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amino-compound相关的网络例句

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According to the concept that the subcellular location of an apoptosis protein is mainly determined by its amino acid sequence, the six kind of subcellular locations of apoptosis proteins were predicted by using the algorithm of the increment of diversity combined with support vector machines based on the n-peptide components of local amino acid sequence and hydropathy and hydrophobicity.

根据凋亡蛋白的亚细胞位置主要决定于它的氨基酸序列这一观点,基于局部氨基酸序列的n肽组分和序列的亲疏水性分布信息,采用离散增量结合支持向量机算法,对六类细胞凋亡蛋白的亚细胞位置进行预测,结果表明,在Re-substitution检验和Jackknife检验下,ID—SVM算法的总体预测成功率分别达到了94.6%和84.2%;在5-fold检验和10-fold检验下,其总体预测成功率也都达到了83%以上。

OrLPT1 ORF encods a polypeptide with 535 amino acid residues (molecular mass of 57.6KDaltons), which shares more than 64% amino acid identity with some other high-affinity Pi transporters of plants. Hydropathy analysis of the deduced polypeptides showed that the OrLPT1 is highly hydrophobic and contains 12 putative membrane-spanning regions.

OrLPT1 ORF 编码长为535 个氨基酸(分子量57.6 KDaltons)的蛋白,与其他植物物种磷酸盐转运蛋白的同源性在64%以上;多肽链的疏水性分析表明,OrLPT1 具有12 个疏水的跨膜区及高亲和力磷酸盐转运蛋白中保守的3 个磷酸化作用位点:蛋白激酶C作用位点、N端糖基化部位和酪蛋白激酶II 作用部位; 3。

The 3D structure of N protein shows that the domain of Ep703 is exposed on the surface of the protein, making the epitope to be readily recognized by antibody. No homology is found between the mimotopes and native epitope. However, they all contain high content of hydrophile amino acids and low content of hydrophobile amino acids.

蛋白的三维结构显示,Ep703的9个氨基酸多肽暴露于蛋白的表面。3个模拟表位与表位Ep703的序列&IQTAFNQGA&相比,相同的氨基酸很少,但是各表位氨基酸的极性却有一个共同的特征:亲水性氨基酸比例较大,疏水性氨基酸比例较少。

The polar hydrophilous amino acid Thr is replaced by an unpolar hydrophobous amino acid Ile, a hydrogen bond changed in the higher structure and the point is far away from the active center, so it doesn't influence the activity and thermostability a lot.

亲水的Thr108突变成非极性的Met,导致与该位点空间相邻的N116亲水氨基酸His的极性残基——咪唑环产生空间电位排斥,从而造成His所在的β折叠构象发生改变。

It looks like that the molecular weight of these immunopeptides were very small, and it also showed that the hydrophobe amino acid on the bottom and alkaline amino acid were important structurals of the immunopeptides.

论文主要研究结论如下:目前已报道的140余种免疫活性肽其相对分子质量都较小,通常在肽链中含有碱性氨基酸或在末端具有疏水性氨基酸。

It is shown by Infrared spectra that relative concentration of amino formic acid ester has prominent relationship with compressive stress at 10% strain in the process of accelerated hygrothermal tests, which means that hydrolysis of amino formic acid ester is main factor resulting in decrease of compressive properties.

经红外光谱测定,在人工加速湿热老化试验过程中,材料的活性基团氨基甲酸酯的相对浓度与10%定应变压缩应力的相关性显著,氨基甲酸酯水解是材料室内贮存过程中力学性能下降的主要原因。

One of the amino acids, called prolene, is not really an amino acid, but imino acid.

有一种称为脯氨酸的氨基酸实际上并不是氨基酸,而是亚氨基酸。

E. the activation of amino acid, the elongation of peptide chain and the termination of the chain reaction, among which the activation of amino acid—the formation of imino acetoxyphosphoranes was the key step.

在这三步中,氨基酸的活化即氨基酸磷烷的形成是整个自组装成肽反应的最重要一步。

Racemic backbones 2-amino-2'-hydroxy-6,6'-dimethyl-l,l'-biphenyl la and 2-amino-2'-hydroxy-4,4',6,6'-tetramethyl-l,1'-biphenyl 1b were synthesized from o-methylaniline and 2,4-dimethylaniline via nitration, diazotation/iodination, Ullmann coupling, selective reduction, diazotation/hydrolysis and hydrogenation.

从邻甲苯胺及2,4-二甲基苯胺出发,经过硝化,重氮化-碘代,偶联,单还原,重氮化-水解及还原反应合成了消旋体骨架2-氨基-2'-羟基-6,6'-二甲基-1,1'-联苯1a和2-氨基-2'-羟基-4,4',6,6'-四甲基-1,1'-联苯1b。

One route was that the amino-groups on the silica gel were transformed to tertiary amines by Eschweiler-clarke reaction that amine-groups react with formaldehyde and methanoic acid to prepare tertiary amines; the silica gel intermediates with tertiary amine groups reacted with chorohydrocarbons to prepare insoluble silica gel quaternary ammonium salt bactericides. Another route was that the amino-groups on the silica gel reacted with excessive chlorohexadecane; the preparing intermediates were quaternized with iodomethane to obtain insoluble silica gel quaternary ammonium salt bactericides.

一条路线是根据埃施韦勒-克拉克(Eschweiler-clarke)胺甲基化反应,进行胺基叔胺化反应,制成带有叔胺官能团的硅胶中间体,此中间体上的叔胺与卤代烷反应生成杀菌活性官能团季铵盐,制成硅胶类水不溶性季铵盐杀菌剂;另一条路线是带有胺反应活性中心的硅胶与过量正氯代十六烷反应,得到的中间体再用碘甲烷季铵化,得到最终产品——水不溶性季铵盐杀菌剂。

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