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1 re most important in determining the near-UV circular dichroism spectrum.
2 corroborated by the corresponding electronic circular dichroism spectrum.
3 tants and native proteins had a very similar circular dichroism spectrum.
4 with seven 12-residue coils and a comparable circular dichroism spectrum.
5 ibility to limited trypsin digestion and its circular dichroism spectrum.
6                 The near-ultraviolet/visible circular dichroism spectrum also supported the proposed
7                                              Circular dichroism spectrum analyses were performed to e
8                                 Furthermore, circular dichroism spectrum analysis shows that LC8 stab
9 The alpha subunit has a well-defined near-UV circular dichroism spectrum and a higher intrinsic fluor
10 he Val(121) --> Ala mutant that has a normal circular dichroism spectrum and AdoMet affinity.
11  with a small but reproducible change in the circular dichroism spectrum and an increase in the 1-ani
12                                          The circular dichroism spectrum and catalytic constants of t
13 sociated with Ac-SVAFS-COO(-) had an altered circular dichroism spectrum and enhanced thermal resista
14                                          The circular dichroism spectrum and measurements of fluoresc
15 ndistinguishable from wild-type TIP47 in its circular dichroism spectrum, and mutant proteins that sh
16 phan fluorescence quantum yield, and natural circular-dichroism spectrum as a function of temperature
17 lution, as is evident from its alpha-helical circular dichroism spectrum, blue shift of the native st
18 t threshold, PG-1 exhibits a unique oriented circular dichroism spectrum called the S state.
19                                The oC far UV circular dichroism spectrum could be modeled as the sum
20                                              Circular-dichroism spectrum deconvolution and secondary-
21                                              Circular dichroism spectrum experiments were performed t
22 ium, and the concentration dependence of its circular dichroism spectrum follows a cooperative monome
23  doping leads to a significant change of the circular dichroism spectrum; however, the anisotropy fac
24      This was correlated with changes in the circular dichroism spectrum imposed by the K601A mutatio
25                                Moreover, the circular dichroism spectrum in membranes is different, i
26 ed by monitoring changes in the nucleic acid circular dichroism spectrum in the 240-300 nm region.
27  data as well as investigation of the UV and circular dichroism spectrum in trifluoroethanol for comp
28                                              Circular dichroism spectrum indicated an A-form helical
29 eme to AeIMUC1 was accompanied by an altered circular dichroism spectrum indicating a change in prote
30 ha-chain fragment, there is no change in the circular dichroism spectrum, indicating that the conform
31  fragment is monomeric in solution and has a circular dichroism spectrum indicative of a mixture of a
32 ar to those of the wild-type Fe protein, the circular dichroism spectrum is markedly different in the
33 a-sheet secondary structure as judged by its circular dichroism spectrum, is monomeric, and undergoes
34 ystal structure are not isolated, nor is the circular dichroism spectrum known.
35 compute from first principles the electronic circular dichroism spectrum of a (modeled or experimenta
36 or the effect of a Ru(III) cross-link on the circular dichroism spectrum of a previously reported 17
37 sity and produced significant changes in the circular dichroism spectrum of BkdR.
38                                          The circular dichroism spectrum of hSTAT4(1-124) indicates t
39 (II)Blm caused little perturbation of the UV circular dichroism spectrum of I or II.
40                                          The circular dichroism spectrum of Jun a 3 is consistent wit
41                                          The circular dichroism spectrum of lumirhodopsin, obtained a
42 avin, whereas the ferrous heme dominates the circular dichroism spectrum of reduced enzyme.
43                                          The circular dichroism spectrum of reduction and carboxyamid
44                                          The circular dichroism spectrum of the dimeric MjMAT indicat
45                                          The circular dichroism spectrum of the E70A aporepressor at
46                                   The far-UV circular dichroism spectrum of the intermediate indicate
47                                          The circular dichroism spectrum of the oxidized fragment is
48 agnitude of the ellipticity at 223 nm in the circular dichroism spectrum of the peptide.
49 lack of free sulfhydryl groups, and atypical circular dichroism spectrum of the recombinant product r
50 ent fit to the temperature dependence of the circular dichroism spectrum of the Ru(III)-cross-linked
51               Furthermore, comparison of the circular dichroism spectrum of the W139F enzyme at 280 n
52                         The near-ultraviolet circular dichroism spectrum of this protein suggests tha
53                                          The circular dichroism spectrum of this protein was similar
54  cations do not affect the oligomeric state, circular dichroism spectrum, or fluorescence spectrum of
55 dark difference spectrum was normal, and its circular dichroism spectrum retained a bilobed feature c
56                                   The far-UV circular dichroism spectrum revealed that tapasin posses
57           However, alteration in the near-UV circular dichroism spectrum suggested the presence of di
58                          On the basis of the circular dichroism spectrum, this region of the polypept
59 t although C403S displays a nearly identical circular dichroism spectrum to that of the wild type enz
60 me, which exhibits a pronounced shift in its circular dichroism spectrum under a modest level of exci
61  of a protein's secondary structure from its circular dichroism spectrum usually requires accurate kn
62 e alpha-chains, the ellipticity of the Soret circular dichroism spectrum was decreased and CO binding
63 as assessed by equilibrium dialysis, and its circular dichroism spectrum was sensitive to the presenc
64                                  The near-UV circular dichroism spectrum was virtually unchanged at e
65 ecreased tetramer-dimer dissociation and its circular dichroism spectrum, which measure the strength
66 DNA aggregates without changes in its B-form circular dichroism spectrum, while short DNA demonstrate