1 trategy and generated abundant fragments for
structural analysis.
2 f RD3 to aggregate in solution has prevented
structural analysis.
3 active-site residues identified through the
structural analysis.
4 onstitution to define lipids appropriate for
structural analysis.
5 fications (PTMs) are key elements in protein
structural analysis.
6 several antibody clonotypes for epitope and
structural analysis.
7 ution, as revealed by 3D electron microscopy
structural analysis.
8 assemblies and the need for high-resolution
structural analysis.
9 zirconium phosphonates that are suitable for
structural analysis.
10 solution of this technique enabling detailed
structural analysis.
11 rtases, but its oligomeric nature challenges
structural analysis.
12 sequence variations within it to facilitate
structural analysis.
13 ses a formidable challenge for comprehensive
structural analysis.
14 a renewed emphasis on detailed GSL headgroup
structural analysis.
15 linical and population genetics with protein
structural analysis.
16 protein sequences that are more amenable to
structural analysis.
17 iables in each group; which enables in-depth
structural analysis.
18 structure was determined via single crystal
structural analysis.
19 ter for reactivation, was confirmed by X-ray
structural analysis.
20 s pose a major analytical challenge to their
structural analysis.
21 lar structure viewer focusing on interactive
structural analysis.
22 ded into XlinkDB for interaction network and
structural analysis.
23 uates gene function, consistent with protein
structural analysis.
24 Based on our
structural analysis,
a magnesium-assisted S(N)2-type mec
25 The mutagenesis and
structural analysis allow us to propose a novel UQ-bindi
26 Structural analysis allowed us to explain the specificit
27 e cholesterol binding to the CRD in a recent
structural analysis also dictate SMO activation, both in
28 Structural analysis also indicated that HLA polymorphism
29 Our
structural analysis also provides novel insight into the
30 The
structural analysis also reveals a glycan-binding domain
31 In addition, our
structural analysis and accompanying biochemical assays
32 Here we report the rational design,
structural analysis and antigenic evaluation of HIV-1 tr
33 ombinant food allergens can accelerate their
structural analysis and benefit specific studies in alle
34 Both
structural analysis and biophysical simulations generate
35 3-D
structural analysis and comparison with unreacted epoxid
36 Structural analysis and computational studies of MalA' i
37 Recent
structural analysis and coupled mass spectrometry studie
38 da(max) =622 nm under 450 nm excitation, and
structural analysis and DFT calculations support the con
39 pectroscopy were performed for comprehensive
structural analysis and energy-transfer (ET) studies of
40 ectrochemical impedance spectroscopy, atomic
structural analysis and in situ X-ray diffraction, prese
41 osed approach will be useful for an improved
structural analysis and it will be the enabling technolo
42 Structural analysis and modeling of EhACK indicated ster
43 Previous
structural analysis and modeling of GCPs suggest that al
44 Here, through
structural analysis and molecular dynamics simulation as
45 Structural analysis and molecular dynamics simulations r
46 This is significant, as accurate RNA
structural analysis and prediction is likely to become a
47 Structural analysis and protein homology modeling showed
48 Here, we report a method for in-depth
structural analysis and quantitation of O-glycans derive
49 We describe the use of comparative
structural analysis and structure-guided molecular desig
50 organic calibrant for IM-MS allowing sizing,
structural analysis,
and discovery of molecular nanostru
51 Mutant studies,
structural analysis,
and molecular modeling revealed tha
52 ure of PHEV S1(A) We then took a comparative
structural analysis approach to map the beta1CoV S RBS,
53 rements and single-crystal X-ray diffraction
structural analysis as well as nuclear magnetic resonanc
54 live-cell fluorescence imaging and cryoEM/ET
structural analysis,
as demonstrated by visualizing huma
55 Here, we use
structural analysis,
as well as biophysical and cell-bas
56 Structural analysis based on the homology model suggests
57 thelium are very resistant to evidence-based
structural analysis because of their inherent flexibilit
58 ered to be complementary methods for protein
structural analysis,
because one probes the protein back
59 ing, and to facilitate this process, careful
structural analysis beyond the antibody binding site is
60 ese methods to increase yield, allowing full
structural analysis by (1)H NMR.
61 the matrix layer of intact virions prompted
structural analysis by cryo-electron microscopy (cryo-EM
62 Structural analysis by high-resolution imaging defines t
63 rom both HN13 and JGS4143 were isolated, and
structural analysis by MALDI-TOF-MS, GC-MS, and 2D NMR r
64 We demonstrate both
structural analysis by MS, as well as functional analysi
65 cetylation followed by online separation and
structural analysis by MS/MS.
66 Structural analysis by negative-stain electron microscop
67 Structural analysis by NMR spectroscopy confirmed that t
68 Furthermore, their large size prohibits
structural analysis by NMR spectroscopy.
69 Structural analysis by single-particle cryo-electron mic
70 Colloidal stabilization enables detailed
structural analysis by synchrotron X-ray diffraction and
71 Detailed
structural analysis by x-ray crystallography and molecul
72 While
structural analysis by X-ray crystallography shows that
73 to GH99 endo-alpha-1,2-mannanases, and their
structural analysis by X-ray crystallography.
74 Detailed
structural analysis combined with dynamic measurements f
75 Structural analysis combined with site-directed mutagene
76 Structural analysis combined with site-directed mutagene
77 Structural analysis,
combined with structure-guided muta
78 Solid-state
structural analysis confirms both methylidene and methyl
79 Structural analysis confirms the high crystalline qualit
80 Structural analysis,
consistent with biochemical inhibit
81 lication in an interlaboratory study on mAbs
structural analysis coordinated by the Consortium for To
82 Our
structural analysis coupled with in silico docking studi
83 In addition,
structural analysis coupled with the results of phosphor
84 Unexpectedly,
structural analysis demonstrated that the Glu(3) --> Ala
85 Structural analysis demonstrated thermal instability of
86 Structural analysis demonstrates a modification in the h
87 Comparative
structural analysis demonstrates how metazoan-specific a
88 Nano-
structural analysis exhibited tight and ordered lamellar
89 the next generation of ligand screening and
structural analysis experiments to be accomplished in a
90 In this study, we developed a
structural analysis for cereal-derived (A)XOS by negativ
91 om sequenced reads, solely or in addition to
structural analysis from genome data.
92 Structural analysis further showed that the RIM-BP fibro
93 Our NMR
structural analysis identified E17 within the PSD-95 N-t
94 In addition,
structural analysis identifies core elements that define
95 Our
structural analysis illustrates distinct mechanisms of t
96 n sequence comparisons and three-dimensional
structural analysis.
IMPORTANCE Low-pathogenicity avian i
97 e process with biochemical assays and cryoEM
structural analysis in parallel.
98 Structural analysis in situ, maintaining Golgi topology,
99 the further development of FPOP for protein
structural analysis in vivo (IV-FPOP) with Caenorhabditi
100 Structural analysis indicated that plant-produced hOPN h
101 Substrate
structural analysis indicated that Vv2KGR uses two modes
102 Comparative
structural analysis indicates that nucleotide sugar dono
103 Structural analysis indicates that the 3 disease-associa
104 Structural analysis indicates that the function of the x
105 ey player in the GDH regulation process. Our
structural analysis indicates that, binding to the regul
106 Their
structural analysis is challenging because the accessibl
107 Based on extensive
structural analysis it was proposed that RING E3 ligases
108 Importantly, our
structural analysis leads to the identification of a pot
109 Here we introduce ISAMBARD, a tool for
structural analysis,
model building and rational design
110 Using
structural analysis,
molecular dynamics, and biochemistr
111 keynotes that covered topics on 3D genomics
structural analysis,
next generation sequencing (NGS) an
112 Structural analysis of 6 HECT-UbV complexes revealed UbV
113 Altogether, the present
structural analysis of 7SK HP1 highlights an original me
114 We report the first
structural analysis of a carbocyclic mechanism-based GH
115 Structural analysis of a known apoptosis signal-regulati
116 Cryo-electron microscopy
structural analysis of a phosphorylated B-Raf kinase dom
117 A computational DFT-B3LYP
structural analysis of a poly phenol, Gallic acid (GA) h
118 Structural analysis of a prototypical Vbeta8.1(+) TCR-H-
119 Structural analysis of a representative TRBV11-2(+) TCR
120 -ray crystallography has been applied to the
structural analysis of a series of tetrapeptides that we
121 Structural analysis of a three-dimensional model of rhGF
122 Structural analysis of additional two mutants with a sin
123 ndent alterations of conformational space by
structural analysis of all relevant transcription interm
124 xample of food allergenic proteins for which
structural analysis of allergenicity has only partially
125 Consequently,
structural analysis of antibodies is crucial for therape
126 Additionally,
structural analysis of antibody binding to CXCR4 is disc
127 Structural analysis of both RBDs suggests that the recep
128 Recent
structural analysis of CD81 indicates that it contains a
129 ic analyses, CRISPR-assisted recombineering,
structural analysis of cell wall-associated polysacchari
130 timized as a data-independent method for the
structural analysis of compounds in complex samples.
131 Finally, our
structural analysis of disease mutations leads to a mech
132 These findings, thus, uncover limitations of
structural analysis of drug binding using X-ray structur
133 In this work, we detail a
structural analysis of E. coli enolase bound to both SF2
134 Functional
structural analysis of E2 based on a Wimley-White interf
135 Chemical protection studies and
structural analysis of everninomicin P revealed that eve
136 High-resolution
structural analysis of flexible proteins is frequently c
137 Structural analysis of Fpn reveals a His-Cys catalytic d
138 Structural analysis of Gn complexed with four Gn-specifi
139 bined LC-MS/MS experiments and comprehensive
structural analysis of HMOs.
140 Structural analysis of HpMTAN shows inhibitors extending
141 The design, synthesis, and X-ray
structural analysis of hybrid HIV-1 protease inhibitors
142 MS) an increasingly popular approach for the
structural analysis of ionic species as well as for sepa
143 Moreover, crystallographic
structural analysis of isomaltase predicts that another
144 Structural analysis of lead analogs provided important i
145 based lipidomics is the primary tool for the
structural analysis of lipids but the effective localiza
146 Structural analysis of mannans from moss and Selaginella
147 Further
structural analysis of mCST's unique lumen-facing partia
148 ic material useful for the stabilization and
structural analysis of membrane proteins.
149 ful complementary technique for chemical and
structural analysis of milk powders and allows improved
150 Structural analysis of mPDE revealed that four Ser/Thr r
151 we present a convenient workflow for cryo-EM
structural analysis of MPs embedded in liposomes, using
152 Structural analysis of myovirus P-SSM2 Fd (pssm2-Fd), wh
153 Through detailed chemical and
structural analysis of natural specimens sampled at dept
154 Structural analysis of NFS indels revealed that they pre
155 nserved motif which we term the "DK switch."
Structural analysis of nSMase2 and the extended N-SMase
156 For comparison, a
structural analysis of O-H/pi interactions and of cation
157 ance spectroscopy is a powerful tool for the
structural analysis of organic compounds and biomolecule
158 essures, recombination and reassortment, and
structural analysis of OROV variants.
159 Structural analysis of our 3D reconstructions revealed i
160 buried surface area of 3094 A(2) Comparative
structural analysis of p59-p261C with the corresponding
161 Our biochemical and
structural analysis of PARP inhibitor potencies establis
162 nal (3D) imaging is difficult to achieve and
structural analysis of pathological myocardial structure
163 conducted a biochemical and high-resolution
structural analysis of PBP2 variants derived from the de
164 Structural analysis of PiuA Fe(III)-bis-catechol and Ga(
165 trophysiological studies in brain slices and
structural analysis of post-mortem tissues obtained from
166 Unlike
structural analysis of proteins using chemical reagents
167 ctrometry is increasingly being used for the
structural analysis of proteins.
168 This information has been combined with a
structural analysis of RNase R, based on its homology to
169 Structural analysis of RT(Y115F/F116Y/Q151M/F160M/M184V)
170 Our work presents the first detailed
structural analysis of sand fly salivary glycans.
171 Structural analysis of SERPINA1 identified 3 amphipathic
172 Specifically, the morphology and
structural analysis of several examples applying MGNs as
173 thods are equally useful for high-resolution
structural analysis of smaller, dynamic protein complexe
174 us, DESSO improves in the identification and
structural analysis of TF binding sites, by integrating
175 Here, we performed a global biochemical and
structural analysis of Tfp in a recently emerged Gram-po
176 X-ray crystallographic
structural analysis of the apo Ega3 and an Ega3-galactos
177 Structural analysis of the AtIPMDH2 K232M mutant and iso
178 Structural analysis of the C-terminal domain reveals a d
179 Structural analysis of the Cas4-Cas1-Cas2 complex reveal
180 ore this question, we report biochemical and
structural analysis of the catalytic core of hpol eta.
181 In addition, the
structural analysis of the complex helped us to explain
182 We perform the
structural analysis of the ComRS system from S. vestibul
183 X-ray
structural analysis of the CsoS2 interaction motif bound
184 Structural analysis of the CsrA/FliW heterotetramer show
185 Here, we present a
structural analysis of the FtsLB complex, performed with
186 We sequence its genome, and based on
structural analysis of the GAX, identify six enzymes tha
187 unds and present the high-resolution cryo-EM
structural analysis of the human immunoproteasome.
188 ic, and kinetic experiments as well as X-ray
structural analysis of the intermediate alkylcobalt(III)
189 Through a functional and
structural analysis of the mechanism of ATP activation i
190 Msm) open promoter complex (RPo), along with
structural analysis of the Msm RPo and a previously repo
191 MALDI-TOF MS-based
structural analysis of the mutant CWPS combined with seq
192 Structural analysis of the MvcA-UBE2N-Ub complex reveals
193 examples, we perform the first cross-kingdom
structural analysis of the OTU fold that highlights comm
194 Structural analysis of the p53 REs in solution shows tha
195 Structural analysis of the prenylated stilbenoids sugges
196 Structural analysis of the resulting crystalline sponge
197 X-ray
structural analysis of the Senphos-Pd(0) complex reveals
198 Structural analysis of the stabilized mutant at 3.6 A re
199 Morphological and
structural analysis of the synthesized nanocomposites sh
200 Multiparametric
structural analysis of these aptamers revealed that A1 a
201 The
structural analysis of these glycosaminoglycans is chall
202 Structural analysis of these variants provides insight i
203 Small angle X-ray scattering (SAXS)-based
structural analysis of this protein indicated a DAH7PS-C
204 Structural analysis of this variant revealed an altered
205 ith the Volta phase plate enabled a detailed
structural analysis of TPPII despite its low abundance.
206 novel polymerization of vancomycin dimers by
structural analysis of vancomycin-Zn(II) crystals and fi
207 e linear alpha-peptides, the main results of
structural analysis on cyclic systems as well as on beta
208 Here we have completed a detailed
structural analysis on native MUC5B polymers purified fr
209 In vitro and
structural analysis on reconstituted Mig1 suggests that
210 s review will first outline the atomic scale
structural analysis on single-atom alloys using microsco
211 Our comparative
structural analysis outlines phylum-specific CYP51 featu
212 Moreover, the
structural analysis provides insights into how LysRS wor
213 The
structural analysis quantitatively revealed an energy tr
214 unusual molecular size, single-crystal X-ray
structural analysis (
resolution 0.9 angstrom) and baseli
215 Structural analysis reveal that individual VHHs variably
216 Structural analysis revealed a bilobed architecture with
217 Its
structural analysis revealed a sophisticated interaction
218 Excitingly, our kinetic, thermodynamic, and
structural analysis revealed an array of different prefe
219 Furthermore, mutagenesis and
structural analysis revealed conservation of the helicas
220 Structural analysis revealed that 3 of these 6 putative
221 Molecular dynamics simulations and
structural analysis revealed that a precise intramolecul
222 Structural analysis revealed that all five known arabino
223 Structural analysis revealed that Calhm1(-/-) brains had
224 Structural analysis revealed that Cmpd-1 binding results
225 Structural analysis revealed that inhibitor 3 binds to h
226 Quantitative
structural analysis revealed that interphase NPC assembl
227 te nucleotide analog ADP-AlF(4) Overall, the
structural analysis revealed that nsP2h adopts a uniquel
228 Protein
structural analysis revealed that Phe10Leu mutation may
229 Our
structural analysis revealed that six GDP nucleotides bo
230 ow activities toward pSer(7) and pSer(2) The
structural analysis revealed that Ssu72 requires that th
231 X-ray cocrystal
structural analysis revealed that the basis for this hig
232 The
structural analysis revealed that the Ni(2+) ion is unde
233 In addition,
structural analysis revealed that the orientation of N6
234 Structural analysis revealed that the RNA motif was not
235 An EM-based
structural analysis revealed that TraB tends to assemble
236 Structural analysis revealed that TTC5 binds near the ri
237 Structural analysis revealed the amino acids clustered i
238 experimental results by enabling in-depth 3D
structural analysis,
revealing energetic mechanisms for
239 Solution
structural analysis reveals a ppi Cl [Formula: see text]
240 Structural analysis reveals open and closed gate conform
241 Structural analysis reveals SART3 contains 12 half-a-tet
242 X-ray
structural analysis reveals that 1 features a multi-shel
243 IR secondary
structural analysis reveals that compact conformations a
244 onal perovskite solar cells (average n = 4).
Structural analysis reveals that different packing arran
245 Structural analysis reveals that ppGpp binds the PRPP bi
246 Structural analysis reveals that Smurf2 has Nedd8-bindin
247 Structural analysis reveals that the Axin segment respon
248 Structural analysis reveals that the fine specificity is
249 Structural analysis reveals that the methyl, hydroxymeth
250 Protein
structural analysis reveals that the missense mutations
251 Crystal
structural analysis reveals that the spiro-structures fa
252 Structural analysis reveals that while the SprT domain i
253 The gene
structural analysis separated these 52 genes into an int
254 Structural analysis showed that homeodomain specificity
255 Structural analysis showed that Phactr1 binding remodels
256 Mutational and
structural analysis showed that potent and selective inh
257 The
structural analysis showed that the sugars are bound to
258 Structural analysis shows FcRn is a nonclassical major h
259 the complex enables UbcH10 association, and
structural analysis shows how the Cdc20 subunit intrinsi
260 Structural analysis shows how the Sam50 beta-barrel open
261 Structural analysis shows that Ad4 E3-19K adopts a terti
262 Structural analysis shows that some analogs of this fami
263 Microscopic
structural analysis shows that the crystal lattice twist
264 Structural analysis shows that, in the presence of palmi
265 preribosomes using affinity purification and
structural analysis,
studies on mammalian ribosome bioge
266 Structural analysis suggested that both mutations affect
267 Structural analysis suggests a mechanism by which residu
268 need for active nuclear import, sequence and
structural analysis suggests that a monopartite nuclear
269 Structural analysis suggests that ATP binding and hydrol
270 Structural analysis suggests that in mUHRF1 V1, in contr
271 Structural analysis suggests that the ankyrin repeat dom
272 Structural analysis suggests that the local fitness land
273 Our
structural analysis supports the assertion that MrNV may
274 ors combined with genome-enabled proteomics,
structural analysis,
targeted gene knockouts and treatme
275 s and aggregates, making traditional protein
structural analysis techniques challenging.
276 Supported by mutational data and
structural analysis,
these direct observations reveal th
277 Structural analysis through X-ray diffraction and Raman
278 with dengue and performed in-silico protein
structural analysis to identify epitope similarities.
279 We use quantitative comparative
structural analysis to localize the origins of L1 stalk
280 Structural analysis together with computational and muta
281 Here, we combine
structural analysis,
unbiased genetic approaches in yeas
282 The
structural analysis unveils the role of conserved residu
283 In silico DNA
structural analysis upstream of this motif showed that t
284 Structural analysis using molecular dynamics simulations
285 Further
structural analysis using mutagenesis studies and molecu
286 Our
structural analysis using photoactivable anesthetics and
287 :viral RNA complex on a scale sufficient for
structural analysis using small-angle X-ray scattering a
288 henotype in Torsin-deficient cells enables a
structural analysis via electron microscopy tomography a
289 Structural analysis was performed using high-resolution
290 oseltamivir, zanamivir, or sialic acid, and
structural analysis was performed.
291 Structural analysis was used to identify positions for c
292 opy and circular dichroism (CD) spectroscopy
structural analysis we were able to separate proteins ba
293 mology, evolutionary statistics, and protein
structural analysis,
we could track changes in substrate
294 ownian dynamics simulation and computational
structural analysis,
we found that deoxy-hydrolysis prod
295 me mistakes CO(2) for O(2) Using genomic and
structural analysis,
we identify regions around the cata
296 says, coimmunoprecipitation experiments, and
structural analysis,
we probed the GAP mode and found th
297 In this study, by combining biochemical and
structural analysis,
we revealed distinct transcriptiona
298 meningeal Alzheimer's brain tissue and their
structural analysis with cryo-electron microscopy.
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