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- W156922172 abstract "The most widely described artificial ribonucleases are designed on the basis of RNA-binding domains and low molecular weight constructs bearing functional groups of amino acid residues from catalytic centers of natural RNases: conjugates containing imidazole and carboxylate ions, guanidinium groups (see review Silnikov and Vlassov 200l). This chapter is devoted to proteins displaying ribonuclease activity and peptide-based conjugates which are capable of hydrolyzing RNA. The basic requirements showed by any artificial ribonucleases are high efficiency and specificity of RNA cleavage. The efficiency of hydrolysis is determined by the catalytic properties of active groups, and the specificity is determined by the affinity of compounds for certain RNA sites.KeywordsRibonuclease ActivityPhosphodiester BondAnticodon LoopNatural RNasesSingle Zinc FingerThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves." @default.
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- W156922172 date "2004-01-01" @default.
- W156922172 modified "2023-09-25" @default.
- W156922172 title "RNA-Cleaving Oligonucleotide-Peptide Conjugates" @default.
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- W156922172 doi "https://doi.org/10.1007/978-3-642-18510-6_10" @default.
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