1 a renewed emphasis on detailed GSL headgroup
structural analysis.
2 linical and population genetics with protein
structural analysis.
3 solution of this technique enabling detailed
structural analysis.
4 rtases, but its oligomeric nature challenges
structural analysis.
5 sented a significant challenge for NMR-based
structural analysis.
6 Si2H2 characterized by single crystal X-ray
structural analysis.
7 ile N-glycans in biological fluids with deep
structural analysis.
8 proteins is often challenging and may limit
structural analysis.
9 e for statistical, quantitative genetic, and
structural analysis.
10 onfirming predictions derived from in silico
structural analysis.
11 onene by cellular detoxification using ultra-
structural analysis.
12 The records were subjected to a process of
structural analysis.
13 the development of methods for comprehensive
structural analysis.
14 e previously been used for three-dimensional
structural analysis.
15 sequence variations within it to facilitate
structural analysis.
16 zirconium phosphonates that are suitable for
structural analysis.
17 ses a formidable challenge for comprehensive
structural analysis.
18 The mutagenesis and
structural analysis allow us to propose a novel UQ-bindi
19 Structural analysis allowed us to explain the specificit
20 e cholesterol binding to the CRD in a recent
structural analysis also dictate SMO activation, both in
21 Our
structural analysis also provides novel insight into the
22 Here we report the rational design,
structural analysis and antigenic evaluation of HIV-1 tr
23 ombinant food allergens can accelerate their
structural analysis and benefit specific studies in alle
24 Both
structural analysis and biophysical simulations generate
25 Structural analysis and comparison with HSV gB suggest t
26 3-D
structural analysis and comparison with unreacted epoxid
27 Structural analysis and computational studies of MalA' i
28 contribution to best practices in NMR-based
structural analysis and dereplication.
29 pectroscopy were performed for comprehensive
structural analysis and energy-transfer (ET) studies of
30 Structural analysis and free-energy calculations indicat
31 We report detailed
structural analysis and glycan microarray data for recom
32 osed approach will be useful for an improved
structural analysis and it will be the enabling technolo
33 Structural analysis and modeling of EhACK indicated ster
34 Previous
structural analysis and modeling of GCPs suggest that al
35 This is significant, as accurate RNA
structural analysis and prediction is likely to become a
36 Structural analysis and spectroscopic studies of ligands
37 We describe the use of comparative
structural analysis and structure-guided molecular desig
38 organic calibrant for IM-MS allowing sizing,
structural analysis,
and discovery of molecular nanostru
39 Mutant studies,
structural analysis,
and molecular modeling revealed tha
40 Gs, uncovering their mechanisms of gelation,
structural analysis,
and tailorable properties, and thei
41 n mass spectrometry, microscopy, and protein
structural analysis are rapidly advancing the amount and
42 task can be completed using online top-down
structural analysis,
as demonstrated using stressed inte
43 Here, we use
structural analysis,
as well as biophysical and cell-bas
44 Streptococcus pneumoniae (SpPaaI), including
structural analysis based on crystal diffraction data to
45 thelium are very resistant to evidence-based
structural analysis because of their inherent flexibilit
46 d, as demonstrated, in excellent quality for
structural analysis by electron microscopy.
47 cetylation followed by online separation and
structural analysis by MS/MS.
48 Structural analysis by negative-stain electron microscop
49 Structural analysis by NMR spectroscopy confirmed that t
50 Furthermore, their large size prohibits
structural analysis by NMR spectroscopy.
51 of localized molecules are further used for
structural analysis by single particle procedures such a
52 to GH99 endo-alpha-1,2-mannanases, and their
structural analysis by X-ray crystallography.
53 This
structural analysis combined with biochemical and cellul
54 Detailed
structural analysis combined with dynamic measurements f
55 Structural analysis combined with molecular dynamics ide
56 Structural analysis combined with recent real-time singl
57 Structural analysis combined with site-directed mutagene
58 Structural analysis,
combined with structure-guided muta
59 NMR and CD
structural analysis confirmed that each alpha-ImI moiety
60 Solid-state
structural analysis confirms both methylidene and methyl
61 Structural analysis confirms the high crystalline qualit
62 Structural analysis,
consistent with biochemical inhibit
63 In addition,
structural analysis coupled with the results of phosphor
64 e from two congeneric PAC dimers, a detailed
structural analysis decoded the stereochemistry, spatial
65 Motif and
structural analysis define expanded pairing rules for ov
66 Structural analysis demonstrated that human alpha2C-AR h
67 Unexpectedly,
structural analysis demonstrated that the Glu(3) --> Ala
68 Structural analysis demonstrates a modification in the h
69 Structural analysis demonstrates that binding of extende
70 Protein
structural analysis demonstrates that water molecules ar
71 Structural analysis demonstrates that YKL-39 interacts w
72 The detailed
structural analysis demonstrates the applicability of SA
73 pology was confirmed by single-crystal X-ray
structural analysis,
demonstrating halogen bonding betwe
74 h nanomolar affinity; biochemical assays and
structural analysis establish that glutamate is occluded
75 A region-of-interest MRI
structural analysis found cingulate cortex to be thinner
76 om sequenced reads, solely or in addition to
structural analysis from genome data.
77 Extensive in vitro
structural analysis has led to a working model of Hsp90'
78 is at positions predicted as critical by the
structural analysis have allowed the identification of H
79 Our NMR
structural analysis identified E17 within the PSD-95 N-t
80 Our
structural analysis illustrates distinct mechanisms of t
81 Structural analysis implicated Arg511 as a required resi
82 Structural analysis in a membrane revealed that all extr
83 lume thus demonstrating new possibilities of
structural analysis in biomedical science.
84 lar analytic tools, has been widely used for
structural analysis in both physical and biological scie
85 The
structural analysis in combination with comparison of di
86 e process with biochemical assays and cryoEM
structural analysis in parallel.
87 Structural analysis in situ, maintaining Golgi topology,
88 Structural analysis,
in conjunction with biochemical stu
89 Structural analysis indicated that CT009 shares high lev
90 Structural analysis indicated that plant-produced hOPN h
91 Structural analysis indicates that after Pol II encounte
92 Structural analysis indicates that the 3 disease-associa
93 Three-dimensional (3D)
structural analysis is essential to understand the relat
94 pite important progress, especially in their
structural analysis,
it is still unknown how the substra
95 Structural analysis leads to identification of a key tyr
96 Importantly, our
structural analysis leads to the identification of a pot
97 s extracted from hip DXA scans using the hip
structural analysis method.
98 lar electronic materials, the multitechnique
structural analysis methodology elaborated here must be
99 Here we introduce ISAMBARD, a tool for
structural analysis,
model building and rational design
100 Using
structural analysis,
molecular dynamics, and biochemistr
101 Structural analysis,
molecular modeling, and mutational
102 Structural analysis,
multiangle light scattering coupled
103 Through
structural analysis,
mutational, biochemical and enzymat
104 keynotes that covered topics on 3D genomics
structural analysis,
next generation sequencing (NGS) an
105 Structural analysis of 6 HECT-UbV complexes revealed UbV
106 Altogether, the present
structural analysis of 7SK HP1 highlights an original me
107 Structural analysis of a 'minimal' TRP vanilloid subtype
108 Recent
structural analysis of a Be-specific TCR interacting wit
109 We report the first
structural analysis of a carbocyclic mechanism-based GH
110 A computational DFT-B3LYP
structural analysis of a poly phenol, Gallic acid (GA) h
111 Structural analysis of a prototypical Vbeta8.1(+) TCR-H-
112 Structural analysis of a representative TRBV11-2(+) TCR
113 -ray crystallography has been applied to the
structural analysis of a series of tetrapeptides that we
114 ndent alterations of conformational space by
structural analysis of all relevant transcription interm
115 xample of food allergenic proteins for which
structural analysis of allergenicity has only partially
116 We have completed a
structural analysis of almost 200 small molecule inhibit
117 A
structural analysis of Arn revealed that its shape and n
118 Structural analysis of BVU_4064 and BF1687 points to pos
119 The
structural analysis of complex carbohydrates typically r
120 Structural analysis of complexes of the FBG domain of L-
121 timized as a data-independent method for the
structural analysis of compounds in complex samples.
122 These findings, thus, uncover limitations of
structural analysis of drug binding using X-ray structur
123 A
structural analysis of duplexes with DNA and RNA by CD-s
124 We demonstrate through
structural analysis of dykes exposed within the Santorin
125 Functional
structural analysis of E2 based on a Wimley-White interf
126 P identification was performed by functional
structural analysis of E2.
127 By combining our genetic data with a
structural analysis of eRF1 mutants, we were able to for
128 A
structural analysis of fibrous proteins often requires l
129 Structural analysis of Fpn reveals a His-Cys catalytic d
130 Here, through functional and
structural analysis of GhV-G, we show how this African H
131 f complex oligosaccharide structures, making
structural analysis of glycoproteins and their glycans c
132 Structural analysis of HLA-B*57:01, HLA-B*08:01, and mut
133 Structural analysis of HS showed about 40% down-regulati
134 We performed a large-scale
structural analysis of human single amino acid variation
135 ture of various anti-GSL antibodies, and (4)
structural analysis of immunostained GSLs directly on th
136 Moreover, crystallographic
structural analysis of isomaltase predicts that another
137 ide mixtures, online separation and detailed
structural analysis of isomeric and epimeric HS mixtures
138 utant at host physiological temperature, but
structural analysis of lipid A in the mutant revealed on
139 ormatic analysis of amino acid conservation,
structural analysis of LPS-binding proteins, and MD simu
140 Ns provide not only a starting point for the
structural analysis of membrane proteins in a phospholip
141 ic material useful for the stabilization and
structural analysis of membrane proteins.
142 ful complementary technique for chemical and
structural analysis of milk powders and allows improved
143 Structural analysis of mPDE revealed that four Ser/Thr r
144 An ultra-
structural analysis of muscle biopsies from DMD patients
145 Structural analysis of NFS indels revealed that they pre
146 Here we report the synthesis and
structural analysis of novel thioether bond-linked cycli
147 nserved motif which we term the "DK switch."
Structural analysis of nSMase2 and the extended N-SMase
148 ctrophoresis (CE) is a powerful approach for
structural analysis of nucleic acids, with recent high-t
149 For comparison, a
structural analysis of O-H/pi interactions and of cation
150 of activation by high-energy photons for the
structural analysis of oligosaccharides, even in unsepar
151 Structural analysis of oncogenic M918T and wild-type RET
152 A
structural analysis of OprP and OprO revealed two crucia
153 ance spectroscopy is a powerful tool for the
structural analysis of organic compounds and biomolecule
154 ch lays the foundation for atomic-resolution
structural analysis of other microtubule-associated moto
155 Structural analysis of oxidized and reduced PcrAB with a
156 buried surface area of 3094 A(2) Comparative
structural analysis of p59-p261C with the corresponding
157 Our biochemical and
structural analysis of PARP inhibitor potencies establis
158 nal (3D) imaging is difficult to achieve and
structural analysis of pathological myocardial structure
159 different wavelengths, 930 and 1,325 nm, for
structural analysis of periodontal tissue in porcine jaw
160 the first detection, isolation, and complete
structural analysis of poly- and oligosaccharides of Shi
161 ght the potential of UVPD to be used for the
structural analysis of proteins in the gas phase.
162 Unlike
structural analysis of proteins using chemical reagents
163 used by a non-monodispersed sample, allowing
structural analysis of PrP alone and in complex with Fab
164 Here, we present a detailed
structural analysis of R2lox in the nonactivated, reduce
165 yloxy amides were ascertained based on X-ray
structural analysis of representative beta-acyloxy amide
166 Structural analysis of Rio2 indicated a role as a confor
167 This information has been combined with a
structural analysis of RNase R, based on its homology to
168 thods are equally useful for high-resolution
structural analysis of smaller, dynamic protein complexe
169 on as well as compositional, functional, and
structural analysis of splicing complexes at distinct st
170 X-ray crystallographic
structural analysis of the analogue bearing a cmF moiety
171 Structural analysis of the AtIPMDH2 K232M mutant and iso
172 Structural analysis of the C-terminal domain of wild-typ
173 Structural analysis of the C-terminal domain reveals a d
174 ore this question, we report biochemical and
structural analysis of the catalytic core of hpol eta.
175 NMR
structural analysis of the chemically synthesized three
176 Structural analysis of the complex between C-epitope I a
177 In this study we performed
structural analysis of the complex between the ASK1 kina
178 In addition, the
structural analysis of the complex helped us to explain
179 le resonance spectra permitted a dynamic and
structural analysis of the crystallization pathway to ho
180 Structural analysis of the CsrA/FliW heterotetramer show
181 e of an entire dimeric photoreceptor through
structural analysis of the Deinococcus radiodurans phyto
182 Drawing on
structural analysis of the dimer interface, we identifie
183 x-ray scattering and chemical cross-linking
structural analysis of the discrete dimer.
184 Here, we present a
structural analysis of the FtsLB complex, performed with
185 bly, phylogenetic inference supported by the
structural analysis of the genome ends provides evidence
186 ch molecules, we carried out a comprehensive
structural analysis of the highly stabilized anti-CXCL13
187 unds and present the high-resolution cryo-EM
structural analysis of the human immunoproteasome.
188 vages, thus providing the most comprehensive
structural analysis of the lipid A.
189 family GH76 alpha-mannanases studied through
structural analysis of the Michaelis complex and synthes
190 Msm) open promoter complex (RPo), along with
structural analysis of the Msm RPo and a previously repo
191 Structural analysis of the p53 REs in solution shows tha
192 Structural analysis of the prenylated stilbenoids sugges
193 X-ray
structural analysis of the purified protein has revealed
194 In contrast, cryo-EM
structural analysis of the R141H mutation at approximate
195 X-ray
structural analysis of the Senphos-Pd(0) complex reveals
196 Structural analysis of the stabilized mutant at 3.6 A re
197 teady-state analysis, stability analysis and
structural analysis of the stoichiometric matrix.
198 the light of published experimental results,
structural analysis of the transmembrane cavity suggests
199 culations of the transport site residues and
structural analysis of the water molecules showed that t
200 cell alphabetaTCR repertoire sequencing, and
structural analysis of these four epitopes in complex wi
201 The
structural analysis of these glycosaminoglycans is chall
202 Structural analysis of these variants provides insight i
203 We perform a
structural analysis of thiG to determine its potential p
204 Structural analysis of this domain alone and in complex
205 Biochemical and
structural analysis of this loop variant and GCK variant
206 This study provides the first
structural analysis of this poorly characterized subfami
207 Structural analysis of this region revealed that it is i
208 Structural analysis of this variant revealed an altered
209 ith the Volta phase plate enabled a detailed
structural analysis of TPPII despite its low abundance.
210 Structural analysis of typical seeds reveals the prevale
211 novel polymerization of vancomycin dimers by
structural analysis of vancomycin-Zn(II) crystals and fi
212 Three-dimensional (3D)
structural analysis of VP1 showed that residue 178 was l
213 A
structural analysis of wild-type fibrils by solid-state
214 rview of the Hippo pathway, the sequence and
structural analysis of YAP/TAZ, the known pharmacologica
215 In vitro and
structural analysis on reconstituted Mig1 suggests that
216 of such H-bonding interactions are based on
structural analysis or correlations between IR and NMR s
217 Our comparative
structural analysis outlines phylum-specific CYP51 featu
218 b complex for different incubation times and
structural analysis provide a model for a hyperstabiliza
219 At the same time, our
structural analysis provides information about the bindi
220 ), with further crystallographic studies and
structural analysis providing insight into the racemic c
221 Structural analysis revealed a bilobed architecture with
222 Our
structural analysis revealed a pre-activation state of N
223 Excitingly, our kinetic, thermodynamic, and
structural analysis revealed an array of different prefe
224 The comparative
structural analysis revealed both the conserved features
225 with other members of the ALDH1A family, our
structural analysis revealed few peculiar residues in th
226 Structural analysis revealed hydrophobic interaction bet
227 Solution-phase NMR
structural analysis revealed key interactions in residue
228 The
structural analysis revealed mechanisms of allergen-anti
229 Mutagenesis and
structural analysis revealed NendoU active site residues
230 Structural analysis revealed that although the CM fits i
231 Structural analysis revealed that Az1 sterically blocks
232 Structural analysis revealed that both aldolases adopt a
233 Structural analysis revealed that Calhm1(-/-) brains had
234 Structural analysis revealed that Cmpd-1 binding results
235 Quantitative
structural analysis revealed that interphase NPC assembl
236 Computational
structural analysis revealed that MHC-E provides heterog
237 Protein
structural analysis revealed that Phe10Leu mutation may
238 Our
structural analysis revealed that six GDP nucleotides bo
239 In addition,
structural analysis revealed that the orientation of N6
240 Structural analysis revealed that this key glutamic acid
241 In particular, the EM
structural analysis revealed that two p53 tetramers bind
242 Structural analysis revealed the amino acids clustered i
243 Structural analysis revealed the similarity between the
244 The
structural analysis revealed two different and coupled c
245 Solution
structural analysis reveals a ppi Cl [Formula: see text]
246 Structural analysis reveals SART3 contains 12 half-a-tet
247 Structural analysis reveals that acetylated Lys9 is sand
248 IR secondary
structural analysis reveals that compact conformations a
249 Structural analysis reveals that FG-repeats of the nups
250 Our
structural analysis reveals that MCV sT also displaces t
251 Structural analysis reveals that Smurf2 has Nedd8-bindin
252 Structural analysis reveals that the Axin segment respon
253 Structural analysis reveals that the fine specificity is
254 Protein
structural analysis reveals that the missense mutations
255 Crystal
structural analysis reveals that the spiro-structures fa
256 Our
structural analysis reveals the interdependency of prote
257 The gene
structural analysis separated these 52 genes into an int
258 Structural analysis showed that different forms of CM ha
259 Structural analysis showed that homeodomain specificity
260 Structural analysis showed that TCR binding or phosphory
261 The
structural analysis showed that the sugars are bound to
262 The
structural analysis shows an unprecedented flexibility o
263 the complex enables UbcH10 association, and
structural analysis shows how the Cdc20 subunit intrinsi
264 Structural analysis shows that Ad4 E3-19K adopts a terti
265 A comprehensive
structural analysis shows that high density of oxygen va
266 Structural analysis shows that the conserved hydrophobic
267 Structural analysis shows that the nucleodyes are sound
268 Our in silico
structural analysis shows that XLG3 aligns closely to th
269 A combination of
structural analysis,
small angle X-ray scattering, mutag
270 Computational
structural analysis suggested that G288D in AcrB heavily
271 Structural analysis suggested that p.Glu344Ala and p.Arg
272 Structural analysis suggests a mechanism by which residu
273 need for active nuclear import, sequence and
structural analysis suggests that a monopartite nuclear
274 Structural analysis suggests that ATP binding and hydrol
275 Structural analysis suggests that several key residues o
276 Structural analysis suggests that the ankyrin repeat dom
277 Comparative
structural analysis suggests that these receptors may sh
278 Our
structural analysis supports the assertion that MrNV may
279 s and aggregates, making traditional protein
structural analysis techniques challenging.
280 tion of local structure is better suited for
structural analysis than continuous descriptions.
281 rained modeling, isothermal calorimetry, and
structural analysis,
that decreasing the affinity of CAP
282 Structural analysis through X-ray diffraction and Raman
283 ance profiling of patient cells ex vivo with
structural analysis to establish the VEGFR tyrosine kina
284 ofactor binding domain, and are predicted by
structural analysis to have a destabilizing effect.
285 t al. couple next-generation sequencing with
structural analysis to illuminate the key processes that
286 We use quantitative comparative
structural analysis to localize the origins of L1 stalk
287 sed epitope prediction and computer-assisted
structural analysis to screen five dominant epitopes and
288 ular Dynamics (MD) simulations together with
structural analysis to shed light on NTP entry pathways.
289 Here, we combine biophysical and
structural analysis to uncover the architecture of SAS-5
290 The
structural analysis,
together with biochemical and bioph
291 Structural analysis,
together with structure-guided bioc
292 henotype in Torsin-deficient cells enables a
structural analysis via electron microscopy tomography a
293 Structural analysis was performed to identify those SDPs
294 oseltamivir, zanamivir, or sialic acid, and
structural analysis was performed.
295 mology, evolutionary statistics, and protein
structural analysis,
we could track changes in substrate
296 ysis, negative-stain electron microscopy and
structural analysis,
we demonstrate that this unique ope
297 iterative rounds of computational design and
structural analysis,
we identified a protein in which th
298 Using kinetic, proteomic, and crystal
structural analysis,
we were able to show that the Met -
299 mass spectrometry-based approach for glycan
structural analysis with immense potential.
300 se from the bacterium Neisseria meningitidis
Structural analysis with X-ray crystallographic diffract