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1 erwhelming contributor to the R - T UV Raman difference spectrum.
2 s no substantial influence on the FTIR redox difference spectrum.
3 on of the heme c(n) Soret band in a chemical difference spectrum.
4 iorhodopsin, was observed as a trough in the difference spectrum.
5 to improve spectral resolution by means of a difference spectrum.
6 in the visible P(700)(+) - P(700) absorbance difference spectrum.
7 m, but are absent in the (P700(+)-P700) FTIR difference spectrum.
8 derably more so than the (P700(+)-P700) FTIR difference spectrum.
9 s at D1 His198 affect the P(+)--P-absorbance difference spectrum.
10 ion of the anion radical are observed in the difference spectrum.
11 tribution to the tryptophan features in this difference spectrum.
12 ching feature which escapes detection in the difference spectrum.
13 te tyrosines to the R - T UV resonance Raman difference spectrum.
15 QNO leads to strong shifts in the FTIR redox difference spectrum, 2-methyl-3-undecylquinolone-4 induc
16 ln mutation has little effect on the optical difference spectrum, (3)P--(1)P, of the reaction center
18 similar to that of the static (reduced - CO) difference spectrum, although the peak intensities were
19 e appearance of a "type I" substrate-induced difference spectrum analogous to those seen upon substra
21 he cross-peaks in the pure heterodimer 2D IR difference spectrum and the splitting of the homodimer p
28 named as a pigment having a carbon monoxide difference spectrum at about 450 nm and no known functio
32 and 1489 cm(-1), respectively, in the Raman difference spectrum between superhelical and relaxed DNA
33 nd 2715(-) cm(-1) in the (P740(+)-P740) FTIR difference spectrum, but are absent in the (P700(+)-P700
34 minima; and (iv) a reduced-oxidized optical difference spectrum characterized by DeltaepsilonmM = 3.
35 ; binding is accompanied by a type I optical difference spectrum consistent with binding near the hem
37 erium-induced changes in (P740(+)-P740) FTIR difference spectrum could also indicate that one of the
38 band at 1654 cm(-1) in the A(1)(-)/A(1) FTIR difference spectrum downshifts 28 cm(-1) on (18)O labeli
39 D(2)O does not alter the (P700(+)-P700) FTIR difference spectrum, even with approximately 50% proton
43 tral signatures, we produce an A1(-)/A1 FTIR difference spectrum for PS I particles with plastoquinon
47 variations in the amide I region of the FTIR difference spectrum, however, reflect a more general per
48 Raman OH-band, (ii) the integrated absolute difference spectrum, (iii) the intensity ratio of two re
49 ent on the concentration of peptide, in a UV difference spectrum in a solution of PFTase and the pept
51 ed at pH values above 7.5, the light-induced difference spectrum indicates a pH-dependent equilibrium
52 uced modification of the (P740(+)-P740) FTIR difference spectrum indicates that only the highest freq
53 ith isoniazid failed to produce a measurable difference spectrum indicating an altered active site co
54 (Ki = 22.6 +/- 1.9 nM), reversed the type II difference spectrum induced by imidazole (Kd = 17.7 nM),
56 he peak-to-trough magnitude of the R - T MCD difference spectrum is equal to 30% of the total R-state
57 band at 1494 cm(-1) in the A(1)(-)/A(1) FTIR difference spectrum is found to downshift 14 cm(-1) and
59 ifferences also: 1), The (P740(+)-P740) FTIR difference spectrum is significantly altered upon proton
60 band at 1654 cm(-1) in the A(1)(-)/A(1) FTIR difference spectrum is therefore due to a C=O mode of ne
61 band at 1494 cm(-1) in the A(1)(-)/A(1) FTIR difference spectrum is therefore due to the antisymmetri
62 band shift at 681 nm, observed in the P(+)-P difference spectrum, is attributed to an electrochromic
64 rough magnitude of the Soret band photolysis difference spectrum measured as a function of the delay
65 sed expression of hemoprotein with a reduced difference spectrum of 450 nm (P450 species) and a corre
66 pectrum, interpreted as the (A(0)(-) - A(0)) difference spectrum of a chlorophyll a molecule, consist
67 characteristic of the oxidized minus reduced difference spectrum of a semiquinone, consistent with ch
68 observed between the shape of the absorption difference spectrum of BPB and the polarity of the envir
69 e assignment of methionine bands in the FTIR difference spectrum of BR provides a means to study meth
70 spectrum of SRII is similar to the BR-->O640 difference spectrum of BR, especially in the configurati
71 band is present in the S(2)-minus-S(1) FTIR difference spectrum of D1-Asp61Ala but absent from the c
72 d states, gives rise to a new maximum in the difference spectrum of Einactive minus E at 57.0 ppm.
73 pectra were distinctly different from the IR difference spectrum of F that formed with extended treat
74 y subtraction of the spectra, the redox FTIR difference spectrum of heme a(3) can be resolved from th
76 The nondecaying component is ascribed to the difference spectrum of P(700) and the quinone or A(1) el
77 ficans oxidase, the major features of the IR difference spectrum of P(M) were similar when produced b
78 s often observed in the S(2)-minus-S(1) FTIR difference spectrum of PSII from the cyanobacterium Syne
79 4 was identified in the S(2)-minus-S(1) FTIR difference spectrum of PSII particles having Sr substitu
80 both room temperature and -20 degrees C, the difference spectrum of SRII is similar to the BR-->O640
85 appearance of a new band in the P700 - P700+ difference spectrum of the HN(B656) PSI are discussed.
98 nus wild type (WT) Q(A)(-) minus Q(A) double-difference spectrum; this assignment provides new eviden
99 d the Trp alpha14 contributions to the T - R difference spectrum to be negligible and confirmed Trp b
100 to a bilin pigment, which produced a native difference spectrum upon assembly with oat apophytochrom
101 3(+)/1638(-) cm(-1) in the P700(+)/P700 FTIR difference spectrum upshifts by approximately 30-40 cm(-
102 d H(2)O, a ((1)H-(2)H) isotope edited double difference spectrum was constructed, and it is shown tha
104 ive to the wild-type lattice, its light-dark difference spectrum was normal, and its circular dichroi
107 from that with unlabeled substrate, a simple difference spectrum was obtained with features involving
108 are superimposed on a subsequently evolving difference spectrum which is characteristic of PPII, alt
109 ents of E222D can be described with only one difference spectrum, with the nu(sym) mode at 1435 cm(-1