ライフサイエンスコーパス: histidine kinase

1 nced the autophosphorylation activity of the histidine kinase.

2 suggest the phosphodonor is instead the EspA histidine kinase.

3 for analysing ligand regulation of a sensor histidine kinase.

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

5 eraction between transmembrane receptors and histidine kinase.

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

7 Trimers activate and control the histidine kinase.

8 ly functioning via interaction with the AgrC histidine kinase.

9 different from those observed in prokaryotic histidine kinases.

10 ing methyl-accepting chemotaxis proteins and histidine kinases.

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

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

13 r specificity in vitro relative to canonical histidine kinases.

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

15 0.10 min(-1)] and typical of those of other histidine kinases.

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

17 lation via a phosphorelay involving multiple histidine kinases.

18 ns of response regulators with their cognate histidine kinases.

19 SR pathways mediated by multiple HWE/HisKA_2 histidine kinases.

20 been identified that directly interact with histidine kinases.

21 gh it has slower kinetics than other similar histidine kinases.

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

23 The hybrid histidine kinase 3 (HHK3) is a highly conserved sensor k

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

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

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

27 ETR1 histidine kinase activity and phosphotransfer through th

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

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

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

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

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

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

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

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

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

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

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

39 nto the signal transduction mechanism of the histidine kinase AfGcHK from Anaeromyxobacter.

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

41 s by sensing the accumulation of AIP via the histidine kinase AgrC and the response regulator AgrA.

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

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

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

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

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

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

48 tion pathway is conserved in Shewanella, and histidine kinase and flagella-mediated motility are esse

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

50 nitrite modifies the activity of a bacterial histidine kinase and mediates T3SS1 repression.

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

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

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

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

55 e signal transduction system consisting of a histidine kinase and two response regulators, named here

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

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

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

59 ting to summarize an emerging picture of how histidine kinases and cognate response regulators achiev

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

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

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

63 Implicating sensory histidine kinases and response regulator proteins, both

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

65 Histidine kinases and response regulators have an intrin

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

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

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

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

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

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

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

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

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

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

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

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

78 Sensor histidine kinases are central to sensing in bacteria and

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

80 Histidine kinases are key regulators in the bacterial tw

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

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

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

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

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

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

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

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

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

92 been demonstrated to occur by their cognate histidine kinases but also by low molecular weight phosp

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

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

95 Although the EspC histidine kinase can efficiently autophosphorylate in vi

96 fundamentally from previously defined linear histidine kinase cascades.

97 ospho-signalling proteins, the transmembrane histidine kinase CckA and the cytoplasmic phosphotransfe

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

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

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

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

102 ges from a strict linear organization of the histidine kinase CheA in Treponema denticola cells, whic

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

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

105 Bacterial chemoreceptors, the histidine kinase CheA, and the coupling protein CheW for

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

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

108 phosphorylated form of the receptor-coupled histidine kinase CheA, thereby providing a biochemical l

109 regulate autophosphorylation of the dimeric histidine kinase CheA.

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

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

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

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

114 ing increases the autophosphorylation of the histidine kinase CheA2, followed by CheY2-mediated depho

115 nt derivatives lacking the chemotaxis master histidine kinase, CheA4, or the central response regulat

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

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

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

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

120 n transporter PiaA, or competence regulatory histidine kinase ComD significantly decreased transmissi

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

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

123 Bioinformatics analysis showed that the SrrB histidine kinase contains several domains, including an

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

125 1 and D2), followed by conserved cytoplasmic histidine kinase core, REC, and Hpt domains.

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

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

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

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

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

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

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

133 g a complex that directly interacts with the histidine kinase domain of RcsC.

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

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

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

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

138 autophosphorylation within the intracellular histidine-kinase domain.

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

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

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

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

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

144 G antagonizes the bacterial receptor QseC, a histidine kinase encoded within the core Enterobacteriac

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

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

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

148 activation of a minimal, blue-light-sensing histidine kinase from Erythrobacter litoralis HTCC2594,

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

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

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

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

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

154 Histidine kinases have a number of biochemical activitie

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

156 requires the presence of a group III hybrid histidine kinase (HHK) and the high osmolarity glycerol

157 Cytosolic hybrid histidine kinases (HHKs) constitute major signaling node

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

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

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

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

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

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

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

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

166 lves two-component systems in which a sensor histidine kinase (HK) autophosphorylates in response to

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

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

169 ponent systems (TCS) which comprise a sensor histidine kinase (HK) containing a phosphorylatable cata

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

171 ntrol plant development via sensors from the histidine kinase (HK) family.

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

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

174 Histidine kinase (HK) receptors are used ubiquitously by

175 ed approach to disrupt a subset of cytokinin histidine kinase (HK) receptors in rice (Oryza sativa) i

176 One component is a sensory histidine kinase (HK) that autophosphorylates when activ

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

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

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

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

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

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

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

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

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

186 Bacterial histidine kinases (HKs) are quintessential regulatory en

187 Histidine kinases (HKs), together with their partner pro

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

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

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

191 en sensor protein AfGcHK is a globin-coupled histidine kinase in the soil bacterium Anaeromyxobacter

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

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

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

195 tation and computation we here show that the histidine kinase is activated by piston-like displacemen

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

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

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

199 contact with P. chlororaphis is mediated by histidine kinases KinA and KinB.

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

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

202 AI-2 also binds to the dCACHE domains of histidine kinase KinD from Bacillus subtilis and diguany

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

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

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

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

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

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

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

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

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

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

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

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

215 mutations in bfmS, which encodes the sensor histidine kinase of the BfmRS two-component system (TCS)

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

217 The histidine kinases of these systems depend entirely on th

218 Histidine kinases, often membrane associated, detect env

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

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

221 nce to various antibiotics, and requires the histidine kinase PA1396.

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

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

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

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

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

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

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

229 date regulatory controls, mutant strains for histidine kinases PhoR and AioS were employed, and illus

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

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

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

233 n the tandem sensor domains of a dual-sensor histidine kinase PPHK (phosphorylation-responsive photos

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 Although their Histidine Kinase receptors are substantially localised t

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

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

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

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

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

249 rate, perhaps by the activity of a divergent histidine kinase-response regulator gene pair.

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

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

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

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

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

255 and ground-state dynamics of the UV form of histidine kinase rhodopsin 1 (HKR1) from eukaryotic alga

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

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

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

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

260 More specifically, nitrite activates histidine kinase sensor VbrK through S-nitrosylation on

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

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

263 nd to and inhibited the intramembrane sensor histidine kinase SGO_1180, thus preventing activation of

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

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

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

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

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

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

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

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

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

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

274 ivity and localization of two key regulatory histidine kinases that control cell fate and differentia

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

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

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

278 K (phosphorylation-responsive photosensitive histidine kinase) that operates a molecular logic OR, by

279 The activated sensory histidine kinase then transfers the phosphoryl group to

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

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

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

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

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

285 Bacterial histidine kinases transduce extracellular signals into t

286 hing mechanism, involving HWE/HisKA_2-family histidine kinases, underlies sigma(EcfG) activation.

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

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

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

290 Thr kinase-phosphatase pair PrkC/PrpC, and a Histidine kinase WalK of a two-component system.

291 gain-of-function mutations in the essential histidine kinase WalK, which also elevates expression of

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

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

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

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

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

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

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

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

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