ライフサイエンスコーパス: histidine

1 n when the residues are good ligands such as histidine.

2 m were prepared by hydrothermal treatment of histidine.

3 nal rearrangements that include the reactive histidine.

4 mediate proton relay to the proton-selective histidine.

5 m, caused by a sulfation of a copper binding histidine.

6 ereas TbAAT2-4 transports both ornithine and histidine.

7 eonine (Tpt) or serine (Spt) in place of the histidine.

8 gment 4 (domain 1), the voltage sensor, with histidine.

9 amino acids, especially serine, arginine and histidine.

10 cupancy of the allosteric sites by TIH and L-histidine.

11 er with an iron cofactor coordinated by four histidines.

12 f MPnS and discover that it has an unusual 2-histidine-1-glutamine iron-coordinating triad.

13 The side chain of histidine-123 in the MIO domain dictated the distance be

14 ular health-related interest is the mutation Histidine 147 to Arginine (H147R) in human TRiC subunit

15 The reciprocal substitution of aspartate-to-histidine-193 in Pto abolished AvrPto recognition, confi

16 Val254 or LACC1 with mutations of the nearby histidines (249,250) have reduced PRR-induced outcomes.

17 m involving two water molecules and residues histidine-42, arginine-38, and serine-71 was proposed.

18 nverting these two residues to those in Pto (histidine-49/valine-51) did not restore recognition of A

19 ational-experimental study demonstrates that histidine-547 (H547) of hDAT plays a crucial role in the

20 n subunits with a C-terminally appended hexa-histidine (6His) tag are still assembled into functional

21 Two oligopeptides, hepta-histidine (7H) and Angiotensin III, rescued the morpholo

22 tagenomes indicated phoA, phoD and phoX, and histidine acid and cysteine phytase genes were most abun

23 es, as their altered pKa values, relative to histidine, allow for studies of the role of proton trans

24 Hz to the exchangeable proton of a conserved histidine and conclude that the histidine is hydrogen-bo

25 evealed a conserved region unusually rich in histidine and cysteine residues in the TMA-L1 region of

26 e contains a diiron cluster ligated by three histidine and four glutamate residues and activates diox

27 tion of a C-S bond between N-alpha-trimethyl histidine and gamma-glutamyl cysteine, which is the key

28 Novel cross-links between an oxidized histidine and intact histidine, lysine, or cysteine resi

29 oing sizable reductions, including loss of L-histidine and L-tryptophan biosynthesis.

30 ed mutagenesis established the importance of histidine and methionine containing motifs for Ag(+) -bi

31 formation of the ion pair associate between histidine and the nano optical samarium tetracycline [Sm

32 ile [2Fe-2S] cluster which is ligated by one histidine and three cysteine residues.

33 ysis gave high levels of cystine/methionine, histidine and tyrosine/phenylalanine.

34 as inhibited by the singlet oxygen scavenger histidine and was accompanied by vacuolar collapse and t

35 sRS from Burkholderia thailandensis bound to histidine, and a LysRS from Burkholderia thailandensis b

36 is essential for the biosynthesis of serine, histidine, and methionine; (iv) catabolic end products o

37 d in animals for nutrient signaling, and the histidine- and glutamine-rich domain of TCP20, which is

38 dicationic His4 filter where two of the four histidines are protonated is more proton-selective than

39 ligand derived from the natural amino acid l-histidine, are replaced by CH3NH3(+).

40 for increasing the impact and assessment of histidine as a biomarker for early diagnosis of histidin

41 itivity (98.88%) and specificity (97.41%) of histidine as a biomarker were calculated.

42 The mechanism involves a histidine as acid/base catalyst, which is unique for gly

43 amphoteric carriers, glutamic acid, aspartyl-histidine (Asp-His), cycloserine (cSer), and arginine, w

44 s an ssDNA-specific nuclease activity in the histidine-aspartate (HD) domain of the Cmr2 subunit of t

45 mid assay showed that mutation either in the histidine-aspartate acid (HD) domain (a quadruple mutati

46 ain-like fold with a characteristic cysteine-histidine-aspartate catalytic triad comprising Cys-73, H

47 We found that sterile alpha motif and histidine-aspartate domain-containing protein 1 (SAMHD1)

48 Sterile alpha motif (SAM) and histidine-aspartic (HD) domains protein 1 (SAMHD1) was p

49 Histidine at position 435 (H435) provides for optimal Fc

50 Some haplotypes of IgG3 have histidine at position 435.

51 CRF01_AE strains have a naturally occurring histidine at this position (H375).

52 e which is very selective and sensitive for [histidine](-) at pH 9.2 in serum and urine samples of hi

53 Cvi-0, one of the two copies of a duplicated histidine biosynthesis gene, HISN6A, is mutated, making

54 With H2/CO2, flavodoxin and histidine biosynthesis genes were upregulated.

55 the enzyme closely resembles the inhibited L-histidine-bound closed conformation, revealing the uncou

56 ained several conserved motifs including the histidine-box motif HXXHH.

57 modynamic appraisal of copper binding to the histidine-brace in an auxiliary activity family 10 (AA10

58 ansporters, one of which can be modulated by histidine, but both of which affect sensitivity to impor

59 rocesses, including myoinositol and 1-methyl-histidine, by targeted mass spectrometry.

60 n, decrease incorporation in response to the histidine CAC codon, and improve cell health and growth

61 mplexes demonstrated that heme binding via a histidine can be supported by hydrogen bond interactions

62 tate, as seen in WT M2, but left half of all histidines cationic, unambiguously demonstrating C-termi

63 p variants that increase reassignment of the histidine CAU codon, decrease incorporation in response

64 auxotrophic for the aromatic amino acids and histidine, causes scrub typhus, a potentially deadly inf

65 the cavity to form NTA-metal complexes with histidine clusters on the Fc domain.

66 A third histidine completes the protein ligand environment, leav

67 Substitution of a histidine, comprising part of the catalytic base group i

68 Our data indicate that carnosine, a histidine containing dipeptide available through the die

69 Herein, we report that C-2 arylated histidines containing tripeptides His(2-Ar)-Trp-His(2-Ar

70 ) has eight "Xpt" domains; six are canonical histidine-containing phosphotransfer (Hpt) domains and t

71 equence, revealing marked differences in the histidine-containing transmembrane helix behavior betwee

72 itratable amino acid residues in lieu of the histidines could bind protons and how they affect proton

73 posed that involves nucleophilic addition by histidine, cysteine, or lysine residues to the carbonyl-

74 It is the first time that histidine-cysteine (His-Cys) and histidine-lysine (His-L

75 Wild-type (WT) and l-histidine decarboxylase (Hdc(-/-)) mice were fed a contr

76 Histidine decarboxylase (HDC) and histamine receptor (HR

77 Histidine decarboxylase (HDC) deficiency has been shown

78 od FCER1A, carboxypeptidase A3 (CPA3), and L-histidine decarboxylase (HDC) gene expression; and serum

79 A premature termination codon in the human histidine decarboxylase (Hdc) gene has been identified i

80 Histidine decarboxylase (HDC) is the main enzyme involve

81 HSCs and hematopoietic progenitors marked by histidine decarboxylase (Hdc).

82 We also analyzed the expression of the Histidine decarboxylase and ECP by flow cytometry and fl

83 iodontitis patients express higher levels of histidine decarboxylase and ECP than those from healthy

84 Here, we show that cholangiocytes express histidine decarboxylase and its inhibition reduces CCA g

85 athymic mice treated with saline, histamine, histidine decarboxylase inhibitor, or cromolyn sodium.

86 In vitro, cultured MCs were transfected with histidine decarboxylase short hairpin RNA to decrease hi

87 lhistidine (a-FMHis), a suicide inhibitor of histidine decarboxylase, displayed impaired IA memory wh

88 MC supernatant fluids increased CCA histidine decarboxylase, vascular endothelial growth fac

89 nic mouse line expressing cre recombinase in histidine decarboxylase-expressing neurons (Hdc-Cre) fol

90 cle di-peptides composed of beta-alanine and histidine derivatives such as anserine are extremely imp

91 ata indicates that protonation of the buried histidine destabilizes both PrP variants, but produces a

92 sed to quantitate two biologically important histidine dipeptides, carnosine and anserine, using capa

93 the formation of a covalent phosphoramidate histidine-DNA adduct for cell-to-cell transfer.

94 hanism in GMC enzymes in which the conserved histidine does not act as a base.

95 Histidine enhances the luminescence intensity of the nan

96 nanocomposite probe comprised of amino acid (histidine) functionalized perylenediimide (PDI-HIS), cop

97 oxylic acid residues but, uniquely, a single histidine functions as the only discernable catalytic am

98 The resulting variant, which has cysteine-histidine-glutamic acid triads on each helix, hydrolyses

99 SAMHD1 (sterile alpha motif and histidine (H) aspartate (D) domain-containing protein 1)

100 n 375, those from CRF01_AE strains possess a histidine (H) at this location.

101 Herein, we describe a simple histidine (H) conjugated perylene diimide (PDI) bolaamph

102 A single buried highly conserved histidine, H187/H186 in GHaPrP/RaPrP, exhibited a marked

103 ime in transmembrane cytochrome, one natural histidine has been replaced by lysine without loss of th

104 Consistent with competition for histidine, high extracellular concentrations of this ami

105 s, bacteria, and archaebacteria synthesise L-histidine (His) in a similar, multistep pathway that is

106 Histidine (His) is proposed to be a key residue in cross

107 11556924), resulting in an arginine (Arg) to histidine (His) substitution in its encoded protein, NIP

108 ominent network-guided GWAS signal was for a histidine (His)-related trait in a region containing two

109 uptake from conserved tyrosine (Tyr-87) and histidine (His-38) residues within the active site.

110 mportantly, BM2 contains a second titratable histidine, His-27, in the tetrameric transmembrane domai

111 d a conserved CXXCH motif of cyt c In cyt c, histidine (His19) of CXXCH acts as an axial ligand to he

112 ences to the presence of a second titratable histidine, His27, which may increase the proton-dissocia

113 Intriguingly, the histidine, His48, is not invariant in GH145; however, wh

114 nd histidine-lysine (His-Lys) in addition to histidine-histidine (His-His) cross-links were discovere

115 For the new strain, histidine hydrogen-deuterium mass spectrometry revealed

116 at position 375 in group M is replaced by a histidine in CRF01_AE Envs.

117 ed as an optical probe for the assessment of histidine in different serum and urine samples of new bo

118 lculations identified a role for a conserved histidine in promoting oxygen activation.

119 GA1 channels by transition metals requires a histidine in the A' helix following the S6 transmembrane

120 be inhibited by the singlet oxygen scavenger histidine in treatments with AO but not with RB In the c

121 By protonation of the four histidines in acidic environments, the overall charge an

122 The pKa of histidines in these domains are determined from titratio

123 or of the dipeptide carnosine (beta-alanyl-l-histidine) in muscle.

124 ies further identified a role for the distal histidine, interacting with the hexacoordinated iron ato

125 a conserved histidine and conclude that the histidine is hydrogen-bonded to N2, tuning its reduction

126 ed setup, we demonstrated that the catalytic histidine is not involved in acyl-enzyme formation, but

127 Considering the two tautomeric forms of histidine, it was found that 2-fluorohistidine primarily

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 membrane-located receptors named ARABIDOPSIS HISTIDINE KINASE2 (AHK2), AHK3, and AHK4/CRE1.

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

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

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

158 Bacterial histidine kinases (HKs) are quintessential regulatory en

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

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

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

162 Sensor histidine kinases are central to sensing in bacteria and

163 Histidine kinases are key regulators in the bacterial tw

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

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

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

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

168 been identified that directly interact with histidine kinases.

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

170 ry backgrounds, combinatorially perturbed in histidine, leucine, methionine and uracil biosynthesis.

171 nt reaction options influenced by the distal histidine ligand.

172 Each Zn(2+) has two bis-coordinated histidine ligands, which bridge adjacent strands to form

173 ed histidine mutants enabled localization of histidines likely to be important for triggering this pH

174 y charged, interacts with positively charged histidine located at position 55, thereby stabilizing KI

175 where oxidized histidines react with intact histidine, lysine, and free cysteine to form cross-links

176 nks between an oxidized histidine and intact histidine, lysine, or cysteine residues were discovered

177 with a small group of amino acids (arginine, histidine, lysine, phenylalanine, tyrosine, and tryptoph

178 t time that histidine-cysteine (His-Cys) and histidine-lysine (His-Lys) in addition to histidine-hist

179 ewise, partially purified spinach extensins (histidine/lysine-rich cationic glycoproteins), strongly

180 at MobM follows a previously uncharacterized histidine/metal-dependent DNA processing mechanism, whic

181 he probe contains a naphthalimide core, an l-histidine methyl ester linker, and an acetylated galacto

182 based recognition element, N-methacryloyl-L-histidine methylester (MAH), 2-Hydroxyethyl methacrylate

183 metal ion, we identify a surface-exposed di-histidine motif in MamO that contributes to metal bindin

184 Reverse genetics and rescue of site-directed histidine mutants enabled localization of histidines lik

185 ygenate to Cu(II) 2 O2 cores bonded by three histidine Ntau-imidazoles per Cu center.

186 lanine 3.33 in CCR5 TM3 by the corresponding histidine of CCR2 converts J113863 from an antagonist fo

187 ysteine for covalent attachment, whereas the histidine of CXXCH positions the second cysteine.

188 the importance of the cysteine and the first histidine of the CX3HX2H motif in the process of copper

189 ates with and dephosphorylates the catalytic histidine on nucleoside diphosphate kinase B (NDPK-B).

190 IV-1, substitution of large residues such as histidine or tryptophan for serine 375 (S375H/W) in the

191 Filling this cavity with a histidine or tryptophan residue in Env with a natural se

192 vative, nonionizable substitutions of the TL histidine (or a neighboring TL arginine conserved in bac

193 The histidine oxidation hot spots were identified, which inc

194 r lysine residues to the carbonyl-containing histidine oxidation intermediates to form the cross-link

195 10 mug/mL of lysine (p < 0.05) and 10 mug/mL histidine (p < 0.001), 100 mug/mL of glutamic acid (p <

196 nt analysis and associations between HAL and histidine, PAH and phenylalanine, and UPB1 and ureidopro

197 argC, argG, argH and argJ) and two arginine/histidine permease genes (SSA_1568 and SSA_1569) were up

198 and aromatic amino acids (alanine, glycine, histidine, phenylalanine, leucine, isoleucine, valine, a

199 The histidine-phosphorylatable phosphocarrier protein (HPr)

200 t time phosphoisoform-specific regulation of histidine-phosphorylated proteins in vivo, and we link t

201 ntracellular copper exhibit increased KCa3.1 histidine phosphorylation and channel activity, leading

202 portant step forward in studying the role of histidine phosphorylation in mammalian biology and disea

203 exceedingly well characterized, the role of histidine phosphorylation in mammalian signaling is larg

204 Histidine phosphorylation is well characterized in proka

205 focused auxin signaling triggers ARABIDOPSIS HISTIDINE PHOSPHOTRANSFER PROTEIN6 (AHP6), which then re

206 the cytokinin signaling pathway mediated by histidine phosphotransferases.

207 vates transcription of sda, and Sda inhibits histidine protein kinases required for activation of the

208 res all four histidines with two of the four histidines protonated and if other titratable amino acid

209 The histidine protonation state responds to the cluster oxid

210 a(+) depends on the selectivity filter's (1) histidine protonation state, (2) solvent exposure, (3) o

211 laced by arginine (Q369R), lysine (Q369K) or histidine (Q369H).

212 a previously uncharacterized arginine 243 to histidine (R243H) mutation in the G-protein alpha subuni

213 s-links in the HMW fractions, where oxidized histidines react with intact histidine, lysine, and free

214 gen bond shape the dominant position of MOBV histidine relaxases among small promiscuous plasmids and

215 An arginine-to-histidine replacement at residue 435 in the binding doma

216 By site-directed mutagenesis we show that a histidine residue (His-347) downstream of S6 reduces inh

217 tion to calcium, phosphorylation of a single histidine residue (His358) in the cytoplasmic region, by

218 ctivity, achieved by introducing a catalytic histidine residue at the terminus of a pH-responsive pep

219 An invariant histidine residue has been proposed to function in the T

220 c role was put forward for a fully conserved histidine residue in MraY (His-289 in BsMraY), which has

221 crepancy, we explored the role of the distal histidine residue in muting the reactivity of human neur

222 The Histidine residue in position 265 of the CdtB catalytic

223 pecific post-translational modification of a histidine residue of eEF2, is involved in translocation.

224 reveal the binding of two ruthenium atoms to histidine residues 146 and 242, which are both located w

225 s we mutated all extracellular glutamate and histidine residues and 4 of 11 aspartates.

226 Four conserved histidine residues are demonstrated to be critical for e

227 is able to bind two b-type hemes through the histidine residues conserved between the MsrQ and NOX pr

228 Histidine residues direct oxidative coupling of boronic

229 m long fibrils with the hydrophobic edge and histidine residues extending in an ordered array as the

230 Specifically, protonation of histidine residues has been implicated in pH-dependent c

231 Histidine residues have been suggested as triggers due t

232 ots were identified, which include conserved histidine residues His292 and His440 in the Fc region an

233 t in canine HSP47, where we have mutated all histidine residues in the collagen binding interface and

234 een GAG anomeric position(s) and one or more histidine residues in the fibrils.

235 tivation causes oxidative damage to specific histidine residues in the key proteins in aldose reducta

236 theoretical and experimental study of the 14 histidine residues present in canine HSP47, where we hav

237 tification, and site-directed mutagenesis of histidine residues, we demonstrated that MsrQ is able to

238 [2Fe-2S] cluster via three cysteine and one histidine residues.

239 ss between one of the photoacids to proximal histidine residues.

240 ayload bound to the Fc region, presumably to histidine residues.

241 r proportion were positive for P. falciparum histidine rich protein 2 (192/246 [78.0%]) vs 811/1154 [

242 diagnostic tests (RDTs) detect P. falciparum histidine rich protein 2 (PfHRP2) and cross react with P

243 n product phosphocholine are identified in a histidine-rich active site.

244 ction enhancer, also called LAH4-A4, a short histidine-rich amphipathic peptide derived from the LAH4

245 Histidine-rich Ca-binding protein (HRC) resides in the l

246 and interface mapping experiments identified histidine-rich cytoplasmic loops within the ZIP6/ZIP10 h

247 The histidine-rich designer peptide LAH4-L1 exhibits antimic

248 Recently, the liver-derived plasma protein, histidine-rich glycoprotein (HRG), was demonstrated, in

249 5, C6, apolipoproteins A-I, A-IV, C-I and M, histidine-rich glycoprotein, heparin cofactor II and att

250 ted form of Ctr1 lacking the methionine- and histidine-rich metal-binding ectodomain, and it exhibits

251 TabZIPs contain the group-defining cysteine-histidine-rich motifs, which are the predicted binding s

252 Modifying antibodies to contain histidine-rich peptides enables reversible loading onto

253 nds on the parasite-derived, knob-associated histidine-rich protein (KAHRP).

254 ged between 6 months and 6 years using rapid histidine-rich protein 2 (HRP2)-based diagnostic tests (

255 sor was used to detect Plasmodium falciparum histidine-rich protein 2 (PfHRP2), an important malaria

256 ing antibodies against Plasmodium falciparum histidine-rich protein 2 (PfHRP2).

257 The most prevalent P. falciparum RDTs detect histidine-rich protein 2 (PfHRP2).

258 asma concentrations of Plasmodium falciparum histidine-rich protein 2 (PfHRP2).

259 d with age, independent of parasite biomass (histidine-rich protein 2 [HRP2]).

260 diagnostic testing with a multiple-antigen (histidine-rich protein 2 and pan-lactate dehydrogenase p

261 a (i) the detection of Plasmodium falciparum histidine-rich protein 2 antigen and (ii) multiplexed an

262 nge in the presence of Plasmodium falciparum histidine-rich protein 2 at a concentration well below c

263 erformance of Plasmodium falciparum-specific histidine-rich protein 2-based rapid diagnostic tests (R

264 , we investigated the diagnostic accuracy of histidine-rich protein 2-based RDTs using qualitative po

265 Knob and knob-associated histidine-rich protein expression, CD36 adhesion, and an

266 gnostic tests based on Plasmodium falciparum histidine-rich protein II (PfHRP-II) and P. falciparum l

267 dy, we assessed the accuracy of a dual-band (histidine-rich protein-2/pan-lactate dehydrogenase [HRP2

268 laria RDT that targets Plasmodium falciparum histidine-rich protein-II (HRPII) and Plasmodium lactate

269 c triad consisting of serine, aspartate, and histidine (SDH) from LCAT enzymes.

270 transmembrane receptors of the two-component histidine sensor kinase family.

271 f methyl jasmonate foliar application, i.e., histidine, serine, tryptophan, phenylalanine, tyrosine,

272 fer takes place with a conserved active-site histidine serving as the second proton donor.

273 ritically important ionization properties of histidine side chains of membrane proteins, when exposed

274 hip desalting, the limit of quantitation for histidine spiked in aCSF is approximately 1 muM, and cal

275 deletion at the C terminus (INTDeltaC15) and histidine substituted at the interaction surface (INT/DS

276 m transfer from the CE1-H group of trimethyl histidine substrate to iron(II)-superoxo.

277 orohistidine primarily forms the common (for histidine) tau-tautomer at neutral pH, while 4-fluorohis

278 one of the aromatic nitrogen atoms of the l-histidine through a hydrolyzable N-glycosidic bond.

279 Mutation of this histidine to alanine has no detectable effect on yeast g

280 -terminal pore at low pH did not convert all histidines to the neutral state, as seen in WT M2, but l

281 nts revealed that a single substitution of a histidine-to-aspartate at position 193 in Pto, which is

282 cysteine, glutamic acid, glutamine, glycine, histidine, total homocysteine, isoleucine, kynurenine, l

283 transcriptional activity is inhibited by the histidine triad nucleotide-binding protein 1 (HINT1) thr

284 We then studied histidine triad protein D (PhtD), an S. pneumoniae adhes

285 petition, YPL067C, uncovered a new family of histidine triad proteins apparently involved in the prev

286 ages employ the 8/4 structure for serine and histidine tRNAs, while minor cysteine and selenocysteine

287 of novel preservation solutions such as new histidine-tryptophan-ketoglutarate (HTK-N) and TiProtec

288 utes of WI, livers were flushed in situ with histidine-tryptophan-ketoglutarate and subsequently pres

289 e preferential COX-2 inhibitor Meloxicam via histidine-tryptophan-ketoglutarate showed the best graft

290 reserved with 8-hour NEVKP or in 4 degrees C histidine-tryptophan-ketoglutarate solution (SCS), follo

291 Only Meloxicam in histidine-tryptophan-ketoglutarate was demonstrated to b

292 A conserved histidine two residues upstream of the autocleavage site

293 ack of complete pathways for biosynthesis of histidine, valine, leucine, isoleucine, lysine and proli

294 -gel matrix by various concentrations of the histidine was successfully used as an optical probe for

295 cine, tyrosine, phenylalanine, ornithine and histidine were low, while values for citrulline, methion

296 atty acids, medium chain acylcarnitines, and histidine were: (1) stable in maternal plasma from pregn

297 he model predictions, except for glucose and histidine, which were depleted more slowly than predicte

298 ation range 1.4x10(-5) - 6.5x10(-10)molL(-1) histidine with a correlation coefficient of (0.998) and

299 ed polar interface houses the Zn(2+)-binding histidines with binding geometries unusual in proteins.

300 ton selectivity absolutely requires all four histidines with two of the four histidines protonated an