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The similarity of nucleotide is 88.1% and the similarity of amino acid is over 90%.

通过在NCBI上进行比对,发现它和拟南芥热激蛋白基因有很高的同源性:核苷酸的同源性在88.1%,氨基酸的同源性在90%以上。

Sequence comparisons showed that the DNA-A sequence of SPLCV-CN were closely related to those of sweet potato leaf curl Georgia virus-[16] (SPLCGV-[16]), Ipomoea yellow vein virus and sweet potato leaf curl virus with nucleotide sequence identity ranging from 88% to 91%.

而由同源性分析得知,SPLCV-CN与SPLCGV-[16]、IYVV和SPLCuV相比对,DNA-A的同源性在88%-91%之间,外壳蛋白的同源性在93%-96%之间。

By using of the Tripos sybyl software, three-dimensional(3D) model of p450nor2 was established based on high sequence similarity to homologous protein p450nor1 structure and the perfect homology modeling was obtained.

基于细胞色素P450nor2与同源蛋白P450nor1氨基酸序列的相似性,采用Tripos sybyl软件对细胞色素P450nor2进行同源模建和分子叠合,获得了理想的同源模建结果。

The predicted amino acid sequence of the gene show a rather high homology(84.47% amino acid identities)with Haemaphysalis longicornis(H.longicornis) TnI (GenBank,GI:14041807).Furthermore, the actin-binding domains of troponin I in predicted amino acid sequence, just the same as H. longicornis ,at the amino acid residues 147-167, suggesting the gene is K haemaphysaloides TnI gene.

经同源性比较,该基因预测的氨基酸序列与长角血蜱肌钙蛋白Ⅰ(GenBank,GI:14041807)有很高的同源性(同源性为84.47%),肌动蛋白结合位点位于147-167氨基酸处,且与长角血蜱肌钙蛋白Ⅰ肌动蛋白结合位点完全相同,表明该基因是镰形扇头蜱肌钙蛋白Ⅰ基因。

When compared with S7 and its putative protein of Lymantria dispar cypovirus 1 and Bombyx mori cypovirus 1, 97.2% and 87.0% identities in the nucleotide level, and 98.7% and 92.8% identities in the amino acid level were found, repectively. BLAST search program revealed some similarity between DpCPV-HN P50 and DnaK-like protein of Mycoplasma hominis.

该基因组与舞毒蛾质多角体病毒1型和家蚕质多角体病毒1型S7节段有很高的同源性,核苷酸序列同源性分别为97.2%和87.0%,氨基酸序列同源性分别为98.7%和92.8%。P50多肽与人型支原体的DnaK样蛋白在C-末端有相似性。

Comparing the nucleotide sequences of 16S rRNA gene and ribosomal protein gene, we could find that these two strains have the highest homology of 99.4% and 99.8%, respectively. The nucleotide sequences of 16S rRNA gene for the CWB-YN strain shared higher homology (98.5%,98.9% and 98.0%) with phytoplasma strains in Tomato big bug 16SrI-A group, Western aster yellow (16SrI-B group and Clover phyllody (16SrI-C group). But it is obviously under 97.0% with other phytoplasma groups. The CWB-GZh strain shared higher homology (98.7%,99.1% and 98.3%) with phytoplasma strains in Tomato big bug(16SrI-A group ),Western aster yellow (16SrI-B group) and Clover phyllody (16SrI-C group).

苦楝丛枝病植原体云南株系与其它组16S rRNA基因序列的同源率进行比较,结果与16SrI-A组中的番茄巨芽病植原体(Tomato big bug,BB)、16SrI-B组中的西方翠菊黄化病植原体(Western aster yellow,SAY)和16SrI-C组中的三叶草变病植原体(Clover phyllody,CPh)同源率达最高,分别为98.5%、98.9%和98.0%,而与其它组的植原体16S rRNA基因序列的同源率均低于95%;苦楝丛枝病植原体贵州株系与16Sr I-A组的番茄巨芽病植原体(Tomato big bug,BB)、16Sr I-B组的西方翠菊黄化病植原体(Western aster yellow, SAY)和16SrI-C组中的三叶草变叶病植原体(Clover phyllody,CPh)的同源率达最高,分别为98.7%、99.1%和98.3%。

In this paper a 1 296 bp cDNA sequence was cloned from bamboo shoot of Phyllostachys violascens by RT-PCR method with degenerated primers based on the sequence conservation of Poaceae TB1 homologous genes.

进化分析进一步表明,竹子TB1相似基因是玉米TB1基因的同源基因,且竹子TB1同源基因的分歧时间介于水稻和现有其他TB1同源基因之间。

Phylogeny analysis indicates that the divergence time of bamboo TB1 homologs are later than rice OsTB1 but earlier than other Poaceae TB1 homologs.

进化分析进一步表明,竹子TB1相似基因是玉米TB1基因的同源基因,且竹子TB1同源基因的分歧时间介于水稻和现有其他TB1同源基因之间。

An identical nucleotide sequence in various passages was obtained by analysis using DNASTAR software, to which the homologies of nucleotides of E2 gene of passages 14, 16, 17, 18 and 23 were 100%, 100%, 99.8%, 99.8%and 99.6%, and those of amino acids were 100%, 100%, 100%, 99.3%and 99.2%, respectively.

结果 Matsuba株E2基因全长846bp,传至23代时仍有很高的同源性,第14、16、17、18和23代与一致序列的核苷酸同源性分别为100%、100%、99.8%、99.8%和99.6%,氨基酸同源性分别为100%、100%、100%、99.3%和99.2%。

The homeodomain is responsible for binding to DNA, and experiments to swap homeodomains between proteins suggest that the specificity of DNA recognition lies within the homeodomain, but (like the situation with phage repressors) no simple code relating protein and DNA sequences can be deduced.

同源域负责结合DNA,在蛋白质之间交换同源域的实验证实了这一结论。但(就像噬菌体阻遏子的情形一样)并没有推出联系蛋白质与DNA序列的简单机理。同源域的C端和原核生物阻遏子α-β-α超二级结构有一定的同源关系。我们回想第13章,λ阻遏子有一个&识别螺旋&(α-螺旋-3)DNA的大构接触,而另一个螺旋(α-螺旋-2)位于 DNA的拐角。

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