ライフサイエンスコーパス: chloroplast protein

1 plant PII-like protein is a nuclear-encoded chloroplast protein.

2 here it accounted for up to 15% of the total chloroplast protein.

3 estimated to constitute <0.02% of the total chloroplast protein.

4 bunit IV of the cytochrome b6/f complex, and chloroplast proteins.

5 ion, and glycosylation, in the regulation of chloroplast proteins.

6 -responsive genes encoding mitochondrial and chloroplast proteins.

7 hared by promoters of nuclear-genes encoding chloroplast proteins.

8 cific DNA affinity chromatography from total chloroplast proteins.

9 hloroplast development and reduced levels of chloroplast proteins.

10 or embryo-defective (emb) mutants altered in chloroplast proteins.

11 rone homolog genes (CGE) in moss that encode chloroplast proteins.

12 and b suggesting a role in the expression of chloroplast proteins.

13 als modulate expression of nuclear genes for chloroplast proteins.

14 uired to maintain nuclear gene expression of chloroplast proteins.

15 ent but did not require ATP, GTP, or soluble chloroplast proteins.

16 ed with the stabilities of two other soluble chloroplast proteins.

17 ps cooperating in the rapid replenishment of chloroplast proteins.

18 anslating ribosomes, ultimately compromising chloroplast protein abundance and thus plant growth and

19 The Arabidopsis thaliana chloroplast protein ACCELERATED CELL DEATH2 (ACD2) modul

20 ng, reduced chloroplast translation, reduced chloroplast protein accumulation, and elevated chloropla

21 t rRNA processing and a drastic reduction in chloroplast protein accumulation.

22 of the expression of nuclear genes encoding chloroplast proteins allows for metabolic adjustment in

23 ondrial protein to replace the function of a chloroplast protein and illustrates the plasticity of th

24 field of posttranslational modifications of chloroplast proteins and points out the importance of th

25 ombinant CPE cleaves in the absence of other chloroplast proteins, and this activity depends on metal

26 of 1,105 proteins were assigned as potential chloroplast proteins, annotated for function, and quanti

27 ic analysis indicated that nuclear genes for chloroplast proteins are down-regulated, and proteins me

28 Most chloroplast proteins are nucleus-encoded and imported fo

29 Most chloroplast proteins are synthesized in the cytosol and

30 Most chloroplast proteins are synthesized in the cytosol as h

31 The majority of nucleus-encoded chloroplast proteins are targeted to the organelle by di

32 he Arabidopsis Thf1 gene encodes an imported chloroplast protein, as shown by in vitro import and loc

33 The accumulation of several chloroplast proteins, as well as most of the chloroplast

34 n vitro analyses reveal different aspects of chloroplast protein biogenesis.

35 -responsive genes encoding mitochondrial and chloroplast proteins but have little effect on more cons

36 occurs in both nuclear- and plastid-encoded chloroplast proteins, but the physiological significance

37 mplex regulatory network systems controlling chloroplast proteins by a range of posttranslational mod

38 Consequently, N termini of mature chloroplast proteins cannot be accurately predicted.

39 Here we report that the chloroplast proteins COR15A and COR15B are necessary for

40 The thioredoxin-regulated chloroplast protein CP12 forms a multienzyme complex wit

41 The chloroplast protein CSP41a both binds and cleaves RNA, p

42 Certain other chloroplast proteins decline with age coordinately with

43 ysis and mass spectrometry identified mainly chloroplast proteins differentially expressed between th

44 with reductions in the accumulation of some chloroplast proteins, directly or indirectly.

45 Once inside the organelle, many chloroplast proteins engage one of four additional prote

46 An extensive overview of BS and M chloroplast protein expression and homeostasis machineri

47 e excision repair of oxidized pyrimidines in chloroplast protein extracts of Arabidopsis thaliana.

48 o DNA replication using a partially purified chloroplast protein fraction.

49 ting as a molecular chaperone and protecting chloroplast proteins from thermal aggregation and inacti

50 Genetic evidence suggests that the chloroplast protein GUN1 integrates signals derived from

51 romal chaperones, suggesting an imbalance in chloroplast protein homeostasis and a well-coordinated n

52 ysically interacts with proteins involved in chloroplast protein homeostasis based on coimmunoprecipi

53 To extend our understanding of chloroplast protein import and the role played by the im

54 of the putative Arabidopsis homologs for the chloroplast protein import apparatus has revealed many q

55 in pea (Pisum sativum) as a component of the chloroplast protein import apparatus.

56 We have used chloroplast protein import assays as a means to identify

57 genetic attributes of Chlamydomonas to study chloroplast protein import by creating a series of delet

58 work showed that SP1-mediated regulation of chloroplast protein import contributes to the organellar

59 GTPases, we provide new insights of how the chloroplast protein import cycle may be regulated.

60 ve begun to take a genetic approach to study chloroplast protein import in Chlamydomonas reinhardtii

61 usly unrecognized roles in the regulation of chloroplast protein import in response to developmental,

62 s was developed to explore the regulation of chloroplast protein import in vivo using two independent

63 This work characterizes a new chloroplast protein import intermediate which has comple

64 derived energy long known to be required for chloroplast protein import is delivered via the Hsp70 ch

65 Our results indicate that chloroplast protein import is responsive to environmenta

66 of two nuclear-encoded preproteins with the chloroplast protein import machinery at three stages in

67 protein (IAP) 100, a 100-kDa protein of the chloroplast protein import machinery of peas.

68 of complex chloroplasts provide barriers to chloroplast protein import not present in the simpler do

69 en demonstrated to be an intermediate in the chloroplast protein import pathway in vitro.

70 Chloroplast protein import presents a complex membrane t

71 suggest that even severely impaired in vivo chloroplast protein import probably does not limit the a

72 In the chloroplast protein import system, a heat shock protein

73 ure applications of this system to analyzing chloroplast protein import, and provide valuable insight

74 at the three components may cooperate during chloroplast protein import.

75 In chloroplasts, protein import is accomplished by the TOC

76 ion arises from changes in the abundances of chloroplast proteins in Emiliania huxleyi strain CCMP 15

77 art at least to de novo protein synthesis of chloroplast proteins in the sea slug.

78 While the import of nuclear-encoded chloroplast proteins is relatively well studied, the tar

79 Biosynthesis of chloroplast proteins is to a large extent regulated post

80 oxidase is nuclear encoded, similar to other chloroplast proteins localized in the lumen.

81 s motivated an extensive characterization of chloroplast protein N termini in Arabidopsis (Arabidopsi

82 UV cross-linking assays revealed that chloroplast proteins of 37 and 38 kDA bind specifically

83 ensive dataset of 381 nuclear genes encoding chloroplast proteins of Arabidopsis associated with embr

84 Nucleus-encoded chloroplast proteins of vascular plants are synthesized

85 amydomonas reinhardtii cells depleted of the chloroplast protein PGRL1 was rescued by the introductio

86 Euglena chloroplast protein precursors are transported as integr

87 All Euglena chloroplast protein precursors have functionally similar

88 An important regulator of chloroplast protein production is the downstream box (DB

89 Here, we report the identification of a chloroplast protein required for Rubisco accumulation in

90 We describe here the diversity of chloroplast proteins required for embryo development in

91 cpRNPs CP31A and CP29A (for 31 kD and 29 kD chloroplast protein, respectively), associate with large

92 ing a maize (Zea mays L.) gene (Zmeftu1) for chloroplast protein synthesis elongation factor, EF-Tu,

93 under long-term treatment with lincomycin, a chloroplast protein synthesis inhibitor.

94 f illumination, carbon source, and levels of chloroplast protein synthesis on trans-acting proteins t

95 ted by the finding that loss of RH50 renders chloroplast protein synthesis sensitive to erythromycin

96 the presence of cycloheximide indicated that chloroplast protein synthesis was broadly reduced in the

97 ersely, photosynthetic proteins and those of chloroplast protein synthesis were significantly lower i

98 tudy the role of initiation codon context in chloroplast protein synthesis, we mutated the three nucl

99 found in all cells except those deficient in chloroplast protein synthesis.

100 center protein of photosystem II or impaired chloroplast protein synthesis.

101 and biochemical approaches for the study of chloroplast protein targeting.

102 sence of Rubisco activase, a nuclear-encoded chloroplast protein that consists of two isoforms arisin

103 Rubisco activase is a nuclear-encoded chloroplast protein that is required for the light activ

104 results suggest that DCP68 is a bifunctional chloroplast protein that participates in reductive sulfu

105 Arabidopsis FZO-LIKE (FZL) was shown as a chloroplast protein that regulates chloroplast morpholog

106 (Nicotiana tabacum) and identified a set of chloroplast proteins that are likely degraded by Clp.

107 The fibrillins are a large family of chloroplast proteins that have been linked with stress t

108 Nucleus-encoded chloroplast proteins that reside in the thylakoid lumen

109 Similar to the authentic chloroplast protein, the reconstituted alpha/beta 14-mer

110 n used to elucidate the function of numerous chloroplast proteins, the characterization of essential

111 and tatC, which are likely to be involved in chloroplast protein translocation.

112 would be a useful model system for studying chloroplast protein transport.

113 Most chloroplast proteins undergo N-terminal maturation, but

114 Many chloroplast proteins were less abundant in the first eme

115 chloroplast genes and nuclear genes encoding chloroplast protein, which sheds light on the understand

116 182-amino-acid-long putative precursor of a chloroplast protein with high sequence similarity to evo

117 wild-type fusion protein was associated with chloroplasts, proteins with transit peptide deletions re