ライフサイエンスコーパス: plasma membrane H ATPase

1 the kidney mediate the transport of H+ by a plasma membrane H+-ATPase.

2 s, and mapped to the PMA1 gene, encoding the plasma membrane H+-ATPase.

3 region of the pma1 locus, which encodes the plasma membrane H+-ATPase.

4 tations in PMA1, which encodes the essential plasma membrane H(+)ATPase.

5 ers and the proton gradient generated by the plasma membrane H(+)-ATPase.

6 luencing root growth via localization of the plasma membrane H(+)-ATPase.

7 al active yeast ion transport protein is the plasma membrane H(+)-ATPase.

8 cade and correlated with the activity of the plasma membrane H(+)-ATPase.

9 stimulus is achieved by the activation of a plasma membrane H(+)-ATPase.

10 ating pH homeostasis between the vacuole and plasma membrane H(+)-ATPase.

11 ips within stalk segment 5 (S5) of the yeast plasma-membrane H(+)-ATPase.

12 PMA1 is an essential gene encoding the yeast plasma membrane [H(+)]ATPase.

13 segment 2 of AHA2 is conserved in all P-type plasma membrane H(+)-ATPases.

14 tn1-Delta strains compensate for the altered plasma membrane H(+)-ATPase activity and vacuolar pH by

15 h arrest, possibly through the inhibition of plasma membrane H(+)-ATPase activity.

16 ngae, wider stomatal apertures, and enhanced plasma membrane H(+)-ATPase activity.

17 In contrast, plasma membrane H+-ATPase activity in isolated plasma me

18 The plasma membrane H(+)-ATPase AHA1 is highly expressed in

19 entify 10 different phosphorylation sites in plasma membrane H(+)-ATPases AHA1, AHA2, AHA3, and AHA4/

20 Mutations in PMA1, which encodes the yeast plasma membrane H+-ATPase, also suppress many growth def

21 Other plasma membrane marker proteins (the plasma membrane H+-ATPase and a GPI-linked protein Gas1p

22 growth promotion through stimulation of the plasma membrane H+-ATPase and resultant acid wall loosen

23 ium acidification, decreases the activity of plasma membrane H(+)-ATPase, and elevates vacuolar pH.

24 ophospholipids specifically activate a plant plasma membrane H(+)-ATPase (Arabidopsis thaliana AHA2)

25 Eukaryotic P-type plasma membrane H(+)-ATPases are primary active transpor

26 for other P-type ATPases, inhibition of the plasma membrane H(+)-ATPase by metal fluorides was partl

27 This all indicates that activation of plasma membrane H(+)-ATPase by unsaturated fatty acids d

28 this study, we have examined M5 of the yeast plasma membrane H+-ATPase by alanine-scanning mutagenesi

29 ) is a fungal toxin that activates the plant plasma membrane H+-ATPase by binding with 14-3-3 protein

30 rol, exocytosis, and activation of the plant plasma-membrane H+-ATPase by fusicoccin.

31 hway and thereby reduces the activity of the plasma membrane H(+)-ATPase complex, thus reducing proto

32 the membrane-spanning segments of the yeast plasma membrane H(+)-ATPase contain seven negatively cha

33 ons conferred resistance because the altered plasma membrane H+-ATPase could more efficiently rid the

34 Mutation of the plasma membrane H+-ATPase did not confer resistance by p

35 lta strains have an elevated activity of the plasma membrane H(+)-ATPase due to an abnormally high va

36 The yeast plasma-membrane H(+)-ATPase, encoded by PMA1, is deliver

37 The plant plasma membrane H(+)-ATPase energizes the secondary upta

38 These data indicate that plant plasma membrane H(+)-ATPases evolved as specific recepto

39 highly expressed isoforms of the Arabidopsis plasma membrane H(+)-ATPase family, have been isolated a

40 ed endomembrane function for a member of the plasma membrane H+-ATPase family.

41 Plasma membrane H(+)-ATPases form a subfamily of P-type

42 In plasma membrane H(+)-ATPases from yeast and plants, simi

43 inking transmembrane segments 2 and 3 of the plasma membrane H+-ATPase from Saccharomyces cerevisiae.

44 irected mutagenesis of the Neurospora crassa plasma membrane H(+)-ATPase has recently been reported.

45 n M4 of the yeast (Saccharomyces cerevisiae) plasma membrane H+-ATPase have been explored by alanine-

46 phosphorylation site (Asp-378) of the yeast plasma-membrane H+-ATPase have been shown previously to

47 or discharged at low pH by stretch-activated plasma membrane H(+)-ATPases, hence a substantial source

48 to other, as yet uncharacterized, changes in plasma membrane H(+)-ATPase hydrolytic activity observed

49 This alteration increases plasma membrane H(+)-ATPase hydrolytic activity.

50 t isoform that incorporates into functional, plasma membrane H(+)ATPases in intercalated cells of the

51 the first genetic evidence for a role of the plasma membrane H+-ATPase in cytoplasmic pH homeostasis

52 The plasma membrane H(+)-ATPase is a P-type ATPase responsib

53 this phenotypic reversal is that activity of plasma membrane H(+)-ATPase is decreased further and vac

54 We propose that the plant plasma-membrane H+-ATPase is regulated in an analogous m

55 machinery of the Arabidopsis thaliana P-type plasma membrane H(+)-ATPase isoform 2 (AHA2) consists of

56 e reconstitution of the Arabidopsis thaliana plasma membrane H(+)-ATPase isoform 2 into soluble nanos

57 The plasma membrane H+-ATPase of yeast assumes distinct conf

58 The plasma-membrane H+-ATPase of Saccharomyces cerevisiae, w

59 The molecular architecture of the yeast plasma membrane H(+)-ATPase phosphorylation region was e

60 provide a mechanistic link between auxin and plasma membrane H(+)-ATPases (PM H(+)-ATPases) in Arabid

61 heory proposed in the 1970s, auxin activates plasma membrane H(+)-ATPases (PM H(+)-ATPases) to facili

62 which N-ethylmaleimide (NEM) reacts with the plasma-membrane H+ATPase (PMA)1 of Saccharomyces cerevis

63 ned in a late Golgi compartment, whereas the plasma membrane H(+) ATPase Pma1, which is transported i

64 The plasma membrane H(+)-ATPase, Pma1, is an essential and l

65 The yeast plasma membrane H(+)-ATPase Pma1p is one of the most abu

66 ation capacity consistent with the augmented plasma membrane H(+)-ATPase proton transport values, and

67 h medium through an elevated activity of the plasma membrane H(+)-ATPase, resulting from a decreased

68 d stomatal opening, then the activity of the plasma membrane H(+)-ATPase should be reduced at this ti

69 edullary intercalated cells with predominant plasma membrane H(+)-ATPase staining was increased signi

70 idneys, relatively few cells had predominant plasma membrane H(+)-ATPase staining.

71 n of the phosphorylation region of the yeast plasma membrane H(+)-ATPase that is consistent with, but

72 In the crystal structure of the plant plasma membrane H(+)-ATPase, this residue is located in

73 ibility of the terminal regulatory domain of plasma membrane H(+)-ATPase to protein kinase action.

74 Plant plasma-membrane H(+)-ATPases, transporters that are acti

75 a rapid, reversible activation of the yeast plasma membrane H(+)-ATPase, very likely mediated by pho

76 The most interesting change in the plasma membrane H+-ATPase was in kinetic behavior.

77 directed mutants in this region of the yeast plasma membrane H(+)-ATPase were constructed and express

78 ne segments 1 (TM1) and 2 (TM2) of the yeast plasma membrane H(+)-ATPase were probed by site-directed

79 icoccin also blocked NIP activity, and plant plasma-membrane H+-ATPases were activated by either fusi

80 Pma1 is a plasma membrane H(+)-ATPase whose activity at the cell s

81 ining a phloem-specific transgene encoding a plasma membrane H+-ATPase with an altered carboxy termin

82 , we observed changes in hexose transporter, plasma membrane H(+)-ATPase, ZmMADS1, and 14-3-3 protein