戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (left1)

通し番号をクリックするとPubMedの該当ページを表示します
1                                              ESEEM also demonstrates ligation of two water molecules
2                                              ESEEM analysis revealed that two histidines are bound eq
3                                              ESEEM measurements support a differential ability of Mn(
4                                              ESEEM of the 2H-labeled substrate radical states in wild
5                                              ESEEM spectra demonstrate that the histidine imidazole c
6                                              ESEEM spectra have been used to determine the orientatio
7                                              ESEEM spectra of altered MoFe proteins, which were produ
8                                              ESEEM spectra of the previously characterized C24A and C
9                                          14N ESEEM from a hyperfine-coupled protein nitrogen in wild
10                              However, an 15N ESEEM peak was observed in parallel chloride-depleted PS
11 ientation-selective Ka- and Q-band ENDOR, 1D ESEEM, and HYSCORE spectra of (14)N and (15)N-labeled mi
12                                       The 2D ESEEM (HYSCORE) experiments with the Q(H) site SQ in the
13  isotope effect for Y(Z) oxidation and by 2H ESEEM measurement of hydrogen-bond exchange.
14 retains four water ligands as measured by 2H ESEEM spectroscopy.
15 sition (adjacent to the sulfonate group), 2H ESEEM spectra show features that arise from dipole-dipol
16                                      With 2H ESEEM modulation comparable to that of Y(D)*, Y(Z)* woul
17                                         2H2O ESEEM spectra showed that the [2Fe-2S] cluster is access
18 terated at both C1 and C2 show an additional ESEEM feature at the deuterium Larmor frequency.
19 ligates the Mn cluster, we have conducted an ESEEM study of D1-H332E PSII particles.
20                              (14)N ENDOR and ESEEM data are most consistent with one of these dicoppe
21                 Analysis of pulsed ENDOR and ESEEM experiments investigating the proximity of deutero
22                          In X-band ENDOR and ESEEM spectra, a weakly coupled nitrogen is visible, mos
23                                    ENDOR and ESEEM spectroscopy of Cu(II)-PcoC and the (15)N- and Met
24 MO have been investigated by EPR, ENDOR, and ESEEM spectroscopies in combination with metal content a
25 ess this issue, we have conducted an EPR and ESEEM (electron spin-echo envelope modulation) study of
26                            Thus, the EPR and ESEEM data indicate the presence of a Mn2+ binding site
27                                  The EPR and ESEEM measurements evince a protein-mediated force on th
28            The interpretation of the EPR and ESEEM spectra was facilitated by a theoretical analysis
29 d forms of the enzyme, and Mn(II) CW-EPR and ESEEM spectra were recorded.
30 s been definitively characterized by EPR and ESEEM spectroscopy.
31 a combination of X-band EPR, S-band EPR, and ESEEM, along with a library of modified peptides designe
32                                      ESR and ESEEM spectroscopies, crystallography, and pH-dependent
33                                      Ka band ESEEM spectroscopy was used to determine the hyperfine (
34                 Companion S-band EPR, X-band ESEEM, and HYSCORE experiments performed on a library of
35 sed the possibility of a correlation between ESEEM spectroscopic properties and the nitrogenase pheno
36 oxin was further characterized by EPR and by ESEEM spectroscopy and was found to differ only marginal
37 ies, designated H, has been characterized by ESEEM spectroscopy using a combination of (14,15)N isoto
38 e too large or anisotropic to be detected by ESEEM analyses conducted at 9.2 GHz.
39 equatorial water on copper, as determined by ESEEM analysis.
40 2+ in this ternary complex was determined by ESEEM studies in D2O to be two fewer than on the average
41 nitrogens, one near the "exact cancellation" ESEEM condition and the other more weakly coupled.
42             In the present study, we combine ESEEM spectroscopy with site-directed spin labeling (SDS
43 rs of the extracted membrane lipids, the D2O-ESEEM intensities of fully charged n-SASL decrease progr
44 alpha-359-arginine is the source of the deep ESEEM N1 modulation; (ii) one or both of the amide nitro
45  model system, we demonstrate that deuterium ESEEM can detect water permeation along the lipid-expose
46                          The two-dimensional ESEEM (HYSCORE) data have directly identified N(epsilon)
47            In the two-pulse frequency domain ESEEM spectrum of the 9.2 GHz S(2) state multiline EPR s
48 Simulation of the time- and frequency-domain ESEEM requires two types of coupled (2)H.
49 coupling constants with results from earlier ESEEM and electron nuclear double resonance (ENDOR) stud
50                              Stimulated echo ESEEM data were divided to eliminate interference from 1
51                                  EPR, ENDOR, ESEEM, and HYSCORE data indicate the presence of two his
52 se variants and investigated by Q-band ENDOR/ESEEM are identical to states, denoted H and I, formed o
53 ch enables its detailed examination by ENDOR/ESEEM spectroscopies.
54 fixed Pi/DP1 ratio of MDP, 25/3, using ENDOR/ESEEM to characterize DP1 ligation to Mn(2+).
55                            We report CW-EPR, ESEEM, and structural NMR results, as well as DFT calcul
56         The results presented here establish ESEEM as a highly informative technique for SDSL studies
57 nd is resolved by the pulsed EPR experiments ESEEM and HYSCORE.
58 N nuclear quadrupole parameters derived from ESEEM simulations and those computed by using density fu
59                                The best (2)H ESEEM time- and frequency-domain simulations are achieve
60                     One peptide nitrogen has ESEEM peaks near 0.7, 2.0, 2.85, and 5.0 MHz with isotro
61 -band EPR and (14/15)N, (1,2)H ENDOR/HYSCORE/ESEEM measurements that characterize the N-atom(s) and p
62 l nitrogen modulation observed near 5 MHz in ESEEM spectra of the S(2) state multiline EPR signal of
63  N1 interaction with FeMo-cofactor; and (iv) ESEEM can be used to detect slight reorientations of FeM
64 n the present work, Q-band CW EPR and (95)Mo ESEEM spectroscopy reveal such samples also contain a co
65 from electron spin echo envelope modulation (ESEEM) allowed to model the N-terminal protein section,
66  and electron spin echo envelope modulation (ESEEM) analyses strongly suggest that the L*-cluster rep
67  and electron spin echo envelope modulation (ESEEM) analysis of Mn(2+)-substituted cytochrome c oxida
68 ulse electron spin-echo envelope modulation (ESEEM) and 4-pulse 2-dimensional hyperfine sublevel corr
69 ulse electron spin echo envelope modulation (ESEEM) and four-pulse two-dimensional hyperfine sublevel
70 h as electron spin echo envelope modulation (ESEEM) and hyperfine sublevel correlation (HYSCORE) spec
71 sing electron spin echo envelope modulation (ESEEM) and hyperfine sublevel correlation spectroscopy (
72  14N electron spin-echo envelope modulation (ESEEM) arising from a nitrogen nucleus (N1) coupled to t
73  and electron spin echo envelope modulation (ESEEM) experiments have been performed.
74      Electron spin echo envelope modulation (ESEEM) experiments suggest that the improved performance
75  the electron spin echo envelope modulation (ESEEM) from (2)H-hyperfine interaction with D2O is deter
76 ated electron spin echo envelope modulation (ESEEM) have been studied in either thylakoid membranes,
77 n of electron spin-echo envelope modulation (ESEEM) spectra from multi-crystalline Cu(2+)-insulin wit
78 band electron spin-echo envelope modulation (ESEEM) spectra of lpH SO were also analyzed.
79      Electron spin-echo envelope modulation (ESEEM) spectra of these Cu-RC proteins have been obtaine
80      Electron spin echo envelope modulation (ESEEM) spectral results indicate multiple weakly hyperfi
81  and electron spin-echo envelope modulation (ESEEM) spectroscopic methods.
82  and electron spin-echo envelope modulation (ESEEM) spectroscopic properties of ethanolamine ammonia-
83  and electron spin-echo envelope modulation (ESEEM) spectroscopies, can help us understand how metal
84 ulse electron spin-echo envelope modulation (ESEEM) spectroscopy in the disordered solid state.
85 ulse electron spin-echo envelope modulation (ESEEM) spectroscopy in the disordered solid state.
86 ver, electron spin-echo envelope modulation (ESEEM) spectroscopy indicates that all nine lectins are
87      Electron spin-echo envelope modulation (ESEEM) spectroscopy is a well-established technique for
88      Electron spin echo envelope modulation (ESEEM) spectroscopy, a pulsed electron spin resonance te
89 ctable by electron spin envelope modulation (ESEEM) spectroscopy, is observed in WT enzyme but not in
90 band electron spin-echo envelope modulation (ESEEM) spectroscopy.
91 sing electron spin echo envelope modulation (ESEEM) spectroscopy.
92 ulse electron spin-echo envelope modulation (ESEEM) spectroscopy.
93 d by electron spin-echo envelope modulation (ESEEM) spectroscopy.
94 ency electron spin echo envelope modulation (ESEEM) studies of this species prepared with (33)S-label
95  and electron spin-echo envelope modulation (ESEEM) studies on the Cu(II) derivative provided evidenc
96 y an electron spin echo envelope modulation (ESEEM) study conducted with [(15)N]histidine-labeled pho
97 ulse electron spin echo envelope modulation (ESEEM) technique was used to detect weakly coupled (2)H-
98      Electron spin-echo envelope modulation (ESEEM) was used to search for spin transitions of 15N nu
99 PR), electron spin-echo envelope modulation (ESEEM), and UV-vis spectroscopies have greatly expanded
100 ave, electron spin-echo envelope modulation (ESEEM), pulsed electron-nuclear double resonance (ENDOR)
101 ar double resonance/ESE envelope modulation (ESEEM)] reveal differential details of the in vivo Mn(2+
102 uces dominating contribution to X-Band (14)N ESEEM spectra.
103                                       The N2 ESEEM pattern is more obvious when unmasked by substitut
104 wo independent approaches: (a) comparison of ESEEM from cob(II)alamin with ESEEM from cob(II)inamide-
105                   Theoretical simulations of ESEEM spectra guided by structure modeling suggest that
106 PR signals and we also advance the theory of ESEEM and HYSCORE to quantitatively describe multiple (1
107                     The "out-of-phase" (OOP) ESEEM attributed to the [P700+ A1-] radical pair has bee
108  electron spin echo envelope modulation (OOP-ESEEM) signal from the NDI(*-)-Sd(*+) spin qubit pair in
109  electron spin echo envelope modulation (OOP-ESEEM).
110                    This study shows that OOP-ESEEM is well-suited for probing the detailed structural
111  extracted by time-domain fitting of the OOP-ESEEM.
112            We further demonstrate that (31)P ESEEM is able to identify channel residues that interact
113                                      Present ESEEM data reveals that two kinds of 14N modulations are
114                                   A previous ESEEM study on altered MoFe proteins generated by substi
115 tion, a compilation of results from previous ESEEM studies of copper proteins reveals that the asymme
116 hrough the use of one-dimensional four-pulse ESEEM and subsequent analysis of the sum combination pea
117                                  Three-pulse ESEEM experiments were performed by using microwave puls
118                                  Three-pulse ESEEM of the natural abundance Sr sample exhibits no det
119                     We performed three-pulse ESEEM on this modified multiline signal of the Mn cluste
120         By comparing the ratioed three-pulse ESEEM spectra of a control, untreated PSII sample in 50%
121                            Using three-pulse ESEEM spectroscopy, we have successfully detected the tw
122                              The three-pulse ESEEM spectrum of the wild-type CF(1)-ATPase with VO(2+)
123                    Simulation of three-pulse ESEEM with a numerical matrix diagonalization procedure
124         Simulation of the (2)H/(1)H quotient ESEEM (obtained at two microwave frequencies, 8.9 and 10
125                                       Recent ESEEM studies of p21 in solution, however, place threoni
126                                We now report ESEEM studies on altered MoFe proteins with substitution
127  spin-echo envelope modulation spectroscopy (ESEEM) to characterize the protein-cofactor interactions
128  spin echo envelope modulation spectroscopy (ESEEM).
129 or the electron spin, analysis of the (87)Sr ESEEM modulation depth via an analytic expression sugges
130                                          The ESEEM spectra of Species 1 prepared in (17)O-enriched wa
131                                          The ESEEM spectra of the mutants do not show evidence of an
132                                          The ESEEM spectra of wild-type ferredoxin displayed weak 14N
133 llumination treatment induces a shift in the ESEEM frequency.
134                               Changes in the ESEEM spectra for different samples correlate directly t
135 s of (14)N features are distinguished in the ESEEM spectra.
136 +/- 0.2 MHz) of the phosphorus signal in the ESEEM spectrum established the formation of an inner sph
137  nuclear quadrupole induced splitting in the ESEEM spectrum of (87)Sr enriched PSII samples is relate
138 etism of Y(.)(z), we are able to observe the ESEEM spectrum of deuterated acetate interacting with on
139                            A good fit of the ESEEM data indicates two (2)H dipolar hyperfine coupling
140 procedure for high-precision analysis of the ESEEM data of the MoFe proteins shows that the deep wild
141                 Numerical simulations of the ESEEM data suggest that the coupling is primarily isotro
142                          Correlations of the ESEEM properties and catalytic activities of the altered
143 ii) explore the mechanistic relevance of the ESEEM signatures to nitrogenase activity; and (iii) stud
144             Furthermore, a comparison of the ESEEM spectra obtained in H(2)O and D(2)O demonstrates t
145 2qQ approximately 3.3 MHz) indicate that the ESEEM effect is most likely due to 14N from the polypept
146                         We conclude that the ESEEM spectrum of QA- is the result of interactions of t
147                                        These ESEEM spectra resemble those observed for Cu(2+) RCs fro
148  MoFe proteins shows that the deep wild-type ESEEM modulation (denoted N1) has a hyperfine-coupling c
149 cetate-treated PSII and untreated PSII using ESEEM.
150 e hydration level of Mn2+ in this site using ESEEM (electron spin-echo envelope modulation) spectrosc
151  peptide nitrogen is that of D2-Ala260, with ESEEM peaks near 0.6 and 1.5 MHz and an isotropic hyperf
152  comparison of ESEEM from cob(II)alamin with ESEEM from cob(II)inamide-ligand model compounds and (b)

 
Page Top