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Titlebook: Macromolecular Biorecognition; Principles and Metho Irwin Chaiken,Emilia Chiancone,Paolo Neri Book 1987 The Humana Press Inc. 1987 Amino ac

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發(fā)表于 2025-3-21 17:15:59 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Macromolecular Biorecognition
副標(biāo)題Principles and Metho
編輯Irwin Chaiken,Emilia Chiancone,Paolo Neri
視頻videohttp://file.papertrans.cn/622/621045/621045.mp4
叢書名稱Experimental Biology and Medicine
圖書封面Titlebook: Macromolecular Biorecognition; Principles and Metho Irwin Chaiken,Emilia Chiancone,Paolo Neri Book 1987 The Humana Press Inc. 1987 Amino ac
出版日期Book 1987
關(guān)鍵詞Amino acid; DNA; Elongation; chemistry; development; enzymes; nucleic acid; protein; proteins; receptor; synth
版次1
doihttps://doi.org/10.1007/978-1-4612-4600-8
isbn_softcover978-1-4612-8944-9
isbn_ebook978-1-4612-4600-8
copyrightThe Humana Press Inc. 1987
The information of publication is updating

書目名稱Macromolecular Biorecognition影響因子(影響力)




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Structural Bases for the Recognition of Inhibitors by Serine Proteinases and their Zymogensind of information, obtained by crystallographic studies (1), has been of primary importance in the understanding of the catalytic steps involved in the hydrolysis of peptide (or ester) bonds by serine proteinases.
板凳
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Transition of Chromatin from the “10 nm” Lower Order Structure, to the “30 nm” Higher Order Structurs been introduced. In this description the persistence length a equals about 40 nm in 0.2M NaCl (5), corresponding to a curvature radius of this order. Short DNA chains are almost rodlike in solution.
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Thermodynamics and Stereochemistry of the Interaction between Anthraquinone Drugs and DNAc ring system of the anthracycline slips into adjacent base pairs of the polynucleotide, whereas the cyclohexene moiety, connected to the amino-sugar is located in the minor groove of the double-helix (6,7). The complex is further stabilized by electrostatic interactions between the positively charged protonated amino group of the polymer chain.
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Studies on the Interaction between Ribosome and Elongation Factor 2 by Fluorescent Labeling of the DF-2 with this fluorescent probe by an efficient and selective enzymatic mechanism which allowed us to confidently attribute the molecular localization of the fluorophore at the level of the diphthamide residue.
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