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Results 1 - 8 of 8
EC Number Application Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 3.1.16.1analysis broadly applicable, robust, and rapid method for complete sequence confirmation of highly modified oligonucleotides containing a mixture of 2'-deoxy, 2'-fluoro, 2'-O-methyl, abasic and ribonucleotides. The sense and antisense strands from synthetic short interfering RNA duplexes are digested individually using both 5'- and 3'-exonucleases and the resulting ladders are analyzed using MALDITOF mass spectrometry. Complete sequence confirmation for the antisense strands of four synthetic RNA duplexes is obtained, whereas a three-base sequence gap in the 5'-end is observed for all four sense strands. Outline of a general strategy for routine sequence confirmation of highly modified oligonucleotides 710529
Display the word mapDisplay the reaction diagram Show all sequences 3.1.16.1analysis detection and assay of RNA-linked nascent DNA pieces in E.coli strains 134158
Display the word mapDisplay the reaction diagram Show all sequences 3.1.16.1analysis end group and sequential analysis of polynucleotides 134140, 134149, 134151
Display the word mapDisplay the reaction diagram Show all sequences 3.1.16.1analysis kinetic studies on macromolecular substrates degradation 134134
Display the word mapDisplay the reaction diagram Show all sequences 3.1.16.1more Ape2 exhibits strong 3'-5' exonuclease and 3'-phosphodiesterase activities and has only a very weak AP-endonuclease activity 682165
Display the word mapDisplay the reaction diagram Show all sequences 3.1.16.1more important role for TRM2 in DNA repair with a potential involvement of its nuclease function in homologous recombination based repair of DNA double-strand breaks, plays no role in the nucleotide excision repair and/or base excision repair pathways 681898
Display the word mapDisplay the reaction diagram Show all sequences 3.1.16.1more Plasmodium FEN-1s have enzymatic activities similar to other species but contain extended C-termini and a more internally located proliferating cell nuclear antigen-binding site. FEN-1 homologs exhibit both endonuclease and exonuclease activities in vitro -, 681823
Display the word mapDisplay the reaction diagram Show all sequences 3.1.16.1more XRNA and XRND are required for trypanosome growth 682836
Results 1 - 8 of 8