同源的

Homologies to Cf-9 reveal motifs useful in the identification of other plant pathogen resistance genes.

与Cf－9的同源性，展示可用于鉴定其他植物病原体抗性基因之基元。

Based on the analysis of ORF , the two cDNAs encode the respective proteins of 541 and 555 amino acids. The two proteins are 77% identical in amino acid sequences, and they have not significant homologies with all known proteins.

根据读码框架分析，这两个cDNA分别编码541和555个氨基酸的蛋白质，两个蛋白质之间氨基酸序列一致率为77％，和已知蛋白无显著同源性。

Based on Database search, five cDNA fragments had high homologies to known genes,while the functions of other six were unknown.

有5个片段在GenBank数据库中发现同源序列，其余的6个功能未知。

Sequences and bioactivity analysis showed that BmK βTX was highly homologous to Ts Ⅶ(aβ-type toxin) with low excitatory toxicity to both mammals and insects, which impled that it belonged to a new subtype of β-type toxin; BmK TX3 might belong to Chraybdotoxin group as specific blockers of potassium channels.

序列与生物活性分析表明BmK βTX与β-型蝎毒素Ts Ⅶ同源性较高，且对哺乳动物和昆虫均有低兴奋性毒性，提示它应属于一类新的β-亚型；BmK TX3应归属于Chraybdotoxin类钾通道特异阻断剂。

Its structure was determined by a combination of MALDI-TOF MS ana lyses, N-terminal Edman degradation and amino acid analyses. Amino acid sequenc e of VAPP was: N-terminus VLSAADKSNVKAAWGKVGGNAPAFGAEALLRM.

结合激光解析电离飞行时间质谱，N-端Edman降解和氨基酸分析结果表明，该多肽是由32个氨基酸残基组成的直链多肽，分子量3 216 u，主要含缬氨酸、丙氨酸、赖氨酸和甘氨酸，无半胱氨酸，其一级结构氨基酸排列顺序为：N端-VLSAA DKSNVKAAWGKVGGNA PAFGAEALLRM，与已知蛋白序列同源性远小于50%。

Sequence comparison revealed that HoMADS2 was highly homologous to the class B MADS box genes.

序列比较分析表明，HoMADS2与B类MADS box蛋白具有较高的同源性。

These findings illustrate the complexity of the homology concept in understanding evolution, particularly the evolution of mineralized tissues.

这些结果显示在进化过程中同源性概念异常复杂，尤其在矿化组织的进化过程中。

In serial passaging experiments, the genome of the chimeric pHBIV-3 could not exist stably. The gag or tat mRNA and the activated proteins could not be detected.

在MT〓细胞中，由于BIVLTR在人细胞中的基础转录活性较弱，尽管存在bTat-bTAR同源反式激活系统，仍不能产生感染性病毒。

Thus Group1,2,3,4 were the four new DNA relation groups different from known rhizobia species.

同时，四个新亚群中心菌株两两之间的 DNA同源性在22.5～62.7%之间。

Methods PCR amplification of drug resistance gene abeM was carried out using chromosomal DNA of Ab 35 and Ab 36 clinical isolates as template. PCR product of abeM gene was sequenced. The nucleotide sequences and deduced amino acid sequences were analyzed by BLAST of NCBI. After cells of Escherichia coli KAM32 transformed with a plasmid carrying the abeM gene PCR product, MICs of various drugs were determined by serial twofold dilution method.

以临床分离的Ab 35、Ab 36染色体DNA为模板扩增abeM基因，对abeM基因扩增产物进行DNA测序及同源性分析；将abeM基因扩增产物与载体连接后转化入大肠埃希菌KAM32感受态细胞中，对转化子进行药敏分析。

She gently rebuff ed him, but agreed that they could be friends

她婉言拒绝了，但同意作为朋友相处。

If in the penal farm, you were sure to be criticized.

要是在劳改农场，你等着挨绳子吧！