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1 to the functional assembly of the human tRNA splicing endonuclease.
2 al of introns catalyzed in yeast by the tRNA splicing endonuclease.
3 ation and characterization of the human tRNA splicing endonuclease.
4 ircularization site is processed by the tRNA splicing endonuclease.
5 ty from that of previously characterized RNA splicing endonucleases.
7 ition and cleavage, is performed by the tRNA-splicing endonuclease, a tetrameric enzyme composed of t
8 l BHB constructs showed that the N. equitans splicing endonuclease accepts a broader range of substra
9 ite of the enzyme is similar to that of tRNA splicing endonucleases, and concordantly, Cas6 activity
10 lytically active ribonucleoprotein (RNP) has splicing, endonuclease, and reverse transcriptase activi
13 re performed on the RNA structures both in a splicing endonuclease complex and in the aqueous solutio
14 1 is associated with the transfer RNA (tRNA) splicing endonuclease complex and the cleavage and polya
17 r results demonstrate that the eucaryal tRNA splicing endonuclease contains two functionally independ
18 d a similar enzyme assembly, currently known splicing endonuclease families have limited RNA specific
19 hallmark structure required by the archaeal splicing endonuclease for recognition and excision of al
20 olution of 2.85 angstroms the structure of a splicing endonuclease from Archaeglobus fulgidus bound w
22 rized splicing endonucleases in Archaea, the splicing endonuclease from archaeum Sulfolobus solfatari
23 he previously determined homotetrameric tRNA splicing endonuclease from Methanococcus jannaschii (MJ)
27 uggest an intriguing hypothesis in which the splicing endonuclease is an intermediate in the transiti
30 found in the gene encoding the archaeal tRNA splicing endonuclease of H. volcanii and in other Archae
31 ly shown that a defect in the essential tRNA splicing endonuclease of yeast results in transcriptome
32 -157), the first for a subunit of a eukaryal splicing endonuclease, revealed that the protein possess
33 tured known 5'-OH fragments produced by tRNA Splicing Endonuclease (SEN) during processing of intron-
35 We demonstrate here that an inactive RNA splicing endonuclease subunit can be switched "on" solel
37 recently identified (alphabeta)(2) family of splicing endonucleases that require two different subuni
38 catalysis of pre-tRNA by the eukaryotic tRNA-splicing endonuclease therefore requires a previously un
39 us (AF) belongs to the homodimeric family of splicing endonucleases, thought to have evolved from the
40 tRNA precursors involves cleavage by a tRNA splicing endonuclease to yield tRNA 3'-halves beginning
41 ecursors (pre-tRNAs) are excised by the tRNA splicing endonuclease TSEN in complex with the RNA kinas
42 to a loss of CLP1 interaction with the tRNA splicing endonuclease (TSEN) complex, largely reduced pr
45 Through its role in intron cleavage, tRNA splicing endonuclease (TSEN) plays a critical function i
46 requires the action of the heterotetrameric splicing endonuclease, which is composed of two catalyti
48 d two avatar (av) or model pre-tRNAs and two splicing endonucleases with distinct mechanisms of recog