作者
Guillaume Gabant, Sylvie Auxilien, Irina Tuszynska, Marie Locard, Michal J Gajda, Guylaine Chaussinand, Bernard Fernandez, Alain Dedieu, Henri Grosjean, Beatrice Golinelli-Pimpaneau, Janusz M Bujnicki, Jean Armengaud
发表日期
2006/1/1
期刊
Nucleic acids research
卷号
34
期号
9
页码范围
2483-2494
出版商
Oxford University Press
简介
The tRNA:m 22 G10 methyltransferase of Pyrococus abyssi (PAB1283, a member of COG1041) catalyzes the N2 , N2 -dimethylation of guanosine at position 10 in tRNA. Boundaries of its THUMP (THioUridine synthases, RNA Methyltransferases and Pseudo-uridine synthases)—containing N-terminal domain [1–152] and C-terminal catalytic domain [157–329] were assessed by trypsin limited proteolysis. An inter-domain flexible region of at least six residues was revealed. The N-terminal domain was then produced as a standalone protein (THUMPα) and further characterized. This autonomously folded unit exhibits very low affinity for tRNA. Using protein fold-recognition (FR) methods, we identified the similarity between THUMPα and a putative RNA-recognition module observed in the crystal structure of another THUMP-containing protein (ThiI …
引用总数
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