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Titlebook: DNA-Ligand Interactions; From Drugs to Protei Wilhelm Guschlbauer (Director),Wolfram Saenger (Co Book 19871st edition The Editor(s) (if app

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書目名稱DNA-Ligand Interactions
副標(biāo)題From Drugs to Protei
編輯Wilhelm Guschlbauer (Director),Wolfram Saenger (Co
視頻videohttp://file.papertrans.cn/261/260233/260233.mp4
圖書封面Titlebook: DNA-Ligand Interactions; From Drugs to Protei Wilhelm Guschlbauer (Director),Wolfram Saenger (Co Book 19871st edition The Editor(s) (if app
描述This volume contains the texts of the nineteen lectures presented at the NATO-ASI - FEBS Course on "DNA - ligand interactions: from drugs to proteins." The Advanced Study Institute (ASIl was held from August 30th to September 11th. 1986 in the Abbey of Fontevraud (France). The ASI was attended by 112 participants from a wide scientific horizon and from twentyone different countries. It was in some way a follow-up of the ASI held in Maratea. Italy in May 1981 and which was published in the NATO ASI Life Science series as volume 45. While much has been learned about the way the cellular machinery maintains and transmits the genetic heritage. as well as how these processes are regulated. little is Known about how the interactions between the various partners involved are taKing place. The interactions of drugs and proteins with nucleic acids are of evident importance in the understanding of these problems. The spectacular advances in recombinant DNA technology and the increased sophistication of biophysical techniques. in particular >:-ray diffraction and nuclear magnetic resonance. have created a scientific environment which is highly promising for the future of research in molecular
出版日期Book 19871st edition
關(guān)鍵詞DNA; biology; molecular biology; nucleic acid; protein; proteins
版次1
doihttps://doi.org/10.1007/978-1-4684-5383-6
isbn_softcover978-1-4684-5385-0
isbn_ebook978-1-4684-5383-6
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Busines
The information of publication is updating

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Mechanism and Specificity of two Restriction Enzymes, ,I and ,II, that Recognize Asymmetrical DNA Seom their recognition sites (2). Hence, the study of type II restriction enzymes was initially motivated by their unique applications in the analysis of DNA and in the construction of recombinant DNA molecules (3). However, these enzymes also provide examples of DNA-protein interactions whose mechanisms are amenable to molecular analysis.
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DNA Methylation and Mismatch Repair: Molecular SpecificitiesDNA replication a single heteroduplex molecule segregates genetically, i.e. yields mixed progeny consisting of DNA duplexes with the sequence of individual heteroduplex strands. The mismatch repair process transforms a heteroduplex molecule into a homoduplex which yields pure progeny of a single genotype.
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Antibodies to Nucleic Acidslins are biologically active glycoproteins capable of carrying out several different functions. They can bind specifically to antigens, activate the complement systems, mediate cytotropic reactions and act as antigen receptors on lymphocyte membranes.
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https://doi.org/10.1007/978-3-030-00238-1underlying their mode of recognition.. Among approximately 500 type II restriction endonucleases described, EcoRI is the so far best studied enzyme. EcoRI is a dimeric protein with two identical sub-units, the aminoacid sequence of which is known..
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