ライフサイエンスコーパス: mitochondrial ribosome

1 s previously assigned to be a subunit of the mitochondrial ribosome.

2 of mt-rRNA variations on the function of the mitochondrial ribosome.

3 sis and function of the large subunit of the mitochondrial ribosome.

4 G in both the A- and P-sites of the metazoan mitochondrial ribosome.

5 nd the major binding partner of ATAD3 is the mitochondrial ribosome.

6 n the biogenesis of the large subunit of the mitochondrial ribosome.

7 the respiratory chain are translated by the mitochondrial ribosome.

8 ified as the major acetylated protein in the mitochondrial ribosome.

9 gated if the Oxa1 complex interacts with the mitochondrial ribosome.

10 lude that HLL and HLP encode L14 subunits of mitochondrial ribosomes.

11 re presented as a model system for mammalian mitochondrial ribosomes.

12 ion of mitochondrial encoded mRNAs occurs on mitochondrial ribosomes.

13 he small subunit of either E. coli or bovine mitochondrial ribosomes.

14 mutations and possessing low affinity toward mitochondrial ribosomes.

15 because of a decrease in fully assembled 55S mitochondrial ribosomes.

16 n a significant inhibition of translation on mitochondrial ribosomes.

17 ranslated regions and promote translation on mitochondrial ribosomes.

18 Very little is known about biogenesis of mitochondrial ribosomes.

19 ify a third gene essential for expression of mitochondrial ribosomes.

20 the Oxa1L-CTT derivatives bind to mammalian mitochondrial ribosomes.

21 in targets the peptidyltransferase center of mitochondrial ribosomes.

22 the protein-rich small subunit of mammalian mitochondrial ribosomes.

23 le of assembly proteins in the biogenesis of mitochondrial ribosomes.

24 c ribosomes (80S), as well as other kinds of mitochondrial ribosomes.

25 hile providing insight into the evolution of mitochondrial ribosomes.

26 bditis elegans, and Saccharomyces cerevisiae mitochondrial ribosomes.

27 bditis elegans, and Saccharomyces cerevisiae mitochondrial ribosomes.

28 ts (MRP-S22 through MRP-S36) are specific to mitochondrial ribosomes.

29 present in the 39 S subunits are specific to mitochondrial ribosomes.

30 k interactions with the large subunit of the mitochondrial ribosome (39S) (K(d) = 1.5 muM).

31 The mammalian mitochondrial ribosomes (55S) differ unexpectedly from b

32 remodeling during the evolution of mammalian mitochondrial ribosomes (55S).

33 The ancestral mitochondrial ribosome (70S) underwent major structural

34 nthesis by the reversible acetylation of the mitochondrial ribosome and characterize MRPL10 as a nove

35 est regulatory mechanisms for assembling the mitochondrial ribosome and illustrate dynamic changes in

36 (mt) shifts the equilibrium between the 55 S mitochondrial ribosome and its subunits toward subunit d

37 -purified with the small, 28S subunit of the mitochondrial ribosome and the endogenous protein co-fra

38 rose gradients with the large subunit of the mitochondrial ribosome and the monosome.

39 s was 1.10 +/- 0.01 x 10(-7) cm(2) s(-1) for mitochondrial ribosomes and 1.72 +/- 0.03 x 10(-7) cm(2)

40 The three core subunits are synthesized on mitochondrial ribosomes and inserted into the inner memb

41 e C-terminal tail of Oxa1L (Oxa1L-CTT) binds mitochondrial ribosomes and is believed to coordinate th

42 l features that are characteristic solely of mitochondrial ribosomes and other features that are char

43 mino acid tail of Oxa1L (Oxa1L-CTT) binds to mitochondrial ribosomes and plays a role in the co-trans

44 reviews the distinctive properties of human mitochondrial ribosomes and ribosomal proteins, and the

45 Mitochondrial ribosomes and translation factors co-purif

46 ransiently, via RNA, with editing complexes, mitochondrial ribosomes, and several ancillary factors t

47 Because the protein:RNA ratio in the mitochondrial ribosome (approximately 69:approximately 3

48 MPV17L2 proteins of the small subunit of the mitochondrial ribosome are trapped in the enlarged nucle

49 The extra proteins in mitochondrial ribosomes are 'new' in the sense that they

50 The ribosomal RNA components of the mitochondrial ribosomes are coded for by mitochondrial D

51 Human mitochondrial ribosomes are highly divergent from all ot

52 Bovine mitochondrial ribosomes are presented as a model system

53 s highlighting the cytosolic rather than the mitochondrial ribosome as the primary drug target.

54 provide a checkpoint for proper 28S and 55S mitochondrial ribosome assembly.

55 l protein synthesis associated with impaired mitochondrial ribosome assembly.

56 cytosolic ribosome and for the A1555G mutant mitochondrial ribosome associated with hypersusceptibili

57 n C7orf30 is, on the contrary, essential for mitochondrial ribosome biogenesis and mitochondrial tran

58 ate that this is one mechanism to coordinate mitochondrial ribosome biogenesis and transcription in h

59 Mitochondrial ribosome biogenesis is therefore critical

60 les in inflammation and infection processes, mitochondrial ribosome biogenesis, and regulation of apo

61 e ribosomal subunit in a process crucial for mitochondrial ribosome biogenesis.

62 We propose that Mtg2p is involved in mitochondrial ribosome biogenesis.

63 that POLRMT associates with h-mtTFB1 in 28S mitochondrial ribosome complexes that are stable in the

64 Mitochondrial ribosomes comprise the most diverse group

65 ty and that the decreased specificity toward mitochondrial ribosome confers the lowered cytotoxicity.

66 This finding suggests that mammalian mitochondrial ribosomes contain several novel proteins.

67 Mammalian mitochondrial ribosomes contain two prokaryotic-like rRN

68 stimulate mitochondrial Met-tRNA binding to mitochondrial ribosomes, exhibiting a 50-fold preference

69 specific antibodies are present in a petunia mitochondrial ribosome fraction.

70 ple of a ribosomal protein that is shared by mitochondrial ribosomes from lower and higher eukaryotes

71 Sucrose gradient sedimentation of mitochondrial ribosomes from temperature-sensitive mtg3

72 auses maternally inherited deafness disrupts mitochondrial ribosome function, in part, via increased

73 iae GTPase Mtg2p (Yhr168wp) is essential for mitochondrial ribosome function.

74 Mitochondrial ribosomes had a particle composition of 75

75 The human mitochondrial ribosome has 29 distinct proteins in the s

76 of the small subunit (28 S) of the mammalian mitochondrial ribosome has been achieved by carrying out

77 of the large subunit (39 S) of the mammalian mitochondrial ribosome has been achieved by carrying out

78 The bovine mitochondrial ribosome has been developed as a model sys

79 s of association with mtDNA nucleoids and/or mitochondrial ribosomes in cell fractionation studies.

80 to an increase in translational activity of mitochondrial ribosomes in Sirt3(-/-) mice.

81 IF-2mt can bind to mitochondrial ribosomes in the absence of GTP, initiator

82 mammalian mitochondrial ribosomes, the human mitochondrial ribosome is one of the most protein-rich r

83 The mitochondrial ribosome is responsible for the biosynthes

84 The binding of Oxa1L-CTT to mitochondrial ribosomes is an enthalpy-driven process wi

85 Mammalian mitochondrial ribosomes lack several of the major RNA st

86 ses in the monosome and both subunits of the mitochondrial ribosome, leading to impaired protein synt

87 The Leishmania tarentolae mitochondrial ribosome (Lmr) is a minimal ribosomal RNA

88 c concept that postulates a key role for the mitochondrial ribosome (mitoribosome) in aminoglycoside

89 The RNA component of the mitochondrial ribosome (mitoribosome) is reduced in size

90 The mammalian mitochondrial ribosomes (mitoribosomes) are responsible

91 Mitochondrial ribosomes (mitoribosomes) perform protein

92 horylation (OXPHOS) system is carried out by mitochondrial ribosomes (mitoribosomes).

93 ied 13 proteins that cofractionated with the mitochondrial ribosome, most of which play a role in tra

94 e of the unusual proteins contained in human mitochondrial ribosomes, MRPS29.

95 berrant assembly of the large subunit of the mitochondrial ribosome (mt-LSU).

96 lly associates with the large subunit of the mitochondrial ribosome (mt-LSU).

97 the additional and/or larger proteins of the mitochondrial ribosome must compensate for the shortened

98 ce that assembly of the small subunit of the mitochondrial ribosome occurs at the nucleoid.

99 Mitochondrial ribosomes of Trypanosoma brucei are compos

100 rthermore, unlike cytoplasmic ribosomes, the mitochondrial ribosome possesses intersubunit bridges co

101 Using a mitochondrial ribosome profiling and mitochondrial poly(

102 Interaction of oxazolidinones with the mitochondrial ribosomes provides a structural basis for

103 sed and increased abundance of plastidic and mitochondrial ribosomes, respectively.

104 tudies with both Escherichia coli and bovine mitochondrial ribosomes revealed that the f(5)C(34) faci

105 ribosomes and a cryo-EM map of the mammalian mitochondrial ribosome show that (i) the overall structu

106 A methyltransferase required for small (28S) mitochondrial ribosome subunit assembly.

107 fications of the 16 S rRNA core of the large mitochondrial ribosome subunit.

108 ere we show that, following its synthesis on mitochondrial ribosomes, subunit 6 of the ATPase (Atp6p)

109 Mitochondrial ribosomes synthesize a subset of hydrophob

110 Typical of mammalian mitochondrial ribosomes, the human mitochondrial ribosom

111 We propose that mitochondrial ribosomes themselves recognize a common fe

112 ped as a model system for the study of human mitochondrial ribosomes to address several questions rel

113 LRMT interacts directly with h-mtTFB1 in 28S mitochondrial ribosomes to augment its 12S rRNA methyltr

114 didates for mitochondrial disease, since the mitochondrial ribosome translates mRNAs for the 13 essen

115 MPV17L2 contributes to the biogenesis of the mitochondrial ribosome, uniting the two subunits to crea

116 A calculated hydration factor of 3.3 g/g for mitochondrial ribosomes was also obtained utilizing a ca

117 molecular weight and buoyant density of rat mitochondrial ribosomes were determined.

118 , the physiochemical properties of rat liver mitochondrial ribosomes were examined and compared with

119 e found in the mammalian and D. melanogaster mitochondrial ribosomes while C. elegans has two S18 hom

120 to the small (28S) subunit of the mammalian mitochondrial ribosome with K(d) values similar to that