups of methyltransferases (MTases) are known: (guanine-N7)-methyltransferases (N7MTases), adding a methyl group onto the N7 atom of guanine, and (nucleoside-2'-O-)-methyltransferases (2'OMTases), adding a methyl group to a ribose hydroxyl. We have expressed and purified two constructs of Meaban virus (MV; genus Flavivirus) NS5 protein MTase domain (residues 1-265 and 1-293, respectively). We report here the three-dimensional structure of the shorter MTase construct in complex with the cofactor S-adenosyl-L-methionine, at 2.9 angstroms resolution. Inspection of the refined crystal structure, which highlights structural conservation of specific active site residues, together with sequence analysis and structural comparison with Dengue virus 2'OMTase, suggests that the crystallized enzyme belongs to the 2'OMTase subgroup. Enzymatic assays show that the short MV MTase construct is inactive, but the longer construct expressed can transfer a methyl group to the ribose 2'O atom of a short GpppAC(5) substrate. West Nile virus MTase domain has been recently shown to display both N7 and 2'O MTase activity on a capped RNA substrate comprising the 5'-terminal 190 nt of the West Nile virus genome. The lack of N7 MTase activity here reported for MV MTase may be related either to the small size of the capped RNA substrate, to its sequence, or to different structural properties of the C-terminal regions of West Nile virus and MV MTase-domains.

PubMed: 17473012
DOI: 10.1110/ps.072758107

実験手法

X-RAY DIFFRACTION (2.9 Å)