ライフサイエンスコーパス: chemical shift of

1 -j, a highly shielded signal with an average chemical shift of 0.05 ppm was observed.

2 values correlate well with the alpha-carbon chemical shift of 1, but polarity measures such as E(N)(

3 The (13)C NMR chemical shifts of 1 and 2 were calculated by the GIAO-C

4 t is frequently discussed in connection with chemical shifts of (1)H nuclear magnetic resonance spect

5 by continuous changes in the (15)N and/or NH chemical shifts of 12 residues, revealed fast exchange,

6 Here we exploit the solubility and chemical shift of (129)Xe, the magnetic resonance signal

7 The (13)C chemical shifts of (13)C, (15)N-labeled residues in the

8 Measured at 2 degrees C in water, NMR chemical shifts of (13)C=O labeled central alanine resid

9 fractionation factor increases to 1.2 with a chemical shift of 15.0.

10 Mutation of Lys 153 to Met results in a 13C chemical shift of 150.8 ppm, which is 0.9 ppm downfield

11 ured by the nuclear magnetic resonance (NMR) chemical shifts of 158 protons.

12 wild type enzyme with MgCl2 show changes in chemical shifts of 15N and NH resonances in regions clos

13 The NMR chemical shifts of 15N-labeled histidine show that His21

14 The NMR chemical shifts of 15N-labeled tryptophan are consistent

15 A downfield chemical shift of 19.45 ppm (Deltadelta(H) = 7.43 ppm) o

16 and BHandHLYP/6-311+G(d,p) computed (1)H NMR chemical shifts of 1a and three other low-lying isomers

17 forward mode, SPARIA is used to predict the chemical shifts of 1H and 13C on aromatic moieties conta

18 isolated molecule to plane changes in the 1H chemical shift of 2.0 and 2.2 ppm are determined for the

19 Upfield chemical shifts of 2.4 ppm for T16 N3H, 1.1 ppm for T17

20 te of the caged compound exhibits an altered chemical shift of -2.6 ppm as compared with 2.3 ppm dete

21 Phosphate-dependent changes in the chemical shifts of 22 amide groups were observed in (1)H

22 We show that the chemical shifts of 4- and 3-trifluoromethylbenzoate and

23 The calculated (13)C NMR chemical shifts of 5 agree rather well with the experime

24 utT induces changes in backbone (15)N and NH chemical shifts of 62 residues widely distributed throug

25 Changes in the chemical shifts of (7)Li NMR signals as functions of [Li

26 that the lowest predicted (13)C and/or (1)H chemical shift of a heterocycle correlates qualitatively

27 m for a hydrogen is known to perturb the NMR chemical shift of a neighboring hydrogen atom.

28 t is shown that the difference in the 1H NMR chemical shift of a protic hydrogen in DMSO and CDCl3 so

29 s at 15.9 ppm, an unusually large N-H proton chemical shift, of a magnitude previously observed only

30 We report here the 1H-NMR chemical shifts of a 20-bp oligodeoxynucleotide containi

31 lts in small changes in the amide 1H and 15N chemical shifts of a few residues from helices B and C,

32 at of the wild type, although changes in the chemical shifts of a number of resonances indicate local

33 nances from much of helix 4 vanish while the chemical shifts of a possibly nascent helical segment im

34 proposed to account for decreased downfield chemical shifts of a proton bound by noncovalent interac

35 ouplet (due to the two Trp residues) and the chemical shifts of a Trp Hepsilon3 site (shifted upfield

36 ssibility to base-catalyzed exchange nor the chemical shifts of active site residues are affected by

37 related with the N epsilon(2) and N delta(1) chemical shifts of all 13 surface histidines per alpha b

38 The chemical shifts of all of the Arg Nepsilon resonances in

39 The Nzeta and Hzeta chemical shifts of all six lysines are similar and are n

40 s based on a cooperative transition of (15)N chemical shifts of amide protons as a function of urea c

41 The (15)N- and (1)H-chemical shifts of amide signals from (15)N-containing a

42 The relative (1)H NMR chemical shift of an exchangeable proton was used to ver

43 The difference in the chemical shifts of an OH or NH group in these two solven

44 The amide 1H and 15N chemical shifts of an uniformly 15N-labeled sample of p5

45 nterpreted using the known dependence of the chemical shifts of anomeric carbon on the conformation a

46 e effects of many common substituents on the chemical shifts of aromatic carbon and hydrogen are well

47 corresponds to changes in the calculated 1H chemical shifts of at most 0.1 ppm.

48 Changes in the NMR chemical shift of backbone amide nuclei (1H and 15N) hav

49 Phospholipid binding led to changes in chemical shifts of backbone atoms in residues Arg233 and

50 ased on interproton NOE's and differences in chemical shifts of backbone H alpha, C alpha, C beta, an

51 Changes in the chemical shifts of backbone signals provided evidence of

52 ly the expected crosscorrelation between the chemical shifts of bonded amide(1)H and (15)N spins but

53 Upfield chemical shifts of both (31)P and H-2' (1)H resonances i

54 The close statistical match of the (13)C chemical shifts of both polymorphic forms with those cal

55 d with cholesterol-containing membranes, the chemical shifts of both residues correlated with beta st

56 its carboxylate exposed at the surface: the chemical shift of bound [18-13C]-stearate; dicarboxylic/

57 ting the mechanism we postulate; and (c) the chemical shift of bound [N4'-(15)N]ThDP provides plausib

58 In both cases, the (15)N chemical shift of bound cyanide was reminiscent of that

59 r the pH range of 5-11, and from the (3)(1)P chemical shift of bound P(i).

60 In addition, on the basis of the chemical shift of C-1 carbon on the amylose backbone, it

61 gh expected to lead to a small change of the chemical shift of C15, in addition to changes of the C4-

62 The (13)C chemical shifts of C3' and C5', considered to be key rep

63 The base and sugar (H6,C6, H1',C1') chemical shifts of C43 for the dominant conformer are si

64 Chemical shifts of CaM bound to a peptide (smMLCKp) corr

65 49 structures by matching the changes in the chemical shifts of CaM upon Ng13-49 binding from nuclear

66 l shifts of the boron nuclei also govern the chemical shifts of carbon nuclei of these hypercoordinat

67 l shifts of the boron nuclei also govern the chemical shifts of carbon nuclei of these hypercoordinat

68 generated by these ring currents affects the chemical shift of carbons on the far side of the fullere

69 The 13C chemical shifts of Cd- and ZnBlm A2 are almost identical

70 conformation substantially, but perturbs the chemical shift of certain backbone and side-chain proton

71 monofunctional binding step from changes of chemical shifts of certain CH(2) linker protons as well

72 ua monochloro species (2) and changes in the chemical shifts of certain DNA (1)H resonances are consi

73 f the relative redox potential and (31)P NMR chemical shifts of corresponding carbene-phosphinidene a

74 The calculated values of (31)P NMR chemical shifts of corresponding phosphinidene adducts o

75 itoring perturbations in the line widths and chemical shifts of cross peaks in the HSQC spectrum of C

76 n order to rationalize the peculiar (1)H NMR chemical shifts of cyclopropane (delta 0.22) and cyclobu

77 Chemical shifts of cyt b(5) backbone resonances and side

78 3), are statistically identical, the carbide chemical shift of delta 501 ppm is much larger than the

79 and are resolved according to the isotropic chemical shifts of different sites in the direct dimensi

80 Upfield chemical shifts of duplex imino protons and the disrupti

81 alue was also calculated from the CD-induced chemical shifts of each RA proton in order to collect in

82 e analysis also provides the limiting proton chemical shifts of EB in each complex which have been us

83 The 13C NMR chemical shifts of enzyme-bound product demonstrate that

84 Chemical shifts of equivalent carbons from 1-4 show that

85 The chemical shifts of exchangeable and non-exchangeable pro

86 d on the basis of the tertiary structure and chemical shifts of folded resonances.

87 ully compared the (1)H, (15)N, and (13)C NMR chemical shifts of four A beta peptides that had the Met

88 onoclonal antibodies (mAbs) by comparing NMR chemical shifts of free OspA and those in Fab complexes.

89 Both (77)Se and (125)Te NMR chemical shifts of given chalcogenide ligands were ident

90 uclear magnetic resonance technique that the chemical shifts of glucose H-6 and alpha-carbon protons

91 We deduce a relationship between the chemical shift of H(-) and the distance from the H(-) io

92 e the link between geometrical structure and chemical shift of H(-) ions in an oxide host, mayenite,

93 was experimentally probed by monitoring the chemical shift of H-bonded Ru-(H2) complexes using NMR s

94 CD spectra without concentration dependence, chemical shifts of H(alpha) that are close to the random

95 plexes were identified by changes in the NMR chemical shifts of H8, H1, H4, 15N7, and 15N4.

96 Comparison with the 15N chemical shifts of halide salts of protonated Schiff bas

97 bition constants (Ki 170-1.2 microM) and the chemical shifts of His 57-Hdelta1 (delta2, 2-dimethylsil

98 omplexes, measurements also were made of the chemical shifts of His 57-Hepsilon1 (delta2,2-dimethylsi

99 tion, we have measured the imidazole (1)H(N) chemical shifts of His37 at different temperatures and p

100 We report here (13)C and (15)N chemical shifts of His37 in the cytoplasmic-containing M

101 euterium isotope effects on the geometry and chemical shifts of hydrogen-bonded protons to probe the

102 We also measured (13)C(alpha) chemical shifts of individual residues as a function of

103 ization magic-angle spinning NMR showed that chemical shifts of inhibitors (13)C-labeled in the sugar

104 In addition, the 1H NMR chemical shifts of isolated zinc knuckle peptides are ve

105 (13)C alpha chemical shifts of isotopically labeled synthetic MLT re

106 Deviations of the chemical shift of key protons in each isomer relative to

107 ter; significant changes are observed in the chemical shifts of key residues in the filter as the pot

108 experiments on Abeta(1-42) oligomers reveal chemical shifts of labeled residues that are indicative

109 The chemical shift of Li polysulfides in (7) Li NMR spectros

110 The 1H NMR chemical shifts of lipid signals were identical to conve

111 However, the C alpha chemical shifts of M60-G73, A83-A90, and other residues

112 The carbon chemical shifts of methyl groups are particularly sensit

113 g, each diastereomer exhibits characteristic chemical shifts of methyl resonances in its (1)H and (13

114 clear magnetic resonance measurements of the chemical shift of methylcyclohexane in solution showed f

115 ent alpha1(V) THP subtly perturbed amide NMR chemical shifts of MMP-12 not only in the active site cl

116 The chemical shifts of most resonances were very close to th

117 (1)H, (15)N, and (13)C chemical shifts of MUP-I were assigned using triple reso

118 Comparison of chemical shifts of mutant and WT proteins reveals that t

119 In contrast, the (1)H and (15)N chemical shifts of N-1H in the PNP.Hx complex are shifte

120 Though the (1)H and (15)N NMR chemical shifts of N-acetyl- and N-sulfoglucosamine resi

121 NMR spectroscopy was used to investigate the chemical shift of nanotube carbons on m- and s-SWNTs (me

122 and completely assign the nonaromatic (15)N chemical shifts of natural abundance bleomycin in the tw

123 derable increases in the nucleus-independent chemical shift of nearby species, in agreement with our

124 e is no marked correlation between the (31)P chemical shifts of neighboring phosphate tetrahedra.

125 The 13C chemical shifts of nicotinamide C4 of NAD+ in these epim

126 Deviation in Shifts (BIRDS), which utilizes chemical shifts of non-exchangeable protons from macrocy

127 The heme substituent 1H NMR chemical shifts of NP2-D1A and those of its imidazole, N

128 A single Mosher ester is made, and the chemical shifts of pairs of resonances related by local

129 Based on the chemical shift of peaks in the (31)PMRS spectrum, intrac

130 Chemical shifts of perdeuterated [U-15N]CYP101 backbone

131 The patterns of changes in the chemical shifts of protein resonances and, particularly,

132 ) has been developed to predict (13)C(alpha) chemical shifts of protein structures.

133 faces can be mapped out by comparison of the chemical shifts of proteins within solid-state complexes

134 ion, and the significant perturbation of the chemical shifts of protons at C-11, H2C, and H20 of U466

135 The chemical shifts of protons in the thiolane 1-oxide ring

136 its native structure was found to revert the chemical shifts of R249S back towards the wild-type valu

137 Perturbations of chemical shifts of residues coordinating the methionine

138 Chemical shifts of residues involved in the ptyr binding

139 and E44D mutants with dGTP showed changes in chemical shifts of residues lining the active site cleft

140 Binding of specific DNA caused significant chemical shifts of residues on the DNA-binding interface

141 enzymes with dGTP show changes in 15N and NH chemicals shifts of residues in a cleft formed by beta-s

142 ike organic molecule leads to changes in the chemical shift of resonances from multiple residues in t

143 using sequence-dependent differences in the chemical shifts of resonances for the backbone CalphaH p

144 (13)C and (15)N anisotropic chemical shifts of RTD-1 in oriented PC bilayers indicat

145 in the spectra of the denatured protein with chemical shifts of sequenced peptides derived from the p

146 a showed both line broadening and changes in chemical shifts of several peptide amide proton resonanc

147 Signal intensity characteristics and chemical shifts of silicone in the two locations were id

148 The sulfamate group (1)H and (15)N chemical shifts of six GAG microenvironments were assign

149 The (13)C chemical shifts of six tertiary amines of unambiguous co

150 MR spectroscopy to assign all (1)H and (13)C chemical shifts of Snn and isoAsp and found characterist

151 Comparison of the chemical shifts of sNRE and b2NRE in complex with nucleo

152 ure, anomalous temperature dependence of the chemical shifts of some resonances, and exchange contrib

153 The chemical shifts of specific (13)C and (15)N labels distr

154 The NMR chemical shift of spin 1/2 nuclei in a polyprotic molecu

155 r coupling turns out to be a function of the chemical shift of spin S.

156 d has been utilized to predict the beryllium chemical shifts of structurally characterized complexes

157 The chemical shifts of subtilisin complexes with peptidyl TF

158 The (13)C NMR chemical shifts of synthetic 3 matched closely those cor

159 ning of the 13CO NMR resonance; however, the chemical shift of the 13CO resonance is unchanged, indic

160 Fortuitously, the 1H chemical shift of the acetate methyl resonance depends o

161 The (13)C NMR chemical shift of the alkylidyne carbon increases with i

162 The chemical shift of the amino nitrogen was deshielded by N

163 The (129)Xe NMR chemical shift of the aqueous Xe@[2](6+) species (308 pp

164 s are sensitive to protonation, and the (1)H chemical shift of the Bronsted site itself reflects hydr

165 In addition, the (1)H chemical shift of the C3-H is also shifted upfield by 1.

166 s also shifted upfield by 1.31 ppm while the chemical shift of the C4 HD-CoA carbon is unchanged upon

167 sented here permit extraction of the precise chemical shift of the carbonyl environment for each (13)

168 3 labeling studies showed that the (13)C NMR chemical shift of the carbonyl resonance increases with

169 The (13)C chemical shift of the central carbon atom of carbenes in

170 ed" xenon to avidin leads to a change in the chemical shift of the encapsulated xenon in addition to

171 The (15)N NMR chemical shift of the essentially planar nitrogen atom o

172 oop turns of the GCA, AAA and GAG types, the chemical shift of the H4' proton of the loop deoxyribose

173 In addition, the chemical shift of the H8 proton (7.51 ppm) of dA(6) appe

174 ed [(1)H,(1)H]-NOESY experiments, adding the chemical shift of the heavy atom attached to the hydroge

175 Likewise, the major perturbation in chemical shift of the histidine H2 and guanine G5 proton

176 Using the chemical shift of the histidine H2 proton in cells incub

177 Changes in the chemical shift of the inner NH protons as well as the or

178 ed (LBHB) diad His 57-Asp 102 and the 1H NMR chemical shift of the LBHB proton in tetrahedral, hemike

179 surprisingly asymmetric changes in the (13)C chemical shift of the ligand methyl groups indicate that

180 annopyranosides is discussed in terms of the chemical shift of the mannose H5 resonance and the (1)J(

181 bstituents as to significantly influence the chemical shift of the methyl group.

182 The chemical shift of the micropore peak is observed to evol

183 The chemical shift of the modified 15N resonance (delta = 86

184 binding affinity of a receptor and the (15)N chemical shift of the nitrogen atoms of its binding cent

185 change in the J coupling with respect to the chemical shift of the observed (F(2)) and neighboring (F

186 copic differentiation based on the (13)C NMR chemical shift of the parent and protonated derivatives

187 (31)P-MRS measurements of the chemical shift of the pH probe, 3-aminopropylphosphonate

188 onance spectroscopy experiments by the (31)P chemical shift of the pH(e) marker 3-aminopropylphosphon

189 itution, a large upfield change in (31)P NMR chemical shift of the phosphorothioate peak (Delta appro

190 ter), intracellular pH (pHi, measured by the chemical shift of the Pi resonance) and extracellular pH

191 The (15)N chemical shift of the Schiff base in K indicates that co

192 trans retinylidene chromophore and the (15)N chemical shift of the Schiff base nitrogen in the active

193 The (29)Si chemical shift of the silylium cation indicates that it

194 free and tricoordinate, whereas the (119)Sn chemical shift of the stannylium cation indicates that i

195 basic conditions, it is noteworthy that the chemical shift of the Y45 C epsilonH resonance is invari

196 n the pH 4 state, indicated by the secondary chemical shifts of the (13)C(alpha), (13)CO, (1)H(alpha)

197 Chemical shifts of the (19)F resonances exhibited differ

198 emperature dependence of the line widths and chemical shifts of the 19F resonances were used to estim

199 Since (13)C(alpha) chemical shifts of the 20 amino acids, which span a wide

200 The pH dependence of the chemical shifts of the 31P resonances of enzyme-bound su

201 ote a correlation between (1)H and (13)C NMR chemical shifts of the acrylamide with GSH reaction rate

202 nges to both CaM lobes as indicated by amide chemical shifts of the amino acids of CaM in (1)H-(15)N

203 N), (15)N, (13)Calpha, (13)Cbeta, and (13)C' chemical shifts of the ankyrin repeat protein IkappaBalp

204 Varying the donor group does not change the chemical shifts of the aromatic hydrogen and carbon atom

205 measurements of (a) the pD dependence of the chemical shifts of the Asp carboxyl carbons and (b) the

206 rying the acceptor group does not change the chemical shifts of the atoms in the donor-substituted ph

207 Chemical shifts of the backbone (15)N, (1)H, and (13)C r

208 The chemical shifts of the backbone atoms indicate that the

209 We have assigned the chemical shifts of the backbone atoms of the 32 kDa liga

210 Major changes were observed in the chemical shifts of the backbone resonances and in the pa

211 the spectroscopy data by calculation of the chemical shifts of the beta-phosphate peak of ATP.

212 ing that the same factors that determine the chemical shifts of the boron nuclei also govern the chem

213 tes that the same factors that determine the chemical shifts of the boron nuclei also govern the chem

214 On the basis of chemical shifts of the BPP34C10, its internal p-hydroqui

215 The chemical shifts of the C(epsilon1) and C(delta2) protons

216 y, binding to enoyl-CoA hydratase causes the chemical shifts of the C1 and C3 HD carbons to move down

217 Upon binding to oxidized pMCAD, the chemical shifts of the C1, C2, and C3 HD carbons are shi

218 The (13)C NMR chemical shifts of the carbocations were calculated usin

219 (13)C, (17)O, and (33)S NMR chemical shifts of the cations and dications were calcul

220 The structures and (13)C NMR chemical shifts of the cations were calculated at the GI

221 The experimental (1)H chemical shifts of the CH and CH(2) protons are assigned

222 The (13)C' chemical shifts of the coiled-coil backbone carbonyl gro

223 (13)C and (11)B NMR chemical shifts of the compounds were also calculated us

224 on of a particular J coupling with the (31)P chemical shifts of the considered nucleus and the couple

225 esulting from functional groups matching the chemical shifts of the constituents making up myelin lip

226 ted hydriodo boron compounds and the 13C NMR chemical shifts of the corresponding isoelectronic and i

227 The (31)P NMR chemical shifts of the corresponding rNHC-phosphinidene

228 ations between the J couplings and the (31)P chemical shifts of the coupled nuclei that are much clea

229 Determination of the13C chemical shifts of the cytosine C6 and C5 and their one-

230 The isotropic 1H and 13C NMR chemical shifts of the DFT-optimized structures were cal

231 but rather to temperature dependence of the chemical shifts of the diastereotopic hydrogens, which a

232 dicated that a temperature dependence of the chemical shifts of the diastereotopic protons results in

233 The 31P chemical shifts of the diphosphate moiety of the protein

234 The (13)C and (15)N chemical shifts of the DNA bases have above-average valu

235 Changes in chemical shifts of the DNA upon complex formation and in

236 A similar trend was noted for the UQ chemical shifts of the DsbA(C33S)-DsbB(WT) heterodimer,

237 (15)N chemical shifts of the EIS obtained from the RD-NMR anal

238 Chemical shifts of the F2 modules and the (1)F2(2)F2 pai

239 The anomalous upfield chemical shifts of the H1' and H4' protons in [GGA]2 mot

240 The chemical shifts of the H1' and H4' protons of the centra

241 ImH ligand could be determined from the (1)H chemical shifts of the heme methyls, and the rate of int

242 ons were then derived using the experimental chemical shifts of the Htt peptide at low and neutral pH

243 Analysis of the H(alpha), H(N) and 15N chemical shifts of the human alpha-LA molten globule at

244 The 11B NMR chemical shifts of the hypercoordinated hydriodo boron c

245 investigation of the origins of the 13C NMR chemical shifts of the imidazole group in histidine-cont

246 The chemical shifts of the imidazole hydrogen atoms exhibite

247 n of Mg(2+) induced selective changes to the chemical shifts of the imino protons of a GCGA tetraloop

248 The range of the chemical shifts of the indole nitrogens suggests that al

249 The 13C NMR chemical shifts of the intriguing dication 14 were calcu

250 The 13C NMR chemical shifts of the isoelectronic analogue tert-butyl

251 ar the lesion site; away from this site, the chemical shifts of the major and minor conformer protons

252 The structure and 13C and 29Si NMR chemical shifts of the model trimethylsilylated carboxon

253 (13)C NMR chemical shifts of the nitrile carbon in cyclohexanecarb

254 Structures and (13)C and (11)B NMR chemical shifts of the onium-carbonium dications and the

255 It is shown that the (13)C chemical shifts of the phenolic residues of A...H...X(-)

256 The solid-state NMR chemical shifts of the PLP pyridine ring nitrogen and ad

257 ta((X)Y)n,s (n = (15)N) and the (13)C(alpha) chemical shifts of the preceding residue X.

258 The 13C chemical shifts of the primary visual photointermediate

259 The chemical shifts of the prochiral hydrogens of authentic

260 The (13)C chemical shifts of the protonated derivatives are solely

261 olecular mechanical calculations of (1)H NMR chemical shifts of the protons in the active site hydrog

262 The chemical shifts of the protons of the methyl group, whic

263 e assigned the imidazole ring (1)H and (15)N chemical shifts of the proximal and distal histidines in

264 The chemical shifts of the pyrenyl moiety were dispersed ove

265 The (31)P chemical shifts of the resting forms of the yeast and hu

266 can be accurately determined, while the (1)H chemical shifts of the Rh...H-C motif can be determined

267 Because the nitrogen chemical shifts of the Schiff base indicate interaction

268 The (1)H NMR chemical shifts of the side-chain amide protons of Asn34

269 The pH dependence of the 13C chemical shifts of the side-chain carboxyl carbons of al

270 We present here the determination using NMR chemical shifts of the structure (PDB code 2K5X) of the

271 (13)C NMR chemical shifts of the structures were also calculated b

272 Significantly, we have shown that the chemical shifts of the substrate-binding domain and the

273 n illustrate the power of the (1)H and (15)N chemical shifts of the sulfamate NH groups for the struc

274 The chemical shifts of the TnC-bound peptide resonances are

275 F3, but not F6, can significantly alter the chemical shifts of the tryptophan indole N-H protons nea

276 ants criteria, but a diagnostic based on the chemical shifts of the two olefinic protons located at t

277 d in the MGS-PGH complex on the basis of the chemical shifts of their Cdelta and C(epsilon) protons.

278 frequencies of their carboxylate groups, the chemical shifts of their protons, and their diffusion co

279 ing the denaturant concentration shifted the chemical shifts of these residues towards theory random

280 mples a single species was detected, but the chemical shifts of these two distinct species differed b

281 Additionally, the chemical shifts of these two residues changed almost ide

282 Change in the chemical shifts of thiophene -CH-protons during the cour

283 Chemical shifts of three C-terminal carbonyl carbons of

284 The chemical shifts of Trp C(gamma) in several proteins, hen

285 st likely that the misassignment of the (1)H chemical shifts of two methyl groups has led to the wron

286 rR and found similar, minor changes in (19)F chemical shifts of tyrosine residues in the free protein

287 The calculated (15)N and (13)CO chemical shifts of Val(16) in DLPC reveal that there are

288 The (13)CO and (15)N chemical shifts of Val-16 labeled PG-1 indicate that the

289 ffects have significant contributions to the chemical shift of Xe in the cage and enabled the replica

290 use the linear temperature dependence of the chemical shift of xenon dissolved in adipose tissue to d