6.5.1.3 ATP + (ribonucleotide)n + (ribonucleotide)m RNA substrates containing a 5'-phosphate terminus at one end and either a 2',3'-cyclic phosphate or a 2'-phosphate terminus at the other end. In the latter case the reaction is about 30% as active as with the cyclic derivative Triticum aestivum AMP + diphosphate + (ribonucleotide)n+m - ? 813 6.5.1.3 ATP + (ribonucleotide)n + (ribonucleotide)m participates in an in vitro splicing of yeast transfer RNA precursors containing intervening sequences. Covalently ligates tRNA5' and 3' half-molecules produced by a yeast endonuclease Triticum aestivum AMP + diphosphate + (ribonucleotide)n+m - ? 813 6.5.1.3 ATP + (ribonucleotide)n + (ribonucleotide)m conversion of linear polyribonucleotides into covalently closed circles, formation of a 2'-phosphomonoester,3',5'-phosphodiester linkage Triticum aestivum AMP + diphosphate + (ribonucleotide)n+m - ? 813 6.5.1.3 ATP + (ribonucleotide)n + (ribonucleotide)m converts linear molecules of polyriboadenylate to circular form by the intramolecular covalent linkage of the 5'-phosphate end to the 3'-hydroxyl terminus Tequatrovirus T4 AMP + diphosphate + (ribonucleotide)n+m - ? 813 6.5.1.3 ATP + (ribonucleotide)n + (ribonucleotide)m formation of a phosphodiester bond between a 5'-PO4-terminated oligonucleotide and a 3'-OH terminated oligonucleotide. Intramolecular formation of single-stranded circles with longer oligonucleotides of the type pAp(Ap)nAOH, where n is about 15 or greater. Intermolecular joining of pAp(Ap)3AOH, where the 5'-PO4-terminated oligonucleotide is short enough to prevent apposition of its 3' and 5' ends, to UpUpUOH Tequatrovirus T4 AMP + diphosphate + (ribonucleotide)n+m - ? 813 6.5.1.3 ATP + (ribonucleotide)n + (ribonucleotide)m cylization of poly(A) Tequatrovirus T4 AMP + diphosphate + (ribonucleotide)n+m - ? 813 6.5.1.3 ATP + (ribonucleotide)n + (ribonucleotide)m the best substrate is [5'-P]polyriboadenylate Tequatrovirus T4 AMP + diphosphate + (ribonucleotide)n+m - ? 813 6.5.1.3 ATP + (ribonucleotide)n + (ribonucleotide)m ligates two substrate RNAs, promoting the attack of the 3'-hydroxyl of one substrate upon the 5'-triphosphate of the other substrate with release of diphosphate, reverse of ligation has been detected, but very inefficient, not saturable by soluble amounts of diphosphate synthetic construct AMP + diphosphate + (ribonucleotide)n+m - ? 813 6.5.1.3 ATP + (ribonucleotide)n + (ribonucleotide)m only the di-magnesium-coordinated form Mg2ATP0 reacts with the enzyme, forming the covalent complex E-AMP, the reverse reaction, ATP synthesis, occurs between the mono-magnesium-coordinated diphosphate from MgP2O72- and the enzyme-MgAMP complex Tequatrovirus T4 AMP + diphosphate + (ribonucleotide)n+m - r 813 6.5.1.3 ATP + (ribonucleotide)n + (ribonucleotide)m catalyzes RNA end-joining Vibrio phage KVP40 AMP + diphosphate + (ribonucleotide)n+m - ? 813