ライフサイエンスコーパス: histidine kinase

1 suggest the phosphodonor is instead the EspA histidine kinase.

2 for analysing ligand regulation of a sensor histidine kinase.

3 are sometimes fused into a so-called hybrid histidine kinase.

4 eraction between transmembrane receptors and histidine kinase.

5 n) is phosphorylated by the WalK(Spn) (VicK) histidine kinase.

6 Trimers activate and control the histidine kinase.

7 nced the autophosphorylation activity of the histidine kinase.

8 um between the inactive and active states of histidine kinases.

9 r specificity in vitro relative to canonical histidine kinases.

10 with a two-state model for ligand control of histidine kinases.

11 0.10 min(-1)] and typical of those of other histidine kinases.

12 le is known about the signals sensed by WalK histidine kinases.

13 lation via a phosphorelay involving multiple histidine kinases.

14 been identified that directly interact with histidine kinases.

15 ryl donor but not with two other recombinant histidine kinases.

16 ce with the GHKL domain of bacterial sensory histidine kinases.

17 different from those observed in prokaryotic histidine kinases.

18 ing methyl-accepting chemotaxis proteins and histidine kinases.

19 lar architecture of KinB is similar to other histidine kinases.

20 The hybrid histidine kinase Arabidopsis histidine kinase 5 (AHK5) is known to mediate stomatal r

21 modular proteins consisting of rhodopsin, a histidine kinase, a response regulator, and in some case

22 orelay based on genetic analysis of receptor histidine kinase activity and mutants involving the type

23 ETR1 histidine kinase activity and phosphotransfer through th

24 alyses of gene expression support a role for histidine kinase activity in eliciting the ethylene resp

25 To resolve the role of histidine kinase activity in signaling by the receptors,

26 reversal frequencies, an in vivo measure of histidine kinase activity in the phototaxis system, indi

27 yte phytochromes also retain light-regulated histidine kinase activity lost in the streptophyte phyto

28 These data indicate that the histidine kinase activity of ETR1 is not required for bu

29 1) and ETHYLENE RESPONSE SENSOR1 (ERS1) have histidine kinase activity, unlike the subfamily 2 member

30 mployed to study, and ultimately to control, histidine kinase activity.

31 tant effector domain, thereby regulating its histidine kinase activity.

32 a transmembrane region; a cytoplasmic HAMP (histidine kinase, adenylyl cyclases, methyl-accepting ch

33 ely 55 amino acid motifs first identified in histidine kinases, adenylyl cyclases, methyl-accepting c

34 MP domains mediate input-output signaling in histidine kinases, adenylyl cyclases, methyl-accepting c

35 model for PAS (Per-Arnt-Sim) and poly-HAMP (histidine kinase-adenylyl cyclase-methyl-accepting chemo

36 The heme-based oxygen sensor histidine kinase AfGcHK is part of a two-component signa

37 he histidine phosphotransferase AHP2 and the histidine kinases AHK2 and AHK3, previously reported to

38 the extracellular domain of the Arabidopsis histidine kinase (AHKs) receptors induces autophosphoryl

39 Although the involvement of histidine kinases (AHKs) in drought stress responses has

40 requires the CYTOKININ INDEPENDENT 1 (CKI1) histidine kinase, an activator of the cytokinin signalin

41 cally composed of a membrane-spanning sensor histidine kinase and a cytoplasmic response regulator.

42 signal transduction pathways consisting of a histidine kinase and a response regulator are used by pr

43 idization probes were designed to target the histidine kinase and glyceraldehyde-3-phosphate dehydrog

44 lutionary relationship as well as containing histidine kinase and receiver domains.

45 ine kinase that is predicted to contain both histidine kinase and response regulator domains, but it

46 scribed with scnK and scnR, which encode the histidine kinase and response regulator, respectively, o

47 cifically designed to predict pairing of the histidine kinase and response-regulator proteins forming

48 ition and phosphotransfer between the sensor histidine kinase and the response regulator.

49 eiver and downstream output domains, e.g. in histidine kinases and bacterial adenylyl cyclases.

50 g network that involves integration from two histidine kinases and branching to three response regula

51 e receptors form ternary complexes with CheA histidine kinases and CheW adaptor proteins.

52 the two-component signaling system involving histidine kinases and cognate response regulators.

53 Direct phosphorylation of Spo0A by histidine kinases and dephosphorylation by kinase-like p

54 tional design of light-regulated variants of histidine kinases and other proteins.

55 wo-component systems (TCS) comprising sensor histidine kinases and response regulator proteins are am

56 first assess the algorithm's performance on histidine kinases and response regulators from bacterial

57 Histidine kinases and response regulators have an intrin

58 In both histidine kinases and response regulators, modular domai

59 TCS both modulate phosphorelays comprised of histidine kinases and response regulators, some of which

60 nal transduction systems consist of pairs of histidine kinases and response regulators, which mediate

61 ed by two-component systems (TCS) comprising histidine kinases and response regulators.

62 ed insight into the functioning of bacterial histidine kinases and response regulators.

63 , high-quality domain models for identifying histidine kinases and response regulators; neighboring t

64 interactions between response regulators and histidine kinases and the specificity therein.

65 These networks comprise histidine kinases and their cognate response regulators.

66 ound a core phosphotransfer reaction between histidine kinases and their output response regulator pr

67 of the algZ [fimS] gene, encoding a putative histidine kinase), and PAO1 DeltaalgR for swarming motil

68 VirA, a hybrid histidine kinase, and its cognate response regulator, Vi

69 axis, transmembrane chemoreceptors, the CheA histidine kinase, and the CheW coupling protein assemble

70 The hybrid histidine kinase Arabidopsis histidine kinase 5 (AHK5) i

71 ncoding the NarL response regulator and NarS histidine kinase are hypothesized to constitute a two-co

72 phosphotransfer activities of a conventional histidine kinase are split onto two distinct proteins th

73 osphorelay in which phosphoryl groups from a histidine kinase are successively transferred via relay

74 Sensor histidine kinases are central to sensing in bacteria and

75 avin-binding LOV (light, oxygen, or voltage) histidine kinases are competent to perceive cytoplasmic

76 Histidine kinases are key regulators in the bacterial tw

77 Yet in almost all known examples, histidine kinases are thought to function as homodimers.

78 These findings suggest that histidine kinases are under selective pressure to mainta

79 Sensor histidine kinases are widely used by bacteria to detect

80 l transduction system, comprised of a sensor histidine kinase (ArsS) and a response regulator (ArsR),

81 a to favorable environments by controlling a histidine kinase as a function of chemoreceptor ligand o

82 xygen and regulates the activity of the FixL histidine kinase as part of a two-component signaling sy

83 n addition, we identified His390 of the LytS histidine kinase as the site of autophosphorylation and

84 ically thought to be mediated exclusively by histidine kinases as part of two-component signaling sys

85 e TipN polar marker, and indirectly the PleC histidine kinase, at the cell pole, but it is not requir

86 redicted to be a hybrid sensor kinase with a histidine kinase/ATPase (HATPase) domain, a receiver (Re

87 One conformer inhibits a histidine-kinase attached to its bound transducer HtrI a

88 receipt of a stimulus, a homodimeric sensor histidine kinase autophosphorylates and then transfers i

89 This dimeric protein histidine kinase autophosphorylates via an intersubunit

90 Histidine kinase autothiophosphorylation is regulated by

91 nd could show that the permease BceB and the histidine kinase BceS interact directly.

92 The vast majority of the sensor histidine kinases belong to the bifunctional HisKA famil

93 lubolar C-terminal structure, and the sensor histidine kinase BovK contains eight transmembrane segme

94 ls binding to sensor domains activate sensor histidine kinases by causing localized strain and unwind

95 A membrane bound two-component sensor histidine kinase called CqsS detects CAI-1, and the CqsS

96 Although the EspC histidine kinase can efficiently autophosphorylate in vi

97 lts emphasize how the bifunctional nature of histidine kinases can help switch cells between mutually

98 fundamentally from previously defined linear histidine kinase cascades.

99 The histidine kinase CckA controls the phosphorylation not o

100 Two phosphorelays, each initiating with the histidine kinase CckA, promote CtrA activation by drivin

101 ughter cells depend on the polarly-localized histidine kinase CckA.

102 egions (PIRs), the latter of which binds the histidine kinase CheA and adaptor CheW.

103 d by signalling complexes of chemoreceptors, histidine kinase CheA and coupling protein CheW.

104 Retrophosphorylation of the histidine kinase CheA in the chemosensory transduction c

105 The histidine kinase CheA is a central component of the bact

106 rs form ternary signaling complexes with the histidine kinase CheA through the coupling protein CheW.

107 ciate with the coupling protein CheW and the histidine kinase CheA to form an ultrasensitive, ultrast

108 ay, involving the receptor signaling domain, histidine kinase CheA, and adaptor protein CheW, as well

109 Bacterial chemoreceptors, histidine kinase CheA, and coupling protein CheW form cl

110 heW that interact with the large multidomain histidine kinase CheA, as well as with the transmembrane

111 n CheW, which bridges the chemoreceptors and histidine kinase CheA, is essential for chemotaxis.

112 ivation, in signalling complexes, of sensory histidine kinase CheA.

113 regulate autophosphorylation of the dimeric histidine kinase CheA.

114 its are composed of transmembrane receptors, histidine-kinase CheA, and coupling protein CheW, but it

115 nt of the component transmembrane receptors, histidine kinases (CheA) and CheW coupling proteins.

116 e chemoreceptors associated with a dedicated histidine kinase, CheA, and a linker protein, CheW, that

117 The dimeric five-domain histidine kinase, CheA, plays a central role in the path

118 tners of TlpD, which included the chemotaxis histidine kinase CheAY2, the central metabolic enzyme ac

119 The Pil-Chp histidine kinase (ChpA) has eight "Xpt" domains; six are

120 he Chp chemosensory system, which includes a histidine kinase, ChpA, and two CheY-like response regul

121 Mutation of the histidine kinase CikA creates an insensitive clock-input

122 The YycG sensor histidine kinase co-ordinates cell wall remodelling with

123 y this phosphodiesterase is dependent on the histidine kinase component of the chemotaxis machinery,

124 ea-nodulating endosymbiont, encodes a sensor histidine kinase containing a LOV domain at the N-termin

125 of two-component systems, in which multiple histidine kinases converge to PhyR, the phosphorylation

126 1 and D2), followed by conserved cytoplasmic histidine kinase core, REC, and Hpt domains.

127 nce, we have examined cross-talk between the histidine kinase CpxA and non-cognate response regulator

128 se system is comprised of the inner membrane histidine kinase CpxA, the cytosolic response regulator

129 erminus of signaling proteins such as sensor histidine kinases, cyclic-di-GMP synthases/hydrolases, a

130 hosphorylation of the receiver domain of the histidine kinase CYTOKININ-INDEPENDENT 1 (CKI1RD) from A

131 ansduction proteins such as bacterial sensor histidine kinases, designed to transition between multip

132 rylation is conserved in orthologous sets of histidine kinases despite highly dissimilar loop sequenc

133 The AgrC receptor histidine kinase detects its autoinducing peptide (AIP)

134 have multiple Per/Arnt/Sim (PAS) domains, a histidine kinase domain and a C-terminal receiver (REC)

135 irected mutagenesis, we demonstrate that the histidine kinase domain of ChpA and the phosphoacceptor

136 d extent of structural change orientates the histidine kinase domain to elicit the desired light-acti

137 he light-oxygen-voltage sensor domain to the histidine kinase domain via a 40 degrees -60 degrees rot

138 st transmembrane helix, whereas those in the histidine kinase domain were mostly clustered to a regio

139 ophytochrome structure, including its output histidine kinase domain, suggests how local structural c

140 eracts with the ATP-binding site of the CKI1 histidine kinase domain.

141 coiled coil that links the LOV domain to the histidine kinase domain.

142 sed on conservation of features within their histidine kinase domain.

143 autophosphorylation within the intracellular histidine-kinase domain.

144 that the coiled coil linker and the attached histidine kinase domains undergo a left handed rotation

145 slower conformational change in the PHY and histidine kinase domains.

146 nditions, its induction is controlled by two histidine kinases, DosS and DosT, and recent experimenta

147 e these signals to control the activity of a histidine kinase effector.

148 ays for Spo0A activation, one dependent on a histidine kinase encoded by cac0323, the other on both h

149 kinase encoded by cac0323, the other on both histidine kinases encoded by cac0903 and cac3319.

150 erization specificity, focusing on the model histidine kinase EnvZ and RstB, its closest paralog in E

151 ted by a comparison with another A. thaliana histidine kinase, ETR1.

152 specific sensing of ethanolamine by a sensor histidine kinase (EutW), resulting in autophosphorylatio

153 KinB is the cognate histidine kinase for the transcriptional activator AlgB.

154 cription factor (AbPro1) and a two-component histidine kinase gene (AbNIK1) were discovered.

155 l biosynthesis operon, a bacteriophytochrome-histidine kinase gene and the fnr-type regulatory gene,

156 he N terminus, was phosphorylated by another histidine kinase, GHK3.

157 p phosphorelay system, was phosphorylated by histidine kinase GHK4, which was essential for flagellar

158 ever, the detailed mechanism(s) by which the histidine kinase, GraS, senses specific HD-CAPs is not w

159 The autophosphorylation of histidine kinases has been reported to occur both in cis

160 Histidine kinases have a number of biochemical activitie

161 alyses reveal that up 1.7% of all identified histidine kinases have the potential to be split and bif

162 Furthermore, Mst50 interacted with histidine kinase Hik1, and the mst50 mutant was reduced

163 ity of downstream signaling proteins such as histidine kinases (HisKa) in a NO-dependent manner.

164 tates of the two catalytic domains of sensor histidine kinases, HisKA and HATPase.

165 in two-component response pathway, including histidine kinases, histidine phosphotransfer proteins an

166 TCSs are comprised of a receptor histidine kinase (HK) and a partner response regulator (

167 gnaling pathways composed of two proteins: a histidine kinase (HK) and a response regulator (RR).

168 nal transduction system (TCST) consists of a histidine kinase (HK) and a response regulator (RR).

169 TCS consist of a sensor histidine kinase (HK) and an effector response regulator

170 ble this reconstitution, coding sequences of histidine kinase (HK) and response regulator (RR) compon

171 we aimed to target the TCS signal transducer histidine kinase (HK) by focusing on their highly conser

172 pically used very high concentrations of the histidine kinase (HK) compared to the RR approximately P

173 which in bacteriophytochromes typically is a histidine kinase (HK) domain.

174 gnal-induced autophosphorylation of a sensor histidine kinase (HK) followed by phosphoryl transfer to

175 In this motif, a single histidine kinase (HK) phosphotransfers reversibly to two

176 Histidine kinase (HK) receptors are used ubiquitously by

177 The three signals are sensed by the QseC histidine kinase (HK) sensor.

178 A typical pathway includes a sensor histidine kinase (HK) that phosphorylates a response reg

179 flow of information observed in conventional histidine kinase (HK)-RR systems and coupling a complex

180 Histidine kinases (HK) are the sensory component, transf

181 Bacteria use membrane-integral sensor histidine kinases (HK) to perceive stimuli and transduce

182 The other TCS consists of a hybrid histidine kinase, Hk1, and the response regulator Rrp1.

183 One is comprised of a histidine kinase, Hk2, and the response regulator Rrp2.

184 mbined NMR and crystallographic study on the histidine kinase HK853 and its response regulator RR468

185 arly through phosphotransfer between cognate histidine kinases (HKs) and response regulators (RRs) to

186 e paralogous signaling systems, comprised of histidine kinases (HKs) and their cognate response regul

187 Although histidine kinases (HKs) are critical sensors of external

188 Bacterial histidine kinases (HKs) are quintessential regulatory en

189 Most of these signals are sensed through histidine kinases (HKs), which comprise the main sensory

190 Tools to study histidine kinases, however, are currently quite limited.

191 The cytoplasmic histidine kinase, HP0244, which until now was thought on

192 pend on expression of the cytoplasmic sensor histidine kinase, HP0244.

193 iously uncharacterized sensing domain of the histidine kinase HssS for HssS function.

194 the HisKA and HATPase-ATP-binding domains of histidine kinases identified amino acid interactions for

195 Despite the essential role of the CckA histidine kinase in the control of cell cycle events, th

196 o identify the downstream target of the DifE histidine kinase in the regulation of exopolysaccharide

197 tivity of the largest family of bifunctional histidine kinases in response to the change of environme

198 y simple orthologous relationships among the histidine kinases in rice and Arabidopsis (Arabidopsis t

199 ation of DNA replication, the essential CckA histidine kinase is activated by phosphorylation, which

200 udies showed that cheA(2), a gene encoding a histidine kinase, is essential for the chemotaxis of B.

201 ct positions in the Bacillus subtilis sensor histidine kinase KinA and by restoration of activity in

202 N-terminal sensor domain of the cytoplasmic histidine kinase KinA is responsible for detection of th

203 Histidine kinase KinB of the KinB-AlgB two-component sys

204 iofilm formation was dependent on the sensor histidine kinase KinD and in particular on an extracellu

205 gene expression and do so by activating the histidine kinase KinD.

206 matrix genes via the activation of a sensor histidine kinase, KinD.

207 ranscription of either response regulator or histidine kinase leads to the coexistence of an approxim

208 presence of homologous domains in bacterial histidine kinase-like ATP binding region-containing prot

209 e demonstrate that the flavin-binding sensor histidine kinase, LovhK (bab2_0652), functions as a prim

210 We report that the soluble histidine kinase LovK and the single-domain response reg

211 Caulobacter crescentus encodes a soluble LOV-histidine kinase, LovK, that regulates the adhesive prop

212 ain interfaces, and they are not observed in histidine kinase-mediated phosphotransfer.

213 f microrchidia Gyrase, Heat Shock Protein90, Histidine Kinase, MutL (GHKL) ATPases, were previously s

214 e requires the multisensor CHASE3/GAF hybrid histidine kinase named CfcA.

215 Here we show that the histidine kinase, nucleoside diphosphate kinase B (NDPK-

216 PhoQ is the transmembrane sensor histidine kinase of the bacterial phoPQ two-component sy

217 We hypothesized that the five orphan histidine kinases of C. acetobutylicum interact directly

218 The histidine kinases of these systems depend entirely on th

219 Histidine kinases, often membrane associated, detect env

220 tomach, the organism expresses two pH-sensor histidine kinases, one, HP0165, responding to a moderate

221 s known about the signals sensed by the WalK histidine kinase or the function of the WalJ ancillary p

222 which alters the position of the downstream histidine kinase output module.

223 ain response regulator (SDRR) SdrG and seven histidine kinases, PakA to PakG, belonging to the HWE/Hi

224 domain of the Bacillus subtilis PhoR sensor histidine kinase, part of a two-component system involve

225 ese data indicate that Nla28S is the in vivo histidine kinase partner of Nla28 and that the primary f

226 d through phosphorylation from their cognate histidine kinase partners, which in turn facilitates an

227 Protein histidine kinases (PHKs) function in Two Component Signa

228 erichia coli, it was recently shown that the histidine kinase PhoQ is also modulated by at least two

229 er colistin removal and was dependent on the histidine kinase PhoQ.

230 orrespond to different states of the sensory histidine kinase PhoR: an inhibition state, an activatio

231 of changes of function of two bi-functional histidine kinases, PleC and CckA.

232 ect the localization of two polar cell cycle histidine kinases, PleC and DivJ, and the pole-specific

233 The DivL pseudo-histidine kinase, positioned at one cell pole, regulates

234 rA and the FPI-encoded pdpD, and KdpD is the histidine kinase primarily responsible for phosphorylati

235 interaction screen we further identified the histidine kinase protein KdpD that in many bacteria is a

236 has the in vitro biochemical properties of a histidine kinase protein: it hydrolyzes ATP and undergoe

237 Among signal relay proteins, sensor, histidine kinase proteins (HK) are auto-phosphorylated u

238 how a single amino acid substitution in the histidine kinase receptor AgrC of ST22 strains determine

239 oorganisms, and each comprises a homodimeric histidine kinase receptor and a cytoplasmic response reg

240 Furthermore, we evaluated Arabidopsis histidine kinase receptor mutant lines ahk2/3, ahk2/4 an

241 CS) are signalling complexes manifested by a histidine kinase (receptor) and a response regulator (ef

242 ins of the three classes of Escherichia coli histidine kinase receptors (HKRs).

243 ational change that modulates the C-terminal histidine kinase region.

244 xperimental and calculated distances for the histidine-kinase region when both subunits are in a para

245 le, while the C-terminal module, including a histidine kinase-related domain (HKRD), does not partici

246 Included are the downstream C-terminal histidine kinase-related domain known to promote dimeriz

247 Two-component signaling pathways involve histidine kinases, response regulators, and sometimes hi

248 designated Rrp1, and BB0420 encodes a hybrid histidine kinase-response regulator designated Hpk1.

249 Here we describe WigK/WigR, a histidine kinase/response regulator pair that enables Vi

250 The histidine kinase/response regulator system YehU/YehT of

251 We also establish that KinD is a principal histidine kinase responsible for sensing the presence of

252 indicated that the TCS comprising the sensor histidine kinase RgfC and the response regulator RgfA me

253 are recognized by a membrane-bound receptor histidine kinase (RHK), AgrC.

254 covered but so far uncharacterized family of histidine kinase rhodopsins (HKRs).

255 and some other S. aureus strains, the sensor histidine kinase SaeS has an L18P (T53C in saeS) substit

256 e its importance, the mechanism by which the histidine kinase SaeS recognizes specific host stimuli i

257 ion of RpaA is regulated by two antagonistic histidine kinases, SasA and CikA, which are sequentially

258 periplasmic sensor domain of a transmembrane histidine kinase sensor, which in turn relays a signal t

259 a template for signal transduction in sensor histidine kinases.Sensor histidine kinases (SHK) consist

260 lases, c-di-GMP-specific phosphodiesterases, histidine kinases, serine/threonine protein kinases and

261 nsduction in sensor histidine kinases.Sensor histidine kinases (SHK) consist of sensor, linker and ki

262 In these, a membrane-bound sensor histidine kinase (SK) autophosphorylates in response to

263 The pathway consists of a hybrid histidine kinase SLN1, a histidine-containing phosphotra

264 , usually via phosphotransfer from a cognate histidine kinase, stabilizes the active conformation.

265 where they are often found in operons with a histidine kinase, suggesting that H-NOX proteins serve a

266 In Vibrio species, CqsS is a membrane-bound histidine kinase that acts as the receptor for the CAI-1

267 l system consists of a membrane-bound sensor histidine kinase that autophosphorylates in response to

268 The E. coli MG1655 envZ gene encodes a histidine kinase that is a member of the envZ-ompR two-c

269 sitive autoregulatory loop involving KinC, a histidine kinase that is activated by potassium leakage.

270 VpsS is a hybrid sensor histidine kinase that is predicted to contain both histi

271 This gene encodes a putative orphan histidine kinase that lies adjacent to a predicted ABC t

272 y, we identified and characterized Nla28S, a histidine kinase that modulates the activity of this imp

273 ion pathways, typically composed of a sensor histidine kinase that receives the input stimuli and the

274 g pathways, which typically involve a sensor histidine kinase that specifically phosphorylates a sing

275 ulation is regulated by at least five sensor histidine kinases that are activated in response to vari

276 ial phytochromes are dimeric light-regulated histidine kinases that convert red light into signaling

277 Most species encode numerous paralogous histidine kinases that exhibit significant structural si

278 ermosensor DesK is a multipass transmembrane histidine-kinase that allows the bacterium Bacillus subt

279 ammable redirection of phosphate flux from a histidine kinase to response regulators based on targeti

280 to follow the flow of phosphate groups from histidine kinases to the cognate response regulators in

281 gate the contribution of the localization of histidine kinases to the establishment of cellular asymm

282 A interacts with DcuS, the membrane embedded histidine kinase, to transfers DcuS to the responsive st

283 rotein was engineered as a functional sensor histidine kinase (TolRSK) and an independent response re

284 Bacterial histidine kinases transduce extracellular signals into t

285 The FsrC sensor histidine kinase, upon activation by the gelatinase bios

286 Here, we report that CckA, the histidine kinase upstream of CtrA, employs a tandem-PAS

287 is activated by phosphorylation by multiple histidine kinases via a multicomponent phosphorelay.

288 dy, we report the identification of a sensor histidine kinase, VpsS, which can control biofilm format

289 sion levels (> 10-fold) of phoR, a P-sensing histidine kinase, were only observed under conditions of

290 autophosphorylation of the operon-associated histidine kinase, whereas the ligand-free H-NOX has no e

291 old greater than the amount of the WalK(Spn) histidine kinase, which is present at approximately 460

292 d RpBphP3, are configured as light-regulated histidine kinases, which initiate a signal transduction

293 We show that many histidine kinases will accept ATPgammaS as a substrate t

294 Salmonella PhoQ is a histidine kinase with a periplasmic sensor domain (PD) t

295 sma0114, encode the proteins Sma0113, an HWE histidine kinase with five PAS domains, and Sma0114, a C

296 echanism underlying interaction of a protein histidine kinase with this tight-binding inhibitor.

297 es that occur when the light-sensitive model histidine kinase YF1 is activated by blue light.

298 ilarly, photoreduction of the engineered LOV histidine kinase YF1 to the NSQ modulates activity and d

299 mesS) encoding the predicted cognate sensor (histidine) kinase yielded a mutant with the same inabili

300 The YycG (sensor histidine kinase)-YycF (response regulator/transcription