ライフサイエンスコーパス: cAMP receptor protein

1 sion of the homodimeric transcription factor cAMP receptor protein.

2 endent of the global cAMP signal transducer, cAMP receptor protein.

3 ntP requires activation by cyclic AMP (cAMP)-cAMP receptor protein.

4 diated at least in part by cyclic AMP (cAMP)-cAMP receptor protein.

5 transcription by competing for binding with cAMP receptor protein, a global activator.

6 of transcriptional regulators similar to the cAMP receptor protein and fumavate nitrate reduction fro

7 regulated by two transcription factors, the cAMP receptor protein and the fumarate and nitrate reduc

8 similar to the arrangement of class II CRP (cAMP receptor protein)- and FNR (fumarate and nitrate re

9 lon genes, its modulation by the cyclic AMP (cAMP) receptor protein-cAMP complex (CRP-cAMP) global re

10 irect, whereas repression by the cyclic AMP (cAMP) receptor protein-cAMP complex (CRP-cAMP) was likel

11 esting that neither RpoS nor the cyclic AMP (cAMP) receptor protein-cAMP complex is required for expr

12 t cstA is regulated by the cyclic AMP (cAMP)-cAMP receptor protein complex and transcribed by Esigma(

13 synthesis of SecB may be related to the cAMP-cAMP receptor protein complex-mediated activation.

14 with the osmolarity-dependent binding of the cAMP receptor protein CRP to a site within the proP P1 p

15 ose) activation, and three binding sites for cAMP receptor protein (CRP or CAP) were identified upstr

16 binding sites of Mycobacterium tuberculosis cAMP receptor protein (CRP(Mt)) at endogenous expression

17 The Escherichia coli cAMP receptor protein (CRP) activates transcription init

18 Binding of cAMP receptor protein (CRP) and CytR mediates both posit

19 of such diverse DNA-binding molecules as the cAMP receptor protein (CRP) and Din-family site-specific

20 Many of these genes were members of the cAMP-cAMP receptor protein (CRP) and guanosine tetraphosphate

21 measurements were performed on solutions of cAMP receptor protein (CRP) and on solutions of the T127

22 ia coli CytR regulon is activated by E. coli cAMP receptor protein (CRP) and repressed by a multiprot

23 ns between two gene regulatory proteins, the cAMP receptor protein (CRP) and the cytidine repressor (

24 wn, the structural homology of PrfA with the cAMP receptor protein (Crp) and the finding of constitut

25 efine a CRP(Mt) DNA motif that resembles the cAMP receptor protein (CRP) binding motif model for Esch

26 ork, sequences matching the Escherichia coli cAMP receptor protein (CRP) binding motif were identifie

27 We show that the cAMP receptor protein (Crp) binds to DNA as several diff

28 ctivated by binding of the cyclic AMP (cAMP)-cAMP receptor protein (CRP) complex to a CRP binding sit

29 adenosine cyclic-3',5'-monophosphate (cAMP)-cAMP receptor protein (CRP) complex.

30 es may be regulated by the cyclic AMP (cAMP)-cAMP receptor protein (CRP) complex.

31 Escherichia coli cAMP receptor protein (CRP) controls more than 20 genes.

32 The Escherichia coli cAMP receptor protein (CRP) displays biphasic characteri

33 for a transcription factor belonging to the cAMP receptor protein (CRP) family caused growth defects

34 CooA, a member of the cAMP receptor protein (CRP) family, is a CO-sensing tran

35 Activation of the cAMP receptor protein (CRP) from Escherichia coli is hig

36 In the transcription factor cAMP receptor protein (CRP) from Escherichia coli, the a

37 The cAMP receptor protein (CRP) from Mycobacterium tuberculo

38 hermodynamic role of binding of an operon to cAMP receptor protein (CRP) in the activation of transcr

39 The effects of varying amounts of cAMP receptor protein (CRP) in the presence and absence

40 Although cAMP binding to wild type cAMP receptor protein (CRP) induces specific DNA binding

41 in the cAMP-induced allosteric activation of cAMP receptor protein (CRP) involve interfacial communic

42 A homologue of the Escherichia coli cAMP receptor protein (CRP) is linked to the guanylyl cy

43 n Escherichia coli, the transcription factor cAMP receptor protein (CRP) is responsible for much of t

44 The cAMP receptor protein (CRP) of Escherichia coli exists i

45 The cAMP receptor protein (CRP) of Escherichia coli is a tra

46 The cAMP receptor protein (CRP) of Escherichia coli undergoe

47 lator HapR, as well as the cyclic AMP (cAMP)-cAMP receptor protein (CRP) regulatory complex.

48 FixK2 belongs to the cAMP receptor protein (CRP) superfamily.

49 in-protein interactions between CytR and the cAMP receptor protein (CRP) that underlie differential r

50 he cAMP-ligated T127L/S128A double mutant of cAMP receptor protein (CRP) was determined to a resoluti

51 Potential Fnr, cyclic AMP (cAMP)-cAMP receptor protein (Crp), and sigma(F) regulatory sit

52 gulator of the arr operon, cyclic AMP (cAMP)-cAMP receptor protein (CRP), could bind simultaneously w

53 f transcription by a mechanism that requires cAMP receptor protein (CRP), cyclic AMP (cAMP) and a CRP

54 AMP) interacts with the transcription factor cAMP receptor protein (CRP), forming active cAMP-CRP com

55 ide a feedback loop to the global regulator, cAMP receptor protein (CRP), in carbon source transition

56 By analogy to the homologous cAMP receptor protein (CRP), it has been proposed that e

57 ion is repressed by a three-protein complex (cAMP receptor protein (CRP)-CytR-CRP) that is stabilized

58 extension analysis confirmed that P1 is the cAMP receptor protein (CRP)-dependent promoter.

59 cherichia coli molecular chaperone GroEL and cAMP receptor protein (CRP).

60 quired integration host factor (IHF) and the cAMP receptor protein (CRP).

61 map ligand-induced conformational changes in cAMP receptor protein (CRP).

62 with the cyclic AMP (cAMP) activated form of cAMP receptor protein (CRP).

63 of three synthetic promoters by cNMP-ligated cAMP receptor protein (CRP)/mutant complexes was determi

64 igh-level ompT transcription is dependent on cAMP receptor protein (CRP); (ii) ToxR not only interfer

65 regulatory molecules, including cyclic AMP (cAMP) receptor protein (CRP) and c-di-GMP, were substant

66 ant of 3',5'-cyclic adenosine monophosphate (cAMP) receptor protein (CRP) by cAMP changes from an exo

67 ine-responsive protein (Lrp) and cyclic AMP (cAMP) receptor protein (CRP) in the transcriptional acti

68 The cyclic AMP (cAMP) receptor protein (CRP) indirectly increases ltxA e

69 In this study, the cyclic AMP (cAMP) receptor protein (CRP) is shown to be involved in

70 ctivation can be enhanced by the cyclic AMP (cAMP) receptor protein (CRP) protein.

71 The cyclic AMP (cAMP) receptor protein (CRP) strongly enhanced hapA tran

72 onstrate that the binding of the cyclic AMP (cAMP) receptor protein (CRP) to a site centered at -34.5

73 A gene encoding a cyclic AMP (cAMP) receptor protein (CRP) was identified as the site

74 mologous to the Escherichia coli cyclic AMP (cAMP) receptor protein (CRP), regulates many aspects of

75 encode adenylate cyclase and the cyclic AMP (cAMP) receptor protein (CRP), respectively, derepressed

76 We show here that Fis and cyclic AMP (cAMP) receptor protein (CRP)-cAMP collaborate to activat

77 to be subject to control by the cyclic AMP (cAMP) receptor protein (CRP)-cAMP complexes.

78 at the level of transcription by cyclic AMP (cAMP) receptor protein (CRP).

79 ntrolled by the global regulator cyclic AMP (cAMP) receptor protein (Crp).

80 wth were not affected by loss of cyclic AMP (cAMP) receptor protein (CRP).

81 encode adenylate cyclase and the cyclic AMP (cAMP) receptor protein (CRP).

82 ulated in response to glucose by cyclic AMP (cAMP) receptor protein (CRP).

83 bal transcription regulator Escherichia coli cAMP-receptor protein (CRP) and RNA polymerase along the

84 r by the regulators Lac repressor (LacR) and cAMP-receptor protein (CRP).

85 te activator protein (CAP; also known as the cAMP receptor protein, CRP) is a textbook example of mod

86 The activated Escherichia coli cAMP receptor protein, CRP, is capable of regulating the

87 create a consensus recognition site for the cAMP-receptor protein, CRP (CC-site), and one that was r

88 ncoding adenylate cyclase) and crp (encoding cAMP receptor protein) deletion mutants revealed that cA

89 regulated by CooA, which is a member of the cAMP receptor protein family of transcriptional regulato

90 to determine the specificity within the CRP (cAMP receptor protein)/FNR (fumarate and nitrate reducta

91 r to the consensus core motifs recognized by cAMP receptor protein/FNR family.

92 owledge, of PDEs directly interacting with a cAMP-receptor protein in a mammalian system, and highlig

93 s between critical residues in CytR and CRP (cAMP receptor protein), is disrupted by exogenous cytidi

94 by two ubiquitously expressed intracellular cAMP receptors, protein kinase A (PKA) and exchange prot

95 The cAMP receptor protein of Escherichia coli, CRP, was empl

96 The recent discovery of Epac, a novel cAMP receptor protein, opens up a new dimension in study

97 ntext constant in Escherichia coli cAMP-CRP (cAMP receptor protein) regulated gal promoters by in vit

98 ced in a mutant defective in the cyclic AMP (cAMP) receptor protein, suggesting that intracellular cA

99 ied affinities of Synechocystis sp. PCC 6803 cAMP receptor protein (SyCrp1), the Escherichia coli Crp

100 dition to SiaR-mediated repression, CRP, the cAMP receptor protein, was shown to activate expression