编码氨基酸

2个分离物的CP基因均由582nt组成，其核苷酸和推导编码氨基酸序列同源性分别为87.8%和95.9%。

The similarities of nucleotide and deduced amino acid sequences of CP genes among these isolates are 87.8 % and 95.9 % respectively .

该引物还在301位点上均有T碱基插入现象，引起了编码氨基酸的改变，由原来的CCT脯氨酸→TCC丝氨酸。

The primer also has 301 points on the T insertion phenomenon , caused changes in amino acid from the CCT proline → TCC serine .

spiralis的序列P49有一定的差异，经同源性分析，二者核苷酸序列同源性为98.63%，推导其所编码氨基酸序列同源性为99.05%。

Spiralis with 98.63 % nucleotide identity and 99.05 % derived amino acid identity respectively .

核苷酸比对分析发现，NAC基因的变异主要发生在内含子区域，少数发生在编码氨基酸的密码子的第三位，属于同义突变范畴。

Nucleotide comparison analysis , NAC gene mutation occurred in intron regions , a few mutation is in the third site of codon , belonging to synonymous mutation .

另一个管家基因的序列及对应的氨基酸序列与人、大鼠和小鼠转录激活因子-4部分cDNA序列及对应的编码氨基酸序列高度同源。

The other housekeeping gene sequence and its corresponding amino acid sequence in deer shared high homology with a group of partial cDNA sequences encoding activating transcription factor 4 of human , rat , mouse and their corresponding amino acid sequences , respectively .

推测的其编码氨基酸序列，5株之间100%一致，与国外已报告的HGV比较，同源性为94.9%～100%。

Compared with the published HGV isolates , the nucleic acid sequences of HGV-C1 ~ C5 are 79 % to 91 % identical and the deduced amino acid sequences exhibit 94.9 % ~ 100 % homology .

东北马鹿肌肉生长抑制素基因序列的克隆、编码氨基酸序列及结构特征分析

Cloning , sequence and structure analysis on myostatin gene of Manchurian wapiti

利用定点突变技术对造成编码氨基酸的碱基定点突变修复。

The mutational basic groups resulting in encoding alteration with site-specific mutagenesis technology were repaired .

核苷酸同源性分别为核苷酸序列同源性分别为98.97%、98.75%、98.69%，推导的编码氨基酸同源性分别为98.12%、97.60%、97.60%。

The deduced amino acid sequences were 98.12 % 、 97.60 % and 97.60 % correspondingly .

它们推断的编码氨基酸序列同源性在796～951%之间。

The identity of their deduced amino acid sequences was 79 6 % ~ 95 1 % .

4个突变热点全部导致了编码氨基酸的突变。

All 4 hot spots of mutation in VP_1 gene led to mutations of deduced amino acid .

与已报道的序列高度同源：其核苷酸序列及推论的编码氨基酸序列的同源率分别为99.6%和99.3%。

The cloned DNA fragment has 99.6 % and 99.3 % homologies in nucleotide sequence and amino acid sequence compared with Led .

对68例发育缺陷胎儿成功测序样本进行分析，共存在20个突变位点，其中引起编码氨基酸改变的突变点共15个。

68 cases of target DNA fragment were successful sequencing , there were 20 mutations , which caused 15 amino acid changes in sites .

神经网络的输入层编码氨基酸序列中的一个移动窗口和预测窗口中的中心残基。可能的窗口的大小为5,7,9,11,15,17,19和21。

The input layer of the ANN encodes a moving window in the amino acid sequence and prediction is made for the central residue in the window .

他们由不同的基因编码，氨基酸序列高度相似，特别是在DNA结合域和配体结合域。

They are encoded by separate genes , highly similar in amino acid sequences , particularly in the DNA binding domain and ligand binding domains .

由DNA顺序推知，linker区编码的氨基酸顺序SerGInAlaCys可能是新的信号肽酶识别位点；

A new signal peptidase recognition site has been found in the linker-encoded amino acid sequence .

编码蛋白氨基酸与来自GenBank的Kestrel、Obese和SC品系的来杭鸡比较，氨基酸的突变主要发生在28～32位。

The deduced amino acid sequences were compared with strains Kestrel , Obese and SC Leghorn chickens from GenBank .

结果显示，15个毒株的E基因核苷酸序列之间的相似性为84.1%～100%，推导编码的氨基酸序列之间的相似性为81.1%～100%；

Nucleotide sequences comparison revealed a sequence homology of 84.1 % - 100 % among all 15 local isolates , with a similarity of 81.1 % - 100 % in deduced amino acid sequences .

该基因编码的氨基酸序列含有3个蛋白激酶C磷酸化位点；2个酪蛋白激酶Ⅱ磷酸化位点；5个N-肉豆蔻酰位点；2个叶绿素a/b结合蛋白位点。

The gene-encoded amino acid sequence contains three Protein kinase C phosphorylation sites , two Casein kinase ⅱ phosphorylation sites , five N-myristoylation sites and two Chlorophyll a / b binding protein and a yiaA / B two helix domain .

与Genebank中报道的番鸭IL-2基因序列有100%的同源性，与绿头鸭IL-2基因序列进行比较，在ORF内有7个碱基不同，但其推导编码的氨基酸二级结构完全相同。

Comparing with the sequences of Anas platyrhynchos reported in gene bank , there are mutation nucleotides of seven , but the predicted second structure of encoding amino acid is similar .

survivin定位于17q25，是一个凋亡抑制基因，属于IAP家族。它编码142氨基酸贱基16.5KD的胞浆蛋白。

Survivin encode 142 amino acids , 16.5 kDa intracellular protein that belongs to the inhibitor of apoptosis ( IAP ) gene family .

并对测序结果进行基因型及血清型分析、全基因序列同源性及差异性比较、HBV各编码区氨基酸变异等生物信息学分析。

The related biological information was analyzed , including the homogeneity and heterogeneity of the HBV DNA sequence before and during PMEA therapy , and variance of amino acids coded by HBV sequence .

由flor基因编码的氨基酸序列与GenBank报道的flor基因存在3个氨基酸替代。

There were three amino acid substitutions in the flor gene between the sequences coloned and reported by GenBank .

目的：克隆编码Nogo-66氨基酸多肽基因，构建原核重组表达载体，并诱导其在大肠埃希菌BL21（DE3）中表达。

Objective : To clone Nogo-66 gene , construct the recombinant prokaryotic expressive vector and express its products in E. coli .

一个位于3257，发生C到A的颠换。比较人IRS&1基因的阅读框发现，这两个SNP均可引起编码的氨基酸改变，可能具有重要生物学意义。

One is G / A in position 2650 , another is C / A in position 3257 . Comparing to the ORF of human 's , both of the SNPs can cause the amino acid change , and maybe affect the functions of IRS-1 .

HCV武汉株和日本株（HCV-J型）E1基因核苷酸的同源性为74.48%，编码的氨基酸的同源性为78.13%。

74.48 % nucleotide acids of El cDNA and 78 . 13 % amino acid of El protein are homologous between WH strain and Japan strain ( HCV-J type ) .

结果：克隆的luffin-a基因及其所编码的氨基酸序列与国外报道的核苷酸序列及氨基酸序列同源性分别为95%和92%，因而所获得的luffin-a基因是丝瓜籽核糖体失活蛋白luffin-a一个新的cDNA序列。

Results : The cDNA and amino acid sequence of the novel luffin-a obtained showed 95 % and 92 % homology with those reported by others .

目的克隆和分析HPV11的晚期表达基因序列L1及其编码的氨基酸序列，为HPV感染的检测和基因工程疫苗研制提供基础。

Objective To clone and analyze the whole sequence of L1 gene and its deduced L1 protein of HFV 11 , for the purpose of detection and prophylactic and therapeutic vaccine against papillomavirus infections .

来自SS-ori菌的D-海因酶基因全长1374bp，编码457氨基酸。

Whilst D-hydantoinase from strain SS-ori contains an open reading frame of 1374 bp encoding 457 amino acids .

将其序列与6株A型流感病毒NP基因序列进行比较，各毒株之间NP基因核苷酸序列同源性为925%～959%，编码的氨基酸同源性为970%～984%。

The results of comparative sequence analysis indicated that the nucleotide sequence of NP gene of this strain shared 92.5 % ~ 95.9 % homology with other six AIV strains , and putative amino acid sequence shared 97.0 % ~ 98.4 % homology with other six strains .