ライフサイエンスコーパス: phosphate transporter

1 ive product shows homology to the glycerol-3-phosphate transporter.

2 al, and structural studies of the glycerol-3-phosphate transporter.

3 onse, a marked increase in mRNA levels for a phosphate transporter.

4 se (P46), and putative glucose and inorganic phosphate transporters.

5 rs it easily incorporated into cells via the phosphate transporters.

6 er from the unrelated lactose and glycerol 3-phosphate transporters.

7 creases in cells that are defective in other phosphate transporters.

8 atalysing Pi uptake in chlorophytes, whereas PHOSPHATE TRANSPORTER 1 (PHT1) proteins are the H(+) /Pi

9 ch is a phosphate analog and a substrate for Phosphate transporter 1 (Pht1) transporters.

10 Whereas KoRV-A uses the sodium-dependent phosphate transporter 1 (PiT1) as a receptor, KoRV-B emp

11 nucleotides (ASOs) specific to the glucose 6-phosphate transporter-1 (G6PT1) enabled reduction of hep

12 ith structural similarity to a type 1 sodium phosphate transporter, 12 novel histone genes, and a gen

13 the binding affinity to the sodium-dependent phosphate transporter 2a (Npt2a) as compared with WT PDZ

14 argets including the Npt2a (sodium-dependent phosphate transporter 2a).

15 ntified NaSIPP, a mitochondrial protein with phosphate transporter activity, as a novel NaStEP-intera

16 RPTECs express the NPT2A phosphate transporter, alphaKlotho, FGFR1, FGFR3, FGFR4,

17 Ram-1 acts as both a sodium-dependent phosphate transporter and a receptor for amphotropic ret

18 sive disease caused by mutation of glucose-6-phosphate transporter and characterized by altered glyco

19 t mutant revealed that MtPT1 is a functional phosphate transporter and Northern analyses revealed tha

20 l stores via the production of high-affinity phosphate transporters and the synthesis of intracellula

21 mutants indicated that MtPT4 functions as a phosphate transporter, and estimates of the K(m) suggest

22 PHO84 encodes a high-affinity phosphate transporter, and mutations in PHO86 cause many

23 ding the PHOX alkaline phosphatase, the PTB2 phosphate transporter, and the regulatory element PSR1.

24 PHO84 gene encodes a high affinity inorganic phosphate transporter, and we find that its disruption r

25 enes encoding glycogen biosynthetic enzymes, phosphate transporters, and the RNA polymerase sigma-38

26 (A-MuLV) utilizes the Pit-2 sodium-dependent phosphate transporter as a cell surface receptor to infe

27 el that used the Escherichia coli glycerol 3-phosphate transporter as a template has been described.

28 (A-MuLV) utilizes the PiT2 sodium-dependent phosphate transporter as its cell surface receptor to in

29 ter structures (lactose permease, glycerol-3-phosphate transporter) as well as to a low resolution pr

30 PHOSPHATE TRANSPORTER B (PTB) proteins are hypothesized

31 Hence, the data support the glycerol 3-phosphate transporter-based homology model of PCFT and t

32 brate brain-specific Na+-dependent inorganic phosphate transporter (BNPI).

33 significantly different from the plant root phosphate transporters cloned to date.

34 nces from phoA, senX3, and the high-affinity phosphate transporter component pstS, demonstrating dire

35 dy of neutrophils deficient in the glucose-6-phosphate transporter, describe a novel role for the per

36 as a plasma membrane Na+-dependent inorganic phosphate transporter (differentiation-associated Na+/P(

37 s with short sequence motifs shared by known phosphate transporters enabled the identification of a n

38 regulate expression of 3 members of the PHT1 phosphate transporter family SiPHT1;2 SiPHT1;3 and SiPHT

39 orters enabled the identification of a novel phosphate transporter from M. truncatula, MtPT4.

40 ion was accompanied by delocalization of the phosphate transporter from the plasma membrane.

41 ucose homeostasis, is comprised of glucose 6-phosphate transporter (G6PT) and G6Pase.

42 1b is caused by a deficiency in a glucose 6-phosphate transporter (G6PT) that translocates glucose 6

43 ) is caused by a deficiency in the glucose-6-phosphate transporter (G6PT), a 10 transmembrane domain

44 type-Ib (GSD-Ib), deficient in the glucose-6-phosphate transporter (G6PT), is characterized by impair

45 ciency in a ubiquitously expressed glucose-6-phosphate transporter (G6PT).

46 ) is caused by a deficiency in the glucose-6-phosphate transporter (G6PT).

47 transcription factor that mediates arsenate/phosphate transporter gene expression and restricts arse

48 Recently, a phosphate transporter gene in potato was shown to be ind

49 Mutations of Fgf23, Klotho and phosphate transporter genes have been identified to caus

50 Previously, we cloned two phosphate transporter genes, MtPT1 and MtPT2 from Medica

51 e, several phosphate-starvation response and phosphate-transporter genes displayed reduced induction

52 ve phosphate sensor), and the uhpT (a hexose phosphate transporter) genes.

53 lease correlated with the level of glucose 6-phosphate transporter (Glc-6-PT) mRNA, which was found t

54 ency in the ubiquitously expressed glucose 6-phosphate transporter (Glc-6-PT).

55 to that of the distantly related glycerol 3-phosphate transporter GlpT.

56 ures of the related transporters, glycerol-3-phosphate transporter (GlpT) and lactose permease (LacY)

57 In the sn-glycerol-3-phosphate transporter (GlpT) from Escherichia coli, the

58 n to the crystal structure of the glycerol 3-phosphate transporter (GlpT) from Escherichia coli.

59 Glycerol 3-phosphate transporter (GlpT) mediates the import of glyc

60 glycerol metabolism, including a glycerol-3-phosphate transporter (GlpT), a glycerol-3-phosphate deh

61 ster phosphodiesterase (GlpQ) and glycerol-3-phosphate transporter (GlpT), respectively.

62 Using the x-ray structure of the glycerol 3-phosphate transporter (GlpT), we devised a model for the

63 e one hand, and up-regulation of a GLUCOSE-6-PHOSPHATE TRANSPORTER (GPT2), on the other hand.

64 The bidirectional phosphate transporter has an intrinsic dissociation cons

65 Two cDNAs (AtPT1 and AtPT2) encoding plant phosphate transporters have been isolated from a library

66 The sodium-dependent phosphate transporter (HOST5/SLC34A2) expression was ass

67 We further characterized putative phosphate transporters, identifying two new phosphate tr

68 m that controls expression of the UhpT sugar phosphate transporter in Escherichia coli in response to

69 The similarity of Pho84p, a high-affinity phosphate transporter in Saccharomyces cerevisiae, to th

70 began these studies to determine the role of phosphate transporters in signaling phosphate starvation

71 as well as that of PiT1 and PiT2 (inorganic phosphate transporters), in blood and airway neutrophils

72 In addition, the glycerol-3-phosphate transporter is monomeric and stable over a wid

73 this approach, we find that the affinity of phosphate transporters is related to the concentration o

74 coli uhpT gene, encoding the inducible sugar phosphate transporter, is dependent on the response regu

75 s of root symbioses, it is apparent that the phosphate transporters known to operate at the root-soil

76 White lupin phosphate transporter (LaPT1) and secreted acid phosphat

77 operon, encoding homologues of an inorganic phosphate transporter, leads to constitutive expression

78 y we identified MtPT4, a Medicago truncatula phosphate transporter located in the periarbuscular memb

79 ate uptake through solute carrier family 20 (phosphate transporter), member 1 (SLC20a1) supports oste

80 domain" that contains the symbiosis-specific phosphate transporter, MtPT4, and an "arbuscule trunk do

81 In addition, analysis of phosphate transporter mutants implicates the trans-Golgi

82 ion, we investigated the effect of glucose-6-phosphate transporter mutation on immune cell homeostasi

83 activity and protein of the principal renal phosphate transporter NaPi-2a.

84 by the action of the apical sodium-dependent phosphate transporters, NaPi-IIa/NaPi-IIc/Pit2.

85 , reduced expression of the sodium-dependent phosphate transporter NPT2a in the proximal tubules, and

86 nd increased protein expression of the renal phosphate transporter Npt2a.

87 kidney by retrieval of the sodium-dependent phosphate transporters (Npt2a and Npt2c) from the apical

88 (PTH)-responsive sequestration of the renal phosphate transporter, Npt2a, with ensuing urinary phosp

89 nternalization of the major sodium-dependent phosphate transporter, Npt2a.

90 UhpT, the sugar phosphate transporter of Escherichia coli, acts to excha

91 from the soil and is distinct from the other phosphate transporter of this class described to date.

92 acid sequence similarity with high-affinity phosphate transporters of Saccharomyces cerevisiae, Neur

93 thin the plant in part through the action of phosphate transporters of the PHT1 family.

94 Overexpression of unrelated phosphate transporters or a glycerophosphoinositol trans

95 d rice genome at hand, only the Oryza sativa phosphate transporter (OsPT) gene OsPT11 was specificall

96 The double mutants of PGK3 and the triose-phosphate transporter (pgk3.2 tpt3) displayed a drastic

97 ession of Arabidopsis (Arabidopsis thaliana) phosphate transporter PHO1;H3 comprising MYB15, MYB84, b

98 1 signaling in C. albicans revealed that the phosphate transporter Pho84 is required for normal TORC1

99 coding-region polymorphism in the inorganic phosphate transporter PHO84 underlies sensitivity to two

100 y of S. cerevisiae transporters, including a phosphate transporter (Pho84p), and both inositol transp

101 phosphate transporters, identifying two new phosphate transporters, PHO90 and PHO91.

102 -affinity phosphate-binding component of the phosphate transporter, phoA, an alkaline phosphatase, an

103 rol 3-phosphate dehydrogenase and glycerol 3-phosphate transporter/phosphodiesterase, respectively.

104 all subunit RBCS2B [RBCS]) or heterotrophic (phosphate transporter PHT1.2 [PHT]) cell-specific promot

105 MVB-mediated sorting of high-affinity phosphate transporters (PHT1) to the vacuole limits thei

106 The Arabidopsis phosphate transporter PHT4;1 was previously localized to

107 ransmembrane monomeric Piriformospora indica phosphate transporter (PiPT), a member of the major faci

108 fungal (Piriformospora indica) high-affinity phosphate transporter, PiPT, in an inward-facing occlude

109 ormal cellular functions as sodium-dependent phosphate transporters (Pit-1 and Pit-2, respectively).

110 ns bind specifically to cells expressing the phosphate transporter protein Pit1, demonstrating for th

111 ls expressing either of two widely expressed phosphate transporter proteins, Pit1 or Pit2.

112 Expression of an inorganic phosphate transporter (PTA3) was enriched approximately

113 red to phosphate, modifies the expression of phosphate transporters (PTs).

114 etitive index assays, mutation of a putative phosphate transporter reduced in vivo competitiveness by

115 rst in plants, in coordination with arsenate/phosphate transporter repression, which immediately rest

116 ndent inorganic phosphate (Pi) cotransporter phosphate transporter/retrovirus receptor 1 (PiT-1).

117 utants implicates the trans-Golgi network in phosphate transporter secretion.

118 t SPX domains--which are found in eukaryotic phosphate transporters, signaling proteins, and inorgani

119 he human type III sodium-dependent inorganic phosphate transporter, SLC20A1, formerly known as PiT1.

120 ns specifically maintained expression of the phosphate transporter SLC20A2 at higher levels relative

121 knocked into the sodium-dependent inorganic phosphate transporter SLC34a1 locus, which is expressed

122 d HOST5 codes for a type II sodium-dependent phosphate transporter (SLC34A2).

123 quisition (the Pho1 acid phosphatase and the phosphate transporter SPBC8E4.01c), without affecting th

124 FT, based upon theEscherichia coliglycerol 3-phosphate transporter structure, predicted that PCFT tra

125 contains a unique set of proteins including phosphate transporters such as Medicago truncatula MtPT4

126 We have identified a phosphate transporter (TcPho91) localized to the bladder

127 by Pi deficiency and arsenate, and encodes a phosphate transporter that has a high affinity for arsen

128 he lumen, and putative glucose and inorganic phosphate transporters that allow exit of the products o

129 rieved genome does not contain all inorganic phosphate transporters that are characteristic of PAOs (

130 as well as the eukaryotic organellar triose phosphate transporter (TPT) and nucleotide-sugar transpo

131 anscription-factor gene is flanked by triose-phosphate transporter (TPT) and RNA helicase genes [9].

132 in phosphate transporter1 (PHT1) family and phosphate transporter traffic facilitator1 (PHF1) in pho

133 hypothesis that the bacterium-derived hexose-phosphate transporter UhpC might have been the primordia

134 tein is required for expression of the sugar phosphate transporter UhpT in Escherichia coli and is re

135 the Escherichia coli uhpT gene for the sugar phosphate transporter UhpT in response to extracellular

136 Expression of the Escherichia coli sugar phosphate transporter UhpT is induced by extracellular g

137 In the sugar phosphate transporter UhpT, gain-of-function derivatives

138 otein which controls production of the sugar phosphate transporter UhpT.

139 that tightly regulate expression of a hexose phosphate transporter (UhpT).

140 ative feedback loops leads to bistability in phosphate transporter usage--individual cells express pr

141 on of transcripts encoding plant PHT1 family phosphate transporters varied among lines.

142 The uhpT gene, which encoded a sugar phosphate transporter, was the most frequently isolated

143 etic lethal phenotype was observed when five phosphate transporters were inactivated, and the contrib

144 exposed to As(V), transcript levels of As(V)/phosphate-transporters were similar or even higher than

145 We evaluated the expression of two phosphate transporters which we have found to be associa

146 Expression and activity of intestinal phosphate transporter, which did not change after nephre

147 te (apparently by both passive diffusion and phosphate transporters), with bulk root tissue Se concen