ライフサイエンスコーパス: RNA-dependent ATPase

1 e show that purified recombinant Prp43 is an RNA-dependent ATPase.

2 rom Escherichia coli and determined to be an RNA-dependent ATPase.

3 ome, and is driven by a family of DExD/H-box RNA-dependent ATPases.

4 e no effect on DNA-independent ATPases or on RNA-dependent ATPases.

5 iated by members of the DExD/H-box family of RNA-dependent ATPases.

6 in globin synthesis, as well as the in vitro RNA-dependent ATPase activities of eIF4A, eIF4B, and eIF

7 The RNA-dependent ATPase activities of wild-type and mutant

8 Rho utilizes its RNA-dependent ATPase activities to translocate along the

9 that removes only the basic tail leaves high RNA-dependent ATPase activity and causes only a modest r

10 DbpA mutants shows the expected decrease in RNA-dependent ATPase activity and helix unwinding activi

11 emonstrated that the mutations abolished the RNA-dependent ATPase activity and RNA unwinding activity

12 Members of these protein families exhibit an RNA-dependent ATPase activity and some possess an ATP-de

13 ATP-binding motif of Prp16 inhibits both the RNA-dependent ATPase activity and the ATP-dependent RNA

14 lex at high pH and increases Delta247-Brr2's RNA-dependent ATPase activity and the extent of RNA unwi

15 l RNA helicase activities, as exemplified by RNA-dependent ATPase activity and unwinding of the DNA-R

16 Gle1 and InsP6 act together to stimulate the RNA-dependent ATPase activity of the essential DEAD-box

17 Dhh1 has weaker RNA-dependent ATPase activity than other well characteri

18 been purified to homogeneity and has a weak RNA-dependent ATPase activity which is not specific for

19 All show substantial RNA-dependent ATPase activity with several homoribopolym

20 Prp28 and Prp28-(127-588) have an intrinsic RNA-dependent ATPase activity, albeit with a low turnove

21 mda-5 displays RNA-dependent ATPase activity, and ectopic expression of

22 DP97 has RNA-dependent ATPase activity, and mapping studies local

23 a-helical region of Mss116p strongly inhibit RNA-dependent ATPase activity, leading to loss of functi

24 re, we purified Mss116p and show that it has RNA-dependent ATPase activity, unwinds RNA duplexes in a

25 hat purified recombinant Prp22 protein is an RNA-dependent ATPase and an ATP-dependent RNA helicase.

26 Its RNA folding activity, RNA-dependent ATPase and dATPase activities, and its tra

27 (b) Both the RNA-dependent ATPase and RNA helicase activities of RH70

28 Both the RNA-dependent ATPase and RNA helicase activities of the

29 two-domain catalytic core that enables their RNA-dependent ATPase and RNA helicase activities.

30 member of the "DEAD box" family of putative RNA-dependent ATPases and helicases.

31 Most of these proteins are RNA-dependent ATPases and some of them have RNA helicase

32 show that purified human UAP56 is an active RNA-dependent ATPase, and we also report the crystal str

33 ors belonging to the DExD/DExH-box family of RNA-dependent ATPases are thought to have a central role

34 An HTS campaign using an RNA-dependent ATPase assay and initial SAR study identif

35 The DExD/H-box RNA-dependent ATPase Dbp5 plays an essential role in the

36 li transcription termination protein Rho, an RNA-dependent ATPase, disrupts transcription complexes,

37 DEAD-box proteins are RNA-dependent ATPase enzymes that have been implicated i

38 plicing requires the function of a number of RNA-dependent ATPases/helicases, yet no three-dimensiona

39 hese Psis interact genetically with Prp5, an RNA-dependent ATPase involved in monitoring the U2 BSRR-

40 a member of the DExD/H box protein family of RNA-dependent ATPases, is required for the stable bindin

41 cient numbers of rC residues to activate the RNA-dependent ATPase of rho; and (ii) a downstream seque

42 e this assembly step, we focused on Prp5, an RNA-dependent ATPase of the DExD/H family.

43 a member of the DEAH-box family of putative RNA-dependent ATPases or helicases.

44 n these studies we have shown that Mtr4p has RNA-dependent ATPase (or dATPase) activity that is stimu

45 DEAD-box proteins, a large class of RNA-dependent ATPases, regulate all aspects of gene expr

46 Brr2 is an RNA-dependent ATPase required to unwind the U4/U6 snRNA

47 Saccharomyces cerevisiae Prp22 and Prp16 are RNA-dependent ATPases required for pre-mRNA splicing.

48 the wild-type Upf1p demonstrated that it has RNA-dependent ATPase, RNA helicase, and RNA binding acti

49 the wild-type Upf1p demonstrates that it has RNA-dependent ATPase, RNA helicase, and RNA binding acti

50 One such protein, the DECD box RNA-dependent ATPase Sub2p/UAP56, is involved in both ea

51 gene in Saccharomyces cerevisiae encodes an RNA-dependent ATPase that activates spliceosomes for the

52 ces cerevisiae spliceosomal protein Prp2, an RNA-dependent ATPase that activates the spliceosome befo

53 Prp2 is an RNA-dependent ATPase that activates the spliceosome befo

54 Saccharomyces cerevisiae Prp43 is a DEAH-box RNA-dependent ATPase that catalyzes the release of excis

55 MDA-5 is a double-stranded RNA-dependent ATPase that contains both a caspase recrui

56 A recent study has found an RNA-dependent ATPase that functions in this manner.

57 eIF4A is a DEAD-box RNA-dependent ATPase thought to unwind RNA secondary str

58 A number of RNA-dependent ATPases which are involved in several dist

59 tes it is a member of the DEAD box family of RNA-dependent ATPases, which mediate ATP hydrolysis duri

60 in E. coli, and all were found to be active RNA-dependent ATPases with k(cat) values ranging from 13