Titlebook: RNA Biochemistry and Biotechnology; Jan Barciszewski,Brian F. C. Clark Book 1999 Springer Science+Business Media Dordrecht 1999 DNA.Elonga

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Why RNA?,he 3-dimensional structure of the key protein or nucleic acid. The data bases of structures are expanding rapidly as X-ray and NMR developing technologies allow structural analysis of more and more proteins, nucleic acids and their complexes. Recently, complex structures have involved various ribonucleic acid molecules.

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Specific Interaction Between Damaged Bases in DNA and Repair Enzymes,ed in a cavity on the protein surface. These structural features allow an understanding of the catalytic mechanism and implicate a general mechanism of how other repair enzymes recognize damaged DNA duplexes.

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1388-6576 acting with specific RNA species. Papers deal withDNA protein interactions, telomerase, aminoacyl-tRNA synthetases,elongation factor Tu, DNA repair, RNA structure, NMR technology, RNAaptamer interaction of biological macromolecules with metal ions. Twopapers deal with theoretical aspects of RNA stru

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Algorithms and Thermodynamics for RNA Secondary Structure Prediction: A Practical Guide,parameters over the past dozen years. Both RNA and DNA rules are discussed, with some mention of parameters for RNA/DNA hybridization. Although the thermodynamic model has grown in complexity to accommodate new types of information, the folding algorithm has not yet incorporated some features, such

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Towards the 3D Structure of 5s rRNA,without the terminal hairpin-loop has been determined at 1.6Å and Helix V of domain E including the terminal hairpin-loop has been determined at 3.0Å [8]. Furthermore it was possible to observe a general mode of intermolecular interaction, which occur only in RNA structures and it was possible to de

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Protein-DNA Recognition,sign proteins with novel recognition specificities. Despite this considerable practical success, the thermodynamic and kinetic properties of protein/DNA recognition remain poorly understood (reviewed in 1).

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,Aminoacylation of tRNA Induces a Conformational Switch on the 3’-Terminal Ribose,e of the fluorescence intensity of formycin in tRNA-CCF. upon aminoacylation is explained by partial destacking of the 3’-terminal base moiety. Several analogues of anminoacyl-tRNA which were modified on 3’-terminal ribose were tested in their ability to interact with elongation factor Tu.GTP comple