1 charge distribution from the Te ions at the
crystallographic 8 f sites to the neighboring Co and O i
2 ing of the crystalline series shows that the
crystallographic a-axis, along the channel, can be varie
3 below T C for magnetic fields applied in the
crystallographic ab-plane.
4 When particles assemble in
crystallographic alignment, expulsion of the intervening
5 Subsequent
crystallographic analyses of AChE complexes with the TZ2
6 putational model of the nucleosome, based on
crystallographic analyses of the structure and elasticit
7 NMR and X-ray
crystallographic analyses of the tetrafluorinated methyl
8 Crystallographic analyses with succinate, fumarate, L-ma
9 se complexes could be characterized by X-ray
crystallographic analysis and employed as catalysts for
10 The X-ray
crystallographic analysis confirms that while CIP and CI
11 Furthermore,
crystallographic analysis demonstrated atomic accuracy t
12 Crystallographic analysis demonstrated that the Crwn-THF
13 insights provide simple and accurate optical
crystallographic analysis for liquid-dispersed nanomater
14 An X-ray
crystallographic analysis has shown the compound to be a
15 Crystallographic analysis of 35 different peptide sequen
16 steric inhibitors, a finding rationalized by
crystallographic analysis of allosterically inhibited L-
17 nimized insulin receptors (IRs) have enabled
crystallographic analysis of insulin-bound "micro-recept
18 Traditionally,
crystallographic analysis of macromolecules has depended
19 ency to form fibrils were coupled with X-ray
crystallographic analysis of nine TTR.ligand complexes.
20 lysozyme, and has been employed for routine
crystallographic analysis of organic and inorganic mater
21 annot phosphorylate PtdIns(4,5)P2 Therefore,
crystallographic analysis of the yeast and plant enzymes
22 X-ray
crystallographic analysis of these scaffold nucleoporins
23 Crystallographic analysis provided insights into the inh
24 X-ray
crystallographic analysis revealed that Abeta42 binding
25 Crystallographic analysis reveals architectural features
26 X-ray
crystallographic analysis reveals that 12 adopts a simil
27 The
crystallographic analysis reveals that the thiolate liga
28 Our
crystallographic analysis unveiled the exact position of
29 repare single crystals suitable for accurate
crystallographic analysis was missing.
30 tional significance that extend recent x-ray
crystallographic analysis.
31 es that was unambiguously confirmed by X-ray
crystallographic analysis.
32 We report X-ray
crystallographic and (19) F NMR studies of the G-protein
33 Crystallographic and AFM data were used to build a struc
34 Here we report on a series of
crystallographic and biochemical analyses of an evolutio
35 Crystallographic and biochemical studies on the Pseudomo
36 Here, we report through
crystallographic and biochemical studies that K-80003 bi
37 rward approach to the discrimination between
crystallographic and biological dimers by docking the tw
38 to the fungus Candida albicans Complementary
crystallographic and biophysical characterization of Bsp
39 This combined
crystallographic and computational study provides valuab
40 Consistent with previous
crystallographic and cryo-EM studies, the obtained force
41 Crystallographic and docking studies revealed the main i
42 Here we present
crystallographic and electron microscopic structures of
43 Here, we present our
crystallographic and enzymatic studies of TTPA.
44 Here, we present
crystallographic and functional data showing that the K(
45 Here, we report
crystallographic and functional studies of the TRIM5alph
46 Targeted modifications to CP2 based on
crystallographic and mass spectrometry analyses results
47 We report here on an X-ray
crystallographic and molecular modeling investigation in
48 Crystallographic and mutagenesis studies elucidated a ke
49 Crystallographic and native ion-mobility mass spectromet
50 Crystallographic and quantum chemical studies reveal tha
51 Crystallographic and small-angle X-ray scattering (SAXS)
52 This article describes X-ray
crystallographic and solution-state NMR studies of pepti
53 X-ray
crystallographic and spectroscopic analyses demonstrate
54 We use X-ray
crystallographic and spectroscopic approaches to show th
55 The
crystallographic and spectroscopic characteristics of li
56 Crystallographic and spectroscopic characterization toge
57 e transport domains consistent with previous
crystallographic and spectroscopic studies.
58 nd Selectfluor is presented, together with a
crystallographic and spectroscopic study.
59 experimental data obtained in spectroscopic,
crystallographic,
and calorimetric measurements during e
60 Comparisons of their magnetic,
crystallographic,
and computational characterization to
61 heir microstructures by photophysical, X-ray
crystallographic,
and computational means.
62 and studied them using biochemical, kinetic,
crystallographic,
and computational studies.
63 plexes were assigned by using spectroscopic,
crystallographic,
and magnetic analyses.
64 Results from calorimetric,
crystallographic,
and theoretical analyses suggest that
65 -dependent surface energy and the subsequent
crystallographic anisotropy via ab-initio calculations b
66 We describe here the
crystallographic application of "atom replacement" mimet
67 Using biophysical and
crystallographic approaches, we identify that PrimPol po
68 ntations of the nanocrystals, as well as the
crystallographic axes of the ensuing triclinic colloidal
69 it ferroelectric behavior along two distinct
crystallographic axes.
70 culations and experimentally by a normalized
crystallographic B-factor analysis.
71 redict related data (NMR order parameter, or
crystallographic B-factor).
72 Analyses of the
crystallographic B-factors indicated several regions wit
73 Significantly, the
crystallographic binding poses are distinguished not onl
74 Here we combine
crystallographic,
biochemical and genetic analyses to sh
75 Trends in
crystallographic bond lengths and angles shed light on t
76 oscale AFM results confirm the alteration of
crystallographic characteristics, and the ability of dis
77 stinct, has allowed for the isolation, X-ray
crystallographic characterization and comprehensive spec
78 Herein we report the spectroscopic and
crystallographic characterization of [(N4Py)Fe(III) -O-C
79 ssemblies can also form, as evidenced by the
crystallographic characterization of a Pt10L5 complex an
80 R, infra-red, (57) Fe-Mossbauer, EPR), X-ray
crystallographic characterization of the cluster in both
81 Crystallographic characterization showed the two hydride
82 However, standard
crystallographic characterization through diffraction yi
83 A combination of x-ray
crystallographic,
computational and electrophysiological
84 t the influence of other receptor domains or
crystallographic conditions.
85 However, the resultant reduced
crystallographic control in mussels raises concerns for
86 allography are of comparable quality to cryo-
crystallographic data and can be routinely collected at
87 n interaction were designed, guided by X-ray
crystallographic data and molecular dynamics simulations
88 Using
crystallographic data and the virtual screening of a che
89 Biochemical and
crystallographic data demonstrate a mechanism in which d
90 Here MS, thioflavin T fluorescence, and
crystallographic data demonstrate that while the X-ray s
91 Serial
crystallographic data for molecular replacement already
92 The
crystallographic data identified most of the monosacchar
93 the handling of MOF crystals and analysis of
crystallographic data obtained from single-crystal X-ray
94 irm the current picture derived from NMR and
crystallographic data of domain docking upon ATP binding
95 Furthermore, we report the
crystallographic data of the chiral [Ru(I)H(CO)((S,S)-f-
96 Our analysis of a pilot collection of
crystallographic data sets demonstrates that the informa
97 plete glycoprotein was achieved by combining
crystallographic data with molecular modeling.
98 ment reported here are consistent with X-ray
crystallographic data, and suggest that crystal packing
99 ties that are derived from spectroscopic and
crystallographic data.
100 ructural conservation and localisation using
crystallographic data.
101 x are revealed by the combination of NMR and
crystallographic data.
102 epitaxial nature, low strain character, and
crystallographic defect content of the resultant solid G
103 tions can change at kinks with no observable
crystallographic defect.
104 fness is 'defect-driven', i.e., dominated by
crystallographic defects such as bridging site vacancies
105 Crystallographic defects such as dislocations can signif
106 These novel H2 O2 solvates have high
crystallographic densities (1.96 and 2.03 g cm(-3) , res
107 provide an experimentally validated complete
crystallographic detail of a highly strained BiFeO3 that
108 mal motion and low occupancies, the reliable
crystallographic determination of the guest can be very
109 meningitidis Structural analysis with X-ray
crystallographic diffraction data to 2.0-A revealed that
110 s in cells, and that both occurs through the
crystallographic dimer interface.
111 basis than previously suggested by the MLA10
crystallographic dimer.
112 niform and random orientation of the lattice
crystallographic direction enabled by a photoalignment t
113 way to realize designed micropatterning of a
crystallographic direction of a soft, cubic liquid-cryst
114 Uniform and patterned orientation of a
crystallographic direction of ordered materials is of fu
115 , acetylene molecules react along a specific
crystallographic direction that is perpendicular to thos
116 ctures were tested along the [001] austenite
crystallographic direction using a custom designed magne
117 ansport Jc of 10(5) A/cm(2) at 15 T for main
crystallographic directions of the applied field, which
118 where it contracts and expands in different
crystallographic directions when hosting the inserted Mg
119 The NWs form along the <11-20> 2H-MoTe2
crystallographic directions with lengths in the micromet
120 kappa, located at ~15 K at zero-H along all
crystallographic directions, moves gradually toward lowe
121 e reaction or lithium diffusion in different
crystallographic directions.
122 h is fully incommensurate (ICM) in all three
crystallographic directions.
123 locities of optical phonons in the different
crystallographic directions.
124 validated by both the Harvey-Gray method of
crystallographic-
distance-to-force-constant correlation
125 ogress in experimental investigations on the
crystallographic,
dynamic and kinetic aspects of substra
126 e of the whole molecule, alone or within the
crystallographic environment.
127 ch structural changes were suppressed in the
crystallographic environment.
128 Crystallographic evidence for the protonation of nearby
129 Furthermore, we provide
crystallographic evidence of an organometallic aryl-Co(I
130 Crystallographic evidence suggests that IREDs may be abl
131 and high frame-rate detector allows typical
crystallographic experiments to be performed at room-tem
132 ystals expressing the (001), (012), or (110)
crystallographic face.
133 Crystallographic,
full spectroscopic characterization, a
134 ut is packed as a high 70% solvent content,
crystallographic heptamer.
135 acroscopic etch pit hexagonal profile to the
crystallographic hexagon.
136 The bases are labeled
crystallographic hexagons.
137 s and coactivator peptides, examined through
crystallographic,
hydrogen-deuterium exchange mass spect
138 e we report a fundamental study coupling the
crystallographic imaging capability of laboratory diffra
139 The nanoparticles' ability to remove
crystallographic imperfections renders them more durable
140 Crystallographic imperfections significantly alter mater
141 We selected the nucleants on the basis of
crystallographic information and assembled them onto 707
142 g, as well as the functional significance of
crystallographic interprotomer interfaces.
143 Comparative
crystallographic investigation of CB[7].Diam(NMe3)2, CB[
144 Crystallographic investigations indicate that the S672R
145 ty in primary sequence and cofactor content,
crystallographic,
kinetic, and mass spectrometry analyse
146 ginates from chirality interplay between the
crystallographic lattice and geometric morphology at dif
147 110 cm(3)/g by cobalt insertion in the MoS2
crystallographic lattice, which induces the formation of
148 With this strategy, different
crystallographic lattices using the same particles can b
149 f ENAM mutation on the enamel structure at a
crystallographic level.
150 lly preferred binding modes that differ from
crystallographic ligands.
151 High pressure
crystallographic measurements confirm uniform compressio
152 Our time-resolved
crystallographic measurements with a 10-second delay cap
153 Using low-temperature magnetisation and
crystallographic measurements, we show here for the firs
154 c coordinates of real systems beyond average
crystallographic measurements.
155 Notably, the recent progress in
crystallographic methods led to a breakthrough in elucid
156 tlenecks to structure determination by X-ray
crystallographic methods-that of crystal growth.
157 he extent of cavitation, the orientation and
crystallographic misorientation of each boundary is char
158 zed glycosyltransfer and present an improved
crystallographic model for inhibition of the PBP1b glyco
159 n of this MDFF model with an earlier-derived
crystallographic model for the planar assembly, the indu
160 es (both in the physical crystals and in the
crystallographic model) and (2) crystallographic twinnin
161 C-terminal domain is in good agreement with
crystallographic models derived from ExoU in complex wit
162 Knowledge of the basic
crystallographic modes of slip is critical to understand
163 ain with phosphorylated XRCC1 peptides using
crystallographic,
NMR, and fluorescence polarization stu
164 Possible
crystallographic nomenclatures, to be used to describe l
165 nt a hierarchy of assembly criteria based on
crystallographic observations and subsequently quantify
166 The
crystallographic observations are reinforced by protein-
167 ades, borides have been primarily studied as
crystallographic oddities.
168 The printed films exhibit similar
crystallographic order and chemistry as the original pow
169 We explore how
crystallographic order and orientation affect the tribol
170 s in the xenolith had the same chemistry and
crystallographic orientation as those for inclusions in
171 This revealed a strong
crystallographic orientation dependence of the sliding p
172 he elastic and shear moduli as a function of
crystallographic orientation gleaned from experiments an
173 and sensitivity of this metal's stiffness to
crystallographic orientation help explain why the existi
174 The
crystallographic orientation of a metal affects its surf
175 ric properties through composition, size and
crystallographic orientation of domains made it possible
176 oxidation state, the coordination number and
crystallographic orientation of metal sites, and bonding
177 s strongly influences the angular spread and
crystallographic orientation of TES-ADT spherulites.
178 ications are achieved based on the patterned
crystallographic orientation of the cubic blue phase, so
179 rably enhance the conductance in a preferred
crystallographic orientation of the layered solid.
180 e show that Li-metal texturing (preferential
crystallographic orientation) occurs during electrochemi
181 ard/soft nanocomposites often exhibit random
crystallographic orientations and monomorphological equi
182 lar complexes aligned along several discrete
crystallographic orientations and that, consequently, co
183 at sites of high stored energy and they have
crystallographic orientations from those present in the
184 omprised of different materials with varying
crystallographic orientations on the overall thermal bou
185 ly scattered by Umklapp processes in all the
crystallographic orientations.
186 various perovskite substrates with different
crystallographic orientations.
187 st tissue biopsies, and related this to both
crystallographic parameters measured previously in the s
188 Such microstructure depends on the shape,
crystallographic phase and orientation, and interfacing
189 The non-
crystallographic phase problem arises in numerous scient
190 dge dislocations that glide on two different
crystallographic planes.
191 th preferred orientation between hk0 and 00l
crystallographic planes.
192 g of lithium electrocrystallization from the
crystallographic point of view provides significant insi
193 ns successfully reverted back to near-native
crystallographic poses after being perturbed.
194 e without the GIST term was wrong, and three
crystallographic poses differed from both predictions.
195 Crystallographic preferred orientation (CPO) of post-per
196 Quantitative characterization of the
crystallographic properties from enamel with known genot
197 oscopy and multiple conformer simulations of
crystallographic protomers as described in the companion
198 o determine which structure fits two sets of
crystallographic raw data best.
199 ducts is also observed, but the mechanism of
crystallographic realignment is unknown.
200 We have employed quantum refinement (
crystallographic refinement enhanced with quantum-mechan
201 o be similar to the oxidation, with the same
crystallographic relationship between the two phases.
202 the confined nanovoids has been observed at
crystallographic resolution, leading to a highly efficie
203 nalized metal-organic framework, MFM-188, at
crystallographic resolution.
204 X-ray
crystallographic screening identified three distinct "ho
205 To fill this gap, we report
crystallographic,
sedimentation-velocity, and kinetics d
206 ead to more complex defect structures, e.g.,
crystallographic shear planes or modules with differing
207 while the higher temperature (Wadsley-Roth,
crystallographic shear structure) H-phase shows high int
208 Here, we identify two possible
crystallographic signatures of geometric frustration: ex
209 rder, but that correlated disorder has clear
crystallographic signatures.
210 and Li are completely disordered on a common
crystallographic site (3c).
211 es associated with shearing on nine distinct
crystallographic slip modes in the hexagonal omega-Zr cr
212 Our
crystallographic,
small angle x-ray scattering, and NMR
213 Crystallographic,
spectroscopic, and computational analy
214 unusual hydrogen bond donor, as confirmed by
crystallographic,
spectroscopic, and computational metho
215 Crystallographic,
spectroscopic, and computational studi
216 Crystallographic,
spectroscopic, and DFT studies reveal
217 Our results from mutagenesis,
crystallographic,
spectroscopic, and kinetic experiments
218 Moreover,
crystallographic structural analysis of isomaltase predi
219 , the ferric enterobactin complex has eluded
crystallographic structural characterization.
220 as a model system, we have used solution and
crystallographic structural methods to delineate the ran
221 Crystallographic structural studies during the developme
222 ools; and clustering on the basis of similar
crystallographic structure (for example, zeolite structu
223 the enzyme active site could be explained by
crystallographic structure analysis, which highlighted t
224 as Fe3 O4 and CoFe2 O4 , which have similar
crystallographic structure and lattice constants as NiFe
225 Its
crystallographic structure determination is the first fo
226 One way to depict a
crystallographic structure is by a periodic (di)graph, i
227 tein, which had been used to solve the X-ray
crystallographic structure of 5-LOX, and examined the bi
228 The
crystallographic structure of a rice (Oryza sativa) cell
229 ing with a comparative analysis of the X-ray
crystallographic structure of compound 5 in complex with
230 We determined the electron
crystallographic structure of H(+),K(+)-ATPase at 6.5 A
231 This paper reports the X-ray
crystallographic structure of oligomers formed by a pept
232 n solubility and function, we determined the
crystallographic structure of one such LGK mutant.
233 The
crystallographic structure of RbkR from Thermoplasma aci
234 We report the first X-ray
crystallographic structure of the "head-to-middle" preny
235 Here we present the
crystallographic structure of the Arabidopsis TPL N-term
236 Here we present the X-ray
crystallographic structure of the human alpha4beta2 nico
237 Here we present a
crystallographic structure of the minimal adhesive fragm
238 precluded conclusive determination of their
crystallographic structure to date, but here we analyze
239 hips and used alternate conformations from a
crystallographic structure to grow a fragment into a mor
240 -diazabicyclo[2.2.2]octane (DABCO), an X-ray
crystallographic structure was obtained.
241 The X-ray
crystallographic structures confirm the mutual columnar
242 This is consistent with time-lapse
crystallographic structures following insertion of Sp-dC
243 Twenty-five X-ray
crystallographic structures have been obtained to confir
244 the role of loop motion in TCR binding, and
crystallographic structures have raised questions about
245 A Bayesian inference method for refining
crystallographic structures is presented.
246 packaged by the nucleoprotein N) we present
crystallographic structures of HMPV N in its assembled R
247 This paper presents the X-ray
crystallographic structures of oligomers formed by a 20-
248 s a beta-hairpin is described, and the X-ray
crystallographic structures of oligomers it forms are re
249 Novel protein
crystallographic structures of the prototypical PC famil
250 Here, we determined the X-ray
crystallographic structures of two catalytically inactiv
251 High-resolution
crystallographic structures provide invaluable insight o
252 The X-ray
crystallographic structures reveal that the stabilized t
253 Through biochemical analyses and X-ray
crystallographic structures we show that to hydrolyze th
254 s that combine high-accuracy priors (such as
crystallographic structures) with medium-resolution cryo
255 paper describes the design, synthesis, X-ray
crystallographic structures, and biophysical and biologi
256 ule Na3 Cit not only helps to manipulate the
crystallographic structures, but also to initiate the tr
257 as identified in some DNA polymerase product
crystallographic structures, but its role is not known.
258 mbination of atomic-resolution protein X-ray
crystallographic structures, ligand-dependent LBD stabil
259 4 of BRD4 as revealed by peptide binding and
crystallographic studies and enhances BRD4's stability b
260 Crystallographic studies and mutational analyses have co
261 The comparison of X-ray
crystallographic studies at low and high temperatures an
262 the molecular basis of this regulation using
crystallographic studies augmented by computational anal
263 Docking and
crystallographic studies corroborate favorable binding t
264 Mutant yeast and co-
crystallographic studies demonstrate binding to the bc1
265 To date,
crystallographic studies have focused on conserved trans
266 pecies, but previous spectroscopic and X-ray
crystallographic studies have not been able to unambiguo
267 Recent EPR and
crystallographic studies have observed that oxidized Pdx
268 However, in contradiction, biochemical and
crystallographic studies have shown that heme decreases
269 We present biochemical and
crystallographic studies indicating that irrespective of
270 X-ray
crystallographic studies of CorA show similar conformati
271 Crystallographic studies of GTF180-DeltaN show that at t
272 Mass spectrometric and
crystallographic studies of Pt(II) binding to the RecA i
273 y NMR (including DOSY) experiments and X-ray
crystallographic studies of several model lithio interme
274 On the basis of X-ray
crystallographic studies of the complex of hCA II with 4
275 Crystallographic studies of the CRBN-DDB1-CC-885-GSPT1 c
276 X-ray
crystallographic studies of the isolated DHO and of the
277 formatic, biochemical, mutational, and X-ray
crystallographic studies on the unicellular alga Chlamyd
278 Crystallographic studies revealed that the specificity o
279 modeling, along with enzymatic, genetic and
crystallographic studies, have established a mechanism-o
280 Mutagenesis and
crystallographic studies, including the structure of BT3
281 wever, by combining genetic, biochemical and
crystallographic studies, we demonstrate that MTM and PK
282 d by deuterium labeling experiment and X-ray
crystallographic studies.
283 ination of biochemical experiments and X-ray
crystallographic studies.
284 FAM) distorts DNA into a U-turn, as shown by
crystallographic studies.
285 This first X-ray
crystallographic study of a single human CCT subunit in
286 Through a combined NMR and
crystallographic study on the histidine kinase HK853 and
287 Our recent
crystallographic study showed that CaM embraces helices
288 enzyme, particularly in light of a previous
crystallographic study that placed the cofactor-binding
289 This allowed a comparative X-ray
crystallographic study to delineate the successive struc
290 Thus, we conclude that there is no
crystallographic support for a dinuclear Cu site in pMMO
291 ent structure-guided optimization using this
crystallographic surrogate.
292 When molecular motion and
crystallographic symmetry are both accounted for, the J(
293 he DQF J splitting is influenced by both the
crystallographic symmetry of the system and the presence
294 perovskite films, featuring strong uniaxial-
crystallographic texture, micrometer-grain morphology, h
295 We report the pressure-induced
crystallographic transitions and optical behavior of MAP
296 athing'-typically occur through well-defined
crystallographic transitions.
297 s and in the crystallographic model) and (2)
crystallographic twinning.
298 Crystallographic unit cells can be assembled into a regu
299 In contrast to previous
crystallographic views, we found that the selectivity fi
300 -49-Asn, and Arg-126-Lys, we inferred that a
crystallographic water acts as a general base during GSH