Replication initiator proteins of Acinetobacter baumannii plasmids: An update note

IF 1.8 4区 生物学 Q3 GENETICS & HEREDITY
Semiramis Castro-Jaimes , Gabriela Guerrero , Elena Bello-López , Miguel A. Cevallos
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引用次数: 4

Abstract

The bioinformatic analysis that we made of 492 Acinetobacter baumannii plasmid sequences identified 418 genes encoding Replication Initiator (Rep) proteins that fell into at least fourteen groups according to the protein domains that they contained. The most abundant group of Rep proteins contained a Rep_3 superfamily domain, followed by Rep proteins containing Replicase/PriCT_1 superfamily domains, and then by Reps possessing only an HTH_MerR-SF superfamily domain. The remaining eleven groups contain only a few members. To evaluate the diversity of these Rep proteins, we classify them using the current scheme of GR homology groups, which contains 34 groups. However, we needed to create 22 additional GR homology groups to capture all the Rep protein diversity of the plasmid collection. Finally, our bioinformatic analysis suggests that a large fraction of the plasmids seem to have a restricted host range limited to Acinetobacter species, except for those belonging to GR38 that have a very wide host range. To facilitate the future analysis of the Rep proteins, we included a list of the DNA and protein sequences, in fasta format, of the representatives of each one of the GR homology groups.

鲍曼不动杆菌质粒的复制启动蛋白:更新说明
我们对492个鲍曼不动杆菌质粒序列进行了生物信息学分析,鉴定出418个编码复制启动器(Rep)蛋白的基因,根据它们所含的蛋白结构域至少分为14组。最丰富的Rep蛋白组含有Rep_3超家族结构域,其次是含有Replicase/PriCT_1超家族结构域的Rep蛋白,然后是仅具有hth_mrer - sf超家族结构域的Rep蛋白。剩下的11个小组只有少数成员。为了评估这些Rep蛋白的多样性,我们使用了目前的GR同源群方案对它们进行分类,该方案包含34个基团。然而,我们需要创建22个额外的GR同源基团来捕获质粒收集的所有Rep蛋白多样性。最后,我们的生物信息学分析表明,除了那些属于GR38的宿主范围非常广泛的质粒外,大部分质粒似乎具有局限于不动杆菌物种的限制性宿主范围。为了便于将来对Rep蛋白进行分析,我们以fasta格式列出了每个GR同源群代表的DNA和蛋白质序列。
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来源期刊
Plasmid
Plasmid 生物-遗传学
CiteScore
4.70
自引率
3.80%
发文量
21
审稿时长
53 days
期刊介绍: Plasmid publishes original research on genetic elements in all kingdoms of life with emphasis on maintenance, transmission and evolution of extrachromosomal elements. Objects of interest include plasmids, bacteriophages, mobile genetic elements, organelle DNA, and genomic and pathogenicity islands.
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