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determined only the Co hyperfine parameters
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0038562106
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F3 primary sequence, KNFTCDSDGCDLRFTTKANMKKHFNRFHNI
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F3 primary sequence, KNFTCDSDGCDLRFTTKANMKKHFNRFHNI.
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16
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0032113850
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18
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3042934967
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2 and incubated for 48 h. The apo-peptide was purified by G-25 gel filtration using 0.01 N HCl for elution to maintain the thiol groups in their protonated form, which inhibits oxidation. The peptide was then concentrated in an Amicon concentrator. DTNB, 5,5′-dithio-bis(2-nitrobenzoic acid), was used to analyze the sulfhydryl content of the peptide (Ellman, G. Arch. Biochem. Biophys. 1959, 82, 70-77).
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Ellman, G.1
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0029960036
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The C-block oligonucleotide was synthesized using a Millipore Cyclone Plus DNA Synthesizer (Mao, Q.; Fulmer, P.; Li, W.; DeRose, E. F.; Petering, D. H. J. Biol. Chem. 1996, 271, 6185-6191).
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0023375317
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21
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0037885872
-
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note
-
2. X-band EPR spectra at 77 K and 35 GHz Q-band EPR and ENDOR spectra were recorded as described.
-
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22
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33751158030
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23
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0035823678
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23
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3+, see: Drew, S. C.; Pilbrow, J. R.; Newman, P. J.; MacFarlane, D. R. J. Phys. D: Appl. Phys. 2001, 34, 2987-2994(23).
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Drew, S.C.1
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24
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12044255398
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Werst, M. M.; Davoust, C. E.; Hoffman, B. M. J. Am. Chem. Soc. 1991, 113, 1533-1538.
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25
-
-
0037885874
-
-
note
-
31P) likely is an experimental consequence of the Mims pulse sequence.
-
-
-
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27
-
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0032506974
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For an analogous result, see: Veselov, A.; Burger, R. M.; Scholes, C. P. J. Am Chem. Soc. 1998, 120, 1030-1033
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Veselov, A.1
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0034815814
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Krepkiy, D.; Antholine, W. E.; Myers, C.; Petering, D. H. Mol. Cell. Biochem. 2001, 222, 213-219.
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Krepkiy, D.1
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Petering, D.H.4
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