ライフサイエンスコーパス: DEAD-box RNA helicase

1 dependent on sigB and cshA, which encodes a DEAD box RNA helicase.

2 PNPase), enolase, phosphofructokinase, and a DEAD box RNA helicase.

3 ontain four exons with similarity to a plant DEAD box RNA helicase.

4 lemented the function of Ded1p, an essential DEAD box RNA helicase.

5 ure revealed only one protein, RhlE, another DEAD-box RNA helicase.

6 t has been observed for many double-stranded DEAD-box RNA helicases.

7 d positively and negatively by multiple host DEAD-box RNA helicases.

8 or of SecA is strongly homologous to that in DEAD-box RNA helicases.

9 gous to the "Q motif" recently identified in DEAD-box RNA helicases.

10 ticles, Xp54, which belongs to the family of DEAD-box RNA helicases.

11 y, mass spectrometry analysis identified the DEAD-box RNA helicase 6 (DDX6) that interacts with the V

12 We have identified a novel DEAD box RNA helicase (97 kDa, DP97) from a breast cance

13 visiae is a nucleic acid helicase related to DEAD box RNA helicases and type I DNA helicases.

14 Recently, our group established the DEAD-box RNA helicase and microRNA (miRNA) microprocesso

15 ase polynucleotide phosphorylase (PNPase), a DEAD-box RNA helicase and the Krebs cycle enzyme aconita

16 Mtr4p shares characteristic motifs with DEAD-box RNA helicases and associates with RNA.

17 Taken together, we propose that DEAD-box RNA helicases are directly coupled to transcrip

18 The DEAD-box RNA helicases are enzymes involved in many crit

19 Here, we show that several DEAD-box RNA helicases are sensitive to AMP, which is no

20 DEAD-box RNA helicases are vital for the regulation of v

21 tudies and identified DDX5, an ATP-dependent DEAD-box RNA helicase, as a component of the MAML1 prote

22 Vasa is a broadly conserved DEAD-box RNA helicase associated with germ line developm

23 al activities of human DDX3X are typical for DEAD-box RNA helicases, but diverge quantitatively from

24 Importantly, we identify the conserved DEAD-box RNA helicase, CGH-1/DDX6, as a key CK2 substrat

25 D-alanine carboxypeptidases (dac1 and dac2), DEAD-box RNA helicases (csdA and Psyc_0943), and energy-

26 s, we identified among multiple proteins the DEAD box RNA helicase CshA (NWMN_1985 or SA1885) by mass

27 iously, our laboratory demonstrated that the DEAD-box RNA helicase Dbp2 in Saccharomyces cerevisiae i

28 DEAD-box RNA helicase Dbp4 is required for 18S rRNA synt

29 on of select RNA chaperones, including three DEAD box RNA helicases (DBRHs) (CsdA, SrmB, RhlB) and th

30 DEAD-box RNA helicases (DBRHs) modulate RNA secondary st

31 Here we show that the DEAD-box RNA helicase DDX21 can sense the transcriptiona

32 In contrast to A52, K7 forms a complex with DEAD box RNA helicase DDX3, thereby suppressing DDX3-med

33 Rev/CRM1 activity utilizes the ATP-dependent DEAD box RNA helicase, DDX3.

34 The DEAD-box RNA helicase DDX3X is frequently mutated in ped

35 116 colon carcinoma cells, we identified the DEAD-box RNA helicase DDX41 as a novel regulator of p21

36 Here, we show that the DEAD box RNA helicase, DDX6 is necessary for maintaining

37 We show that two DEAD-box RNA helicases, DeaD and SrmB, activate csrB/C e

38 DEAD-box RNA helicases, defined by the sequence Asp-Glu-

39 roteins that activate decapping, such as the DEAD-box RNA helicase Dhh1, have been postulated to func

40 eat domain 3 protein (PTCD3), and a putative DEAD-box RNA helicase, DHX30.

41 ions in the HRxGRxxR motif of the prototypal DEAD box RNA helicase eIF-4A abolish or severely inhibit

42 DEAD-box RNA helicases eIF4A and Ded1 are believed to pr

43 ranslation initiation involves two conserved DEAD-box RNA helicases, eIF4A and Ded1p.

44 In this study, a virulence-associated DEAD-box RNA helicase-encoding gene (VAD1) was isolated

45 Most aspects of RNA metabolism involve DEAD-box RNA helicases, enzymes that bind and remodel RN

46 DEAD-box RNA helicases eukaryotic translation initiation

47 t least seven nucleus-encoded members of the DEAD box RNA helicase family.

48 nsistent activation of DDX3, a member of the DEAD box RNA helicase family.

49 creen we isolated SUB2, encoding a conserved DEAD-box RNA helicase family member having roles in both

50 n evolutionarily conserved member of the SF2 DEAD-box RNA helicase family that contributes to the reg

51 egulation by other members of the ubiquitous DEAD-box RNA helicase family.

52 We reported earlier that LAF-1, a DEAD box RNA helicase in C. elegans, dynamically interac

53 ependent and ATP-dependent roles of the Has1 DEAD-box RNA helicase in consecutive pre-rRNA processing

54 n this issue of the JCI identifies the first DEAD-box RNA helicase in the pathogenic fungus Cryptococ

55 siRNA) library screen targeting the 58 human DEAD-box RNA helicases in two permissive human cancer ce

56 DDX3X is a conserved DEAD-box RNA helicase involved in translation initiation

57 This DEAD-box RNA helicase is known to be associated with var

58 the single-copy bobcat gene, which encodes a DEAD-box RNA helicase, is embedded within the first Manx

59 In many species examined, Vasa, a DEAD-box RNA helicase, is found in these morphologically

60 itiation factor 4A (eIF4A), an ATP-dependent DEAD-box RNA helicase; its messenger RNA selectivity is

61 Unlike a previously reported DEAD box RNA helicase (LOW EXPRESSION OF OSMOTICALLY RES

62 DEAD-box RNA helicases of the bacterial DbpA subfamily a

63 Here we show that DHH1, encoding a DEAD-box RNA helicase orthologous to the human putative

64 Here we showed that the DEAD-box RNA helicase p68 (DDX5) and its associated nonc

65 The DEAD-box RNA helicases p68 (DDX5) and p72 (DDX17) have b

66 The DEAD box RNA helicase, p68, has been implicated in vario

67 The DEAD box RNA helicase, p68, is upregulated in exponentia

68 Here, we show that the abundant DEAD-box RNA helicase p72, but not its close relative p6

69 DEAD box RNA helicases play central roles in RNP biogene

70 is a Saccharomyces cerevisiae mitochondrial DEAD-box RNA helicase protein that is essential for effi

71 DEAD-box RNA helicase proteins use the energy of ATP hyd

72 1 and established that it encodes a putative DEAD-box RNA helicase related to Saccharomycescerevisiae

73 fied as the Kreb's cycle enzyme aconitase, a DEAD-box RNA helicase RhlB and the exoribonuclease polyn

74 Here, we show that the DEAD box RNA helicase smut-1 functions redundantly in th

75 nwinding by DbpA, a non-processive bacterial DEAD-box RNA helicase specifically activated by the pept

76 Eukaryotic initiation factor (eIF) 4A is a DEAD box RNA helicase that works in conjunction with eIF

77 is the second example of a Asp-Glu-Ala-Asp (DEAD) box RNA helicase that unwinds RNA duplexes in a bi

78 Gemin3 is a DEAD-box RNA helicase that binds to the Survival of Moto

79 Vasa is a DEAD-box RNA helicase that functions in translational re

80 DDX3X is a DEAD-box RNA helicase that has been implicated in multip

81 ISE1 encodes a putative plant-specific DEAD-box RNA helicase that localizes specifically to mit

82 soforms of the eIF4A family of ATP-dependent DEAD-box RNA helicases that are required for translation

83 Amplifier is nucleated by the DEAD box RNA helicase Vasa and contains the two Piwi pro

84 rosophila orthologue GUSTAVUS binding to the DEAD-box RNA helicase VASA (DINNNN).

85 ISE1 encodes a mitochondrial DEAD-box RNA helicase, whereas ISE2 encodes a DEVH-type

86 DEAD-box RNA helicases, which are involved in virtually

87 DDX3 is a DEAD box RNA helicase with oncogenic properties.

88 The DEAD-box RNA helicase Xp54 is an integral component of t