ライフサイエンスコーパス: small ribosomal subunit

1 iates the recruitment of capped mRNAs by the small ribosomal subunit.

2 3 is required for recruitment of eIF1 to the small ribosomal subunit.

3 re GTPases that bind Met-tRNA(i)(Met) to the small ribosomal subunit.

4 tRNA, appears to be an essential core of the small ribosomal subunit.

5 eins and Var1p, a hydrophilic protein in the small ribosomal subunit.

6 r these conditions, BipA associates with the small ribosomal subunit.

7 binding of eIF4G and the recruitment of the small ribosomal subunit.

8 nit, and is required for the assembly of the small ribosomal subunit.

9 16S rRNA mapped the AMI binding site to the small ribosomal subunit.

10 enger RNA codon present in the A site of the small ribosomal subunit.

11 14, YqeH, has been linked to assembly of the small ribosomal subunit.

12 pre-rRNA that results in the assembly of the small ribosomal subunit.

13 he factor's interaction with 18S rRNA of the small ribosomal subunit.

14 lects and delivers the initiator tRNA to the small ribosomal subunit.

15 tiple translation initiation factors and the small ribosomal subunit.

16 n the ribosome includes that of the isolated small ribosomal subunit.

17 the translational GTPases on the body of the small ribosomal subunit.

18 F-G binding-induced ratcheting motion of the small ribosomal subunit.

19 osome that clamp P-site tRNA and mRNA on the small ribosomal subunit.

20 action of mutations affected assembly of the small ribosomal subunit.

21 tation of a key bridge between the large and small ribosomal subunits.

22 in that is required for joining of large and small ribosomal subunits.

23 orm for the interactions between both of the small ribosomal subunits.

24 ectly binds ribosomes and isolated large and small ribosomal subunits.

25 ch its binding specificity from ribosomes to small ribosomal subunits.

26 parates the rRNA components of the large and small ribosomal subunits.

27 Methylation of the bacterial small ribosomal subunit (16S) rRNA on the N1 position of

28 Here we demonstrate the engineering of the small-ribosomal subunit (16S) RNA of Mycoplasma mycoides

29 the final processing step to produce mature small ribosomal subunit 18S rRNA.

30 sts is a multigenic cluster that encodes the small ribosomal subunit 2 followed by four ATP synthase

31 s on the binding of IF3(mt) to mitochondrial small ribosomal subunits (28S) was studied using derivat

32 The movement of the small ribosomal subunit (30S) relative to the large ribo

33 t, and domain II is oriented more toward the small ribosomal subunit (30S).

34 l Ribosomal Entry Site (CrPV-IRES) binds the small ribosomal subunit (40S) and the translocation inte

35 Two conformational rearrangements in the small ribosomal subunit, a closing of the head and body

36 Upon joining of the large and small ribosomal subunits, a 100-nt long expansion segmen

37 itive noncoding ribosome, proto-mRNA and the small ribosomal subunit acted as cofactors, positioning

38 in IV of EF-G moves toward the A site of the small ribosomal subunit and facilitates the movement of

39 PS20, which encodes a component (S20) of the small ribosomal subunit and is a new colon cancer predis

40 The A/U-tail enables mRNA binding to the small ribosomal subunit and is essential for translation

41 itiator methionyl-tRNA (tRNA(i)(Met)) to the small ribosomal subunit and is necessary for protein syn

42 mRNA and initiator transfer RNA bound to the small ribosomal subunit and provide insights into the de

43 ethionyl initiator tRNA (Met-tRNA(i)) to the small ribosomal subunit and releases it upon GTP hydroly

44 th previous in vitro assembly studies of the small ribosomal subunit and six 50S assembly groups that

45 Escherichia coli protein Y (pY) binds to the small ribosomal subunit and stabilizes ribosomes against

46 TFB1M mediates an rRNA modification in the small ribosomal subunit and thus plays a role analogous

47 llular protein synthesis by sequestering 30S small ribosomal subunits and 70S ribosomes in nonfunctio

48 r resulted in accumulation of both large and small ribosomal subunits and also affected the stability

49 urs in a preinitiation complex that includes small ribosomal subunits and multiple translation initia

50 eference only occurs when both ppGpp and the small ribosomal subunit are present.

51 Initial recruitment of the small ribosomal subunit as well as two translocation ste

52 The small ribosomal subunit assembles cotranscriptionally on

53 Protein S4 is essential for bacterial small ribosomal subunit assembly and recognizes the 5' d

54 is of the concerted early and late stages of small ribosomal subunit assembly.

55 PS19-mutated iPSCs exhibited defects in 40S (small) ribosomal subunit assembly and production of 18S

56 uring eukaryotic translation initiation, the small ribosomal subunit, assisted by initiation factors,

57 espectively, and bind to the same regions of small ribosomal subunits, between the platform and initi

58 We report that eIF3 and the small ribosomal subunit bind HIV RNA within gag open rea

59 ng translation initiation in eukaryotes, the small ribosomal subunit binds messenger RNA at the 5' en

60 Nop9 is a conserved small ribosomal subunit biogenesis factor, essential in

61 IO kinases (Rio1, Rio2 and Rio3) function in small ribosomal subunit biogenesis.

62 (<3-A diffraction) and Thermus thermophilus small ribosomal subunit bound to the antibiotic paromomy

63 The latter then interacts with small ribosomal subunit-bound proteins, thereby promotin

64 aryotic protein S4 initiates assembly of the small ribosomal subunit by binding to 16 S rRNA.

65 le, organizes the assembly of the eukaryotic small ribosomal subunit by coordinating the folding, cle

66 elated conformational changes induced in the small ribosomal subunit by factor binding.

67 The eukaryotic small ribosomal subunit carries only four ribosomal (r)

68 Because the 40S small ribosomal subunit contains the key regulatory ribo

69 the initiator Met-tRNA to the P site on the small ribosomal subunit during a rate-limiting initiatio

70 A to interact with both the ribosome and the small ribosomal subunit during stress response.

71 universally conserved rRNA structure of the small ribosomal subunit essential for protein synthesis.

72 ssors, enabling the factor to engage the 40S small ribosomal subunit for translation initiation.

73 cts to switch the decoding preference of the small ribosomal subunit from elongator to initiator tRNA

74 subunit from Haloarcula marismortui and the small ribosomal subunit from Thermus thermophilus has pe

75 ribosomes was accompanied by the release of small ribosomal subunits from the ER membrane; the major

76 in NusE (identical to the protein S10 of the small ribosomal subunit) from the pathogenic mycobacteri

77 versus S4/S5) in two distinct regions of the small ribosomal subunit function independently to promot

78 teins of the large and three proteins of the small ribosomal subunit have been analyzed in this manne

79 bosome is sufficient to lock the head of the small ribosomal subunit in a single conformation, thereb

80 ansfers methionyl-initiator tRNA(Met) to the small ribosomal subunit in a ternary complex with GTP.

81 15 is a key component in the assembly of the small ribosomal subunit in bacteria.

82 re required for complete modification of the small ribosomal subunit in Escherichia coli.

83 ified KRIPP1 and KRIPP8 as components of the small ribosomal subunit in mammalian and insect forms, b

84 o dimethylate two adjacent adenosines of the small ribosomal subunit in the normal course of ribosome

85 olvement of RNAs from both the large and the small ribosomal subunits in catalysis of peptidyl-tRNA h

86 -LRP, also termed p40, is a component of the small ribosomal subunit indicating that it may be a mult

87 ational switch in the decoding center of the small ribosomal subunit induced by cognate but not by ne

88 It interacts with the small ribosomal subunit interacting protein, eIF3, and t

89 After export, the 20S rRNA in the small ribosomal subunit is cleaved to yield 18S rRNA and

90 st that the timely removal of ERAL1 from the small ribosomal subunit is essential for the efficient m

91 uitment of several components, including the small ribosomal subunit, is thought to allow migration o

92 ited a high-affinity binding to the isolated small ribosomal subunit (K(d) of 1.1 microM).

93 Stress granules are aggregates of small ribosomal subunits, mRNA, and numerous associated

94 In the small ribosomal subunit of budding yeast, on the 18S rRN

95 ration of ribosomal RNAs in the large or the small ribosomal subunit production pathway, expanding th

96 f all genes and were predominantly large and small ribosomal subunit protein components.

97 Sud1 to catalyze prolyl-hydroxylation of the small ribosomal subunit protein RPS23.

98 eat protein Yar1 directly interacts with the small ribosomal subunit protein Rps3 and accompanies new

99 the 18S rRNA-containing 40S subunit and the small ribosomal subunit protein S27a in the presence of

100 lates serine/threonine residues in the human small ribosomal subunit protein, receptor for activated

101 ing that the sedimentation properties of the small ribosomal subunit protein, S6, are dramatically al

102 NPM interacts with rRNA and large and small ribosomal subunit proteins and also colocalizes wi

103 proteins and also colocalizes with large and small ribosomal subunit proteins in the nucleolus, nucle

104 methylation of Rps2, Rps3, and Rps27a, three small ribosomal subunit proteins in the yeast Saccharomy

105 lar mRNA metabolism, including the large and small ribosomal subunit proteins L10a and S6, the stress

106 a nonpermissive temperature, both large and small-ribosomal-subunit proteins accumulate in the nucle

107 iation linked the evolution of the large and small ribosomal subunits, proto-mRNA, and tRNA.

108 on of factors required for maturation of the small ribosomal subunit (Rcl1, Fcf1/Utp24, Utp23) and th

109 ects of PABP-eIF4G on cap binding to promote small ribosomal subunit recruitment.

110 eukaryotes relies largely on analyses of the small ribosomal subunit RNA (SSU rRNA).

111 smortui and Deinococcus radiodurans, and the small ribosomal subunit RNA of Thermus thermophilus and

112 ose phylogenetic relationships inferred from small ribosomal subunit RNA sequences, and to examine mo

113 udoknot encompassing residues 500-545 of the small ribosomal subunit RNA was used as a target in scre

114 processome is required for production of the small ribosomal subunit RNA, the 18S rRNA.

115 ions in its ATPase motifs lead to defects in small ribosomal subunit rRNA maturation, the absence of

116 E-BPs) and protein kinases that act upon the small ribosomal subunit (S6 kinases).

117 Ribosomal protein S5 is critical for small ribosomal subunit (SSU) assembly and is indispensa

118 the high mobility group protein Hmo1 and the small ribosomal subunit (SSU) processome complex.

119 The small ribosomal subunit (SSU) processome is a large ribo

120 (pre-rRNA) processing as a component of the small ribosomal subunit (SSU) processome.

121 KsgA, a universally conserved small ribosomal subunit (SSU) rRNA methyltransferase, ha

122 While localization of KsgA on 30S subunits [small ribosomal subunits (SSUs)] and genetic interaction

123 es) to be located in separate regions of the small ribosomal subunit that are important for domain cl

124 ine the structures of three complexes of the small ribosomal subunit that represent distinct steps in

125 he binding of initiator tRNA and mRNA to the small ribosomal subunit to form the initiation complex,

126 cells begins with the ordered binding of the small ribosomal subunit to messenger RNA (mRNA) and tran

127 arkable array of initiation factors onto the small ribosomal subunit to select an appropriate mRNA st

128 e cap-binding protein eIF4E, it recruits the small ribosomal subunit to the 5'-end of mRNA and promot

129 in all cells begins with recruitment of the small ribosomal subunit to the initiation codon in a mes

130 initiation complex, i.e., recruitment of the small ribosomal subunit to the messenger RNA (mRNA).

131 volution of the large ribosomal subunit, the small ribosomal subunit, tRNA, and mRNA.

132 n complexes and does not dissociate from the small ribosomal subunit upon mRNA recruitment, as previo

133 ranslocation, relative to protein S12 of the small ribosomal subunit using single-molecule FRET.

134 erein peptidyl-tRNA enters the P site of the small ribosomal subunit via reversible, swivel-like moti

135 agment as an indicator for the export of the small ribosomal subunit, we have identified genes that a

136 which both function during maturation of the small ribosomal subunit, we show here that Rrp5 provides

137 ailed mRNA preferentially interacts with the small ribosomal subunit, whereas edited substrates and c

138 The creation of orthogonal large and small ribosomal subunits, which interact with each other

139 vel sites of protein modification within the small ribosomal subunit will now allow for an analysis o

140 sis factor important for the assembly of the small ribosomal subunit with an uncommon dual ATPase and