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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 d positively and negatively by multiple host DEAD-box RNA helicases.
7 t has been observed for many double-stranded 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.
13 y, mass spectrometry analysis identified the DEAD-box RNA helicase 6 (DDX6) that interacts with the V
17 esults confirmed that OsDB10 is a functional DEAD-box RNA helicase and played vital roles in plant de
18 ase polynucleotide phosphorylase (PNPase), a DEAD-box RNA helicase and the Krebs cycle enzyme aconita
24 tudies and identified DDX5, an ATP-dependent DEAD-box RNA helicase, as a component of the MAML1 prote
26 al activities of human DDX3X are typical for DEAD-box RNA helicases, but diverge quantitatively from
27 this model by identifying such a protein, a DEAD-box RNA helicase called Pitchoune, and show that mo
29 roteolytic degradation of the cyanobacterial DEAD-box RNA helicase CrhR is conditional, being initiat
30 D-alanine carboxypeptidases (dac1 and dac2), DEAD-box RNA helicases (csdA and Psyc_0943), and energy-
31 s, we identified among multiple proteins the DEAD box RNA helicase CshA (NWMN_1985 or SA1885) by mass
32 iously, our laboratory demonstrated that the DEAD-box RNA helicase Dbp2 in Saccharomyces cerevisiae i
34 The adenosine triphosphate (ATP)-dependent DEAD-box RNA helicase DbpA from Escherichia coli functio
35 on of select RNA chaperones, including three DEAD box RNA helicases (DBRHs) (CsdA, SrmB, RhlB) and th
39 In contrast to A52, K7 forms a complex with DEAD box RNA helicase DDX3, thereby suppressing DDX3-med
45 116 colon carcinoma cells, we identified the DEAD-box RNA helicase DDX41 as a novel regulator of p21
46 ocused our analysis on the largely unstudied DEAD box RNA helicase DDX55, and validated its novel rol
51 roteins that activate decapping, such as the DEAD-box RNA helicase Dhh1, have been postulated to func
53 ions in the HRxGRxxR motif of the prototypal DEAD box RNA helicase eIF-4A abolish or severely inhibit
58 ed testicular RNA helicase (GRTH)/DDX25 is a DEAD-box RNA helicase essential for the completion of sp
62 creen we isolated SUB2, encoding a conserved DEAD-box RNA helicase family member having roles in both
63 n evolutionarily conserved member of the SF2 DEAD-box RNA helicase family that contributes to the reg
64 elicase 5 (DDX5) is a founding member of the DEAD-box RNA helicase family, a group of enzymes that re
65 hat DDX5, one of the founding members of the DEAD-box RNA helicase family, is extremely proficient at
69 the gene encoding the sole Asp-Glu-Ala-Asp (DEAD)-box RNA helicase in Synechocystis sp. PCC 6803, cr
70 ependent and ATP-dependent roles of the Has1 DEAD-box RNA helicase in consecutive pre-rRNA processing
71 n this issue of the JCI identifies the first DEAD-box RNA helicase in the pathogenic fungus Cryptococ
72 siRNA) library screen targeting the 58 human DEAD-box RNA helicases in two permissive human cancer ce
74 lasmic roles as a modulator of ATP-dependent DEAD-box RNA helicases involved in messenger (m)RNA expo
76 itiation factor 4A (eIF4A), an ATP-dependent DEAD-box RNA helicase, is a critical component of the eI
77 the single-copy bobcat gene, which encodes a DEAD-box RNA helicase, is embedded within the first Manx
79 itiation factor 4A (eIF4A), an ATP-dependent DEAD-box RNA helicase; its messenger RNA selectivity is
94 es identified frequent mutations in DDX3X, a DEAD-box RNA helicase primarily implicated in translatio
95 is a Saccharomyces cerevisiae mitochondrial DEAD-box RNA helicase protein that is essential for effi
98 1 and established that it encodes a putative DEAD-box RNA helicase related to Saccharomycescerevisiae
99 fied as the Kreb's cycle enzyme aconitase, a DEAD-box RNA helicase RhlB and the exoribonuclease polyn
102 nwinding by DbpA, a non-processive bacterial DEAD-box RNA helicase specifically activated by the pept
103 Eukaryotic initiation factor (eIF) 4A is a DEAD box RNA helicase that works in conjunction with eIF
104 is the second example of a Asp-Glu-Ala-Asp (DEAD) box RNA helicase that unwinds RNA duplexes in a bi
109 soforms of the eIF4A family of ATP-dependent DEAD-box RNA helicases that are required for translation
110 ic initiation factor (eIF)4A, an ATP-powered DEAD-box RNA-helicase that unwinds the messenger RNA sec
111 y RNA-RNA interactions that are modulated by DEAD-box RNA helicases to ensure RNA availability and tr
119 Gle1 is a conserved, essential regulator of DEAD-box RNA helicases, with critical roles defined in m