Kelso Andrew A, Goodson Steven D, Temesvari Lesly A, Sehorn Michael G
Department of Genetics and Biochemistry, Clemson University, Clemson 29634, SC, USA; Eukaryotic Pathogens Innovation Center, Clemson University, Clemson 29634, SC, USA.
Eukaryotic Pathogens Innovation Center, Clemson University, Clemson 29634, SC, USA; Department of Biological Sciences, Clemson University, Clemson 29634, SC, USA; Clemson University School of Health Research, Clemson 29634, SC, USA.
Data Brief. 2016 Dec 8;10:364-368. doi: 10.1016/j.dib.2016.12.002. eCollection 2017 Feb.
This paper contains data related to the research article titled "Characterization of the recombination activities of the Rad51 recombinase" (Kelso et al., in press) [1]. The known and putative amino acid sequence of Rad51, the central enzyme of homologous recombination, from nineteen different higher and lower eukaryotic organisms was analyzed. Here, we show amino acid conservation using a multiple sequence alignment, overall sequence identities using a percent identity matrix, and the evolutionary relationship between organisms using a neighbor-joining tree.
本文包含与题为《Rad51重组酶重组活性的表征》(凯尔索等人,即将发表)[1]的研究文章相关的数据。分析了来自19种不同高等和低等真核生物的同源重组核心酶Rad51的已知和推测氨基酸序列。在这里,我们使用多序列比对展示氨基酸保守性,使用百分比同一性矩阵展示整体序列同一性,并使用邻接法树展示生物之间的进化关系。