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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.
6 of transcriptional regulators similar to the cAMP receptor protein and fumavate nitrate reduction fro
8 regulated by two transcription factors, the cAMP receptor protein and the fumarate and nitrate reduc
9 similar to the arrangement of class II CRP (cAMP receptor protein)- and FNR (fumarate and nitrate re
10 lon genes, its modulation by the cyclic AMP (cAMP) receptor protein-cAMP complex (CRP-cAMP) global re
11 irect, whereas repression by the cyclic AMP (cAMP) receptor protein-cAMP complex (CRP-cAMP) was likel
12 esting that neither RpoS nor the cyclic AMP (cAMP) receptor protein-cAMP complex is required for expr
14 t cstA is regulated by the cyclic AMP (cAMP)-cAMP receptor protein complex and transcribed by Esigma(
16 with the osmolarity-dependent binding of the cAMP receptor protein CRP to a site within the proP P1 p
17 ose) activation, and three binding sites for cAMP receptor protein (CRP or CAP) were identified upstr
18 binding sites of Mycobacterium tuberculosis cAMP receptor protein (CRP(Mt)) at endogenous expression
21 of such diverse DNA-binding molecules as the cAMP receptor protein (CRP) and Din-family site-specific
22 Many of these genes were members of the cAMP-cAMP receptor protein (CRP) and guanosine tetraphosphate
23 measurements were performed on solutions of cAMP receptor protein (CRP) and on solutions of the T127
24 ia coli CytR regulon is activated by E. coli cAMP receptor protein (CRP) and repressed by a multiprot
25 ns between two gene regulatory proteins, the cAMP receptor protein (CRP) and the cytidine repressor (
26 wn, the structural homology of PrfA with the cAMP receptor protein (Crp) and the finding of constitut
27 efine a CRP(Mt) DNA motif that resembles the cAMP receptor protein (CRP) binding motif model for Esch
28 ork, sequences matching the Escherichia coli cAMP receptor protein (CRP) binding motif were identifie
30 ctivated by binding of the cyclic AMP (cAMP)-cAMP receptor protein (CRP) complex to a CRP binding sit
35 for a transcription factor belonging to the cAMP receptor protein (CRP) family caused growth defects
40 hermodynamic role of binding of an operon to cAMP receptor protein (CRP) in the activation of transcr
43 in the cAMP-induced allosteric activation of cAMP receptor protein (CRP) involve interfacial communic
45 n Escherichia coli, the transcription factor cAMP receptor protein (CRP) is responsible for much of t
51 any HapR targets coincide with sites for the cAMP receptor protein (CRP) that regulates the transcrip
52 in-protein interactions between CytR and the cAMP receptor protein (CRP) that underlie differential r
53 he cAMP-ligated T127L/S128A double mutant of cAMP receptor protein (CRP) was determined to a resoluti
55 gulator of the arr operon, cyclic AMP (cAMP)-cAMP receptor protein (CRP), could bind simultaneously w
56 f transcription by a mechanism that requires cAMP receptor protein (CRP), cyclic AMP (cAMP) and a CRP
57 AMP) interacts with the transcription factor cAMP receptor protein (CRP), forming active cAMP-CRP com
58 ide a feedback loop to the global regulator, cAMP receptor protein (CRP), in carbon source transition
60 ), the essential allosteric activator of the cAMP receptor protein (CRP), master regulator of carbon
61 hate (cAMP), the allosteric activator of the cAMP receptor protein (CRP), master regulator of carbon
63 ion is repressed by a three-protein complex (cAMP receptor protein (CRP)-CytR-CRP) that is stabilized
69 of three synthetic promoters by cNMP-ligated cAMP receptor protein (CRP)/mutant complexes was determi
70 igh-level ompT transcription is dependent on cAMP receptor protein (CRP); (ii) ToxR not only interfer
71 regulatory molecules, including cyclic AMP (cAMP) receptor protein (CRP) and c-di-GMP, were substant
72 ant of 3',5'-cyclic adenosine monophosphate (cAMP) receptor protein (CRP) by cAMP changes from an exo
73 ine-responsive protein (Lrp) and cyclic AMP (cAMP) receptor protein (CRP) in the transcriptional acti
78 onstrate that the binding of the cyclic AMP (cAMP) receptor protein (CRP) to a site centered at -34.5
80 mologous to the Escherichia coli cyclic AMP (cAMP) receptor protein (CRP), regulates many aspects of
81 encode adenylate cyclase and the cyclic AMP (cAMP) receptor protein (CRP), respectively, derepressed
89 bal transcription regulator Escherichia coli cAMP-receptor protein (CRP) and RNA polymerase along the
91 te activator protein (CAP; also known as the cAMP receptor protein, CRP) is a textbook example of mod
95 create a consensus recognition site for the cAMP-receptor protein, CRP (CC-site), and one that was r
96 ncoding adenylate cyclase) and crp (encoding cAMP receptor protein) deletion mutants revealed that cA
97 regulated by CooA, which is a member of the cAMP receptor protein family of transcriptional regulato
98 to determine the specificity within the CRP (cAMP receptor protein)/FNR (fumarate and nitrate reducta
101 owledge, of PDEs directly interacting with a cAMP-receptor protein in a mammalian system, and highlig
102 s between critical residues in CytR and CRP (cAMP receptor protein), is disrupted by exogenous cytidi
104 by two ubiquitously expressed intracellular cAMP receptors, protein kinase A (PKA) and exchange prot
107 ntext constant in Escherichia coli cAMP-CRP (cAMP receptor protein) regulated gal promoters by in vit
108 ced in a mutant defective in the cyclic AMP (cAMP) receptor protein, suggesting that intracellular cA
109 ied affinities of Synechocystis sp. PCC 6803 cAMP receptor protein (SyCrp1), the Escherichia coli Crp
110 dition to SiaR-mediated repression, CRP, the cAMP receptor protein, was shown to activate expression