ライフサイエンスコーパス: histidine

1 hibited a 13-fold preference for lysine over histidine.

2 ational change of the conserved neighbouring histidine.

3 ty for SETD3 and inhibited SETD3 activity on histidine.

4 ess is known about other amino acids such as histidine.

5 an affordable linker prepared from natural l-histidine.

6 idazole propionate biosynthesis from dietary histidine.

7 a clear reporter of the protonation state of histidine.

8 central metal cofactor coordinated by three histidines.

9 amino acid residues containing two conserved histidines.

10 eract with and bind Zn(2+) via the essential histidines.

11 rises six K-segments, each with two adjacent histidines.

12 atically via pH-dependent protonation of the histidines.

13 ed environmental changes surrounding residue histidine 266 of POT1 that were dependent on telomere ss

14 Recently, a 2-histidine (2H) phosphoesterase motif was identified with

15 A Zn(II)(histidine)(3)(H(2)O) centre can be incorporated at a rem

16 cysteine residues 29 and 128 in addition to histidine 42 and glutamate 65.

17 These results point to dual functions of histidine-43 in structurally assisting the proper coupli

18 paramagnetic resonance analyses to establish histidine-43 of Methanosarcina acetivorans NifB (MaNifB)

19 for cofactor maturation upon substitution of histidine-43 with alanine; whereas x-ray absorption spec

20 ates of the de novo syntheses of purines and histidine, 5-aminoimidazole-4-carboxamide-1-beta-D-ribof

21 Indeed, histidine 59 in HLA-B*27:03 leads to a series of local c

22 sing the region around KRAS-specific residue histidine 95 at the helix alpha3/loop 7/helix alpha4 int

23 face is characterized by the movement of the histidine 98 residue, which is, after acidification, dec

24 ons in amphipathic character associated with histidines affect the permeabilization properties of p1

25 This site is defined by an N-terminal histidine and a second internal histidine side chain in

26 beta-CASP domains and a cluster of conserved histidine and aspartate residues capable of binding two

27 egulate metabolic partitioning between the l-histidine and coformycin pathways.

28 The proton-selective histidine and gating tryptophan in the open BM2 reorient

29 site-directed mutants identifies a catalytic histidine and how the acceptor site of UGT76G1 achieves

30 vitamin D(3), vitamin C, trytophan, taurine, histidine and hydroxyproline were below the reference ra

31 opic and structural characterization of this histidine and surrounding H-bonding residues, based on a

32 e two target nitrogen atoms-the N(3) atom of histidine and the terminal e-amino nitrogen of lysine-oc

33 Microbiome-associated histidine and tyrosine metabolites were increased in bot

34 sheet and interactions of its dual HxT motif histidines and threonines with phosphate in the active s

35 Carnosine (beta-alanyl-l-histidine) and anserine (beta-alanyl-3-methyl-l-histidin

36 to the bulkier or charged residues tyrosine, histidine, and glutamic acid.

37 sensors that detect pH, NAD(+), NADH, NADPH, histidine, and glutathione redox potential.

38 imilar in GB to basic amino acids lysine and histidine, and phosphatidic acid and phosphatidylglycero

39 ntaining combinations of cysteine, tyrosine, histidine, and serine residues react with octafluorocycl

40 al, pRpp-derived metabolites, including UTP, histidine, and tryptophan.

41 We conclude that these two histidines, and TM6b more broadly, help trigger the bulk

42 member-specific metabolic bottlenecks (e.g. histidine- and transport-related reactions) and compensa

43 ongly inhibited at pH 6.0 when the conserved histidines are partially charged and H17 is predominantl

44 tidine) and anserine (beta-alanyl-3-methyl-l-histidine) are abundant peptides in the nervous system a

45 stem is required for energy generation using histidine as a carbon and nitrogen source.

46 In subtype I-D systems, however, the histidine-aspartate (HD) nuclease domain is encoded as p

47 Here we show that a turgor-sensing histidine-aspartate kinase, Sln1, enables the appressori

48 Sterile alpha motif and histidine-aspartic acid domain-containing protein 1 (SAM

49 d tripeptide stretches that contain multiple histidines associate negatively with crystallizability.

50 366 (L366H) can interact with the introduced histidine at position 370 (stabilizing that portion of t

51 er the kinase and substrate domains to limit histidine autophosphorylation.

52 o identify candidate genes for a reaction in histidine biosynthesis lacking an annotated gene and hig

53 aps significantly with the early stages of l-histidine biosynthesis.

54 IB 3610 cells revealed that genes from the L-histidine biosynthetic pathway, the purine, pyrimidine d

55 amic properties exist in the ligand-free and histidine-bound enzymes.

56 insight into the biological significance of histidine brace-mediated copper coordination.

57 ine side chain in a configuration called the histidine brace.

58 behavior of Deionized (DI) water and 10mM L-Histidine buffer solution which were subjected to drop s

59 ophan, phenylalanine + tyrosine, isoleucine, histidine, but limiting for lysine, leucine, and threoni

60 They contain poly-histidine chains (poly-His), whose imidazole groups gene

61 pany proton transport in the +0, + 1, and +2 histidine charge states.

62 core aggregates via its conserved C-terminal histidine cluster (HisC).

63 NKD HisC cores co-aggregate with a conserved histidine cluster within Axin, to destabilize it along w

64 We show that surface-exposed histidine clusters are essential for robust inhibition o

65 Substitution of either conserved histidine compromised the ability of Sts-1 to suppress s

66 ZnO@PLP and ZnO@Py showed good linearity to histidine concentration from 2.49 to 24.4 muM and 7.44 t

67 physiological role of carnosine and related histidine-containing dipeptides (HCDs) is not clear.

68 immunofluorescence microscopy to identify a histidine-containing motif ((398)HTH) in the first extra

69 vity can be controlled through the number of histidine-containing networks and the strength of the su

70 However, after synthesizing a C2-deuterated-histidine-containing peptide, we were able to follow the

71 Modulating histidine content thereby influenced the resultant MOF p

72 n (IgV)-like domain and extraordinarily high histidine content, suggesting that unique structural fea

73 spectra indicate that removal of the second histidine converted the protonation and tautomeric equil

74 n the current block is the formation of a Cu-histidine coordination complex.

75 rrangement that involves a co-axial tyrosine/histidine coordination strategy and a complex electronic

76 HA using an anti-HA antibody and a probe for histidine decarboxylase (HDC), a synthetic enzyme for HA

77 Certain host cells express the histidine decarboxylase enzyme (HDC), which is responsib

78 Histidine decarboxylase-containing varicosities diffusel

79 ss-related arousal states, is synthesized in histidine decarboxylase-expressing hypothalamic neurons

80 eries that synthesize two "genes", e.g., the histidine-dependent DNAzyme g1 and the Zn(2+)-ion-depend

81 but whether the Hut system is important for histidine-dependent energy generation or vertebrate colo

82 Herein, the potential of double-histidine (dHis)-based Cu(II) spin labeling for the iden

83 atients and controls did not differ in their histidine dietary intake, the elevated levels of imidazo

84 We show that simultaneous mutation of these histidines drastically weakens the cis interaction and e

85 ate transition of hemes through deprotonated histidine (e.g. Cytochrome c).

86 These results demonstrate that a histidine-enhanced hydroxyl reactivity can contribute to

87 measures, participants consumed encapsulated histidine for 4 wk followed by a 3-wk recovery period.

88 tible indispensable AA (IAA) score was 1.03 (histidine) for WPI and close to 0 for zein, owing to its

89 acteria to synthesize; therefore, scavenging histidine from the environment is likely advantageous.

90 se, the highly prevalent FcgammaRIIa (CD32a) histidine (H)-131 variant (CD32aH) is strongly linked to

91 nificantly more permeabilizing, has a fourth histidine (H17).

92 They share three histidines (H3, H4, and H11), but p1, which is significa

93 t-shifted resonances tentatively assigned to histidine Hdelta1 display a two-state chemical exchange

94 The BM2 channel also contains a second histidine (His), H27, equidistant from the gating trypto

95 TM6b contains two highly conserved histidines, His(232) and His(237) We found that differen

96 xylate group of 2OG is trans to the proximal histidine (His134) of the 2-His-1-carboxylate facial tri

97 the C1 carboxylate group trans to the distal histidine (His211); (2) The decay rate constant of the f

98 e processes reflect the rotational motion of histidine imidazole rings that coordinate the coppers in

99 determine the tolerance to graded dosages of histidine in a healthy adult population.

100 duct complex, SETD3 generates the methylated histidine in an N(1)-protonated (N(1)-H) and N(3)-methyl

101 method for the determination of the pK(a) of histidine in complex or heterogeneous systems amenable t

102 g the nepenthesin loop of plasmepsin V and a histidine in place of a catalytic aspartate in plasmepsi

103 duced by bacteria through decarboxylation of histidine in spoiled foods such as fish is known to caus

104 These results suggest that bioavailable histidine in the lung promotes Acinetobacter pathogenesi

105 ressing the alpha-chain segment TRAV9-2 or a histidine in their alpha- or beta-chain complementarity

106 rleucine (HHL), but only from species with a histidine in their alpha1(I) C-telopeptide sequence.

107 HutH is required for acquiring nitrogen from histidine in vitro, and strains inactivated for hutH are

108 We also find that extra N-terminal histidines in pathological familial mutations involving

109 Histidines in proteins play a crucial role in the observ

110 e demonstrate here that two highly conserved histidines in the C-terminal domain of PrP(C) are essent

111 ssays and cysteine accessibility placed both histidines in the extracellular half of the cytoplasmic

112 tidines than the monomer or a dimer with the histidines in the periphery.

113 ues from I360 to F370 in the S4 segment into histidine, in i, i + 3 and i, i + 6 or i, i + 4 and i, i

114 lementation; however, the clinical safety of histidine intake above the average dietary intake (1.52-

115 crobial metabolism of histidine, rather than histidine intake per se.

116 etal ion bridges, and we have found that the histidine introduced at position 366 (L366H) can interac

117 We concluded that histidine involved in zinc coordination at the active si

118 Histidine is a versatile residue playing key roles in en

119 Of these, the amino acid histidine is among the most energetically expensive for

120 Histidine is an essential amino acid with health benefit

121 e or pentacoordinate, depending on whether a histidine is coordinating or not at the sixth position o

122 L1 and the A2ML1 H1084N mutant in which this histidine is removed.

123 Each of these histidines is essential for plasmanylethanolamine desatu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

145 Although their Histidine Kinase receptors are substantially localised t

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

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

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

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

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

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

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

153 ly functioning via interaction with the AgrC histidine kinase.

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

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

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

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

158 ns of response regulators with their cognate histidine kinases.

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

160 Proline, L-arginine, L-histidine, L-isoleucine, and tryptophan were accumulated

161 Cu(A) site of Pseudomonas stutzeri N(2)OR, a histidine ligand was found to undergo a conformational f

162 uestion in this field is how the function of histidine ligated Cu centers are modulated by delta vs e

163 as yet to be spectroscopically observed in a histidine-ligated heme enzyme.

164 These enzymes include histidine-ligated heme-dependent dehaloperoxidase and ty

165 rt C-H bonds, reactions that are unknown for histidine-ligated hemes enzymes.

166 Plasma histidine (measured in subjects who completed all dosage

167 This study suggests that perturbations in histidine metabolism selectively target neural tumours t

168 support the broader hypothesis that protein histidine methylation acts as a common regulatory mechan

169 Histidine methylation is essential for catalytic functio

170 -scale CRISPR screens, we identify the actin histidine methyltransferase SET domain containing 3 (SET

171 ntaining 3 (SETD3) is a protein (i.e. actin) histidine methyltransferase.

172 A histidine missense substitution mutation at this locus i

173 was synthesized along with its cysteine and histidine modified versions.

174 through traditional, vertically adsorbed, or histidine-modified peptides, such a molecularly tunable

175 ) in addition to NH(4) (+) Of note, the twin-histidine motif was not essential for ammonium transport

176 ystematic replacements in the conserved twin-histidine motif, a hallmark of most AMT/Mep/Rh, alter su

177 ly demonstrated to be a protein (i.e. actin) histidine-N(3) methyltransferase.

178 erved in translocases, and a family-specific histidine near motif IVa, reminiscent of the "arginine c

179 idues in outer capsid proteins, a pH-sensing histidine of a zinc finger within the receptor-binding V

180 hydrogen-bonding interaction with the target histidine of actin that likely contributes to its >1300-

181 siae numbering), that contacts the catalytic histidine of eIF5B (H480).

182 with PD-L1 did the FSY react with a proximal histidine of PD-L1 selectively, enabling irreversible bi

183 a heme cofactor is allowed to bind to either histidine or cysteine ligands, within a single artificia

184 Cysteine, histidine, phenylalanine, lysine, tryptophan and arginin

185 tral Src homology 3 domain, and a C-terminal histidine phosphatase domain.

186 yphosphate phosphatases (MINPPs) are clade 2 histidine phosphatases (HP2P) able to carry out the step

187 fident site-specific localization of protein histidine phosphorylation remains challenging.

188 estigate the hitherto rather elusive protein histidine phosphorylation.

189 the catalytic pocket, while the pai-methyl-l-histidine (Pmh) moiety transfers the electrophile.

190 t genome revealed, uniquely among mammals, a histidine point variation in the neuronal potassium-chlo

191 addition, changing ANDV residue S386 to the histidine present in MAPV N or the alanine present in ot

192 the enolate intermediate is protonated by a histidine preventing CO(2)-enolate recombination, yieldi

193 arbonyl- and trityl-protected, C2-deuterated histidine produces a vibrational-probe-equipped amino ac

194 This biosensor can be used to isolate L-histidine-producing strains by FACS, showing that TR eng

195 ction of a NME1 site-directed mutant lacking histidine protein kinase activity but retaining nucleosi

196 Histidine protein kinases (HKs) are prevalent prokaryoti

197 mal pH could relax the frustration, allowing histidine protonation and facilitating conformational co

198 To explore the role of histidine protonation in the binding process, the pH-dep

199 tions show a stabilization of the protein by histidine protonation.

200 reinforced following protonation of a nearby histidine, providing a conceptual link between receptor

201 Glutamine-148->histidine (Q148H) and glycine-140->serine (G140S) amino

202 ed and hydrogen-bonded imidazole-imidazolium histidine quaternary structures have been proposed, base

203 ely reflects altered microbial metabolism of histidine, rather than histidine intake per se.

204 rotonation must occur outside of the central histidine region, most likely in the vestibules.

205 A novel steric gate histidine residue (H931 in Thermococcus sp. 9 degrees N

206 l reactivity that is conveyed by a conserved histidine residue and allows conjugation to cell surface

207 to demonstrate that both a C-terminal domain histidine residue and the 2-amino group of OG base are c

208 ce of RIPK1 activation, suggesting that this histidine residue functions as a proton acceptor to modu

209 ferent substrates with the conserved central histidine residue in protonated or neutral form.

210 entially autophosphorylate at each conserved histidine residue in the individual protomers, leading t

211 The pK(a) of the lone histidine residue in the peptide, which is likely respon

212 domains contribute equatorially coordinated histidine residue side-chains, resulting in a novel brid

213 diphosphate (ADP)-ribosylation of a modified histidine residue, diphthamide, at His715, which blocks

214 A thioester bond near an invariant catalytic histidine residue.

215 or but has the hydroxyl reactivity-conveying histidine residue.

216 Multiple histidine residues along the rim of the VISTA extracellu

217 subjects, while the extents of conversion of histidine residues at alpha-His-20, alpha-His-50, and be

218 ly allowing VP5 to sense low pH via specific histidine residues at key positions.

219 conformational change removes one of the two histidine residues from the active site, likely triggeri

220 rmational changes by precisely preorganizing histidine residues in buried hydrogen-bond networks.

221 We found that five histidine residues in helices 5-8 of apoA-I are preferab

222 he receptor-binding VP2 protein, and certain histidine residues in the membrane-penetrating VP5 prote

223 ted mZIP4 variants, we provide evidence that histidine residues in this motif coordinate a zinc ion i

224 microscopy, revealing that highly-conserved histidine residues near the C terminus of each microtubu

225 on via their interaction with the N-terminal histidine residues of amyloid-beta (Abeta).

226 It is characterized by two invariant histidine residues that play a critical role in catalyti

227 of interest and inspired by nature's use of histidine residues within the active sites of various co

228 trate that the highly conserved cysteine and histidine residues within the C-X(8)-C-X(24-75)-H-X-G-G-

229 tion through protonation of CpxA periplasmic histidine residues, and upregulates the fabA and fabB ge

230 ted CC' loop and a striking concentration of histidine residues, located in the complementarity-deter

231 A pair of histidine residues, which are conserved in coronavirus s

232 In the M1 polymer, five histidine residues-contributed by three different monome

233 s acetaldehyde adduct formation on lysine or histidine residues.

234 species that lack an alpha1(I) C-telopeptide histidine, revealed that HHL is a laboratory artifact ra

235 w that TaHRC, a gene that encodes a putative histidine-rich calcium-binding protein, is the key deter

236 Histidine-rich clusters are generally present in at leas

237 to associate predominantly with albumin and histidine-rich glycoprotein (HRG) in mouse and human pla

238 a rapid diagnostic tests (mRDTs) that target histidine-rich protein 2 (HRP2) are important tools for

239 control and elimination, and Haiti relies on histidine-rich protein 2 (HRP2)-based rapid diagnostic t

240 etect Plasmodium falciparum via its abundant histidine-rich protein 2 (HRP2).

241 at detect the Plasmodium falciparum-specific histidine-rich protein 2 (PfHRP2) antigen are the primar

242 uency of Plasmodium falciparum isolates with histidine-rich protein 2 (pfhrp2) gene deletion as one o

243 The membrane-bound histidine sensor kinase, CpxA, is a bacterial serotonin

244 While many divalent metals bind to poly histidine sequences reversibly, oxidation of imidazole-b

245 promotes Acinetobacter pathogenesis and that histidine serves as a crucial nitrogen source during inf

246 n N-terminal histidine and a second internal histidine side chain in a configuration called the histi

247 ime scales, with coupling of the dynamics of histidine side chains and those of remote key backbone e

248 The arrangement of histidine side chains in influenza A M2 tetramer determi

249 wide measurements of mRNA translation during histidine starvation in fission yeast Schizosaccharomyce

250 tion as a defining mycobacterial response to histidine starvation.

251 and n = 20 women) and/or a 16-g/d dosage of histidine (Study 2, n = 21 men and n = 19 women); 27 par

252 vely low domain mobility, and associated the histidine substrate and docking domains with the kinase

253 C/D- and G/H-turn regions hosting the three histidines, suggest a complex way of pH-governed alloste

254 lts aged 21-50 y completed graded dosages of histidine supplement (4, 8, and 12 g/d, Study 1) (n = 20

255 in vitals or body composition occurred with histidine supplementation in either study.

256 o acid with health benefits that may warrant histidine supplementation; however, the clinical safety

257 ich endows it with selectivity toward a hexa-histidine tag (His-tag).

258 ted PfCSP4/38, was produced initially with a histidine tag and purified by a simple two-step procedur

259 16-residue C-terminal extension containing a histidine tag.

260 purity and recoveries than the favorite poly histidine tag.

261 nal cells were exposed to active recombinant histidine-tagged cathepsin B (His-CATB).

262 nickel-binding motifs: a variable C-terminal histidine tail and a strictly conserved H(W/F)X (2)HX (3

263 , we generated an actin variant in which the histidine target of SETD3 was substituted with methionin

264 imidazole hydrogen-bonding geometries in the histidine tetrad at low pH, thus validating the proton c

265 ater catalytic efficiency (k (cat)/K(m) ) on histidine than on lysine.

266 racting and binding Zn(2+) via the essential histidines than the monomer or a dimer with the histidin

267 This cavity also contains a histidine that has previously been identified as essenti

268 ue pairing of an arginine with the catalytic histidine that makes the proteolytic activity of GII.4 p

269 otein motif (pfam10520) with eight conserved histidines that is shared by an alternative type of plan

270 egatively regulated by arginine, lysine, and histidine, the amino acids that PQLC2 transports across

271 In the absence of the histidine, the flavin and disulfide moieties were no lon

272 were able to follow the protonation state of histidine throughout a pH titration using Raman differen

273 in sites of Met, His, and Tyr, conversion of histidine to aspartate and hydroxyaspartate was identifi

274 hydrophobic interaction with cell membranes, histidine to facilitate endosomal escape and cysteine fo

275 nsible for catalysing the decarboxylation of histidine to histamine.

276 Furthermore, the advanced oxidation of histidine to hydroxyaspartate at alpha-His-50 and beta-H

277 To our knowledge, this advanced oxidation of histidine to hydroxyaspartate is a new post-translationa

278 Furthermore, advanced oxidation of histidine to hydroxyaspartate was identified at two site

279 to switch the SETD3 target specificity from histidine to lysine.

280 The amino acid mutation at position 84 from histidine to threonine minimizes the mitogenicity of the

281 (MGL(long)) splice variants, as well as of a histidine-to-threonine mutant (MGL(short) H259T).

282 HAC1 (HAC1i) mRNA and the downregulation of Histidine triad NucleoTide-binding 1 (HNT1) mRNA.

283 We discovered FHIT (fragile histidine triad) as a novel BMPR2 modifier.

284 Organs were flushed with histidine tryptophan ketoglutarate solution and subjecte

285 hen randomly assigned to static storage with histidine-tryptophan-ketoglutarate (HTK) at 4 degrees C

286 ) after 0, 4, and 8 hours of cold storage in histidine-tryptophan-ketoglutarate preservation solution

287 or indica germplasms identified rice Lysine-Histidine-type Transporter 1 (OsLHT1) as a candidate gen

288 ttributed to the protonation of the bridging histidine upon copper reduction, yielding redox centers

289 Transporter-mediated histidine uptake and system L activity were similar in c

290 Amino acid transporter-mediated histidine uptake and system L amino acid transporter act

291 vel protocol to measure transporter-mediated histidine uptake, system L amino acid transporter activi

292 We previously identified the A. baumannii histidine utilization (Hut) system as being linked to nu

293 ive regulons, such as a relationship between histidine utilization and quorum sensing.

294 ingly, both zinc and copper addition shifted histidine UVRR bands in a manner diagnostic for metal co

295 K(+) AMT-specific differences were found for histidine variants.

296 Histidine was also detected extracellularly in the murin

297 trostatic and hydrophobic characteristics of histidine were both required for tau-microtubule binding

298 a novel microbially produced metabolite from histidine, which impairs glucose metabolism.

299 ng a phenylalanine that replaces a conserved histidine, which in typical DSORs is essential for stabi

300 , bovine serum albumin, R-phycoerythrin, and histidine, within minutes.