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1 h encodes for the RNA component of the large ribosome subunit.
2 he 16 S rRNA core of the large mitochondrial ribosome subunit.
3 ouridine residues within helix 69 of the 50S ribosome subunit.
4 repressor Armitage--and proteins of the 60S ribosome subunit.
5 decreased expression of Rps4l, coding for a ribosome subunit.
6 GTPase BipA involved in assembly of the 50S ribosome subunit.
7 ovided evidence for the presence of SecY and ribosome subunits.
8 ing that results in production of proper 30S ribosome subunits.
9 cessing, and assembly of the large and small ribosome subunits.
10 rate limiting for the efficient assembly of ribosome subunits.
11 , and assembled with ribosomal proteins into ribosome subunits.
12 at, following its synthesis on mitochondrial ribosomes, subunit 6 of the ATPase (Atp6p) can be cross-
13 ry site (IRES), which directly binds the 40S ribosome subunit and is a target for candidate therapeut
15 7-cognate codons in high-abundance mRNAs for ribosome subunits and energy metabolism, congruent with
17 associates with a class of mRNAs that encode ribosome subunits and precursors to snoRNAs involved in
18 ion, the ribosomal proteins of the small 30S ribosome subunit, and minor ribosome-associated proteins
19 y understood form of initiation in which 40S ribosome subunits are loaded onto mRNA through interacti
20 prehensive models of the pre-40S and pre-60S ribosome subunits as well as the largest cotranscription
21 increased ribosome density, consistent with ribosome subunit assembly for initiation, the first step
23 messenger RNA synthesis and processing, and ribosome subunit biogenesis, take place within the nucle
25 ciation of cap-binding factors and the small ribosome subunit but before formation of the 80S ribosom
26 tightly associated with some of the free 40S ribosome subunits, but it was not present in the 80S poo
27 n requires ribosomal RNA methylation in both ribosome subunits by TlyA (Rv1694), an enzyme with dual
29 hat may involve faster scanning by the small ribosome subunit due to increased local concentration of
31 ituted IVT systems containing iMet-retaining ribosome subunits from ES27L Deltab1-4 strain, combined
32 ally occurs by 5'-processive scanning of 40S ribosome subunits from the m7GTP-cap to the initiating A
35 ping, involves discontinuous scanning by 40S ribosome subunits, in which large segments of the 5' non
38 of the RBD to 23S rRNA in the late stages of ribosome subunit maturation would position the ATP-bindi
39 al systems, numerous GTPBPs are required for ribosome subunit maturation, with EngB being a GTPBP inv
40 ffect steady-state levels of large and small ribosome subunits, monoribosomes, and polyribosomes.
43 beyond that required for the typical rate of ribosome-subunit production and accumulate in the nucleo
44 ng, nucleophosmin-mediated nuclear export of ribosome subunits, protein synthesis levels, and cell gr
45 Tsc1 promoted the nuclear export of maturing ribosome subunits, providing a mechanistic link between
47 It was shown decades ago that purified 30S ribosome subunits readily interconvert between "active"
49 t that late steps in maturation of the large ribosome subunit rRNAs employ mechanisms that are evolut
50 or 4E (eIF4E), diminishes phosphorylation of ribosome subunit S6, and phosphorylates translation init
51 f tRNA from the A to the P site as the small ribosome subunit spontaneously rotates back from the hyb
52 omplex known to be related to arrangement of ribosome subunits that exhibit extremely high gene expre
53 hibited dramatic reductions in levels of 60S ribosome subunits under non-permissive conditions as wel