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Structure of Saccharomyces cerevisiae mitochondrial Qri7 in complex with AMP

机译:与AMP复合的酿酒酵母线粒体Qri7的结构

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摘要

N 6-Threonylcarbamoyladenosine (t6A) is a modified tRNA base required for accuracy in translation. Qri7 is localized in yeast mitochondria and is involved in t6A biosynthesis. In t6A biosynthesis, threonylcarbamoyl-adenylate (TCA) is synthesized from threonine, bicarbonate and ATP, and the threonyl-carbamoyl group is transferred to adenine 37 of tRNA by Qri7. Qri7 alone is sufficient to catalyze the second step of the reaction, whereas the Qri7 homologues YgjD (in bacteria) and Kae1 (in archaea and eukaryotes) function as parts of multi-protein complexes. In this study, the crystal structure of Qri7 complexed with AMP (a part of TCA) has been determined at 2.94 Å resolution in a new crystal form. The manner of AMP recognition is similar, with some minor variations, among the Qri7/Kae1/YgjD family proteins. The previously reported dimer formation was also observed in this new crystal form. Furthermore, a comparison with the structure of TobZ, which catalyzes a similar reaction to t6A biosynthesis, revealed the presence of a flexible loop that may be involved in tRNA binding.
机译:N 6 -苏糖基氨基甲酰腺苷(t 6 A)是修饰的tRNA碱基,对于翻译的准确性至关重要。 Qri7位于酵母线粒体中,参与t 6 A的生物合成。在t 6 的生物合成中,苏氨酸氨基甲酸酯-腺苷酸(TCA)由苏氨酸,碳酸氢盐和ATP合成,苏氨酸-氨基甲酰基通过Qri7转移至tRNA的腺嘌呤37。单独的Qri7足以催化反应的第二步,而Qri7的同系物YgjD(在细菌中)和Kae1(在古细菌和真核生物中)作为多蛋白复合物的一部分起作用。在这项研究中,与AMP(TCA的一部分)复合的Qri7的晶体结构已经以2.94Å的分辨率确定为新的晶体形式。在Qri7 / Kae1 / YgjD家族蛋白中,AMP的识别方式相似,但有一些细微的差异。还以这种新的晶体形式观察到先前报道的二聚体形成。此外,与催化与t 6 生物合成类似反应的TobZ结构进行比较,发现存在可能与tRNA结合有关的柔性环。

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