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1 to the E site but remains temporarily in the peptidyl transferase center.
2 re with another activity associated with the peptidyl transferase center.
3 n establishing the tertiary structure of the peptidyl transferase center.
4 ics on the scale of seconds at the ribosomal peptidyl transferase center.
5 the L27 N-terminus, which protrudes into the peptidyl transferase center.
6  is located in the immediate vicinity of the peptidyl transferase center.
7  is known to be a component of the ribosomal peptidyl transferase center.
8 ial for the successful assembly of ribosomal peptidyl transferase center.
9 via tertiary interactions to features of the peptidyl transferase center.
10 f the acceptor end of the A-site tRNA at the peptidyl transferase center.
11  within domains IV and V, which contains the peptidyl transferase center.
12 o position helices 77 and 78 relative to the peptidyl transferase center.
13 oning the activated ends of tRNAs within the peptidyl transferase center.
14 f the A-tRNA from entering the A site of the peptidyl transferase center.
15 omal tunnel to the exit port, ~100A from the peptidyl transferase center.
16 S rRNA A-loop, an essential component of the peptidyl transferase center.
17 are elongated, one residue at a time, at the peptidyl transferase center.
18 he modern ribosome this remnant includes the peptidyl transferase center.
19 esidue was separated by 14 residues from the peptidyl transferase center.
20 l RNA (rRNA) that includes hairpin 92 of the peptidyl transferase center.
21 y conserved GGQ motif packs tightly into the peptidyl transferase center.
22 ents are normally performed in the ribosomal peptidyl transferase center.
23  23S ribosomal RNA, an important part of the peptidyl transferase center.
24 somal subunit in the cleft that contains the peptidyl transferase center.
25  the RNA-mediated catalysis of the ribosomal peptidyl transferase center.
26  interplay between the nascent chain and the peptidyl transferase center.
27 3S rRNA at three sites, all located near the peptidyl transferase center.
28 inhibition of TnaC-tRNA(Pro) cleavage at the peptidyl transferase center.
29 he subunit interface, and junctions near the peptidyl transferase center.
30  as a function of the distance away from the peptidyl transferase center.
31 f the ribosome such as the tRNA path and the peptidyl transferase center.
32         Nucleotide A2572 is in the ribosomal peptidyl transferase center.
33  binding sites of several antibiotics in the peptidyl transferase center.
34 e accommodation of decoding factors into the peptidyl transferase center.
35 m to pause before allowing entrance into the peptidyl transferase center.
36 may generalize to other aaRS, as well as the peptidyl transferase center.
37 entified group thought to reside in the rRNA peptidyl transferase center.
38  that docks the catalytic GGQ motif into the peptidyl-transferase center.
39 s access to both the decoding center and the peptidyl-transferase center.
40 RNAs containing deleterious mutations in the peptidyl transferase center (25S NRD).
41             Thus, eIF5B interaction with the peptidyl transferase center A loop increases the accurac
42 ther universally conserved nucleotide in the peptidyl transferase center, A2451.
43 itionally, a nucleotide located close to the peptidyl transferase center, A2572, which was protected
44  All three are at or have been linked to the peptidyl transferase center according to the literature.
45 eptide exit tunnel at some distance from the peptidyl transferase center agrees with the proposed mod
46 contributes to the tertiary structure of the peptidyl transferase center and influences the conformat
47 he C-terminal domain of EF4 reaches into the peptidyl transferase center and interacts with the accep
48 the protein that interacts with the ribosome peptidyl transferase center and mimics the 3'-acceptor s
49                 Both antibiotics bind at the peptidyl transferase center and sterically occlude the C
50 nd the subsequent expansions that shaped the peptidyl transferase center and the conserved core.
51 n of essential functional sites, such as the peptidyl transferase center and the decoding site.
52  end in tRNA interactions with the ribosomal peptidyl transferase center and the elongation factor Tu
53 ubunit along the path it follows between the peptidyl transferase center and the exit site on the dis
54         Two hydrophobic crevices, one at the peptidyl transferase center and the other at the entranc
55  a catalytic water can be coordinated in the peptidyl transferase center and, together with previous
56 d helix 44 of 18S rRNA, domain 4 is near the peptidyl-transferase center and its helical subdomain co
57 omain V (which is known to be a component of peptidyl transferase center) and a loop of the helix 35
58  the A loop and P loop, respectively, of the peptidyl transferase center, and G1735A, mapping near a
59 , including the neighborhood surrounding the peptidyl transferase center, and stable association of r
60 d that the ribosome dynamics detected at the peptidyl transferase center are highly inhomogeneous.
61 es of tRNA substrate located in the ribosome peptidyl transferase center around the 2-fold axis, we h
62 oRNA binding causes little distortion of the peptidyl transferase center but do provide suggestive ev
63 fined to the nascent peptide residues in the peptidyl transferase center but not to the peptide segme
64 e ribosome is catalyzed in the large subunit peptidyl transferase center by release factors on recogn
65 ons of two other nucleotide positions in the peptidyl transferase center, C2471 and U2519 (C2452 and
66  centers in the large subunit, including the peptidyl-transferase center, for unnatural polymer synth
67  confirm the topographical separation of the peptidyl transferase center from the E site domain.
68 S rRNA nucleotides in the 2585 region of the peptidyl transferase center, G2583A and U2584C, were obs
69 bosomal subunits and the conformation of the peptidyl transferase center in the context of the intact
70 nd peptidyl-D-aa-tRNA can trap the ribosomal peptidyl-transferase center in a conformation in which p
71 onstruct that comprises much of the 23S rRNA peptidyl transferase center, including the central loop
72 ce of these results for the structure of the peptidyl transferase center is considered.
73 ce of these results for the structure of the peptidyl transferase center is considered.
74 s to block assembly at a late stage when the peptidyl transferase center is formed, indicating a poss
75                                The ribosomal peptidyl transferase center is responsible for two funda
76 gest that the positioning of Pro-tRNA in the peptidyl transferase center is the major determinant for
77 nity for CCdApPuro comparable to that of the peptidyl transferase center itself (Kd approximately 10
78           Three additional sites were at the peptidyl transferase center itself.
79 -bound tRNAs, whose 3' termini reside in the peptidyl transferase center, label primarily nucleotides
80  in 23S rRNA, which is situated close to the peptidyl transferase center, may participate in one or m
81  to interact with nucleotide residues in the peptidyl transferase center of domain V.
82 to pseudouridine (Psi) in a stem-loop at the peptidyl transferase center of Escherichia coli 23S rRNA
83 lmN and Cfr, both methylate A2503 within the peptidyl transferase center of prokaryotic ribosomes, yi
84 ance of pseudouridine formation (Psi) in the peptidyl transferase center of rRNA was examined by depl
85        These findings directly implicate the peptidyl transferase center of the 50S subunit in the me
86 on binding sites of the 30S subunit with the peptidyl transferase center of the 50S subunit via rRNA-
87 , inhibit protein synthesis by targeting the peptidyl transferase center of the bacterial ribosome.
88  has been implicated as a constituent of the peptidyl transferase center of the Escherichia coli 50 S
89                            The action of the peptidyl transferase center of the large ribosomal unit
90 ffectively an unbranched tube connecting the peptidyl transferase center of the large subunit and the
91 lation of an adenosine nucleotide within the peptidyl transferase center of the ribosome mediated by
92 ired for introducing specific changes in the peptidyl transferase center of the ribosome that activat
93     This nucleotide is positioned within the peptidyl transferase center of the ribosome, which is a
94  catalytically productive orientation in the peptidyl transferase center of the ribosome.
95 o acids are polymerized into peptides in the peptidyl transferase center of the ribosome.
96          This modification is located in the peptidyl transferase center of the ribosome.
97 of domain V, which forms a major part of the peptidyl transferase center of the ribosome.
98 ndividual point mutations, in either the 25S peptidyl transferase center or 18S decoding site, that a
99 aphic structures of antibiotics bound to the peptidyl transferase center or the exit tunnel of archae
100                     Such placement, near the peptidyl transferase center, provides a rationale for th
101 beling, and mutational analyses revealed the peptidyl transferase center (PTC) as the focal point of
102 its peptide-bond formation in the ribosome's peptidyl transferase center (PTC) during its own transla
103        The effect of AAP and Arg on ribosome peptidyl transferase center (PTC) function was analyzed
104  ribosomal exit tunnel and the A-site of the peptidyl transferase center (PTC) in halting translation
105 the CCA-end of the A-site tRNA away from the peptidyl transferase center (PTC) is functionally signif
106       Here we demonstrate that the ribosomal peptidyl transferase center (PTC) is supported by a fram
107 x RNA helicase specifically activated by the peptidyl transferase center (PTC) of 23S rRNA.
108   Peptide bond formation is catalyzed at the peptidyl transferase center (PTC) of the large ribosomal
109 protein synthesis inhibitors that target the peptidyl transferase center (PTC) on the large subunit o
110 nding of neither nucleotide (ATP or ADP) nor peptidyl transferase center (PTC) RNA, the presumed phys
111 ribosomal RNA (rRNA) helix 89 of the nascent peptidyl transferase center (PTC) through Nsa2.
112 tion axes for both subunits pass through the peptidyl transferase center (PTC), indicating a tendency
113 and catalyzing peptide bond formation at the peptidyl transferase center (PTC).
114 none molecule within its binding site in the peptidyl transferase center (PTC).
115 l differences are in the conformation of the peptidyl-transferase center (PTC) and the interface betw
116 the sarcin/ricin loop (SRL) and A2531 in the peptidyl-transferase center (PTC) has adverse effects on
117 owing a disruption of the A-site side of the peptidyl-transferase center (PTC).
118  discovered near the decoding center and the peptidyl transferase center, respectively.
119 es specific nucleotides within the ribosomal peptidyl transferase center that appear to be essential
120 mes, and their effect on conformation in the peptidyl transferase center, the GTPase-associated cente
121 erichia coli 23S rRNA, 14 are located in the peptidyl transferase center, the main antibiotic target
122 iary interactions between nucleotides in the peptidyl transferase center, the SRD, and the GTPase-ass
123 e essential macromolecular components of the peptidyl transferase center to 23S rRNA and ribosomal pr
124 s a hydrolytic reaction in the large subunit peptidyl transferase center to release the finished poly
125  subunit surface, connecting the tRNA in the peptidyl transferase center to the distally located nasc
126  changes occur at several nucleotides in the peptidyl transferase center upon alterations in pH, temp
127 es of 8 rRNA-modifying enzymes targeting the peptidyl transferase center were individually inactivate
128 reates a free tryptophan-binding site in the peptidyl transferase center, where bound tryptophan inhi
129 tRNAs for binding in the A-site cleft in the peptidyl-transferase center, which is universally conser
130 rom the back of the 50 S particle toward the peptidyl transferase center within the 50 S subunit.
131 ming the three- dimensional structure of the peptidyl transferase center within the ribosome.

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