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Cloning and characterization of the cDNA encoding rice elongation factor 1β

机译:水稻延伸因子1β的cDNA的克隆与鉴定

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>We have cloned and sequenced a cDNA coding for rice elongation factor 1β (EF-1β). The clone was 1420 bp long and contained an open reading frame coding for 229 amino acids. The overall identity between rice EF-1β and rice EF-1β' [Matsumoto, S., Oizumi, N., Taira, H. and Ejiri, S. (1992) FEBS Lett. 311, 46-48] is 60% at the amino acid sequence level; a higher percent identical residues (81%) were especially observed in the C-temiinal region. Rice EF-1β has no conserved phosphorylation site for casein kinase II and no leucine zipper motif, although these motifs are well conserved in EF-1δ (= β in plants) subunits of animal EF-1.
机译:>我们已经克隆并测序了编码水稻延伸因子1β(EF-1β)的cDNA。该克隆长1420 bp,并包含一个编码229个氨基酸的开放阅读框。水稻EF-1β与水稻EF-1β'的整体同一性[Matsumoto,S.,Oizumi,N.,Taira,H.和Ejiri,S.(1992)FEBS Lett。 311,46-48]在氨基酸序列水平为60%;特别是在C末端区域中,观察到更高的相同残基百分比(81%)。水稻EF-1β没有酪蛋白激酶II的保守磷酸化位点,也没有亮氨酸拉链基序,尽管这些基序在动物EF-1的EF-1δ(植物中为β)亚基中非常保守。

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