ライフサイエンスコーパス: crystallographic

1 th molecules stacked approximately along the crystallographic a-axis.

2 kness and shear stress, and control over the crystallographic alignment of the confining surfaces, we

3 xible DNA ligand shell, led to an unexpected crystallographic alignment of the entire superlattice, a

4 Finally, X-ray crystallographic analyses of a spectrum of analogues cle

5 Crystallographic analyses of representative structures r

6 Crystallographic analyses of two compounds demonstrated

7 X-ray crystallographic analyses revealed that, similar to 8-ox

8 hemical and biophysical tools, LC-MS/MS, and crystallographic analyses, we identified key residues es

9 a bowl-shaped geometry, as revealed by X-ray crystallographic analysis and density functional theory

10 ge this gap uniquely enabling both nanoscale crystallographic analysis and the low-dose formation of

11 X-ray crystallographic analysis based on Flack parameters assi

12 Crystallographic analysis confirmed that the compound ta

13 Crystallographic analysis demonstrates that P-4G2 binds

14 As the key structural outcome, the X-ray crystallographic analysis discloses the consequences of

15 In this study, X-ray crystallographic analysis has been used to authenticate

16 ation assays, surface plasmon resonance, and crystallographic analysis of a 1.5 angstrom structure de

17 Crystallographic analysis of DdPhyA enables comparisons

18 That is defined by crystallographic analysis of phenylphosphonylated reacti

19 A crystallographic analysis of the LegK7-MOB1A complex rev

20 Crystallographic analysis of the obtained compounds reve

21 X-ray crystallographic analysis of three compounds (11a, 11d,

22 The crystallographic analysis of two IDT derivatives yielded

23 X-ray crystallographic analysis revealed a planar backbone wit

24 Crystallographic analysis revealed structural changes th

25 tic investigation based on spectroscopic and crystallographic analysis revealed that a putative reduc

26 Crystallographic analysis revealed that HIPP interacts w

27 Crystallographic analysis reveals that this specificity

28 Molecular dynamics simulations and crystallographic analysis show how distinct hydrogen-bon

29 hylococcus aureus, and biochemical and X-ray crystallographic analysis showed that SpFakB1 selectivel

30 Single-crystal X-ray crystallographic analysis shows that the cage contains a

31 X-ray crystallographic analysis successfully determined the st

32 of 1 was established by single-crystal X-ray crystallographic analysis using Cu Kalpha radiation.

33 -azotriazapentalene, which was confirmed via crystallographic analysis.

34 Crystallographic and 2D k-space spectroscopic analysis r

35 We use ab initio calculations together with crystallographic and adsorption data to show that the dy

36 Here, using comparative crystallographic and biochemical analyses of WT human CY

37 In this study, we use crystallographic and biochemical techniques to further d

38 er mechanism of action-as elucidated through crystallographic and biological studies-is likely due to

39 We explored this question via crystallographic and biophysical analyses of PKM2 mutant

40 Crystallographic and calorimetric data of wild-type and

41 lauea Volcano, Hawai'i, using an integrative crystallographic and chemical approach places quantitati

42 s acidity through an array of spectroscopic, crystallographic and computational characterization tech

43 tion of Trp9, site-directed mutagenesis, and crystallographic and computational chemical studies to s

44 Here, we present crystallographic and cryo-electron microscopic structure

45 Crystallographic and density functional theory (DFT) ana

46 electron conductivity of 1.10 mS m(-1), with crystallographic and electrochemical stability upon thou

47 NMR, biochemical, crystallographic and genetic data collectively indicate

48 Using results from X-ray crystallographic and isotope labeling experiments, a mec

49 Here, crystallographic and kinetic analyses of 2-nt gap-fillin

50 Crystallographic and NMR analysis confirms an earlier re

51 Crystallographic and NMR spectroscopic characterization

52 nd the results are consistent with the X-ray crystallographic and NMR spectroscopic data.

53 ions, which are in full agreement with X-ray crystallographic and NMR spectroscopic results.

54 X-ray crystallographic and NMR titration studies indicate dist

55 rtiary aliphatic sulfonamides was studied by crystallographic and quantum chemical methods.

56 Through crystallographic and solution-based studies we show that

57 work solids, and the capability of combining crystallographic and spectroscopic analysis, will greatl

58 In this article, we present crystallographic and spectroscopic evidence of a tunable

59 Crystallographic and spectroscopic studies confirm assem

60 epimeric imine (1-pyrroline) forms; previous crystallographic and spectroscopic studies have reported

61 erein we report a comprehensive theoretical, crystallographic and spectroscopic studies on the UO(2)(

62 Here, we present crystallographic and vibrational-spectroscopic insights

63 X-ray crystallographic and vibrational-spectroscopic studies o

64 as to how the symmetry breaking occurs on a crystallographic and, therefore, long-range level.

65 Here we present spectroscopic, crystallographic, and biochemical evidence that the cofa

66 ined NMR spectroscopic, single-crystal X-ray crystallographic, and computational (DFT) investigation

67 A combination of NMR and IR spectroscopic, crystallographic, and computational data reveal that the

68 e importance of this cofactor using kinetic, crystallographic, and computational modeling approaches.

69 A combined spectroscopic, crystallographic, and computational study provides insig

70 presented, based on NMR spectroscopic, X-ray crystallographic, and DFT data.

71 e been subjected to NMR spectroscopic, X-ray crystallographic, and reaction kinetic measurements in o

72 Using crystallographic approaches and radiolabeled competitive

73 lithium layered oxides with different grain crystallographic arrangements and establish a model to q

74 rometallophosphorane 1a(F) .Fp that allows a crystallographic assessment of the variance in the Fe-P

75 n this Letter, the formatting of some of the crystallographic axes was incorrect.

76 ctivity direction does not coincide with any crystallographic axis.

77 the Ni and Re magnetic sublattices along the crystallographic b-axis.

78 (6)] octahedra, which are arranged along the crystallographic c axis, separated by nonmagnetic K ions

79 e range of 295-523 K when measured along the crystallographic c-axis.

80 sign of porphyrin-binding proteins; however, crystallographic characterization has been elusive, limi

81 Detailed crystallographic characterization of a tri-aspartate met

82 ediates, which is supported by isolation and crystallographic characterization of key Au(III) interme

83 We also report spectroscopic and crystallographic characterization of rare Cu-hemiacetala

84 After in-depth crystallographic characterization of single-crystal bloc

85 , which constitute the first achievements of crystallographic characterization of the full 360 degree

86 linker installation were highlighted through crystallographic characterization of the intermediate, a

87 g only six twin systems, tuning for improved crystallographic compatibility will be of limited value.

88 ameters in Ba(Ti(1-x)Zr(x))O(3) for improved crystallographic compatibility, even at low doping level

89 Crystallographic, computational, electrochemical, and op

90 Spectroscopic and crystallographic data and DFT calculations support a "pr

91 NMR and X-ray crystallographic data demonstrate that at least one stru

92 X-ray crystallographic data for relevant Pd-AMPP* complexes an

93 novel series of inhibitors, along with X-ray crystallographic data for selected examples bound to hum

94 Crystallographic data of 8a-bound hDDAH-1 illuminated a

95 ts, as can be deduced from spectroscopic and crystallographic data of various intermediates; this inc

96 Crystallographic data prove the identity of synthetic (-

97 Topographic steric maps derived from crystallographic data provided insights into the basis f

98 Biochemical and crystallographic data show how the mutated residues modu

99 Our spectroscopic and crystallographic data suggest that the local conformatio

100 ecular dynamics simulations, based on recent crystallographic data, on the 8-17 DNAzyme at four state

101 ic, spectroscopic, and high-resolution X-ray crystallographic data, reaction of O(2) with the di-Fe(2

102 ( Oxy-GQ), in agreement with high-resolution crystallographic data.

103 using bond distances from readily-available crystallographic data.

104 d critical analysis during interpretation of crystallographic data.

105 red using exit vector plot analysis of X-ray crystallographic data.

106 l NMR, IR, electrochemical and in some cases crystallographic data.

107 dology that incorporate ensemble modeling of crystallographic data.

108 mentally and computationally with the aid of crystallographic data.

109 atic sulfonamides published in the Cambridge crystallographic database, Paquette's sultams (i.e., bri

110 A joint analysis of ~170 crystallographic datasets probing different signaling st

111 derstanding of the interrelationship between crystallographic defects and redox reactions.

112 study illustrates that a precise control of crystallographic defects and their distribution can pote

113 Through Laue X-ray microdiffraction, many crystallographic defects are spatially identified and st

114 Crystallographic defects exist in many redox active ener

115 The negative effect of crystallographic defects in the heteroepitaxial material

116 The role of crystallographic defects on structure evolution and perf

117 These crystallographic defects play a vital role in determinin

118 Herein, crystallographic defects, such as geometrically necessar

119 e angle between the edge orientation and the crystallographic direction significantly affects the opt

120 ure, and diffuse scattering along the [00 L] crystallographic direction that manifests as a rather br

121 of the stress state are considered (for the crystallographic directions observed here).

122 particular the relative angle between their crystallographic directions, modifies properties of the

123 pace connected by 12-ring openings along all crystallographic directions.

124 ing in-plane dopant placement along specific crystallographic directions.

125 coupling in this system that occurs in all 3 crystallographic directions.

126 Crystallographic dislocation has been well-known to be o

127 be non-centrosymmetric and we herein present crystallographic evidence as to how the symmetry breakin

128 Crystallographic evidence suggests that the polarized [R

129 Kinetic and crystallographic experiments showed that the glycosyltra

130 thin polycrystalline gold films (predominant crystallographic face is (111)) that are triggered to un

131 d, bend, and fracture, mainly along specific crystallographic faces, before releasing N(2).

132 that the two active sites considered on each crystallographic facet demonstrate OER activities remark

133 tiple OER pathways and intermediates on each crystallographic facet of a potential electrocatalyst.

134 the OER activities of the two most abundant crystallographic facets of pristine beta-NiOOH, the (000

135 st overpotential active sites on these three crystallographic facets operate via different mechanisms

136 We show that TcpB is a homotrimer in its crystallographic form as well as in solution and is pres

137 A crystallographic fragment screening campaign against the

138 gaps, magnetic moments, type of magnetic and crystallographic ground state, bond disproportionation a

139 is used to spatially and temporally quantify crystallographic heterogeneities within and between part

140 , we introduce BinaryCIF, a serialization of Crystallographic Information File (CIF) format files tha

141 Crystallographic information, photoproduct distributions

142 Drawing on X-ray crystallographic information, we designed GS-6207 to bin

143 ow that PIP(2) interacts most tightly at the crystallographic interaction sites, outcompeting other l

144 inding assays were then used to validate the crystallographic interface.

145 Time-resolved crystallographic investigations on biological macromolec

146 X-ray crystallographic investigations revealed a nonplanar ori

147 ins (4-10%) of nanomaterials and the uniform crystallographic lattice distortion strains (4-10%) of t

148 ough this analysis, insights into changes in crystallographic lattice parameters, water siting inform

149 cheme and the identification of analogues of crystallographic ligands.

150 The physical, crystallographic, mechanical, electrochemical, and trans

151 human DHFR based on kinetic, NMR, and X-ray crystallographic methods.

152 rtant for their mechanical properties as are crystallographic microstructures in metallic alloys.

153 ps strongly correlate with gradually varying crystallographic misorientations detected by electron ba

154 ementing currently available high-resolution crystallographic models.

155 es of up to 254 gigapascals that reveals the crystallographic nature of the transitions from phase I

156 Reported here is the first crystallographic observation of stereospecific bindings

157 Crystallographic, optical, electrochemical, and computat

158 ssion electron diffraction (PED) techniques, crystallographic orientation and the radiation-induced r

159 ntrol their position, direction, length, and crystallographic orientation and to enable their large-s

160 Architecting grain crystallographic orientation can modulate charge distrib

161 The resultant Bragg-dip shifting has enabled crystallographic orientation mapping of bulk single crys

162 of the substrate nanocrystal must guide the crystallographic orientation of the overgrowth phase(7).

163 eal that cellulose crystals have a preferred crystallographic orientation with the (200) and (110)/([

164 interplay between charge distribution, grain crystallographic orientation, and performance remains a

165 of surface activity, with grains of specific crystallographic orientation, grain boundaries and areas

166 n prevails in polycrystalline particles, the crystallographic orientation-guided redox reaction gover

167 1/3)Nb(2/3))O(3)-0.32PbTiO(3) in a different crystallographic orientation.

168 crystals, aligned exclusively in the zigzag crystallographic orientation.

169 h-quality compact thin films with favourable crystallographic orientation.

170 imeter-sized single-crystal domains and pure crystallographic orientations are achieved, revealing a

171 Analysis of crystallographic orientations show a moderately strong c

172 n-group nitride semiconductors along certain crystallographic orientations.

173 ch as dots, rings or lines, along with other crystallographic orientations.

174 l and garnet crystal structures with varying crystallographic orientations.

175 egardless of the different morphologies, the crystallographic packing is nearly identical and is not

176 ith twinned domains exhibit markedly altered crystallographic phase and phase transition characterist

177 ad to an FCC to hexagonal close packed (HCP) crystallographic phase transformation upon a 10 dpa radi

178 voids the phase separation into two distinct crystallographic phases with different magnetic structur

179 Detailed X-ray crystallographic, photophysical and computational analys

180 Misorientation of the (001) crystallographic plane has been visualised and a new spi

181 GO, each layer of Li atoms grows along (110) crystallographic plane of the Li crystals because of the

182 f matter where the conductivity in its (001) crystallographic planes is protected by crystallographic

183 es have focused on the properties of various crystallographic planes of metallic substrates, as well

184 001) crystallographic planes is protected by crystallographic point group symmetries.

185 It has two different crystallographic polymorphs, alpha- and beta-Ni(OH)(2) ,

186 istribution of the Li atoms over the diverse crystallographic positions between the [AlP(4) ](9-) tet

187 sence of one type of Mo species in different crystallographic positions in the MFI framework.

188 Vacancies created at selected crystallographic positions of MOFs promoted their photoc

189 tal all iron ions, sitting in five different crystallographic positions, are Fe(3+) in the high-spin

190 rrangements that is hidden from conventional crystallographic powder analysis.

191 raphic orientations show a moderately strong crystallographic preferred orientation (CPO) for calcite

192 e), physical properties (physical structure, crystallographic properties, optical absorption, charge

193 Crystallographic refinements of high-resolution synchrot

194 esults suggest that a three-dimensional (3D) crystallographic registry within cage-like superstructur

195 Here, based on the geometric crystallographic relationship, we propose to utilize the

196 The crystallographic results highlight the ability of bicycl

197 ontradictory biochemical, spectroscopic, and crystallographic results.

198 Our crystallographic screen identified 71 hits that span the

199 he Magnetic Materials Database on the Bilbao Crystallographic Server, which contains more than 549 ma

200 Wadsley-Roth crystallographic shear phases form a family of compounds

201 niobium-titanium oxide or pure niobium oxide crystallographic shear phases.

202 stablish arise from the compound-independent crystallographic shear structure and are therefore likel

203 lization of intragranular deformation due to crystallographic slip acts as a precursor for crack init

204 The crystallographic snapshots and kinetic data indicate tha

205 In particular, we have determined crystallographic snapshots of DrDXPS in two states along

206 In this study, we have obtained crystallographic snapshots that reveal ligand-induced or

207 fect CTR dynamics not observed in the static crystallographic snapshots.

208 ure and mechanism of these two enzymes using crystallographic, spectroscopic and fast kinetics techni

209 We introduce the notion of a "crystallographic sphere packing," defined to be one whos

210 We also report in-depth X-ray crystallographic structural analyses of each isoform at

211 Crystallographic structural analyses reveal much about t

212 X-ray crystallographic structural analysis of the apo Ega3 and

213 Using an integrative approach that combines crystallographic structural information about the globul

214 X-ray free-electron lasers (XFELs) enable crystallographic structure determination beyond the limi

215 X-ray crystallographic structure determination revealed that t

216 , the presence of defects, or pinning of the crystallographic structure in metastable phases induced

217 The crystallographic structure is within 0.6 angstrom of the

218 In this work, we present an X-ray crystallographic structure of a cyclic beta-sheet peptid

219 nby were produced, providing the first X-ray crystallographic structure of a zinc corrin.

220 structure of E. coli DnaA, modeled upon the crystallographic structure of Aquifex aeolicus DnaA, pre

221 levan synthesis reaction, we determined the crystallographic structure of Bacillus subtilis LS (SacB

222 The X-ray crystallographic structure of N-Me-d-Gln(4),d-aza-Thr(8)

223 The X-ray crystallographic structure of Pb matches previous models

224 A high-resolution X-ray crystallographic structure of the beta-galactose-contain

225 The crystallographic structure of the BMV capsid shows four

226 erential plasticity, we determined the X-ray crystallographic structure of the CYP3A5 substrate-free

227 The complex crystallographic structure of these materials poses a ch

228 g the 2011 report of a high-resolution X-ray crystallographic structure resolving the site of catalys

229 aper describes the chemical synthesis, X-ray crystallographic structure, and antibiotic activity assa

230 ination of geometric characterization of MOF crystallographic structure, molecular simulation, and vi

231 Here, we present the atomic resolution crystallographic structure, the function, and the ion-bi

232 abilizing molecules as well as the ruthenium crystallographic structure.

233 f the alignment of these dyes imposed by the crystallographic structure.

234 dition to previously observed characteristic crystallographic structure.

235 In particular, all crystallographic structures are consistent with an achir

236 The x-ray crystallographic structures of compounds bound to CA IX

237 induced allosteric networks present in x-ray crystallographic structures of FVIIa, which previously o

238 olution-phase biophysical studies, and X-ray crystallographic structures of hexamers formed by macroc

239 Our studies here sought to utilize X-ray crystallographic structures of HsNudT16 in complex with

240 biophysical analyses of PfHsp70-x, including crystallographic structures of its catalytic domain and

241 We have determined the cGMP-free crystallographic structures of PKG from Plasmodium falci

242 The presence of knots in crystallographic structures of proteins have stimulated

243 e Cre-loxP system has largely been guided by crystallographic structures of tetrameric synaptic compl

244 Here, we solved the X-ray crystallographic structures of the BlaR1 and MecR1 senso

245 ulting kinetic data were consistent with the crystallographic structures of the highly homologous Xan

246 The three PfMyoA crystallographic structures presented here provide a blu

247 Crystallographic structures reveal that the binding pock

248 urthermore, based on the analysis of several crystallographic structures, a distinction between toxin

249 he N-terminal globular domain, unresolved in crystallographic structures, comprises a flexible loop t

250 simulations starting from SAS-6 head domain crystallographic structures, including that of the human

251 Here, ensemble refinement of crystallographic structures, which uses multiple copies

252 y (1)H-(15)N HMBC NMR spectroscopy and X-ray crystallographic structures.

253 proline-centered tripeptides extracted from crystallographic structures.

254 of this secondary site has been indicated by crystallographic studies as two symmetric surface pocket

255 Further X-ray crystallographic studies confirmed the assigned structur

256 Phosphoproteomics, quantitative binding and crystallographic studies demonstrate that 14-3-3 binds t

257 Biophysical and crystallographic studies demonstrated that RABL3 formed

258 The combination of EPR with X-ray crystallographic studies has revealed the mixed Li/Mn co

259 Crystallographic studies have enabled us to identify the

260 Previous crystallographic studies have shown that Escherichia col

261 of the ED with respect to the RBD, previous crystallographic studies have shown that minor group H5N

262 s bearing the MA mutations and by performing crystallographic studies of in vitro-assembled MA lattic

263 Interestingly, crystallographic studies of ligand-dependent TRPV2 gatin

264 Previous crystallographic studies of the CENP-A nucleosome core p

265 nucleosome structures is mainly based on the crystallographic studies of the nucleosomes containing n

266 In vitro DNA binding assays and crystallographic studies reveal the ZNF410-DNA binding m

267 Crystallographic studies revealed a cation bound at the

268 Crystallographic studies revealed that direct intercalat

269 X-ray crystallographic studies show one isomer with 1,8-pendan

270 Crystallographic studies show that the selectivity is ba

271 Although crystallographic studies show that viral capsids are sta

272 4-dimethylaminopyridine, DMAP), which X-ray crystallographic studies show to have markedly elongated

273 However, recent crystallographic studies suggest that N(2) reduction may

274 Protein crystallographic studies suggest that the house dust mit

275 Here we present solution and X-ray crystallographic studies that indicate a potential role

276 ere, we integrate cellular, biophysical, and crystallographic studies to address this conundrum.

277 tly populated states (hidden to conventional crystallographic studies) can be correlated to the patho

278 nteractions have been documented by numerous crystallographic studies, and now NQO2 is one of the bes

279 A comprehensive X-ray crystallographic study (12 crystal structures), involvin

280 A thorough X-ray crystallographic study depicted their binding mode to bo

281 ure-based drug design, we conducted an x-ray crystallographic study of the SARS-CoV-2 nsp16-nsp10 2'-

282 A comprehensive crystallographic study on a state-of-the-art NFA, Y6, an

283 The crystallographic, surface texturing, and electrochemical

284 t simulations on five representative calcite crystallographic surfaces and observed that the adhesion

285 controlled shapes with selectively displayed crystallographic surfaces, tailored surface strains, sur

286 esolved measurements reveal underlying C(2h) crystallographic symmetry-and thus monoclinic stacking o

287 lternating magnetic sublattices generated by crystallographic symmetry.

288 urea have been discussed using NMR and X-ray crystallographic techniques.

289 nces in active and inactive Cre protomers in crystallographic tetramers.

290 d wild (adult) Lake Sturgeon exhibit extreme crystallographic texture as evidenced by X-ray diffracti

291 re recrystallisation sequence and associated crystallographic texture evolution of Mg-0.8Zn-0.2Ca (wt

292 hydrolyze or decarboxylate reactants on the crystallographic time frame preventing determination of

293 t titration have been also used to study the crystallographic transitions, electrochemical activity,

294 th a molecule of cyclohexadiene (CHD) in its crystallographic unit cell to give 1.CHD as a room tempe

295 normalized atomic displacement parameters of crystallographic water molecules.

296 monstrate that it is now possible to recover crystallographic water structure using restrained MD sim

297 For these simulations, the recall of crystallographic waters using strong peaks in the MD wat

298 For this simulation, the recall of crystallographic waters was much lower.

299 est water density peaks were associated with crystallographic waters.

300 A crystallographic X-ray fragment screen was performed, wh