ライフサイエンスコーパス: NMR spectrum

1 shifts present crucial information about an NMR spectrum.

2 that ranged from 0.5 to 4.3 ppm in the (1)H NMR spectrum.

3 h a large 7Li hyperfine shift in the 7Li MAS NMR spectrum.

4 (II) environments, as confirmed by a (113)Cd NMR spectrum.

5 ay cause the broadened peaks of the C-RING1B NMR spectrum.

6 ete consumption of 1-hexene before the first NMR spectrum.

7 ized xenon leads to the effects on the xenon NMR spectrum.

8 which was confirmed by its characteristic 1H NMR spectrum.

9 C-9 hydroxyl group, on the basis of its (1)H NMR spectrum.

10 which to derive the particle shape from the NMR spectrum.

11 t exhibits some loss of dispersion in the 1H-NMR spectrum.

12 ntense H8/H8 ROE cross-peaks in the 2D ROESY NMR spectrum.

13 e at all accessible temperatures in the (1)H NMR spectrum.

14 ative thermal unfolding and a well-dispersed NMR spectrum.

15 tationary phase displayed an amorphous CPMAS NMR spectrum.

16 its protease sensitivity and (1)H-(15)N HSQC NMR spectrum.

17 midpoint potential and (for plastocyanin) 1H-NMR spectrum.

18 sine and histidine chemical shifts in the 1H NMR spectrum.

19 lucono-delta-lactone was observed in the 13C NMR spectrum.

20 wever, 2 becomes S = 2, as shown by its (1)H NMR spectrum.

21 etween a simulated and experimental 1D (13)C NMR spectrum.

22 ds a single, background-free one-dimensional NMR spectrum.

23 in blood using a simple one-dimensional (1D) NMR spectrum.

24 y integration of well-defined regions of the NMR spectrum.

25 ds signals were observed clearly in the (1)H NMR spectrum.

26 ing vinyl resonances that appear in the (1)H NMR spectrum.

27 to-enol form shows significant difference in NMR spectrum.

28 ence of the protein and its referenced (13)C NMR spectrum.

29 abolites using the same one-dimensional (1D) NMR spectrum.

30 ual dipolar coupling constants from a single NMR spectrum.

31 leads to a 10-fold enhancement in the (11)B NMR spectrum.

32 cing a small chemical shift change in the Xe NMR spectrum.

33 m for the coordinated CH3 group in the (13)C NMR spectrum.

34 e cytosol and yields a well-resolved in-cell NMR spectrum.

35 ur peaks were observed in the direct (113)Cd NMR spectrum.

36 tected in a single scan hyperpolarized (13)C NMR spectrum.

37 ded state of wild-type IscU and assigned its NMR spectrum.

38 nd observable in a variable-temperature (1)H NMR spectrum.

39 egular isotropic nuclear magnetic resonance (NMR) spectrum.

40 peak in the 175-212 ppm region of the (31)P NMR spectrum ((2)J(PH) ~14 Hz).

41 lable comprising compound annotation, a (1)H NMR spectrum, 2D and 3D structure with correct stereoche

42 ) the upfield shift of methyl groups in a 1D NMR spectrum, a 2D- HSQC NMR spectrum of ImmE1 in the mi

43 Finally, changes in the (87)Sr NMR spectrum after immersion of the glass in simulated b

44 terns was further inspected by FRET and (1)H NMR spectrum analysis facilitated via genetic code expan

45 IR spectra, (1)H-NMR spectrum and elemental analysis were evaluated for t

46 (calculation of the first derivative of the NMR spectrum and Gaussian shaping of the free-induction

47 amagnetically shifted resonances in the (1)H NMR spectrum and has been characterized by IR spectrosco

48 dged by titration calorimetry, by changes in NMR spectrum and intrinsic tryptophan fluorescence, and

49 hand, complicates the interpretation of the NMR spectrum and means that different samples of the sam

50 Comparison of the (1)H NMR spectrum and NICS(1) zz of 5(2-) with those of 5(2+)

51 and radius of gyration and was supported by NMR spectrum and nuclease assays.

52 f the effects of Co(III) hexammine on the 1H NMR spectrum and results of automatic docking into the I

53 mi-purified ethyl acetate fraction while the NMR spectrum and the LCMS profile revealed the isolation

54 identifying informative regions in the HRMAS NMR spectrum and using them for tumor margin assessment

55 e unsupported bridge (inferred from the (1)H NMR spectrum), and 21 has one unsupported Fe-(mu(2)-SR)-

56 Populations were determined from the (13)C NMR spectrum, and assignments were based on the (13)C sp

57 re observed in a number of resonances in the NMR spectrum, and both chemical shifts and NOEs provide

58 alcium phosphate (OCP), reassigned its (31)P NMR spectrum, and identified an extended hydrogen-bondin

59 wn, we observed dynamic behavior in the (1)H NMR spectrum, and using VTNMR were able to measure a Del

60 ial chemical shift dispersion evident in the NMR spectrum are consistent with the highly structured d

61 resentative X-ray crystal structure and (1)H NMR spectrum are examined that provide evidence for a un

62 at the peak ratios for any metabolite in the NMR spectrum are fixed and proportional to the relative

63 This is demonstrated using 13C NMR spectrum as readily obtainable information.

64 uency-stepped fashion, indirectly maps their NMR spectrum as sizable attenuations of the abundant (1)

65 rcular dichroism, intrinsic fluorescence and NMR spectrum as the protein denatured at high concentrat

66 ved deuterium 2 and 3 resonances in its (2)H NMR spectrum at 14.1 T.

67 The solid-state (13)C CPMAS NMR spectrum at 20 degrees C shows three chemically ineq

68 AAF-12-mer, d(CTTCTTG[FAAF]ACCTC), whose 19F NMR spectrum at 22 degrees C and pH 7.0 gave only two si

69 act human low-density lipoprotein (LDL) (1)H NMR spectrum at 600 MHz enabled the investigation of LDL

70 Broadening of a subset of resonances in the NMR spectrum at low temperature, anomalous temperature d

71 and accurate, including measurement of (1)H NMR spectrum before and after the addition of the analyt

72 ements, it is shown that the visible gelator NMR spectrum below the liquid-gel transition temperature

73 This rate was calculated from the 1D NMR spectrum by measuring the reappearance of biotin's u

74 Peak suppression in the NMR spectrum by sorption of the paramagnetic relaxation

75 , ClFe(III)(meso-NH(2)-OEP) displays an (1)H NMR spectrum characteristic of a high-spin, five-coordin

76 The NMR spectrum confirmed stability of nanofiber as there w

77 The proton NMR spectrum confirms the presence of a strong diamagnet

78 uble in dry CDCl(3) and gave an ill-resolved NMR spectrum, consistent with its nonspecific aggregatio

79 thioate 5' to A7 results in a distinct (31)P NMR spectrum, consistent with thermodynamic studies repo

80 es in its UV spectrum (lambdamax 236 nm) and NMR spectrum (defining a 9,10-epoxy-octadec-10,12Z-dieno

81 The (13)C NMR spectrum (delta = 127.8 ppm at pH 13 vs dioxane at 6

82 The proton NMR spectrum demonstrated that the system has a strong d

83 -(t)Bu(2)bpy derivative 1a has a useful (1)H NMR spectrum, despite being paramagnetic.

84 ents from DO spectra are projected onto a 1D NMR spectrum (diffusion-ordered projection spectroscopy,

85 e formed, the NMR signals disappear from the NMR spectrum, due to the existence of fast transverse re

86 inogen activator inhibitor-1, since the (1)H NMR spectrum, electrophoretic mobility, and proteolytic

87 in the (1)H nuclear magnetic resonance ((1)H NMR) spectrum, enabling itself to be detected at sub-mM

88 ion causes strong upfield shifts in the (1)H NMR spectrum even in the presence of only 5 mol % of 3.

89 prisingly, at ambient temperature, the (13)C NMR spectrum exhibits isotropic motional averaging yield

90 erized complexes for which no measured (9)Be NMR spectrum exists, and to investigate a literature com

91 rresponding area under the peaks in the (1)H NMR spectrum, explains the unusual regioselectivity of h

92 The (2)H NMR spectrum for equimolar [3 alpha-(2)H(1)]cholesterol

93 diphosphate 7b, with no evidence in the 31P NMR spectrum for pentacoordinate chlorooxyanionic phosph

94 oes not require any detailed analysis of the NMR spectrum for the detection and quantification of suc

95 In the proton NMR spectrum for the dication, the internal CH was shift

96 The NMR spectrum for the monoadduct 2b is consistent with re

97 dependence of the chemical shift in the 13C NMR spectrum for the N5-methyl resonance indicates that

98 ies, characterized by J(SeH) coupling in the NMR spectrum for the P(V)-seleno compounds and a bathoch

99 The proton NMR spectrum for this complex also shows the retention o

100 The (13)C NMR spectrum for Y3N@C2-C78 exhibits strongly deshielded

101 ngle NMR peak and reconstructing of the (1)H NMR spectrum from a specific HPTLC spot, enhancing derep

102 also report and analyze the solid-state (2)H NMR spectrum from these spores.

103 NMR spectrum further confirmed the presence of bioactive

104 ly diatropic characteristics, and the proton NMR spectrum gave resonances at -5.74 and -6.24 ppm for

105 k positions and intensities from a reference NMR spectrum generally serves as the identifying signatu

106 s 8-10 min for a simple one-dimensional (1)H NMR spectrum, giving access to metabolite information wh

107 downfield resonance at 556 ppm in the (13)C NMR spectrum has been assigned to the carbide carbon.

108 s there is no change in the (1)H- (15)N HSQC NMR spectrum in comparison to wild-type CaM.

109 On the basis of the downfield 1H NMR spectrum in solution, His 57 is not protonated at Ne

110 iple broad peaks and gave a poorly dispersed NMR spectrum in the presence of calcium.

111 e anomeric bonds, identified in the FTIR and NMR spectrum, indicate that the extracts are a mixture o

112 The proton NMR spectrum indicated that the carbachlorin is strongly

113 The (1)H NMR spectrum indicates that this minor product contains

114 metric bound conformation observed in the 1H NMR spectrum, indicating that the DNA duplex retains its

115 ox domain, there is a striking change to the NMR spectrum indicative of conformational tightening.

116 The single low-field line in the 1H NMR spectrum is assigned by site-directed mutagenesis: T

117 The anomeric (H1) region of the 1H NMR spectrum is band-selected in the F1 dimension.

118 ed in the cytosol, and the resulting in-cell NMR spectrum is broadened.

119 29Si NMR spectrum is consistent with phase pure type I clathr

120 At pH* 4.6, the 1H NMR spectrum is sensitive to complexation of the proteas

121 by thermal and by chemical denaturation, its NMR spectrum is significantly broader than that of the w

122 kappaBalpha, the resonance dispersion in the NMR spectrum is significantly greater, providing definit

123 The complete (195)Pt MAS NMR spectrum is then reconstructed by recording a series

124 The 1H-15N TROSY NMR spectrum is well dispersed and contains signals from

125 The proton NMR spectrum, NICS calculations, and AICD plots indicate

126 eatly altered, paramagnetically shifted (1)H NMR spectrum observed for this species.

127 The broadened 1H NMR spectrum of 2 indicates the presence of a triplet, b

128 The (13)C NMR spectrum of 2-butyl-1,2-(13)C(2) cation (1) is uncha

129 In particular, analysis of the NMR spectrum of 27AQS2 bound to a specially designed syn

130 The (19)F NMR spectrum of 6-(19)F-Trp-labeled mADA reveals four di

131 The (1)H NMR spectrum of 9 using the lanthanide shift reagent Eu(

132 or chemistry and biomedicine, we show a ZULF NMR spectrum of [2-(13)C]pyruvic acid hyperpolarized via

133 Similar to previous reports, the (31)P NMR spectrum of a 12-nucleotide stem-loop sequence 5'-GG

134 The 13C NMR spectrum of a 13C-labeled version of the latter spec

135 a (31)P refocused INADEQUATE solid-state MAS NMR spectrum of a cadmium phosphate glass, 0.575CdO-0.42

136 onsiderably overlapped cross peaks in the 1H-NMR spectrum of a DNA trinucleotide repeat sequence.

137 The impact of specific binding on the NMR spectrum of a membrane protein can be difficult to d

138 A decreased SMR intensity in the 1H NMR spectrum of a protein mixture compared to the added

139 We also acquire a NMR spectrum of a single C. elegans worm at 23.5 T.

140 ppears with PPACK, which is absent in the 1H NMR spectrum of a solution of the enzyme between pH 5.3

141 se results indicate that the E. coli in-cell NMR spectrum of a target protein is a useful tool for mo

142 First, the de-HETCOR NMR spectrum of a ten-site (15)N-labeled sample of p1 al

143 An NMR spectrum of a test polymerization indicates that onl

144 ion was demonstrated by changes in the (31)P NMR spectrum of ATP.

145 The NMR spectrum of bacterially expressed CD2d1, assigned in

146 We now show specific differences between the NMR spectrum of bacterially expressed full-length tail a

147 demonstrated effects of dimerization on the NMR spectrum of bovine neurophysin-I, and preliminary in

148 ith C(3) symmetry as determined by the (13)C NMR spectrum of C(60)H(36) and the (3)He NMR spectrum of

149 Additionally, the line shape of the 2H NMR spectrum of CD3-Ala24 reveals more side chain dynami

150 ic spectrum of CuAbeta, hyperfine-shifted 1H NMR spectrum of CoAbeta, and molecular mechanics calcula

151 The paramagnetic (1)H NMR spectrum of Cu(II) pseudoazurin [PACu(II)] contains

152 CXCR4 induced chemical shift changes in the NMR spectrum of CXCR4 in membranes, disturbed the associ

153 The 1H-NMR spectrum of cyanide-ligated D245N CIP, assigned usin

154 inimizes the effects of Pdx titration on the NMR spectrum of CYP-S-CO, but is competent to replace K+

155 In the (1)H NMR spectrum of D. crassirhizoma PCu(I), there is no sig

156 The 19F NMR spectrum of dG-C8-FAAF [N-(deoxyguanosin-8-yl)-N-ace

157 (31)P NMR data to the chlorides 2, the (1)H NMR spectrum of each features a triplet ((3)JHP = 3.8 Hz

158 Upon DNA binding, the NMR spectrum of each isoform changed to indicate greater

159 The downfield region of the (1)H NMR spectrum of free BChE at pH 7.5 showed a broad, weak

160 matic Ge(II) porphyrin complex, while the 1H NMR spectrum of Ge(TPP)(py)2 clearly indicates the prese

161 The (13)C NMR spectrum of guanine bound to Leuko-PNP, its fluoresc

162 plexes was investigated by obtaining the 19F NMR spectrum of H93G(3-FPyr)CO, whose 19F signal can be

163 A high quality heteronuclear NMR spectrum of HCV NS5B(Delta21) has been obtained and

164 The (1)H-(15)N TROSY NMR spectrum of HO-2 reveals specific residues, includin

165 tions where CPR affects the (1)H-(15)N TROSY NMR spectrum of HO-2, BVR has no effect.

166 While the NMR spectrum of honey and its classical metabonomic anal

167 Changes in the NMR spectrum of HscB upon addition of IscU mapped to the

168 In this study, we measure the (19)F NMR spectrum of hundreds of fluorinated compounds and us

169 thyl groups in a 1D NMR spectrum, a 2D- HSQC NMR spectrum of ImmE1 in the mixed polarity solvent mixt

170 o a pH-dependent line broadening in the (1)H NMR spectrum of iPrNHN(O)=NOMe, suggesting a complex flu

171 The (1)H NMR spectrum of Lu[CH(SiMe3)2]3 shows that the -SiMe3 gr

172 e glucose (MAG), and a single (2)H and (13)C NMR spectrum of MAG provided the following metabolic dat

173 The 31P NMR spectrum of native enzyme exhibits resonances due to

174 The assigned paramagnetic (1)H NMR spectrum of Ni(II) UMC demonstrates that the axial G

175 The temperature-dependent imino proton NMR spectrum of oxoG modified DNA confirms the destabili

176 For the first time, the 13C NMR spectrum of p-QDM 1 was observed.

177 inal (N) domain of Hsp90 does not affect the NMR spectrum of p23 either in the presence or absence of

178 arison, the oriented-sample (OS) solid-state NMR spectrum of Pf1 coat protein in aligned phospholipid

179 The (31)P{(1)H} NMR spectrum of phosphate 3a displayed four resonances d

180 by measuring a diffusion-edited 1H-1H TOCSY NMR spectrum of plasma, it is possible to obtain signals

181 complete assignment of the resonances of the NMR spectrum of proteins for the evaluation of the foldi

182 ntense H8/H8 ROE cross-peaks in the 2D ROESY NMR spectrum of Rh(2)(OAc)(2)[d(GpG)] indicate head-to-h

183 eters from the diamond surface to detect the NMR spectrum of roughly 1 pl of fluid lying within adjac

184 tion) method, which deconvolutes the average NMR spectrum of small flexible molecules into individual

185 The (1)H NMR spectrum of synthetic 5 correlated closely with that

186 The (15)N NMR spectrum of the 1((15)N) (50% Fe identical with(15)N

187 h small sample volumes, we have recorded the NMR spectrum of the 20 nm (6 mug) passivating layer on a

188 At lower temperatures, the proton NMR spectrum of the asymmetrically substituted carbaporp

189 The proton NMR spectrum of the bipyridyl ferrous cyanoheme complex

190 some N-terminal residues to appear in the 1D NMR spectrum of the carboxylated form.

191 In addition, the aromatic 1H NMR spectrum of the cold denatured state at 0 degree C i

192 extremely well resolved imino protons in the NMR spectrum of the complex.

193 eta-pinene for benzene and evaluating the 2D NMR spectrum of the corresponding beta-pinene complex.

194 3)C NMR spectrum of C(60)H(36) and the (3)He NMR spectrum of the corresponding sample of (3)He@C(60)H

195 In contrast, the HSQC NMR spectrum of the covalent complex showed that the rea

196 The NMR spectrum of the cross-linked peptide has been fully

197 The NMR spectrum of the Cu(II) protein does not exhibit any

198 In the (1)H NMR spectrum of the diamagnetic Y complex 1, the equival

199 The solution-state (13)C NMR spectrum of the endofullerene (3)He@C(60) displays a

200 A (13)C NMR spectrum of the enzyme complex with 4-nitrobenzo[(13

201 The (19)F NMR spectrum of the F93A ADH-NAD(+)-pentafluorobenzyl al

202 The (1)H NMR spectrum of the gamma-picoline/trifluoroacetic acid

203 ted resonances (<4%) were found in the (31)P NMR spectrum of the GDP product.

204 and accurate method for calculating the 13C NMR spectrum of the generated structures exists.

205 ading to an unequivocal assignment of the 1H NMR spectrum of the hexasaccharide.

206 The 15N-1H HSQC NMR spectrum of the human alpha-lactalbumin (alpha-LA) m

207 bin with the inhibitors, but in a 600 MHz 1H NMR spectrum of the inhibition adduct at pH 6.7 and 30 d

208 with input of the molecular formula and 13C NMR spectrum of the isolated compound.

209 rization (DNP) at 90 K, we observe the first NMR spectrum of the K intermediate in the ion-motive pho

210 The (1)H NMR spectrum of the Mg-IRE complex revealed, in contrast

211 The 188-MHz 19F NMR spectrum of the microcrystalline, double-labeled enz

212 The WISE NMR spectrum of the native silk exhibits (1)H line width

213 f its (1)H NMR spectrum to the obtained (1)H NMR spectrum of the natural product, as well as matching

214 onstants was obtained by analysis of the ABX NMR spectrum of the new glycine-derived N-p-toluenesulfo

215 ngle quantum correlation spectroscopy (HSQC) NMR spectrum of the non-covalent complex showed that the

216 a few minutes that registration of the (1)H NMR spectrum of the oil takes, in addition to the rest o

217 e EPR spectrum of the oxidized state and the NMR spectrum of the paramagnetically shifted resonances

218 The uniquely well-resolved (99)Tc NMR spectrum of the pertechnetate ion in liquid water po

219 The (31)P NMR spectrum of the product duplex shows that the H-bond

220 Free ethene is detected in the NMR spectrum of the products, and insoluble rhenium prod

221 of the His-72 Cepsilon1H resonance in the 1H NMR spectrum of the protein, consistent with a structura

222 tter resolution than the equivalent solution NMR spectrum of the same protein in micelles.

223 The NMR spectrum of the substituted 2-methylfurans shows an

224 strate mixtures causes upfield shifts in the NMR spectrum of the substrate and often enhances the ena

225 The proton NMR spectrum of the transition-state analogue complex of

226 The (51)V NMR spectrum of this compound in CD(3)CN exhibits multip

227 utyl group chemical shift observed in the 1H NMR spectrum of this enantiomer measured in the presence

228 The 19F NMR spectrum of this enzyme showed five sharp resonances

229 ignment of the complex overlapping (47/49)Ti NMR spectrum of Ti(3)AlC(2).

230 As a typical example, the NMR spectrum of trimethyl derivative Me(2)NN(O)=NOMe rev

231 ppm at pH 6.40 and 42 degrees C) in the 15N NMR spectrum of uniformly 15N-labeled 4-OT.

232 evidence of monohydrogen phosphate in a (1)H NMR spectrum of unmodified bone is presented for the fir

233 The trimethoxy complex (III), the (1)H NMR spectrum of which was observed earlier by Servis, th

234 The (67)Zn NMR spectrum of WT LpxC at pH 6 (prepared at 0 degrees C

235 The 15N-1H HSQC NMR spectrum of WT PI-PLC is also reported at 600 MHz.

236 e changes in the nuclear magnetic resonance (NMR) spectrum of a protein upon binding a set of quasi-d

237 identity for many unknown metabolites in the NMR spectrum, offer new avenues for human serum/plasma-b

238 pool of other metabolites using a single 1D NMR spectrum offers a new avenue in the metabolomics fie

239 ning of ethyl and aromatic signals in the 1H-NMR spectrum on the addition of the paramagnetic probe 4

240 Python 3.5, MixONat analyses a {(1)H}-(13)C NMR spectrum optionally combined with DEPT-135 and 90 da

241 It is generally accepted that a single 1D NMR spectrum or mass spectrum is usually not sufficient

242 A technique is proposed in which an NMR spectrum or MRI is encoded and stored as spin polari

243 es, addition of calcium had no effect on the NMR spectrum or on the pH-induced changes.

244 The effect of pH on the (1)H NMR spectrum, reduction potential, and self-exchange rat

245 However, the analysis of (1)H NMR spectrum remains difficult, mainly due to the differ

246 Remarkably, the native NMR spectrum returns with this slower time constant of c

247 1)B{(17)O} dipolar heteronuclear correlation NMR spectrum revealed the structural connectivity betwee

248 The (113)Cd NMR spectrum reveals a single resonance of delta = 622 p

249 Surprisingly, the first NMR spectrum reveals, aside from uninitiated catalyst, Z

250 In principle, this region of the NMR spectrum should be amenable to detailed analysis, be

251 s with a cis E18-P19 peptide bond, the 1-bar NMR spectrum showed sharp resonances with near random co

252 id (AE-CWI) contained 95% GalA and its (13)C NMR spectrum showed signals at delta 98.9, 78.0, 71.4, 6

253 le bands in the Soret region, and the proton NMR spectrum showed that it has a reduced diamagnetic ri

254 The proton NMR spectrum showed that the carbachlorin is highly diat

255 The 1H NMR spectrum shows a pattern consistent with mobile hydr

256 The one-dimensional exchangeable proton NMR spectrum shows resonances expected for imino protons

257 the fluorinated benzene ring, and the (19)F NMR spectrum shows three resonances for the two bound fl

258 The (29)Si CPMAS NMR spectrum shows two chemically inequivalent resonance

259 First, localized (31)P NMR spectrum signals of pHi and pHe reporter molecules [

260 In the present paper, we review the major NMR spectrum simulation techniques with regard to chemic

261 Important resonances in the (19)F NMR spectrum such as that of trifluoroacetic acid are br

262 The effects detected by the NMR spectrum suggest a biphasic process, involving stron

263 The (13)C NMR spectrum suggested a C(2)-symmetrical structure.

264 avior during Edman sequence analysis and its NMR spectrum suggested that sublancin is a dehydroalanin

265 appear as one equivalent signal in the (1)H NMR spectrum, suggesting that even methane can rotate in

266 henanthryl protons shift upfield in the (1)H NMR spectrum, suggesting that the phenanthrenes pi-stack

267 The (1)H NMR spectrum supports proper folding of the K1 component

268 The ROESY NMR spectrum, tandem MS/MS analysis, and methylation ana

269 mplex results in changes in the IkappaBalpha NMR spectrum that are consistent with dissociation of th

270 traces in a constant-time (13)C-(13)C TOCSY NMR spectrum that are unique for individual mixture comp

271 produces a high-resolution, single-scan (1)H NMR spectrum that can be recorded after a pump-probe del

272 pectra) to generate a pseudo-two-dimensional NMR spectrum that displays the correlation among the int

273 arkable and complicated solvent-dependent 1H NMR spectrum that suggests the existence of hydrogen bon

274 tained from a two-dimensional, heteronuclear NMR spectrum), the inverse mode of SPARIA calculates all

275 allows for the rectification of the 1D (1)H NMR spectrum to a level suitable for a quantitative hydr

276 hese required a careful analysis of the (1)H NMR spectrum to identify the stereoisomers, particularly

277 Following the acquisition of a single 2D NMR spectrum to measure the frequency-dependent homogene

278 remely close match in appearance of its (1)H NMR spectrum to the obtained (1)H NMR spectrum of the na

279 ical shift perturbations in a 2D 1H-15N HSQC NMR spectrum to verify specific interactions of the comp

280 oncentration within the methyl region of the NMR spectrum using the same conversion constant.

281 ), was isolated at -15 degrees C, and its 1H NMR spectrum was recorded at that temperature.

282 s, 6-7 ppm vinylic proton region in the (1)H NMR spectrum was used, where acetone was observed as the

283 al heteronuclear nuclear magnetic resonance (NMR) spectrum was recorded after the rapid initiation of

284 However, the (15)N NMR spectrum we measure (delta = -80.6 ppm at pH 13 vs N

285 obtain a protease construct with a resolved NMR spectrum, we expressed and purified an unlinked prot

286 Based upon perturbations to the NMR spectrum, we propose that the binding site of the C-

287 Two upfield-shifted signals in the (1)H NMR spectrum were used as sensitive probes of the vWF-A

288 n be tackled through the corresponding (13)C NMR spectrum where a significant enantiodifferentiation

289 t comes from the (31)P splitting of the (1)H NMR spectrum, where additional coupling indicates unusua

290 by the H8/H8 NOE cross-peaks in the 2D ROESY NMR spectrum, whereas the formamidinate bridging groups

291 L550, a new SB signal is detected in the 15N NMR spectrum which disappears upon thermal relaxation.

292 nce of broad macromolecule peaks in the (1)H NMR spectrum, which can severely limit the amount of obt

293 The NMR spectrum will display signals from all species in th

294 ion of the apoenzyme with OMP yields a (31)P NMR spectrum with peaks for both free and enzyme-bound O

295 synthesis and comparison of its (29)Si{(1)H} NMR spectrum with that of the in situ reaction mixture.

296 between the two transmembrane helices has an NMR spectrum with well-dispersed peaks, suggesting that

297 osition of a protein from a single, 1D (13)C NMR spectrum without chemical shift assignments.

298 wo-dimensional (2D) [(13)C-(1)H] correlation NMR spectrum without the need for identification and ass

299 The (11)B NMR spectrum, X-ray diffraction analysis and computation

300 The (11)B NMR spectrum, X-ray diffraction analysis, and computatio