ライフサイエンスコーパス: F1F0-ATPase

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1 n in the MTATP6 subunit of the mitochondrial F1F0-ATPase.

2 s dependent on the activity of mitochondrial F1F0-ATPase.

3 T8993G mutation results in loss of assembled F1F0-ATPase.

4 transporter, or by direct inhibition of the F1F0-ATPase.

5 ose genes encode the various subunits of the F1F0-ATPase.

6 carbodiimide (DCCD), a specific inhibitor of F1F0-ATPase.

7 ollowing ATP hydrolysis by the mitochondrial F1F0-ATPase.

8 opy models of either V-ATPase or the related F1F0-ATPase.

9 term or long-term acid survival capacity and F1F0 ATPase activity remained unaffected in the mutants.

10 ntibodies to the beta- and gamma-subunits of F1F0-ATPase (anti-beta, anti-gamma) occur.

11 lta psi m is maintained by the mitochondrial F1F0-ATPase at the expense of ATP reserves.

12 . subtilis deleted in atp genes encoding the F1F0-ATPase (BD99-A), glucose energized Na+ exclusion in

13 clone the gene (atpD) encoding the H. pylori F1F0-ATPase beta subunit.

14 The deduced amino acid sequences of the F1F0-ATPase beta subunits from H. pylori and Wolinella s

15 chia coli mutants in the beta subunit of the F1F0-ATPase can be complemented with the beta subunit fr

16 ADH-ubiquinone oxidoreductase (complex I) or F1F0-ATPase (complex V) also precipitated a 45-kDa prote

17 cassette and sought to construct an isogenic F1F0-ATPase H. pylori mutant by natural transformation a

18 A mutant of the Escherichia coli F1F0-ATPase has been generated (alphaQ2C) in which the g

19 that more c subunits are assembled into the F1F0 ATPase in cells grown on glucose than in cells grow

20 characterize a potential functional role of F1F0-ATPase in H. pylori, H. pylori or Escherichia coli

21 potential energy and the formation of ATP by F1F0-ATPase in heart and skeletal muscle mitochondria.

22 ole of IF1 (the natural inhibitor protein of F1F0-ATPase) in cancer cell metabolism is still uncertai

23 lipoprotein (SmpA), and the C subunit of the F1F0 ATPase indicated that the lowest-density membrane f

24 In the presence of oligomycin (Oligo), an F1F0-ATPase inhibitor, the decrease in pH(i) was attenua

25 dle, which is different from all other known F1F0-ATPase inhibitors.

26 The proton-translocating F1F0-ATPase is an important enzyme for regulating intrac

27 odiazepine derivate blocks the mitochondrial F1F0-ATPase, leads to a surplus production of mitochondr

28 Furthermore, we demonstrate that the F1F0-ATPase monomers present in su e null mutant mitocho

29 ly been demonstrated that the binding of the F1F0-ATPase natural inhibitor protein to purified bovine

30 ntibodies to the beta- and gamma-subunits of F1F0-ATPase occur in anti-M2 positive and -negative PBC

31 e structural data suggest a new mechanism of F1F0-ATPase regulation in alpha-proteobacteria.

32 re recently discovered alpha-proteobacterial F1F0-ATPase-regulatory proteins representing a Pfam prot

33 ate primers derived from conserved bacterial F1F0-ATPase sequences to PCR amplify and clone the gene

34 mechanisms to cope with acidic environments (F1F0-ATPase system, fatty acid biosynthesis, branched ch

35 cessing of only one, the beta subunit of the F1F0 ATPase, was dramatically affected.

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