Titlebook: Chemical Genomics; Reviews and Protocol Edward D. Zanders Book 2005 Humana Press 2005 Escherichia coli.Microarray.Proteomics.genetic inform

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書目名稱Chemical Genomics影響因子(影響力)




書目名稱Chemical Genomics影響因子(影響力)學(xué)科排名




書目名稱Chemical Genomics網(wǎng)絡(luò)公開度




書目名稱Chemical Genomics網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Chemical Genomics被引頻次




書目名稱Chemical Genomics被引頻次學(xué)科排名




書目名稱Chemical Genomics年度引用




書目名稱Chemical Genomics年度引用學(xué)科排名




書目名稱Chemical Genomics讀者反饋




書目名稱Chemical Genomics讀者反饋學(xué)科排名

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Computer-Aided Design of Small Molecules for Chemical Genomicsor creating molecules for chemical genomics. The design process involves manipulation of the input, modification of structural constraints, and further processing of the .-generated molecules using various modular toolkits. The development of a theoretical framework for each of these stages will pro

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Design, Synthesis, and Screening of Biomimetic Ligands for Affinity Chromatographye affinity ligands that represent a promising class of synthetic affinity ligands have been developed to target specific proteins and designed to mimic peptidal templates, natural biological recognition motifs, or complementary surface-exposed residues. These biomimetic ligands have been generated b

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The Role and Application of , Docking in Chemical Genomics Researches can be used to identify the structural features that are important for binding and for . screening efforts in which suitable binding partners can be identified. Here we describe a practical approach for setting up docking simulations using different docking programs. We also cover the analysis an

Mindfulness

Synthesis of Complex Carbohydrates and Glyconjugatesex5 glycoform. Genome analysis identified an open reading frame, HI1578, referred to as LgtD, whose amino acid sequence shows a significant level of similarity to those of a number of bacterial glycosyltransferases involved in lipopolysaccharide biosynthesis. To investigate its function, overexpress

Nonporous

Nonporous

Screening for the Expression of Soluble Recombinant Protein in , in most proteomics pipelines. . (.) is the most convenient and cost-effective host, although optimal conditions for the expression of different proteins vary widely. Proteins vary in their structural stability, solubility, and toxicity in this environment, resulting in differing rates of protein de

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Production of Proteins for NMR Studies Using the Wheat Germ Cell-Free Systemerm cell-free system (without purification). A comparison of .H-.N heteronuclear single-quantum coherence (HSQC) spectra of yeast ubiquitin prepared using each method indicates that this wheat germ cell-free system may be used for rapid nuclear magnetic resonance analyses of proteins without purific