ライフサイエンスコーパス: ferricytochrome

1 tase (EC 1.6.2.2) catalyzes the reduction of ferricytochrome b(5) using NADH as the physiological ele

2 artners, and (iii) the [Zn-deuteromyoglobin, ferricytochrome b(5)] complex, [ZnDMb, Fe(3+)b(5)], whic

3 ochrome b5 and ferricytochrome c that yields ferricytochrome b5 and ferrocytochrome c.

4 The electrochemical reduction of ferricytochrome b5 at the electrode surface is followed

5 arising from the heme propionate carbons in ferricytochrome b5 was carried out by a combination of o

6 ption of the compact acid-denatured state of ferricytochrome c (A-state).

7 persed granuloma cells were unable to reduce ferricytochrome c (as an indicator of O2.-) in response

8 mation of 19 complexes involving yeast iso-1-ferricytochrome c (Cc) and ferricytochrome c peroxidase

9 m catalyzes irreversible oxidative damage to ferricytochrome c (Cc3+) in the presence of H2O2 and 3,4

10 in, we demonstrate that unfolded horse heart ferricytochrome c (Cyt c) is a novel chromophoric probe

11 Horse ferricytochrome c (cyt c) undergoes exchange of one of i

12 e variants of Saccharomyces cerevisiae iso-1 ferricytochrome c (labeled at mutant Cys residues 4, 39,

13 en-am)-Cys-(Glu)(5)-Gly](3-) = RuCE(5)G, and ferricytochrome c = Cyt c.

14 most frequently used scavengers of O(2)(*-), ferricytochrome c and Cu/Zn-SOD, were evaluated as compe

15 ow kinetic studies of azide binding to human ferricytochrome c and its Gly41Ser variant, together wit

16 the presence of saturating concentrations of ferricytochrome c and L-lactate, the catalytic cycle pro

17 relevant redox protein complex between yeast ferricytochrome c and yeast ferricytochrome c peroxidase

18 with superoxide (O2*-) were estimated, using ferricytochrome c as a competitive inhibitor.

19 e 695 nm charge transfer band of horse heart ferricytochrome c as a function of pH between 7.0 and 10

20 e heme environment in bovine and horse heart ferricytochrome c as a function of temperature between 2

21 elevance for characterizing the structure of ferricytochrome c bound to anionic phospholipids.

22 uperoxide dismutase-inhibitable reduction of ferricytochrome c by myocyte monolayers.

23 We discuss our results in relation to ferricytochrome c folding kinetics.

24 granuloma cells, they also failed to reduce ferricytochrome c following PMA stimulation, implying th

25 onic circular dichroism (ECD) of horse heart ferricytochrome c for the Soret and 695 nm charge-transf

26 el for the solution structure of horse heart ferricytochrome c has been determined by nuclear magneti

27 Tuna ferricytochrome c has been used to demonstrate the poten

28 omparison of native and non-native states of ferricytochrome c has thus far not been achieved.

29 e alkaline-induced structural transitions of ferricytochrome c have been studied intensively as a mod

30 cedure, complete heme proton assignments for ferricytochrome c have never been demonstrated by a sing

31 e organism assay for their ability to reduce ferricytochrome c in a superoxide dismutase-inhibitable

32 sugars to solutions of acid-denatured equine ferricytochrome c induces formation of the A-state in th

33 The results indicated that the iso-1-ferricytochrome c magnetic axis system orientation shift

34 lving yeast iso-1-ferricytochrome c (Cc) and ferricytochrome c peroxidase (CcP).

35 rmation of the horse ferricytochrome c/yeast ferricytochrome c peroxidase complex.

36 ng of yeast iso-1-ferricytochrome c to yeast ferricytochrome c peroxidase in dilute solution and in s

37 y defined cytochrome c binding site on yeast ferricytochrome c peroxidase.

38 ex between yeast ferricytochrome c and yeast ferricytochrome c peroxidase.

39 easured with the use of superoxide-dependent ferricytochrome c reduction and flow cytometry with dihy

40 However, Cu(2+) inhibits ferricytochrome c reduction by the full-length nNOS 2 or

41 Cu(2+) and Zn(2+) also inhibit ferricytochrome c reduction by the independent reductase

42 NADPH oxidation by the full-length nNOS and ferricytochrome c reduction by the reductase domain are

43 uld then promote the selective inhibition of ferricytochrome c reduction in full-length nNOS.

44 Serum-induced ferricytochrome c reduction, cellular proliferation, and

45 ronal nitric-oxide synthase (nNOS) including ferricytochrome c reduction, NADPH oxidation, and citrul

46 and superoxide dismutase (SOD)--inhibitable ferricytochrome c reduction, respectively.

47 escence and superoxide dismutase-inhibitable ferricytochrome c reduction, respectively.

48 ultures via superoxide dismutase-inhibitable ferricytochrome c reduction.

49 generation, but rather was interfering with ferricytochrome c reduction.

50 on that pre-steady-state flavin oxidation by ferricytochrome c takes place at 120 s-1.

51 sfer reaction between ferrocytochrome b5 and ferricytochrome c that yields ferricytochrome b5 and fer

52 otochemical electron injection into unfolded ferricytochrome c titrated with 2.3 to 4.6 M guanidine h

53 We used yeast iso-1-ferricytochrome c to test for an evolutionary-invariant

54 thalpy change for the binding of yeast iso-1-ferricytochrome c to yeast ferricytochrome c peroxidase

55 global and local stabilities of a eukaryotic ferricytochrome c variant with an engineered disulfide a

56 The structure of encapsulated ferricytochrome c was determined to high precision (<r.m

57 When ferricytochrome c was entrapped within liposomes prepare

58 free and cytochrome c peroxidase-bound iso-1-ferricytochrome c were elucidated.

59 uperoxide dismutase-inhibitable reduction of ferricytochrome c were not different between cultured tr

60 nts have been made for wild-type yeast iso-1-ferricytochrome c when it is free in solution and when i

61 used to investigate the interaction of horse ferricytochrome c with baker's yeast cytochrome c peroxi

62 One exception to this is ferricytochrome c(552) from Hydrogenobacter thermophilus

63 lysis of NMR line shapes for H. thermophilus ferricytochrome c(552) is performed.

64 by a spectrophotometric assay (reduction of ferricytochrome C).

65 uperoxide dismutase-inhibitable reduction of ferricytochrome c, 2) monitoring fluxes in Ca2+ concentr

66 icytochrome c, while for CcP-complexed iso-1-ferricytochrome c, 70% of heme proton assignments were m

67 t activated cell sorter (FACS), reduction of ferricytochrome C, and bioassay, respectively.

68 ptor is either cupriplastocyanin, pc(II), or ferricytochrome c, cyt(III); and the mobile charge carri

69 rosomal ferrocytochrome b5, with horse heart ferricytochrome c, respectively.

70 sonance assignments were made for free iso-1-ferricytochrome c, while for CcP-complexed iso-1-ferricy

71 ide dismutase (SOD)-inhibitable reduction of ferricytochrome c.

72 ease was measured by use of the reduction of ferricytochrome c.

73 catalytic oxidation of ferrocytochrome c to ferricytochrome c.

74 ne such molecule, the A-state of yeast iso-1-ferricytochrome c.

75 uperoxide dismutase-inhibitable reduction of ferricytochrome C.

76 amagnetic ferrocytochrome c and paramagnetic ferricytochrome c.

77 directly cross-linked to the basic patch in ferricytochrome c.

78 spiratory burst was measured by reduction of ferricytochrome C.

79 compared to those for formation of the horse ferricytochrome c/yeast ferricytochrome c peroxidase com

80 The heme group in paramagnetic (S = 1/2) ferricytochromes c typically displays a markedly asymmet

81 e conformational differences in the hemes in ferricytochromes c3.

82 Bath, analytical ultracentrifugation of the ferricytochrome, the ferrocytochrome, and the ferrocytoc