lrr

Structure and Function of LRR Proteins in Plant Defense Mechanism

参与植物防御反应的LRR型蛋白结构与功能

Mathematics relationship between modulation of LRR and target configuration is established .

建立了低分辨雷达调制特征和目标结构的数学关系。

Studies of modualation characteristics of propeller aircraft returns in the LRR

低分辨雷达螺旋桨飞机回波调制特性的研究

FEM encodes a polypeptide with two LRR domains and two F-Box domains .

FEM蛋白包含两个LRR结构和两个F-box结构域。

Nucleotide diversity of four group have no difference , but the region of LRR show more high variation than the two ends .

四组之间的核苷酸多样性没有显著差异，而亮氨酸重复序列区域的变异较两端大。

This paper presents a new scheduling algorithm , called layering round robin ( LRR ), which is based on current available algorithms .

在综合现有的一些算法的基础上，提出了一种分层循环（LRR）的调度算法。

HRI consists of 15 leucine - rich repeat ( LRR ) .

hRI是由15个亮氨酸重复序列（Leucine-richrepeat，LRR）组成的。

Laser rapid repair ( LRR ) is an advanced laser repair technology that has been developed based on Laser rapid forming ( LRF ) .

激光快速修复技术是在激光快速成形技术的基础上发展起来的一项先进的激光再制造技术。

The internal flow field of hydrocyclone is simulated using LRR Reynolds stress model , applying SIMPLE arithmetic and basing on basic theory of hydrocyclone .

从油水分离旋流器流场分析的基本理论出发，采用LRR雷诺应力湍流模型，应用SIMPLE算法，对其内部流场进行了数值模拟。

In this paper , based on the results of the separation experiment , analyzed nine turbulence models discovered LRR Reynolds Stress model is the best for this problem .

本研究以实验数据为依托，利用CFD方法对描述液体流动的九种湍流模型进行了计算与对比，发现LRR雷诺应力模型的计算精确度要高于其他八种湍流模型。

LRR distributed in all the C terminal sequences , but most were located at - 80 amino acids after the MHD domain .

LRR在整个NBS至C末端序列中均有分布，但多数位于MHD下游大约80个氨基酸左右。

Proteins encoded by resistance genes usually contain leucine-rich repeats ( LRR ) and nucleotide binding site ( NBS ) .

植物抗病基因编码的蛋白质大多含有富亮氨酸重复单位（LRR）和核酸结合位点（NBS）等结构。

Further investigate the flow mechanism of the liquid-liquid hydrocyclone , and the oil and water phases flow field in hydrocyclone for oil water separation is simulated using LRR stress model .

深入研究了液-液水力旋流器的流动机理，并采用LRR应力模型对油水分离旋流器的油水两相流场进行了数值模拟。

Thaliana were highly homologous , with a distinct structure from other plant LRR proteins , suggesting that LRR RL proteins belonged to a new LRR protein family .

序列和结构比较分析表明：该棉花LRRRL蛋白与拟南芥的两个类LRR抗病蛋白高度同源，而与植物的其他LRR蛋白结构不同，推测LRRRL蛋白属于一类新的LRR蛋白。

The Cf proteins , which are anchored at plasma membrane with the main body outside , mainly consist of a leucine-rich repeat ( LRR ) and a transmembrane domain .

Cf蛋白定位于细胞质膜，但主体在膜外，主要结构域为富含亮氨酸重复（LRR）和跨膜结构域。LRR重复单元数目以及N端序列决定了Cf蛋白对Avr的识别特异性。

To date the majority of known plant disease-resistance genes are featured with a nucleotide-binding site ( NBS ) and leucine-rich repeats ( LRR ) .

已知的植物抗病基因大多数具有核苷酸结合位点（NBS）和富含亮氨酸重复区（LRR）。

The clone plasmid DNA was digested with various 6-base restriction enzymes , then transferred to membrane , and conducted southern hybridization with the LRR fragment as a probe .

将该TAC克隆用不同6碱基酶酶切，转膜后，以上述LRR片段作探针进行Southern杂交，每种酶切均有杂交带，表明该克隆为真正的阳性单克隆。

VLRs are leucine-rich repeat ( LRR ) proteins that mediate adaptive immunity in jawless vertebrates ( hagfish and lamprey ) .

可变淋巴细胞受体是富含亮氨酸重复序列（leucine-richrepeat，LRR）蛋白，调控无颌类脊椎动物（八目鳗和七鳃鳗）的获得性免疫。

Most of plant disease resistance ( R ) genes cloned so far belong to NBS LRR group which contains nucleotide binding sites ( NBS ) and a leucine rich repeat ( LRR ) .

大部分已克隆的植物抗病基因都包含有核苷酸结合位点区（NBS）和富含亮氨酸的重复序列区（LRR）。

LR is more adapted in non-rhizosphere soils , and LRR is less competent in healthy cotton rhizosphere than LTR-2 . LR is not effective in controlling cotton damping-off caused by R.

LR比LTR2更能适合非根际土壤环境，而LRR在健康棉花根际的定殖能力上，比LTR2有明显下降。

Amplified products were cloned in pGEM-T vector and then sequenced . Eighteen clones characterized with NBS , three with LRR and one with serine / threonine kinase domain were obtained by sequencing analysis .

扩增产物克隆到pGEM-T载体中，经测序，共获得具有NBS结构域片段的克隆18个，具有LRR结构域片段的克隆3个，具有丝氨酸/苏氨酸蛋白质激酶域片段的克隆1个。

Sequence homology analysis of amino acid showed that R-Fom-2 shared high homology ( 96 % ) with Fom-2 and had a similarity over 91 % compared with different melon breeds in Fom-2 LRR .

氨基酸同源性分析显示，R-Fom-2同Fom-2全长序列具有96%的同源性，对不同甜瓜品种Fom-2的LRR区分析比较，同源性在91%以上。

All of NBS resistance gene analogues contained the conserved motifs of NBS LRR type resistance genes , such as P loop ( Kinase 1a ), Kinase 2 , Kinase 3a and transmembrance domain .

所有11类的抗病基因同源系列均含有NBS-LRR类抗病基因的保守序列，如P-loop、Kinase2、Kinase3a以及跨膜区域等。

VLRs can utilize the LRR module to recognize glycans with an affinity equal to that of lectins and antibodies , and will be a very promising class of natural glycan-binding proteins for basis research and clinical applications .

可变淋巴细胞受体能利用LRR模块以媲美凝集素和抗体的亲和力和选择性识别多糖，将成为在基础研究和临床应用上非常有前景的一类天然多糖结合蛋白。

Mutant LR which is fast growing and grows at low temperature ( 10 ℃), and mutant LRR which is resistant to carbendazim ( 20 μ g / ml ), were obtained from a Trichoderma viride strain LTR-2 by ultraviolet mutation .

通过紫外线诱变处理，获得了可以在低温下（10℃）生长的绿色木霉LTR2的快速生长型突变株LR，以及对多菌灵具有抗性的突变株LRR。

The cloned gene Mi - 1 . 2 which possesses the existence of a nucleotide binding site ( NBS ) and a leucine-rich repeat ( LRR ) manifest that it can cause the localized cell death in host plant and hypersusceptible reaction ( HR ) .

已克隆的Mi-1.2基因，具有核苷酸结合位点（NBS）和亮氨酸重复（LRR）的存在；表现为在寄主植物内引起过敏反应（HR），造成局部细胞坏死；

The proteins encoded by these resistance genes usually contain one or more following conserved domains , such as LRR , STK , NBS , LZs , TIR and so on , and probably mediate the signal recognition , production , and transmission during expression of plant disease resistance .

这些抗病基因编码的蛋白质产物一般具有LRR、STK、NBS、LZs、TIR等一种或多种保守结构，在植物抗病中可能介导抗病信号的识别、产生和传导过程。

Analysis of the sequence for conserved functional domains reveals that the protein is composed of a cysteine-rich amino-terminal leucine-rich repeat ( CR ) flanking domain , followed by a leucine-rich repeat domains ( LRR ) and a serine / threonine - rich region ( S / T ) .

对十四种动物OMgp的蛋白序列分析发现，OMgp由几个部分构成：富含半胱氨酸的结构域（CR）、富含亮氨酸重复序列的结构域（LRR）和富含丝／苏氨酸的结构域。