1 of the protein as we show in biochemical and
structural analyses.
2 structurally mapped after sequence and X-ray
structural analyses.
3 atom of Gly48 of protease as examined in the
structural analyses.
4 9- and K33-linked chains for biochemical and
structural analyses.
5 This was shown by chemical and
structural analyses.
6 ptidoglycan pose a challenge to conventional
structural analyses.
7 ing a direct binding assay, mutagenesis, and
structural analyses.
8 l shift differences, thus paving the way for
structural analyses.
9 6, within the FAK family is explained by our
structural analyses.
10 ylotrophic yeast Pichia pastoris (PpCSP) for
structural analyses.
11 poses a great challenge for biochemical and
structural analyses.
12 identified through genetic, biochemical and
structural analyses.
13 tigated through functional, biophysical, and
structural analyses.
14 ronments and may be useful for other protein
structural analyses.
15 strate and cosubstrate sites, as revealed by
structural analyses.
16 hree main families based on evolutionary and
structural analyses (
A-, B- and C-families), with the B-
17 NMR and small-angle X-ray scattering (SAXS)
structural analyses allowed us to construct models of bo
18 Our
structural analyses also demonstrate that self-intoxicat
19 Based on the X-ray
structural analyses,
an earlier study has made a compell
20 seen for CsF and CsCl, single-crystal X-ray
structural analyses and (1)H NMR spectroscopic studies r
21 Structural analyses and binding experiments comparing th
22 g of mouse brain tissue, and will facilitate
structural analyses and connectomics of large assemblies
23 to serum C1q as judged from biochemical and
structural analyses and exhibits the characteristic shap
24 that begins with extensive laboratory-based
structural analyses and functional assays.
25 Based on
structural analyses and genetic and biochemical experime
26 around axons is currently widely studied by
structural analyses and large-scale imaging techniques,
27 Structural analyses and molecular dynamics simulations s
28 tions as a cardiolipin transporter(6-9), our
structural analyses and physiological studies identify a
29 insights that could prove helpful in further
structural analyses and screening of ECA(LPS) among Ente
30 The combined computer-based
structural analyses and supporting physicochemical prope
31 Structural analyses and theoretical calculations togethe
32 onents (including isomeric NAs) for in-depth
structural analyses,
and a method by which NA analytes,
33 uginosa (SPOR-RlpA) by mass spectrometry and
structural analyses,
and demonstrate that indeed the pre
34 ut not Galphaq, Using sequence conservation,
structural analyses,
and mutagenesis, we identify a hydr
35 preference of FadD10 through biological and
structural analyses,
and the data indicate long chain sa
36 troscopic titrations, ICP-MS, single-crystal
structural analyses,
and theoretical calculations.
37 Moreover,
structural analyses are performed revealing relevant cha
38 ional modeling, including both energetic and
structural analyses,
are compared with novel data from p
39 Morphology and
structural analyses,
as well as IR studies as a function
40 we use a combination of VA RNAI mutagenesis,
structural analyses,
as well as PKR activity and binding
41 Comparative
structural analyses between conventional cobalamin ribos
42 Comparative
structural analyses between iLOV and its progenitors rev
43 Structural analyses by mass spectrometry allowed the ide
44 Evolutionary and protein
structural analyses can provide functional insights into
45 Structural analyses combined with binding assays indicat
46 In this study,
structural analyses combined with site-directed mutagene
47 n, this glycolipid was subjected to detailed
structural analyses,
combining gas-liquid chromatography
48 Through genetic, functional, and
structural analyses,
commonalities among different mutat
49 Structural analyses define the stoichiometry of the comp
50 Biochemical and
structural analyses demonstrate that Cmpd-43 and its clo
51 Recent biochemical, genetic and
structural analyses demonstrate that GA de-represses its
52 Finally,
structural analyses demonstrated CG17282 is a noncanonic
53 Structural analyses demonstrated that one antibody inter
54 However, biochemical and
structural analyses demonstrated the apicomplexan orthol
55 Structural analyses demonstrated the profound influence
56 mbined with the accompanying biochemical and
structural analyses directly correlate VP35 dsRNA bindin
57 Combined with mutagenesis study, our
structural analyses elucidate two distinct inhibitory me
58 Structural analyses,
functional characterizations and co
59 Structural analyses further localize ORF19 and ORF32 pro
60 Structural analyses guided the discovery of a broad, spl
61 -cell imaging, modeling, and high-resolution
structural analyses has revealed more complexity and pro
62 Our in vitro assembly and
structural analyses have been enabled by the creation of
63 Furthermore,
structural analyses have identified biochemically discre
64 Previous CaCC
structural analyses have relied on homology modelling of
65 insolubility of e-gp41, most biophysical and
structural analyses have relied on the production of tru
66 tinct insulin binding sites, 1 and 2, recent
structural analyses have resolved only site 1.
67 V-ATPase is a rotary motor, and recent
structural analyses have revealed different rotary state
68 nce the SARS-CoV outbreak in 2002, extensive
structural analyses have revealed key atomic-level inter
69 High-resolution crystal
structural analyses have revealed that I-CLiPs harbor th
70 These studies, together with
structural analyses,
have yielded comprehensive models o
71 Our
structural analyses highlight differences in the interac
72 Subsequent complementary genetic and
structural analyses in yeast implicate these alleles in
73 as further investigated through the multiple
structural analyses including HPLC, IR and NMR.
74 Herein, we employed phylogenetic and
structural analyses including the use of a novel model f
75 Structural analyses indicate affected residues cluster a
76 Biochemical and
structural analyses indicate how plasticity of hydrophob
77 Structural analyses indicate that Ccp1 forms a homodimer
78 Spectroscopic and x-ray diffraction
structural analyses indicate that despite their non-fibr
79 Structural analyses indicate that fSHAPE precisely detec
80 Structural analyses indicate that MFS transporters evolv
81 Importantly, our
structural analyses indicate that the conformation of th
82 Furthermore, biochemical and
structural analyses indicate that the dimer-of-dimers co
83 Our
structural analyses indicate that the relative shape and
84 Functional predictions from
structural analyses indicate that, contrary to previous
85 rchromicity, the circular dichroism, and the
structural analyses indicated that Psi(39) enhanced the
86 anced or force-independent in labeling, with
structural analyses indicating the force-enhanced sites
87 Furthermore,
structural analyses led to dissection of the induced-fit
88 These
structural analyses led us to test the role of the poly-
89 Structural analyses localized the BH4 interaction site t
90 or binding to arabinoxylan, although protein
structural analyses may be required to confirm some of t
91 ploying population and cancer genomics data,
structural analyses,
molecular dynamics simulations, res
92 A combination of measurements of pKa values,
structural analyses of 2,6-diarylanilinium cations, and
93 Genetic, biochemical, and
structural analyses of an Nbs1-Ctp1 complex show Nbs1 re
94 re-based vaccine design depends on extensive
structural analyses of antigen-antibody complexes.Single
95 Structural analyses of APRs indicate that APRs are three
96 Recent
structural analyses of ARFs and Aux/IAAs have raised que
97 Despite the extensive
structural analyses of b (6) f-lipid interactions, the b
98 nalysis have enabled routine high-resolution
structural analyses of biological macromolecules, result
99 Here, we describe detailed functional and
structural analyses of CCRs from Medicago truncatula and
100 rt the results of genomic, phylogenetic, and
structural analyses of ComGC, the major pilin subunit of
101 Combining
structural analyses of cryo-electron microscopy data wit
102 Solution-state
structural analyses of cyclopentyllithium and cyclopenty
103 Structural analyses of DAD2(N242I) and DAD2(D166A) revea
104 Structural analyses of distinct segments ("protomers") o
105 also report in-depth X-ray crystallographic
structural analyses of each isoform at 1.9 and 2.4 angst
106 Structural analyses of Fab fragments of mAbs 023.102 and
107 Structural analyses of features characteristic for parti
108 Using detailed
structural analyses of FeRh films of varying crystalline
109 Here, we describe
structural analyses of five different extensively retarg
110 This allows
structural analyses of fluorescence-labeled I/R hearts w
111 The combined biochemical and
structural analyses of FrbF provide insights into this p
112 Structural analyses of germline mAb BBE6.12H3 in an Ag-f
113 rate previous physiological, biochemical and
structural analyses of glutamate receptors and provide a
114 re investigated through single-crystal X-ray
structural analyses of guest-exchanged 1S and 1R.
115 In this study, biochemical and
structural analyses of H. pylori HypB (HpHypB) revealed
116 tools for detailed, high-throughput, de novo
structural analyses of highly sulfated GAGs.
117 X-ray
structural analyses of inhibitor-bound crystal structure
118 d organisms, (ii) performing biochemical and
structural analyses of key enzymes to understand thermod
119 Structural analyses of ligand-occupied Klotho extracellu
120 Secondary
structural analyses of locus A recombinant WxL domain-co
121 Previous
structural analyses of NRs, although productive in eluci
122 Structural analyses of nucleoside inhibitor binding prov
123 Previous
structural analyses of Old World arenaviral GP1 glycopro
124 Structural analyses of other cap-binding proteins indica
125 n mechanisms revealed by the biochemical and
structural analyses of replicative and translesion synth
126 Structural analyses of ribosomal complexes indicate that
127 iendly visualization tool and a standard for
structural analyses of simulated systems.
128 ts that the samples are amenable to detailed
structural analyses of spherules engaged in RNA synthesi
129 Biochemical and
structural analyses of sRNPs assembled with mutant sRNAs
130 especially if combined with high-resolution
structural analyses of such inhibitors to shed light on
131 Also,
structural analyses of the altered proteins identified c
132 Structural analyses of the amyloidogenic intermediates u
133 Our detailed
structural analyses of the ASPP-p53 interactions provide
134 igh quality of the maps should enable future
structural analyses of the chemical basis for translatio
135 comprehensive biochemical, biophysical, and
structural analyses of the complex formed between PGC-1a
136 Structural analyses of the complexes with oxaloacetate a
137 We have carried out 3D
structural analyses of the core editing complex or "L (l
138 Structural analyses of the E2 epitope bound to hu5B3.v3
139 tegrative approach of three-dimensional (3D)
structural analyses of the entire phage by cryo-electron
140 Structural analyses of the extracellular region of stem
141 ost & Microbe, Moonens et al. (2016) perform
structural analyses of the Helicobacter pylori adhesin B
142 it can serve as a starting point for further
structural analyses of the HOPS tethering complex.
143 Structural analyses of the hPAH:BH(4) subunits revealed
144 Comprehensive lipidomic and
structural analyses of the lungs revealed aberrant phosp
145 adapter P of Mononegavirales We outline the
structural analyses of the Mononegavirales polymerases s
146 Moreover,
structural analyses of the MSP domain alone or in comple
147 Further, the phylogeny and predicted
structural analyses of the nine paralogs revealed that P
148 y at a similar level to wild-type NFeoB, and
structural analyses of the nucleotide-free and GDP-bound
149 lls in vitro In summary, our biochemical and
structural analyses of the P. luminescens lectin PllA ha
150 X-ray
structural analyses of the PIs complexed with wild-type
151 Structural analyses of the PRL-1.Peptide 1 complex revea
152 Structural analyses of the receptor binding hemagglutini
153 Detailed energetic and
structural analyses of the simulation results indicate t
154 rch on transposable elements, no large-scale
structural analyses of the TE proteome have been perform
155 We report the biochemical and
structural analyses of the TE/CLC domain in polyketide s
156 Prior PS
structural analyses of the vaccine-associated serotype 2
157 Based on the energetic and
structural analyses of the wild-type and mutant enzymes,
158 Our
structural analyses of these networks revealed that the
159 Structural analyses of these revealed primarily an influ
160 However, only medium resolution
structural analyses of this complex have been reported.
161 Structural analyses of transcriptionally competent DLPs
162 X-ray
structural analyses of tridentate halogen bond donors (h
163 Structural analyses of tRNase Z(L) performed by limited
164 Structural analyses of Tse6 show that it resembles mono-
165 Primary sequence comparisons and x-ray
structural analyses of two MERS-CoV 3CLpro and inhibitor
166 Here we present
structural analyses of two rabbit MAbs, R56 and R20, aga
167 Detailed sequence and
structural analyses of Ydr109c and FGGY as well as homol
168 Structural analyses of yeast and mammalian CTD are hampe
169 animal cells and is a strategy for focusing
structural analyses on functionally important glycans.
170 Structural analyses on other riboswitch RNA classes, whi
171 In the present experiments, we focused our
structural analyses on the ventral occipitotemporal regi
172 Structural analyses performed on adults showed that repr
173 Prior biochemical and
structural analyses pinpointed the amidine moiety of bas
174 es for WT and DM, together with the thorough
structural analyses presented herein, we propose that th
175 c studies, which, when combined with ongoing
structural analyses,
promise to provide details for mech
176 Traditional
structural analyses provide a static image of conformers
177 Enzyme kinetic and NA
structural analyses provide an explanation for the high
178 Our
structural analyses provide pseudo-atomic models at vari
179 These classifications and
structural analyses provide rules for assigning current
180 Biochemical and
structural analyses provide unique insights into the sub
181 l calculations, electrical measurements, and
structural analyses provides evidence of room-temperatur
182 The enzymatic and
structural analyses reported here provide a valuable mol
183 Structural analyses reveal a tripartite recognition mech
184 In conclusion, our biochemical and
structural analyses reveal autoinhibitory and activation
185 ular modeling and nuclear magnetic resonance
structural analyses reveal direct hirsutinolide:Stat3 bi
186 Structural analyses reveal glycosaminoglycan binding sit
187 Crystallographic
structural analyses reveal much about the exquisite hexa
188 recognition mechanisms vary from RNA to RNA,
structural analyses reveal recurring strategies that ari
189 PntC
structural analyses reveal steric discrimination against
190 Structural analyses reveal subunit interfaces responsibl
191 Phylogenomic and
structural analyses reveal that F17-like pili are closel
192 Our
structural analyses reveal that in contrast to the heter
193 The solid-state and computational
structural analyses reveal that m-CBPQT(2(+*)) is ideall
194 Structural analyses reveal that m12 sequesters a large N
195 Structural analyses reveal that these sites interact dir
196 Mutagenesis and
structural analyses reveal that, for this infant bnAb, s
197 g the tDED filament structure as a template,
structural analyses reveal the interaction surfaces betw
198 Structural analyses reveal the mechanism of recognition
199 ther with results of genomic, proteomic, and
structural analyses,
reveal several putative virulence f
200 Structural analyses revealed an EB-like +TIP-binding mot
201 Biochemical and
structural analyses revealed cleavage of ESF1 propeptide
202 Structural analyses revealed conformational variations o
203 Biofilm
structural analyses revealed country-specific difference
204 Structural analyses revealed focal hippocampal atrophy w
205 Previous
structural analyses revealed important differences betwe
206 Chromatin
structural analyses revealed interactions within the car
207 Enzyme kinetics and
structural analyses revealed SmCI to be an inhibitor of
208 Ultra-
structural analyses revealed that desmosomes were absent
209 Structural analyses revealed that DupA and SidE ubiquiti
210 Biochemical and
structural analyses revealed that NleD exclusively targe
211 Structural analyses revealed that S-nitrosylated cystein
212 The
structural analyses revealed that steric force inherent
213 The present
structural analyses revealed that TbGMPR forms an octame
214 Structural analyses revealed that the beta-hairpin of 40
215 T cell recognition foot-print and pMHC-I
structural analyses revealed that the cross-reactive T c
216 Detailed
structural analyses revealed that the dyads assemble to
217 Structural analyses revealed that the RhoGAP domain of M
218 Structural analyses revealed that the selected HA mutati
219 Additional
structural analyses revealed that the sequence identity
220 Extensive
structural analyses revealed that this AAV-derived vecto
221 Recent
structural analyses revealed the close proximity of Cys-
222 Structural analyses revealed the mechanism underlying th
223 Genetic and
structural analyses revealed two of these lineages to be
224 rved tertiary structure of these regulators,
structural analyses revealed unexpected diversity in the
225 ere evidenced by morphological, physical and
structural analyses,
revealed elongated structures protr
226 se findings with solvent mapping and various
structural analyses reveals alternative druggable sites
227 This finding, together with comparative
structural analyses,
reveals that the principal site of
228 Our
structural analyses shed light on the genetic mutations
229 X-ray and computational
structural analyses show a "transition-metal-like" cis-b
230 Structural analyses show that eukaryotic SWEETs are comp
231 Structural analyses show that IMes-N2O is able to act as
232 Kinetic, biochemical, and X-ray
structural analyses show that the two expressed proteins
233 Our previous
structural analyses show that TlpB binds urea with high
234 Structural analyses showed an increase in polar side cha
235 Biochemical and
structural analyses showed binding to and inhibition of
236 Sequence and
structural analyses showed differences between the activ
237 The BA9/10 regions identified through
structural analyses showed increases in blood oxygen lev
238 Ultra-
structural analyses showed mitochondrial and endoplasmic
239 Structural analyses showed that one antibody gene family
240 Sequential and
structural analyses showed that residues conserved throu
241 X-ray and NMR
structural analyses showed that the (S)-C5'-Me epimers a
242 Structural analyses showed that the extract contained tw
243 nuclear magnetic resonance measurements and
structural analyses,
showed that many of the DNA mismatc
244 Previous
structural analyses showing little differences between n
245 ERG results are consistent with the
structural analyses showing the greatest attenuation of
246 Structural analyses,
site-directed mutagenesis experimen
247 l-based interferon suppression assays, these
structural analyses strongly support a unified model of
248 Based on these
structural analyses,
substrate-based aldehyde inhibitors
249 Structural analyses suggest a face-to-face stacking of D
250 for sCJD(MM1) prions by more than 100 days;
structural analyses suggest a profound change in the ori
251 Both biochemical and X-ray crystal
structural analyses suggest an unusual mechanism of beta
252 Further
structural analyses suggest that all CNTN ectodomains ad
253 Structural analyses suggest that S305-P forms a charge-l
254 D, and V321I residue changes were found, and
structural analyses suggest that these mutations distort
255 DZ2 mediates the GRASP self-interaction, and
structural analyses suggest that this occurs via a uniqu
256 Further bioinformatics, biochemical, and
structural analyses suggested that phenylalanine (F309)
257 Structural analyses suggested that the mutation disturbs
258 Finally,
structural analyses support findings of previously misse
259 These kinetic measurements, and supporting
structural analyses,
support a mechanism in which some u
260 se rPrP aggregates more amenable to detailed
structural analyses than bona fide PrP(Sc).
261 h genetic complementation and polysaccharide
structural analyses that C. glabrata ANP1, MNN2, and MNN
262 rther demonstrate through in-depth cell wall
structural analyses that OsCAldOMT1-deficient rice plant
263 square deviations combined with the detailed
structural analyses,
the helical bundle of the CB(1) rec
264 enzymatic extractions, followed by detailed
structural analyses,
the newly produced HM polymers were
265 oteins have been analyzed by high-resolution
structural analyses,
the residues involved in RNA-recogn
266 lation signature that couples epigenomic and
structural analyses,
thereby offering insights into the
267 f A. baumannii LPS were limited primarily to
structural analyses;
therefore, studies evaluating the c
268 However,
structural analyses to date have focused on how SF1A hel
269 iral passaging, deep sequencing, and protein
structural analyses to define escape mutations and mecha
270 Here we use functional and
structural analyses to demonstrate that HLA-C expression
271 Here, we use comprehensive biochemical and
structural analyses to demonstrate that PTPRG.CNTN3-6 co
272 elationships requires sensitive and accurate
structural analyses to determine parameters like degree
273 We used X-ray
structural analyses to determine possible modes of irrev
274 ces in susceptibility with multiple in-depth
structural analyses to identify key ACE2 amino acid posi
275 ns using the cell culture infectious HCV and
structural analyses to identify mechanisms of HCV resist
276 We have now used comparative sequence and
structural analyses to study the structure and evolution
277 andom forest predictor trained on rule-based
structural analyses together with structural clustering
278 In the
structural analyses,
Tp-THF of GRL-015, -085, and -097 s
279 The chemical and
structural analyses using HRTEM, Rutherford backscatteri
280 Biochemical and
structural analyses using NMR and fluorescence spectrosc
281 Based on our sequence and
structural analyses using the crystal structure of CA_C2
282 Structural analyses using various X-ray techniques revea
283 nation of molecular dynamics simulations and
structural analyses,
we find that the neck sequentially
284 S-based analyses of O-glycans, and NMR-based
structural analyses,
we identified a B. cenocepacia O-gl
285 - and nuclear magnetic resonance (NMR)-based
structural analyses,
we identified a phosphorylated O-ma
286 On the basis of these kinetic and
structural analyses,
we propose possible mechanistic rol
287 Based on
structural analyses,
we propose that the enhanced rate o
288 Using cellular, biophysical, and
structural analyses,
we show that CDR3alpha residues can
289 Using an array of biochemical and
structural analyses,
we show that Fsq is a member of the
290 erium exchange, fluorescence anisotropy, and
structural analyses,
we show that the flexibility of the
291 Using genetic and
structural analyses,
we solve the mystery here by showin
292 On the basis of our
structural analyses,
we suggest a mechanism whereby mole
293 Based on these kinetic, biochemical, and
structural analyses,
we suggest that these compounds are
294 Whole-brain
structural analyses were also performed.
295 Additional spectroscopic and
structural analyses were done to track the dependencies
296 omprehensive bioinformatics, biochemical and
structural analyses were used to acquire a better unders
297 Here we combine
structural analyses with a "Reconstructed Evolutionary A
298 We combine our
structural analyses with both functional and computation
299 Further
structural analyses with computational docking results u
300 gy approach that combines transcriptomic and
structural analyses with live-cell imaging to predict sm