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1 out the domain, as determined by (2)H methyl NMR relaxation.
2 tional molecular dynamics is not detected by NMR relaxation.
3 different backbone mobility, as monitored by NMR relaxation.
4 G4T4G4) is slow on the timescale of the 23Na NMR relaxation.
5 h measures of side-chain motion derived from NMR relaxation.
6 ized using (15)N nuclear magnetic resonance (NMR) relaxation.
7           Here we show that solid-state (2)H NMR relaxation allows investigation of light-induced cha
8 onditions studied, the order parameters from NMR relaxation analysis are uniformly high (>0.8) for mo
9 ers, structure-based calculations, and (15)N NMR relaxation analysis highlights the energetic contrib
10 ents, multiangle light scattering, and (15)N NMR relaxation analysis indicate that AtraPBP1 forms a s
11 d gradient NMR diffusion experiments and 15N NMR relaxation analysis indicate that Ca2+-bound DREAM f
12                                              NMR relaxation analysis revealed that protein dynamics w
13 ysis combined with dynamic measurements from NMR relaxation and diffusion data provides direct eviden
14                 Hydrodynamic parameters from NMR relaxation and diffusion measurements showed that fA
15  adapted version of H/D exchange experiment, NMR relaxation and diffusion measurements, dynamic light
16 gnetometers as detectors for ultra-low-field NMR relaxation and diffusion measurements.
17                                              NMR relaxation and dispersion experiments compare fast (
18 udies of conformational flexibility from 15N NMR relaxation and H/D exchange experiments.
19  and RLP2-bound SH3 were performed via (15)N NMR relaxation and hydrogen-deuterium (H/(2)H) exchange
20                                          Our NMR relaxation and hydrogen-deuterium exchange studies t
21                                  Using (15)N NMR relaxation and hydrogen/deuterium exchange, we demon
22 ions proposed on the basis of recent elegant NMR relaxation and line-shape analyses, the energetics o
23 in of Trp102 obtained from the fluorescence, NMR relaxation and minimum perturbation data are consist
24 in (ABP) with its ligand, d-galactose, using NMR relaxation and molecular dynamics simulation.
25  T antigens have been investigated using 15N NMR relaxation and molecular dynamics simulation.
26 d electron spin resonance spectroscopy, (1)H NMR relaxation, and (19)F NMR spectroscopy experiments w
27 re further studied by X-ray crystallography, NMR relaxation, and pulse-EPR methods, in conjunction wi
28 ptor-like kinase partner, according to (15)N NMR relaxation at 11.7 and 14.1 T.
29 o barnase, is investigated with (15)N, (13)C NMR relaxation at 11.74 and 18.78 T and with a 1.1 ns mo
30                              Unlike solution NMR relaxation-based order parameters, order parameters
31                          We report a (129)Xe NMR relaxation-based sensing approach that exploits chan
32            These results suggest that F- 19F NMR relaxation can be used to predict the reactivities o
33 nce is much stronger than the case for other NMR relaxation constants, including the "conventional" r
34 thermore, analyses of the spin-label induced NMR relaxation corroborates the presence of a discrete t
35                                    The (15)N NMR relaxation data ((15)N-T(1), (15)N-T(2), and heteron
36 bling may be determined by analysis of (15)N NMR relaxation data according to the Lipari-Szabo model
37 al diffusion model is generally required for NMR relaxation data analysis in single-domain proteins,
38                                        (15)N NMR relaxation data and RDCs show that TM is highly orde
39                                              NMR relaxation data and structural studies of the folded
40                                  As shown by NMR relaxation data collected at two fields, several cle
41    This method offers the possibility to use NMR relaxation data for detailed structure characterizat
42                        The interpretation of NMR relaxation data for macromolecules possessing slow i
43 lography data on the free protein, and (15)N NMR relaxation data for the uncomplexed and HA(8)-bound
44                           Proper analysis of NMR relaxation data for these systems in solution has to
45                                        (15)N NMR relaxation data identify significant motion occurrin
46 ide bases is important for interpretation of NMR relaxation data in terms of local dynamic properties
47 eloped by Freed and others, we interpret the NMR relaxation data in terms of localized water translat
48 ynamic properties were determined from (15)N NMR relaxation data in terms of the extended model-free
49                                      The 13C NMR relaxation data indicate substantial dynamic fluctua
50 parameters of polyunsaturated chains and the NMR relaxation data indicate that both DHA and DPA under
51  structure of this helix is well formed, but NMR relaxation data indicate that there is considerable
52                                        (31)P-NMR relaxation data indicated a change in lipid headgrou
53 ework is presented for the interpretation of NMR relaxation data of proteins.
54                  The approach was applied to NMR relaxation data of ubiquitin collected at multiple m
55                          Our analysis of the NMR relaxation data quantifies subtle changes in the int
56                                              NMR relaxation data reveal a role for conformational pla
57                                              NMR relaxation data reveal that the source of the differ
58                  Our structural analysis and NMR relaxation data show that these motifs do not intera
59                                  Analysis of NMR relaxation data shows that the chemical exchange exh
60                                              NMR relaxation data suggest that structural dynamics are
61 n of the novel RED results and corresponding NMR relaxation data suggests that the loss of collective
62 nt of a peptide sequence, we have used (15)N NMR relaxation data to characterize the backbone motions
63            Detailed analysis of backbone 15N NMR relaxation data using both the Lipari-Szabo model-fr
64 namics of eotaxin-3 were determined from 15N NMR relaxation data using the extended model free dynami
65                                              NMR relaxation data were analyzed by the model-free appr
66 s, their eigenvalues, and correlation times, NMR relaxation data were calculated in accordance with B
67  characterized based on an analysis of (15)N NMR relaxation data which we have interpreted using the
68 ze our simulation trajectories, we reproduce NMR relaxation data without fitting any parameters of ou
69                                        (13)C-NMR relaxation data, analyzed using the model-free forma
70                          Comparison of (15)N NMR relaxation data, reduced spectral density profiles,
71                              On the basis of NMR relaxation data, the alpha2 helix as well as the bet
72 in via a hydrophilic interface and, based on NMR relaxation data, undergoes inter-domain motions enab
73 that provide a microscopic interpretation of NMR relaxation data.
74 etation of dynamics parameters obtained from NMR relaxation data.
75 near models and the distances implied by the NMR relaxation data.
76  or 64TC lesions were investigated using 15N NMR relaxation data.
77 the (3)J(NzetaCgamma)-coupling constants and NMR-relaxation-derived S(2) order parameters of the NH(3
78 arrowed linewidths, and accurate analysis of NMR relaxation dispersion (CPMG) and TROSY-based CEST ex
79                                              NMR relaxation dispersion (RD) spectroscopy based on a C
80                 By applying a combination of NMR relaxation dispersion and fluorescence kinetics meth
81                           The combination of NMR relaxation dispersion Carr-Purcell-Meiboom-Gill (CPM
82 ermined from a linear dependence of the (1)H NMR relaxation dispersion drawn as a function of the squ
83 millisecond dynamics that can by measured by NMR relaxation dispersion experiments and shows a linear
84                                     Solution NMR relaxation dispersion experiments performed under ph
85                           Data gathered from NMR relaxation dispersion experiments show that a subset
86                                              NMR relaxation dispersion experiments with that enzyme s
87                                              NMR relaxation dispersion experiments, coupled with conc
88 in Pol beta have been determined by solution NMR relaxation dispersion for the apo and substrate-boun
89  and off-resonance carbon and nitrogen R1rho NMR relaxation dispersion in concert with mutagenesis an
90 at Carr-Purcell-Meiboom-Gill (CPMG) 13Calpha NMR relaxation dispersion measurements are a viable mean
91                                              NMR relaxation dispersion measurements indicate that res
92                                              NMR relaxation dispersion measurements of millisecond ti
93 ynamics of these states have been studied by NMR relaxation dispersion measurements of the methyl gro
94      Based on these results and pH-dependent NMR relaxation dispersion measurements, we estimate that
95               Here, we use side-chain proton NMR relaxation dispersion measurements, X-ray crystallog
96 ysis using the Modelfree approach and by the NMR relaxation dispersion measurements.
97 ange broadening effects (R(ex)) as probed by NMR relaxation dispersion measurements.
98                             We recently used NMR relaxation dispersion methods and computational tech
99 apture key properties previously measured by NMR relaxation dispersion methods including the structur
100                            Studies employing NMR relaxation dispersion recently showed that wobble dG
101                         In the present work, NMR relaxation dispersion spectroscopy is used to direct
102 ogical function, as demonstrated by numerous NMR relaxation dispersion studies.
103                                   We applied NMR relaxation dispersion to investigate the role of bou
104                                  Here we use NMR relaxation dispersion to probe conformational exchan
105       In this study, we use a combination of NMR relaxation dispersion, model-free analysis, and liga
106                                        Using NMR relaxation dispersion, we have measured the temperat
107                                        Using NMR relaxation dispersion, we show here that wobble dG*d
108 ed with intrinsic millisecond dynamics using NMR relaxation dispersion.
109 the contacts in detail, we used paramagnetic NMR relaxation enhancements, in combination with single-
110                       A ligand-observed (1)H NMR relaxation experiment is introduced for measuring th
111                                          13C-NMR relaxation experiments (T(1), T(2), T(1)(rho), and N
112                                              NMR relaxation experiments and other biophysical measure
113 and side-chain order parameters derived from NMR relaxation experiments are in excellent agreement wi
114                                              NMR relaxation experiments clarified the hypothesis abou
115                                        (19)F NMR relaxation experiments employing an active-site inhi
116                                     Solution NMR relaxation experiments identify a cluster of residue
117                                              NMR relaxation experiments indicated that a flexible loo
118                                              NMR relaxation experiments indicated that the peptide wa
119                                        (15)N NMR relaxation experiments of the (15)N-labeled recombin
120                                              NMR relaxation experiments often require site-specific i
121                       Two-dimensional 1H-15N NMR relaxation experiments on [alpha-15N]histidine-label
122                                              NMR relaxation experiments reveal that HisJ becomes more
123                                              NMR relaxation experiments sensitive to motions of methy
124                                        (15)N NMR relaxation experiments show that PTB1:34 has slow, m
125              Complementary cross-linking and NMR relaxation experiments show that the OmpA beta-barre
126                             The kinetics and NMR relaxation experiments suggest that the weak binding
127                       Moreover, we carry out NMR relaxation experiments to characterize the picosecon
128                                 We have used NMR relaxation experiments to determine the molecular ba
129                           We have used (13)C NMR relaxation experiments to examine changes in the mot
130                   In this study, we used 15N NMR relaxation experiments to probe the fast (i.e., ps-n
131                  In addition, by using (15)N NMR relaxation experiments, we find that binding ubiquit
132                     Furthermore, using (15)N NMR relaxation experiments, we show that, in the mutant
133 ributions to side-chain dynamics measured by NMR relaxation experiments.
134 and during catalysis were characterized with NMR relaxation experiments.
135 monitored by hydrogen/deuterium exchange and NMR relaxation experiments.
136 sin inhibitor (BPTI) were examined using 15N NMR relaxation experiments.
137 and two-dimensional (1)H-(15)N heteronuclear NMR relaxation experiments.
138 ired mobility by both molecular dynamics and NMR relaxation experiments.
139                  Nuclear magnetic resonance (NMR) relaxation experiments show that TF interacts with
140                  Most theoretical models for NMR relaxation in liquids assume that overall rotational
141                                              NMR relaxation indicates compensatory changes in loop fl
142 obility gradient similar to that observed in NMR relaxation, indicating that side chain motions mirro
143                                              NMR relaxation is used here to monitor the effects of hi
144 hly dynamic and mostly extended according to NMR relaxation measurements and analytical ultracentrifu
145 ex with DNA have been characterized by (15)N NMR relaxation measurements and model-free analysis.
146 ere investigated at 30 degrees C using (15)N NMR relaxation measurements and NMR monitored hydrogen-d
147                               Interestingly, NMR relaxation measurements and the results of a model b
148 ely) of carboxyl side chains, based on (13)C NMR relaxation measurements as a function of pH.
149  analogue were determined from heteronuclear NMR relaxation measurements at similar solution conditio
150                                Historically, NMR relaxation measurements have played a dominant role
151                                              NMR relaxation measurements have suggested that changes
152                By use of heteronuclear (15)N NMR relaxation measurements in a series (n = 1-6) of (15
153 ned rotational diffusion tensor derived from NMR relaxation measurements in macromolecular structure
154                                              NMR relaxation measurements of 15N spin-lattice relaxati
155  motion was investigated by 1H, 13C, and 15N NMR relaxation measurements on a DNA decamer d(CATTTGCAT
156                                         (2)H NMR relaxation measurements revealed an additional water
157                                        (15)N NMR relaxation measurements show that full-length HMGB1
158                                  Here we use NMR relaxation measurements to address the kinetics of e
159                                  Here we use NMR relaxation measurements to explore the role of the l
160  hydroxylation and epoxidation, paramagnetic NMR relaxation measurements were conducted.
161 lectron spin resonance spectroscopy and (1)H NMR relaxation measurements, including spin-lattice rela
162                                         23Na NMR relaxation measurements, performed as a function of
163 w temperature as identified by heteronuclear NMR relaxation measurements, secondary chemical shifts,
164 ating those that could be obtained from (1)H-NMR relaxation measurements, were calculated between lig
165 ith a long insertion shown to be flexible by NMR relaxation measurements.
166 ts (CTPR2 and CPTR3, respectively) using 15N NMR relaxation measurements.
167 st equivalent of metal through heteronuclear NMR relaxation measurements.
168 ains on a fast timescale was confirmed using NMR relaxation measurements.
169 namics of TRX(HE) were investigated by (15)N NMR relaxation measurements.
170 ts, PrP(29-231) and PrP(90-231), using (15)N NMR relaxation measurements.
171 m B. fragilis have been examined using (15)N NMR relaxation measurements.
172 bound form of Bcl-x(L) was investigated from NMR relaxation measurements.
173 idaredoxin (Pdx) have been studied by 2D 15N NMR relaxation measurements.
174 scale were compared with those obtained from NMR relaxation measurements.
175  nidulans flavodoxin at pH 6.6, 303 K by 15N NMR relaxation measurements.
176 ligands, which are less commonly analyzed by NMR relaxation measurements.
177 were investigated using backbone amide (15)N-NMR relaxation measurements.
178                                        Here, NMR relaxation methods for characterizing thermal motion
179  of the RNA in the loop and in the stem, 13C NMR relaxation methods have been used to describe the dy
180 es sampled during enzymatic reactions, while NMR relaxation methods reveal the rates of interconversi
181  the unfolded monomer for each variant using NMR relaxation methods revealed that all variants contai
182              Toward this end, we present new NMR relaxation methods that describe ligand flexibility
183           Here, we have used mutagenesis and NMR relaxation methods to investigate the scope and natu
184  combine high resolution field-cycling (31)P NMR relaxation methods with spin-labeled proteins to del
185 ic group-bearing proteins studied with these NMR relaxation methods, the side chains of oxidized flav
186 hey become invisible to traditional solution NMR relaxation methods.
187  in the enzyme dihydrofolate reductase using NMR relaxation methods.
188 hich has not been previously investigated by NMR relaxation methods.
189 ht chain kinase is examined using 15N and 2H NMR relaxation methods.
190 gated using (15)N amide and deuterium methyl NMR relaxation methods.
191 eptide complex using site-specific deuterium NMR relaxation methods.
192 second aromatic-ring dynamics using solution NMR relaxation methods.
193   Several lines of evidence, including (15)N NMR relaxation, NMR chemical shift perturbations, static
194   Results of ligand docking and heme-induced NMR relaxation of drug protons showed that ticlopidine w
195 latus ferrocytochrome c(2) derived from (2)H NMR relaxation of methyl group resonances is presented.
196 elaxivity (i.e., its ability to speed up the NMR relaxation of nearby water molecules).
197 amplitudes of the vibrations, as measured by NMR relaxation or crystallographic B-factors, remain lar
198                         Measurement of (15)N NMR relaxation parameters and backbone hydrogen/deuteriu
199                            Agreement between NMR relaxation parameters and our theoretical results hi
200  behavior of individual domains by measuring NMR relaxation parameters and residual dipolar couplings
201                                          The NMR relaxation parameters are primarily sensitive to rot
202  filtration has allowed the determination of NMR relaxation parameters at an unprecedented number of
203                   Model-free analysis of the NMR relaxation parameters indicated significantly greate
204                      Comparison of the (15)N NMR relaxation parameters of the holo-TrpRs with those o
205 ual structure in the intermediate state, and NMR relaxation parameters T(1) and T(2) and inverted que
206                                        Here, NMR relaxation parameters were acquired for backbone 15N
207                              (15)N and (13)C NMR relaxation parameters were measured for both peptide
208 erase by recording an extensive set of (13)C NMR relaxation parameters.
209 protein, as indicated by the analysis of the NMR relaxation parameters.
210 ) of this oligomer have been determined from NMR relaxation parameters.
211 -3' sequence steps have been determined from NMR relaxation parameters.
212                       Using solid-state (2)H NMR relaxation performed on selectively deuterated methy
213 olactin were investigated by analysis of 15N NMR relaxation phenomena and demonstrated a rigid four-h
214                                    The (15)N NMR relaxation profiles of apo-L75F-TrpR were analyzed a
215  Here we introduce an approach to making the NMR relaxation properties of large proteins amenable to
216 ions and dynamics because of their favorable NMR relaxation properties, which lead to sharp signals i
217 ures of disordered proteins and experimental NMR relaxation properties.
218 (PH) domain from dynamin were studied by 15N NMR relaxation (R1 and R2) and steady state heteronuclea
219 bindin D(9k) have been characterized by (2)H NMR relaxation rate measurements.
220 ) was determined from its effect on the T(2) NMR relaxation rate of either phosphite (HPO(3)(2-)) or
221                               Measurement of NMR relaxation rate of water protons in heating-cooling
222 hibit an ex vivo nuclear magnetic resonance (NMR) relaxation rate (1/T2) as high as 24-39 s-1/mM iron
223                                              NMR relaxation rates ( (15)N R 1, R 2) and (1)H- (15)N h
224                           Moreover, the (2)H NMR relaxation rates are increased by the presence of om
225 residue topology was probed by measuring 19F NMR relaxation rates for site-specifically labeled sampl
226         The paramagnetic enhancements in the NMR relaxation rates for the fluorine in fluorophthalate
227 ISL by analyzing the power dependence of 13C NMR relaxation rates in the rotating frame.
228 onstrate that intermoment distances based on NMR relaxation rates provide a sensitive indicator of in
229 distance, but the distances deduced from the NMR relaxation rates were shorter than expected for ever
230 , predictions for the amide hydrogens of the NMR relaxation-restrained ensemble that become exposed t
231 alysis of protein backbone dynamics based on NMR relaxation reveals a combination of complementary ef
232                We conducted solid-state (2)H NMR relaxation (spin-lattice, T(1Z), and quadrupolar-ord
233                                              NMR relaxation studies are capable of providing "long-ra
234                                              NMR relaxation studies are well suited for examining cha
235                                          31P NMR relaxation studies from 0.005 to 11.7 T are used to
236                                     Previous NMR relaxation studies have identified exchange line bro
237 dynamic was anticipated by previous solution NMR relaxation studies in micelles, these measurements i
238                        Here, we report (13)C NMR relaxation studies of base and ribose dynamics for t
239                                              NMR relaxation studies of the complex were carried out a
240                                     Previous NMR relaxation studies of the isolated RNase H domain of
241 ng 1855 order parameters from 20 independent NMR relaxation studies on proteins whose three-dimension
242                                          15N NMR relaxation studies reveal that the two zinc knuckle
243                          For the first time, NMR relaxation studies show that the viscoelastic proper
244                Previously, we showed through NMR relaxation studies that binding of the RA-GEF2 C-ter
245                       Described here are 15N NMR relaxation studies to compare the backbone dynamics
246                                              NMR relaxation studies were conducted to investigate the
247 ntrifugation, size-exclusion chromatography, NMR relaxation studies, dynamic light scattering, and ci
248                                        Using NMR relaxation studies, the dynamics of the backbone nit
249 xistence of this network comes from previous NMR relaxation studies, where motions in several residue
250 with data from fluorescence polarization and NMR relaxation studies.
251                           Herein we report a NMR relaxation study [(1)H and (13)C T(1), T(2); (13)C{(
252                           Here, we report an NMR relaxation study of dynamics over multiple timescale
253                        Longitudinal (1)H(2)O NMR relaxation time constant (T(1)) values were measured
254 conditions were also studied by 23Na and 7Li NMR relaxation time measurements.
255 the experimentally determined dielectric and NMR relaxation time scales.
256 ng amide hydrogen-deuterium exchange and 15N NMR relaxation times (T1 and T2) and 15N inverted questi
257                                         (1)H NMR relaxation times (T1 and T2) were measured at low fi
258                                 (13)C-[(1)H] NMR relaxation times and steady-state NOE enhancements w
259 by analysis of the power dependence of (13)C NMR relaxation times in the rotating frame (T(1)(rho)).
260 receptor substrate-1 (IRS-PTB), we have used NMR relaxation to determine the dynamics of backbone ami
261                            We used low-field NMR relaxation to investigate CO2 and water interactions
262          This novel approach yields (19)F T2 NMR relaxation values of any fluorinated contaminant, wh
263    Nitrogen-15 backbone and carbon-13 methyl NMR relaxation was measured to investigate the dynamical
264                                              NMR relaxation was used to probe motion on the backbone
265 h measurement of enzyme kinetics, main chain NMR relaxation, X-ray crystallographic studies, and in v

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