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 of membrane transporters, function in the co-
translocational metalation of Mn(2+)-dependent membrane
13 mechanistic differences between co- and post-
translocational O-mannosylation.
14 acks onto nascent G3 in the cytosol during a
translocational pause and enters the ER lumen with G3, a
15 Here we show that during a
translocational pause, the junction between the ribosome
16 nt chain are visible to the cytosol during a
translocational pause.
17 demonstrates the existence of translational/
translocational pausing for a viral glycoprotein and sug
18 Translocational pausing is a mechanism used by certain s
19 en identified and may be responsible for the
translocational pausing observed in this study.
20 ccur at a constant rate but by translational/
translocational pausing that has not previously been sho
21 cule assay that defines, simultaneously, the
translocational position of a protein complex relative t
22 We applied the assay to define
translocational positions and sigma70 contents of bacter
23 en bases of the mRNA may act as "pawls" of a
translocational ratchet.
24 A conceptual framework for
translocational regulation is proposed based on our curr
25 6% clear cell renal cell carcinoma, 75.0% of
translocational renal cell carcinoma, 100% of primitive
26 the signal for transition of the post to pre-
translocational ribosomal state in yeast.
27 locational (tRNAs in A and P sites) and post-
translocational ribosomes (P and E sites occupied) were
28 (PFA, foscarnet) was shown to freeze the pre-
translocational state of the reverse transcriptase (RT)
29 The complex is frozen in the post-
translocational state that usually accommodates the inco
30 Focusing on the post-
translocational state, we extended this assessment to th
31 , including an intermediate state and a post-
translocational state.
32 ic state and only a minor population in post-
translocational state.
33 omain in switching between the pre- and post-
translocational states are discussed.
34 ngation cycle intermediates in pre- and post-
translocational states, but also eEF1A-containing decodi
35 allosteric switch between the pre- and post-
translocational states.
36 ality control mechanisms that resolve faulty
translocational states.
37 In particular, the structures of pre-
translocational (
tRNAs in A and P sites) and post-transl
38 al) unfolding, the major intermediates of co-
translocational unfolding are mainly mediated by non-nat
39 In vivo, co-
translocational unfolding can be affected by the end of
40 Recently, we have shown that co-
translocational unfolding can be followed in a model sys
41 rt through the nanopore, with directional co-
translocational unfolding occurring unit by unit from ei
42 To examine co-
translocational unfolding of individual molecules, we ta