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1 mbinations of one NADH dehydrogenase and one quinol oxidase.
2 , possibly, in the mitochondrial alternative quinol oxidase.
3 echocystis sp. PCC 6803 encodes a functional quinol oxidase.
4  observed in cytochrome bo(3), a respiratory quinol oxidase.
5 tic activity of classical NO targets such as quinol oxidases.
6 her of these residues results in the loss of quinol oxidase activity and can result in the loss of th
7  the more conservative D75E substitution has quinol oxidase activity equal to that of the wild-type e
8                                          The quinol oxidase activity of the W93V mutant is also reduc
9 hrome bd oxidase exhibited cyanide-sensitive quinol oxidase activity.
10 enzymes were found to show very little or no quinol oxidase activity.
11 ctivity but expressing normal levels of aa3 (quinol) oxidase activity.
12 -011992 acts on both, quinone reductases and quinol oxidases and could be very well suited to regulat
13 i, the biogenesis of both cytochrome bd-type quinol oxidases and periplasmic cytochromes requires the
14 that we interpret to be a cytochrome bo-type quinol oxidase, and a putative cytochrome bd quinol oxid
15              GSH transport and cytochrome bd quinol oxidase assembly are abolished in the cydD1 mutan
16  mutant of CyoA still assembles as an active quinol oxidase capable of supporting growth of the cells
17                           Cytochrome bd-type quinol oxidases catalyze the reduction of molecular oxyg
18             The possibility that a primitive quinol oxidase complex evolved to yield two separate com
19 quinol binding subunit of the cytochrome bo3 quinol oxidase complex) and wild-type procoat are slight
20 ane-localized cytochrome c oxidase (COX) and quinol oxidase (Cyd) and the cytoplasmic membrane-locali
21 cytochrome c oxidase (Cox) and cytochrome bd quinol oxidase (Cyd), are present in the photosynthetic
22 quinol oxidase, and a putative cytochrome bd quinol oxidase (Cyd).
23  plastoquinol oxidation in thylakoids by the quinol oxidase CydAB that occurs without upregulation of
24 strate that the widely conserved respiratory quinol oxidase cytochrome bd is required for intracellul
25                          The reaction of the quinol oxidase cytochrome bo3 from Escherichia coli with
26                                          The quinol oxidase, cytochrome bd, functions as a terminal o
27                         As integral membrane quinol oxidases, cytochrome bd and fumarate reductase re
28   Both are members of the diiron carboxylate quinol oxidase (DOX) class of proteins.
29 CuB histidines from the cytochrome aa(3)-600 quinol oxidase from Bacillus subtilis.
30 corresponding region of the cytochrome bo(3) quinol oxidase from Escherichia coli (where E89II is the
31  mutagenesis studies of the cytochrome bo(3) quinol oxidase from Escherichia coli implicated an almos
32                           Cytochrome bd is a quinol oxidase from Escherichia coli, which is optimally
33 Cu(II) and Cu(I) forms of the cytochrome bo3 quinol oxidase from Escherichia coli.
34 nscribed in the cccA deletion mutant and the quinol oxidase genes (cioAB) were up-regulated.
35              Cytochrome bd is one of the two quinol oxidases in the respiratory chain of Escherichia
36 that oxygen consumption by V. fischeri CydAB quinol oxidase is inhibited by NO treatment, whereas oxy
37                            The cytochrome bd quinol oxidase is one of two respiratory oxidases in Esc
38 uence alignment of subunit II of heme-copper quinol oxidases is used as a guide to select conserved r
39           Speculation that subunit II in the quinol oxidases may also be important as an electron ent
40 ific enzyme examined is the cytochrome bo(3) quinol oxidase of E. coli.
41 and CioB are homologous to the cytochrome bd quinol oxidases of Escherichia coli and Azotobacter vine
42 ain contained reduced levels of the terminal quinol oxidases of the electron transport chain.
43 ligands appear to interact directly with the quinol oxidase (Q(o)) binding pocket.
44                                          The quinol oxidase (Q(o)) site in this complex oxidizes a hy
45  ions, which bind at a site distant from the quinol oxidase (Q(o)) site, inhibit plastoquinol (PQH2)
46 position of the substrate, ubiquinol, in the quinol oxidase (Q(o)) site.
47 ce to the proton channels of the heme-copper quinol oxidase (QO), cytochrome bo3, E. coli, has been c
48 sibility that there is a family of bacterial quinol oxidases related to the cytochrome bd of E. coli
49 Protein sequence alignments of cytochrome bd quinol oxidase sequences from different microorganisms h
50  the level of a reactive intermediate in the quinol oxidase site of the enzyme, resulting in "bypass
51 on of reactive intermediates produced at the quinol oxidase site of the enzyme.
52                     Cytochrome bo3 and other quinol oxidases that are members of the heme-copper oxid
53 s containing mammalian complex I, Q10, and a quinol oxidase (the alternative oxidase, AOX) to recycle
54 ffinity ubisemiquinone radical, QH*-, of bo3 quinol oxidase to determine its electronic spin distribu
55 osomes containing complex I, together with a quinol oxidase, to determine the kinetics of complex I c
56      Indeed, mutants lacking the respiratory quinol oxidases were sensitive to H2O2, and NO did not h
57 valens expresses a membrane-bound aa(3)-type quinol oxidase, when grown aerobically, that we have stu