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1 rate but not the sites of processing of the tRNA precursor.
2 enzyme that removes 5' leader sequences from tRNA precursors.
3 r the initial cleavage of some polycistronic tRNA precursors.
4 er growth and affects maturation of multiple tRNA precursors.
5 P) catalyzes the maturation of the 5' end of tRNA precursors.
6 . coli, can participate in the processing of tRNA precursors.
7 can process both CCA-less and CCA-containing tRNA precursors.
8 cleaved less efficiently than, for example, tRNA precursors.
9 n enzyme that catalyzes the 5' maturation of tRNA precursors.
10 ucleolytically process the 5' and 3' ends of tRNA precursors.
11 se P is responsible for the 5'-maturation of tRNA precursors.
12 ble for the removal of leader sequences from tRNA precursors.
13 ble for the removal of leader sequences from tRNA precursors.
14 moves 5' leader sequences from mitochondrial tRNA precursors.
15 lyzes the essential removal of the 5' end of tRNA precursors.
16 N is not required for maturation of phage T4 tRNA precursors, a known specific function of this RNase
17 mation on the ability of RNase BN to process tRNA precursors and help explain the known physiological
19 ding protein that promotes the maturation of tRNA precursors and other nascent transcripts synthesize
20 ugh processing of pre-tRNA(i)(Met) and other tRNA precursors, and the aminoacylation of tRNA(i)(Met)
21 or hcNME1 led to the accumulation of certain tRNA precursors, and their Gcd(-) phenotypes were revers
22 e R can precisely remove the 3'-trailer of a tRNA precursor by recognizing features in the terminal d
24 iological conditions E. coli and B. subtilis tRNA precursors containing a CCA determinant are not sub
26 he N. equitans splicing endonuclease cleaves tRNA precursors containing normal introns, as well as al
28 everal sequence and structural features of a tRNA precursor determine its precise processing at the 3
31 ymes, which process RNA substrates including tRNA precursors for RNase P and 5.8 S rRNA precursors, a
33 ng and maturation of mono- and polycistronic tRNA precursors in Escherichia coli involves initial cle
36 he 3'ETS of the glyW-cysT-leuZ polycistronic tRNA precursor is highly and specifically enriched by co
38 Z) endonucleolytically processes B. subtilis tRNA precursors lacking a CCA determinant both in vivo a
39 t inhibition of the processing of Drosophila tRNA precursor molecules by phosphodiester bond cleavage
40 ed synthesis of TnaC-tRNA(Pro), the peptidyl-tRNA precursor of the leader peptide of this operon.
41 cDNAs derived from unprocessed polycistronic tRNA precursors often lack some of the editing site inse
42 n of RNase BN on bacteriophage and bacterial tRNA precursors, particularly in light of a recent repor
43 eriments conducted in culture, the aminoacyl-tRNA precursor pool is near completely labeled in a few
44 intracellular free amino acid and aminoacyl-tRNA precursor pools in dividing and division-arrested n
47 clease P (RNase P), processes the 5' ends of tRNA precursors (ptRNA) in cells and organelles that car
48 nhibitor and the structure of the particular tRNA precursor substrate for tRNA(Ala), tRNA(Val), and t
50 onuclease is essential for the maturation of tRNA precursors that do not contain a chromosomally enco
52 F-1001, derived from the 3' end of a Ser-TGA tRNA precursor transcript that is not retained in the ma
53 t direct entry at a site on the 5' side of a tRNA precursor triggers a series of 5'-monophosphate-dep
54 em, which precisely cleaves both ends of the tRNA precursor, was engineered as a simple and robust pl
56 f single-stranded RNA and is able to process tRNA precursors with adenosine-rich 3' extensions in vit
57 r, RNase P cleavages separate the individual tRNA precursors with the concomitant formation of their
58 es] add CCA onto the 3' end of transfer RNA (tRNA) precursors without using a nucleic acid template.
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