ライフサイエンスコーパス: elongation factor P

1 translation is carried out in the absence of elongation factor P.

2 cus encodes a protein similar in sequence to elongation factor P, a protein thought to be involved in

3 Elongation factor P (EF-P) accelerates diprolyl synthesi

4 Elongation factor P (EF-P) binds to ribosomes requiring

5 Translation elongation factor P (EF-P) in Bacillus subtilis is requi

6 Elongation factor P (EF-P) is a conserved ribosome-bindi

7 Elongation factor P (EF-P) is a universally conserved ba

8 Elongation factor P (EF-P) is an essential protein that

9 Bacterial elongation factor P (EF-P) is the ortholog of archaeal a

10 Post-translational modification of bacterial elongation factor P (EF-P) with (R)-beta-lysine at a con

11 Strikingly, we show that elongation factor P (EF-P), traditionally known to allev

12 d ribosomes are rescued by the translational elongation factor P (EF-P), which by stimulating peptide

13 nship, we examined the bacterial translation elongation factor P (EF-P), which plays a critical role

14 ia, stalling at PPP motifs is rescued by the elongation factor P (EF-P).

15 ling at poly-Pro motifs is alleviated by the elongation factor P (EF-P).

16 y than the wild-type strain, indicating that elongation factor P is important but not essential for t

17 he requirements for positive transcriptional elongation factor (P-TEF) b activity.

18 the importance of the positive transcription elongation factor (P-TEF)b in control of global RNA synt

19 ated AhR recruits the positive transcription elongation factor (P-TEFb) and RNA polymerase II (RNA PI

20 artner of CDK9 in the positive transcription elongation factor (P-TEFb) complex, and binds cooperativ

21 linT1) subunit of the positive transcription elongation factor (P-TEFb) complex, which then cooperati

22 evealed roles for the positive transcription elongation factor (P-TEFb) component Cyclin T1 (Ccnt1).

23 The positive transcription elongation factor (P-TEFb) is required for the transcrip

24 tors, including the positive transcriptional elongation factor (P-TEFb), the bromodomain-containing p

25 Positive transcription elongation factor (P-TEFb), which is composed of CDK9 an

26 The metazoan transcription elongation factor P-TEFb (CDK-9/cyclin T) is essential f

27 The RNA polymerase II transcriptional elongation factor P-TEFb (cyclin-dependent kinase 9/cycl

28 of the Tat-associated kinase TAK and of the elongation factor P-TEFb (positive transcription elongat

29 nd MePCE captures the positive transcription elongation factor P-TEFb and prevents phosphorylation of

30 In contrast, the positive transcription elongation factor P-TEFb is a local explorer that oversa

31 The human positive transcription elongation factor P-TEFb is composed of two subunits, cy

32 BRCA1 but also associates with the positive elongation factor P-TEFb through interaction with the re

33 se CDK9, is a component of the transcription elongation factor P-TEFb which binds the human immunodef

34 H and Tat-associated kinase (a transcription elongation factor P-TEFb) and requires the carboxyl-term

35 orks by activating the human transcriptional elongation factor P-TEFb, a CDK9-cyclin T1 heterodimer t

36 h components of the positive transcriptional elongation factor P-TEFb, a complex containing cyclin T1

37 e mediated through the binding of TAT-SF1 to elongation factor P-TEFb, a proposed component of the tr

38 sed to respond to the positive transcription elongation factor P-TEFb, and then enter productive elon

39 The human positive transcription elongation factor P-TEFb, consisting of a CDK9/cyclin T1

40 on by recruitment of the human transcription elongation factor P-TEFb, consisting of CDK9 and cyclin

41 on by recruitment of the human transcription elongation factor P-TEFb, consisting of Cdk9 and cyclin

42 Recently, a human transcription elongation factor P-TEFb, consisting of CDK9 kinase, cyc

43 1 (hCycT1), a major subunit of the essential elongation factor P-TEFb, has been proposed to act as a

44 h AFF4, ELLs, and the positive transcription elongation factor P-TEFb, providing evidence that the dy

45 polymerase II or cyclin T, a subunit of the elongation factor P-TEFb, reveals that all three factors

46 block is associated with recruitment of the elongation factor P-TEFb, the co-activator GRIP1, the ch

47 scription is mediated by human transcription elongation factor P-TEFb, which interacts with Tat and p

48 or elongation mediated by the recruitment of elongation factor P-TEFb.

49 er, and blockage of the assembly of the host elongation factor P-TEFb.

50 ion until it is counteracted by the positive elongation factor P-TEFb.

51 CDK9 and as a component of the transcription elongation factor P-TEFb.

52 re also components of positive transcription elongation factor P-TEFb.

53 interaction with the positive transcription elongation factor, P-TEFb, and directs the factor to pro

54 The positive transcription elongation factor, P-TEFb, controls the fraction of init

55 ieves a block to elongation by recruiting an elongation factor, P-TEFb, to the viral promoter.

56 es Tat to recruit the positive transcription elongation factor, P-TEFb, which functions to promote th

57 SCL transcription complex, and the positive elongation factors p-TEFb and FACT.

58 mponents that link this complex to two major elongation factors, P-TEFb and the PAF complex.

59 The translation factor elongation factor P, which alleviates pausing at polypro