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蛋白质计算
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  “蛋白质计算”译为未确定词的双语例句
     Computative and Separative Determination of Proteins in the Mixture of Milk Powder and Soya Powder ──Partial Least Squares(PLS)-High Performance Liquid Chromatography(HPLC) Method
     奶粉和豆粉混合食物中蛋白质计算分离测定──偏最小二乘-高效液相色谱法
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     It is significantly lower in December than in other months and is correlated with the intake of nitrate (r=+0.130, P<0.05) and closely negatively correlated with the ratio of intake of VC/NO_3~- (r=-0.162, P<0.01).
     考虑可能来自蛋白质,计算相关系数,结果发现当能量摄入不足时,尿中硝酸盐排出量与植物蛋白、谷类蛋白摄入量密切相关(P<0.01);
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  相似匹配句对
     for Prokaryotic protein an overall predictive accuracy of 89.9% is obtained.
     在蛋白质
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     We also give a new correction factor to simplify the calculation of the Unstatistic.
     的计算
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     The application of the computational methods in protein-protein interaction study
     计算方法在蛋白质相互作用研究中的应用
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     AN ALGORITHM FOR CALCULATING PROTEINSOLUTION C ONFORMATIONS
     蛋白质溶液构象的核磁共振计算方法研究
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     Mobile Computing
     移动计算
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  protein score
HepG2 cells were co-transfected with plasmids for seven HCV proteins (core protein, NS2, NS3, NS4A, NS4B, NS5A, and NS5B) and the IFN-beta promoter luciferase.
      
Its biological value(72), digestibility coefficient(70) and protein score(58) indicated it to be a good protein.
      
The protein score of the weaning food was 70 calculated according to FAO/WHO (1973) pattern.
      
Incidence of proteinuria represents the number of mice whose urinary protein score reached 1 or more.
      
The protein score is a function calculated from the individual normalized z-scores of validated peptides.
      
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Based on the hypothesis on protein folding initiation, in this paper, a new parameter, conformation potential of amino acid, has been established together with corresponding computer program to search for protein folding initiation-the fragment with the highest conformation potential in protein. An excellent explanation for the folding pathway of BPTI has been presented and the results of other twenty proteins have also been discussed.

基于本文对蛋白质卷曲起始位点的假设,提出了一个新参数——氨基酸的有序结构形成势。利用此参数及相应的程序来寻找蛋白质卷曲起始点——蛋白质中有序结构形成势最高的肽段。用BPTI的计算结果非常吻合地解释了BPTI的二硫键重组过程,对其余20个蛋白质的计算结果也进行了讨论。

The gene coding for oligo-1,6-glucosidase of Bacillus subtilis HB002 was cloned by the shotgun-cloning method and sequenced by the chain-termination method of Sanger et al. It consists of an open reading frame of 1683 bp. The amino acid sequence of oligo-1,6-glucosidase deduced from its nuecleotide sequence predicts a protein of 561 amino acid residues with a Mr of 65.985kD, which is 81% and 67% identical to those of oligo-1,6-glucosidase from Bacillus sp. and Bacillus coagulans, respectively, 89% and 79% similar...

The gene coding for oligo-1,6-glucosidase of Bacillus subtilis HB002 was cloned by the shotgun-cloning method and sequenced by the chain-termination method of Sanger et al. It consists of an open reading frame of 1683 bp. The amino acid sequence of oligo-1,6-glucosidase deduced from its nuecleotide sequence predicts a protein of 561 amino acid residues with a Mr of 65.985kD, which is 81% and 67% identical to those of oligo-1,6-glucosidase from Bacillus sp. and Bacillus coagulans, respectively, 89% and 79% similar to those of oligo-1,6-glucosidase from Bacillus sp. and Bacillus coagulans, respectively. The oligo-1,6-glucosidase gene of Bacillus subtilis HB002 was cloned into Escherichia coli expression plasmid pBV220, the result of SDS-PAGE showed that the oligo-1,6-glucosidase gene had been expressed in Escherichia coli DH5α,the expressed oligo-1,6-glucosidase has enzymatic activity.

本研究用鸟枪法构建了枯草芽孢杆菌 (Bacillussubtilis)HB0 0 2的基因组文库 ,经平板法筛选得到了六株能水解合成底物对 硝基苯 α D 葡萄糖吡喃糖苷的阳性克隆 ,经鉴定均含克隆了寡聚 1 ,6 葡萄糖苷酶基因的重组质粒 (命名为pHBM0 0 1~pHBM0 0 6 )。选择pHBM0 0 3 ,对其插入片段测序分析 ,此片段内有一编码 5 6 1个氨基酸的开放阅读框 ,该蛋白质的计算分子量为 6 5 985kD。HB0 0 2的寡聚 1 ,6 葡萄糖苷酶的氨基酸序列与Bacillussp .和凝结芽孢杆菌 (Bacilluscoagulans)的寡聚 1 ,6 葡萄糖苷酶的氨基酸序列一致性分别为 81 %、6 7% ,相似性分别为 89%、79%。从pHBM0 0 3中扩增出寡聚 1 ,6 葡萄糖苷酶基因 ,克隆到pBV2 2 0上 ,转化大肠杆菌 (Escherichiacoli)DH5α ,得到三个能水解对 硝基苯 α D 葡萄糖吡喃糖苷的阳性克隆HBM0 0 3 1~HBM0 0 3 3 ,将此三个菌株热诱导表达 ,SDS PAGE电泳可检测到特异表达的蛋白...

本研究用鸟枪法构建了枯草芽孢杆菌 (Bacillussubtilis)HB0 0 2的基因组文库 ,经平板法筛选得到了六株能水解合成底物对 硝基苯 α D 葡萄糖吡喃糖苷的阳性克隆 ,经鉴定均含克隆了寡聚 1 ,6 葡萄糖苷酶基因的重组质粒 (命名为pHBM0 0 1~pHBM0 0 6 )。选择pHBM0 0 3 ,对其插入片段测序分析 ,此片段内有一编码 5 6 1个氨基酸的开放阅读框 ,该蛋白质的计算分子量为 6 5 985kD。HB0 0 2的寡聚 1 ,6 葡萄糖苷酶的氨基酸序列与Bacillussp .和凝结芽孢杆菌 (Bacilluscoagulans)的寡聚 1 ,6 葡萄糖苷酶的氨基酸序列一致性分别为 81 %、6 7% ,相似性分别为 89%、79%。从pHBM0 0 3中扩增出寡聚 1 ,6 葡萄糖苷酶基因 ,克隆到pBV2 2 0上 ,转化大肠杆菌 (Escherichiacoli)DH5α ,得到三个能水解对 硝基苯 α D 葡萄糖吡喃糖苷的阳性克隆HBM0 0 3 1~HBM0 0 3 3 ,将此三个菌株热诱导表达 ,SDS PAGE电泳可检测到特异表达的蛋白质 ,其中HBM0 0 3 1、HBM0 0 3 2表达的蛋白约 6 6kD ,为完整的寡聚 1 ,6 葡萄糖苷酶 ,而HBM0 0 3 3表达的蛋白质偏小 ;表达的蛋白质均有寡聚 1 ,6 葡萄糖苷酶活性

The microphase adsorption-spectral correction (MPASC) technique was applied to investigation of the interactions of bromo-pyrogallol red (BPR) with proteins.The aggregation of BPR obeys the langmuir monolayer adsorption at pH 3.85.Results show that the adsorption ratios of BPR to proteins are BPR∶BSA=1∶41,BPR∶OVA=1∶11 and BPR∶Mb=1∶4 with adsorption constants of 6.60×10 4,1.49×10 4,3.25×10 4L/mol and real molar absorptivities at 582nm of ε BSA-BPR=7.61×10 5, ε OVA-BPR=2.43×10 5,ε Mb-BPR=3.25×10...

The microphase adsorption-spectral correction (MPASC) technique was applied to investigation of the interactions of bromo-pyrogallol red (BPR) with proteins.The aggregation of BPR obeys the langmuir monolayer adsorption at pH 3.85.Results show that the adsorption ratios of BPR to proteins are BPR∶BSA=1∶41,BPR∶OVA=1∶11 and BPR∶Mb=1∶4 with adsorption constants of 6.60×10 4,1.49×10 4,3.25×10 4L/mol and real molar absorptivities at 582nm of ε BSA-BPR=7.61×10 5, ε OVA-BPR=2.43×10 5,ε Mb-BPR=3.25×10 5L·mol -1·cm -1 respectively.

研究了蛋白质与溴邻苯三酚红 (BPR)的结合反应及溶液酸碱度、温度和离子强度对结合影响 ,表征了 3种组装产物 ,分析了作用机理。结果表明 ,BPR-蛋白质间作用符合 Langmuir单分子层吸附。蛋白质的计算结合比为 :BPR∶ BSA=1∶ 4 1、BPR∶ OVA=1∶ 11、BPR∶ Mb=1∶ 4 ;结合常数 K分别为 6 .6 0×10 4、1.4 9× 10 4和 3.2 5× 10 4L/ mol。产物在 5 82 nm处的摩尔吸收系数为 :εBSA-BPR=7.6 1× 10 5、εOVA-BPR=2 .4 3× 10 5和εMb-BPR=3.2 5× 10 5L· mol-1· cm-1。

 
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