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1                              Due to the post-translocational activation of CueO, this enzyme contribu
2                                          The translocational and cell cycle properties of knockin Cdk
3 RNA-RNA base pairing associated with (i) the translocational and size fluctuations of the transcripti
4  Sec61 complex, the major constituent of the translocational channel.
5 ng to the classical and hybrid states of the translocational cycle.
6                           In the presence of translocational diffusion during active unwinding, the d
7 TP, the NS3 helicase can display significant translocational diffusion.
8 al feature of this mechanism is that a rapid translocational equilibrium is established after each cy
9 lex in sensitive fungi, stabilizing the post-translocational GDP form.
10 - and GTP-dependent, and is inhibited by the translocational inhibitor thiostrepton.
11                                          The translocational intermediate presented here represents a
12 mechanistic differences between co- and post-translocational O-mannosylation.
13 acks onto nascent G3 in the cytosol during a translocational pause and enters the ER lumen with G3, a
14                   Here we show that during a translocational pause, the junction between the ribosome
15 nt chain are visible to the cytosol during a translocational pause.
16  demonstrates the existence of translational/translocational pausing for a viral glycoprotein and sug
17                                              Translocational pausing is a mechanism used by certain s
18 en identified and may be responsible for the translocational pausing observed in this study.
19 ccur at a constant rate but by translational/translocational pausing that has not previously been sho
20 cule assay that defines, simultaneously, the translocational position of a protein complex relative t
21               We applied the assay to define translocational positions and sigma70 contents of bacter
22 en bases of the mRNA may act as "pawls" of a translocational ratchet.
23                   A conceptual framework for translocational regulation is proposed based on our curr
24 the signal for transition of the post to pre-translocational ribosomal state in yeast.
25 locational (tRNAs in A and P sites) and post-translocational ribosomes (P and E sites occupied) were
26 (PFA, foscarnet) was shown to freeze the pre-translocational state of the reverse transcriptase (RT)
27            The complex is frozen in the post-translocational state that usually accommodates the inco
28                         Focusing on the post-translocational state, we extended this assessment to th
29 omain in switching between the pre- and post-translocational states are discussed.
30 ngation cycle intermediates in pre- and post-translocational states, but also eEF1A-containing decodi
31 ality control mechanisms that resolve faulty translocational states.
32  allosteric switch between the pre- and post-translocational states.
33         In particular, the structures of pre-translocational (tRNAs in A and P sites) and post-transl
34 al) unfolding, the major intermediates of co-translocational unfolding are mainly mediated by non-nat
35                                  In vivo, co-translocational unfolding can be affected by the end of
36              Recently, we have shown that co-translocational unfolding can be followed in a model sys
37                                To examine co-translocational unfolding of individual molecules, we ta

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