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1 uinol oxidation Qo site in cytochrome b with cytochrome c1.
2  mediate electron transfer from ubiquinol to cytochrome c1.
3  two positions, proximal to cytochrome b and cytochrome c1.
4 order to shuttle electrons from ubiquinol to cytochrome c1.
5 iphasic binding of oxidized cytochrome c2 to cytochrome c1.
6 educed cytochrome c2, when it is proximal to cytochrome c1.
7 ation proximal to cytochrome b and distal to cytochrome c1.
8 s in heme synthesis or heme binding abrogate cytochrome c1 accumulation, apparently due to protein de
9 ting only its CycH2 subdomain always produce cytochrome c1 and affect the presence of other cytochrom
10 ,N,N', N'-tetramethyl-p-phenylenediamine via cytochrome c1 and the iron-sulfur protein of complex III
11 monstrates that the kinetics of reduction of cytochromes c1 and bH are fully explained by the modifie
12 sparity between the kinetics of reduction of cytochromes c1 and bH.
13 photosynthetic (Ps) growth that requires the cytochromes c1 and c2 or cy.
14 , subunit 7, a carboxyl-terminal fragment of cytochrome c1, and an amino-terminal fragment of the iro
15 eactions of redox-altered cytochromes c with cytochrome c1 both in vitro and in vivo.
16  mobile, moving between the cytochrome b and cytochrome c1 components during turnover.
17    In all of these mutants except W152F, the cytochrome c1 content, determined by immunoblotting, was
18                              Mutation of the cytochrome c1 cysteines involved in covalent binding to
19               We suggest that iron-dependent cytochrome c1 expression is mediated by heme availabilit
20                               Iron-dependent cytochrome c1 expression was restored in the ALA synthas
21  cytochrome c2 binding site is also near the cytochrome c1 heme but on the opposite side from the Rie
22 assembly factors cytochrome c heme lyase and cytochrome c1 heme lyase (CCHL and CC1HL).
23 n transfer from iron-sulfur protein (ISP) to cytochrome c1 in the bc1 complex.
24 eraction between the iron-sulfur protein and cytochrome c1 is partially impaired.
25                                              Cytochrome c1 is synthesized as a protein precursor fuse
26                                This range of cytochrome c1 ligand mutants exposes both the relative r
27 oth implicated in a recent longevity study), cytochrome c1 (mitochondrial electron transport), calmod
28                                 Furthermore, cytochrome c1 mRNA was not influenced by the iron status
29                                         Only cytochrome c1 of the cytochrome bc1 complex was present
30 r from cytochrome b-bound ubihydroquinone to cytochrome c1 of the cytochrome bc1 complex.
31 on of the heme ligating methionine (M185) in cytochrome c1 of the Rhodobacter sphaeroides cytochrome
32  dehydrogenase (cytosolic GAPDH or GapC) and cytochrome c1 precursor.
33                           Here, we show that cytochrome c1 protein from Bradyrhizobium japonicum was
34 ntation with heme resulted in high levels of cytochrome c1 protein in the wild type and in both mutan
35                                              Cytochrome c1 protein levels were very low in mutants de
36 ding of cytochrome b, ISP, and subunit IV to cytochrome c1, redox potentials of cytochromes b and c1
37  levels of cytochrome oxidase subunit IV and cytochrome c1, reflecting mitochondrial respiratory comp
38 posed of the Fe-S protein, cytochrome b, and cytochrome c1 subunits encoded by petA(fbcF), petB(fbcB)
39            The other site is close enough to cytochrome c1 to allow oxidation of the Fe-S protein by
40 lowed by intracomplex electron transfer from cytochrome c1 to heme c with a rate constant of 1.4 x 10
41      A plasmid-borne construct encoding only cytochrome c1 was expressed in an iron- and heme-depende
42 ollowing results were obtained: (i) When ISP/cytochrome c1 were prereduced or SMP were treated with a
43  terminal exons of GapC have been donated to cytochrome c1, where, in a new protein environment, they
44 1 is sufficient for the proper maturation of cytochrome c1 which is the only known c-type cytochrome
45 n, the Rieske protein binds near the heme of cytochrome c1, while the cytochrome c2 binding site is a

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