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1 VirA is a homodimeric membrane-spanning histidine protein kinase.
2 kinases, BCKD kinase does not function as a histidine protein kinase.
3 on results in autophosphorylation of CheA, a histidine protein kinase.
4 evidence that kinB encodes the AlgB cognate histidine protein kinase.
5 autoinducing peptide (AIP) activates AgrC, a histidine protein kinase.
6 ellular domain of AgrC, a classical receptor histidine protein kinase.
7 similar to the core catalytic domain of the histidine protein kinases.
8 logous expression of full-length RegB or any histidine protein kinases.
9 ArlS exhibits strong similarities with histidine protein kinases.
10 cell surface, which are often membrane-bound histidine protein kinases.
11 the conserved residues typical of the sensor histidine protein kinases.
12 al of the highly conserved motifs typical of histidine protein kinases.
13 ain that is homologous to the transmitter of histidine protein kinases.
14 ubstitutions of the residues conserved among histidine protein kinases abolished KinB autophosphoryla
15 cytokinin signalling through distinct hybrid histidine protein kinase activities at the plasma membra
17 multidomain proteins that typically couple a histidine protein kinase activity to a heme-binding doma
18 was previously correlated with its in vitro histidine protein kinase activity, but physiological sub
19 orylation on serines, and slightly decreased histidine protein kinase activity; significant NDPK acti
21 duct of mtrB displayed similarities with the histidine protein kinases AfsQ2, PhoR, and EnvZ and othe
22 on proteins, we have cloned genes encoding a histidine protein kinase and a response regulator from t
23 a phosphorylation cascade that consists of a histidine protein kinase and a response regulator protei
24 chemes involving two conserved components, a histidine protein kinase and a response regulator protei
25 genes, comD and comE, that encode members of histidine protein kinase and response-regulator families
26 xists instead with key motifs of prokaryotic histidine protein kinases and a family of eukaryotic ATP
27 sphorelay through the opposing activities of histidine protein kinases and aspartyl phosphate phospha
29 stem, in which RegB is the integral membrane histidine protein kinase, and RegA is the cytosolic resp
31 deficient phosphotransfer activity in three histidine protein kinase assays, using succinic thiokina
33 d out of the clock core appears to occur via histidine protein kinase-based phosphorylation relays.
34 despite its sequence similarity to bacterial histidine protein kinases, BCKD kinase does not function
39 of a family of Type I membrane receptors, a histidine protein kinase (CheA), and an Src homology 3-l
40 osphotransfer reactions using a heterologous histidine protein kinase, CheA, as a phosphoryl group do
41 ulated by a phosphorelay network involving a histidine protein kinase, CheA, whose activity is contro
44 complex chemosensory pathway comprising two histidine protein kinases (CheAs) and eight downstream r
45 xis signal transduction pathway has: CheA, a histidine protein kinase; CheW, a linker between CheA an
46 f three-dimensional structures of domains of histidine protein kinase domains and response regulator
47 The Esp signal system consists of the hybrid histidine protein kinase, EspA, two serine/threonine pro
49 th of which are members of the two-component histidine protein kinase family that is prevalent in pro
50 contain all the key motifs identified in the histidine protein kinase family, except for conservative
52 e-rich regions (G1 and G2) of CheA and other histidine protein kinases have been presumed to play imp
53 s, the response regulator (RR) PhoP, and the histidine protein kinase (HK) PhoR, are involved in the
55 the 2CRS mutants showed that mutation of the histidine protein kinase (HPK) had no effect on the indu
56 A possesses three distinct domains: a GAF, a histidine protein kinase (HPK), and a receiver domain si
57 in is homologous to the ubiquitous bacterial histidine protein kinases (HPKs), it differs from previo
59 substitute for the phosphodonor function of histidine protein kinases in in vitro phosphorylation st
60 The sequence of KinB is homologous to the histidine protein kinase members of two-component regula
61 gent bacteriophytochrome with characteristic histidine protein kinase motifs and a cryptic response r
62 kA sequence contains all five characteristic histidine protein kinase motifs with the same relative o
64 d to have similarity to the sequences of the histidine protein kinases of two-component regulatory sy
66 nin perception in Arabidopsis, the action of histidine protein kinase receptors and the downstream si
67 vates transcription of sda, and Sda inhibits histidine protein kinases required for activation of the
70 signal transduction pathway involves hybrid histidine protein kinase sensors, phosphotransfer protei
71 EspA and EspC participate in a novel hybrid histidine protein kinase signaling mechanism involving b
72 can act as a protein kinase to phosphorylate histidine protein kinases such as EnvZ and CheA which ar
73 This gene is predicted to encode a sensor histidine protein kinase that appears to be a key elemen
76 of algB and was shown to encode the cognate histidine protein kinase that efficiently phosphorylates
77 orks is the dynamic localization of multiple histidine protein kinases that control a master response
78 transduction based on phosphotransfer from a histidine protein kinase to a response regulator protein
79 edge, CheA(3)A(4) is the first characterized histidine protein kinase where the subunits are encoded
82 ence analysis of EspA indicates that it is a histidine protein kinase with a fork head-associated (FH
83 eB, a response regulator; and CseC, a sensor histidine protein kinase with two predicted transmembran
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