ライフサイエンスコーパス: lipid transfer protein

1 targeted and exacerbated by an intracellular lipid transfer protein.

2 Here, we demonstrate that human ATG2A is a lipid transfer protein.

3 to M-833 and identify mutations in the START lipid transfer protein.

4 ass 10 allergen, profilin, and a nonspecific lipid transfer protein.

5 re mainly positive for the peach-nonspecific lipid-transfer protein.

6 ylase inhibitors, seed storage proteins, and lipid transfer proteins.

7 s molecule shares some similarity with plant lipid transfer proteins.

8 el genes, ATA7, encodes a protein related to lipid transfer proteins.

9 terol-binding protein-like proteins (OSBPLs) lipid transfer proteins.

10 uncovering the catalytic mechanisms of other lipid transfer proteins.

11 y to accurately model lipid-binding poses in lipid transfer proteins.

12 h another plant food allergy to non-specific lipid transfer proteins.

13 ctrostatic switching mechanism used by other lipid transfer proteins.

14 ansport between the two bilayers mediated by lipid transfer proteins.

15 d oxysterol-binding protein (OSBP) family of lipid transfer proteins.

16 Par j 1 and Par j 2, have been identified as lipid transfer proteins.

17 ilar structure to that of plant non-specific lipid-transfer proteins.

18 rimary structure of a monomeric non-specific lipid transfer protein 1 (nsLTP1), with molecular weight

19 ins (6), plasma membrane receptors (19), and lipid-transfer-proteins (18).

20 lipid transfer protein (PLTP), also known as lipid transfer protein 2 (LTP-2), mediates a transfer of

21 that hypomorphs of the cuticle-related gene LIPID TRANSFER PROTEIN 2 (LTP2) greatly increased variat

22 9 (profilin, 31%) and Act d 10 (nonspecific lipid transfer protein, 22%).

23 To study how elevated StAR-related lipid transfer protein 3 (StARD3) expression affects bre

24 We show that one such protein, bridge-like lipid transfer protein 3A (BLTP3A)/UHRF1BP1 binds VAMP7

25 lipid transfer between the membrane and the lipid transfer protein, a key parameter determining the

26 normalities in cholesteryl ester transfer or lipid transfer protein activities do not underlie the in

27 ty could not be accounted for by nonspecific lipid transfer protein activity.

28 while the Bet v 1 homologue Ara h 8 and the lipid transfer protein allergen, Ara h 9, were detected

29 ein complexes (transmembrane-like channel 2, lipid transfer protein and 'Protein S'), from transgenic

30 TIPE3 can act as a lipid transfer protein and may constitute a novel phosph

31 DIR1 encodes a putative apoplastic lipid transfer protein and we propose that DIR1 interact

32 blt4 barley gene family encodes non-specific lipid transfer proteins and has been shown, by in situ l

33 Understanding the relationship between lipid transfer proteins and lipoprotein metabolism is ex

34 ich protein with some sequence similarity to lipid transfer proteins and now called stigma/stylar cys

35 -cell protein complementation screen between lipid transfer proteins and PPARs uncovered a direct int

36 These include thionins, lipid transfer proteins and snakins.

37 olvement of hydrogen peroxide, nitric oxide, lipid transfer proteins, and aspartic proteases as criti

38 rs, heat shock proteins, DEAD-box helicases, lipid transfer proteins, and membrane-deforming proteins

39 enes include classes of defensins, thionins, lipid transfer proteins, and snakins, plus other proteas

40 a thaumatin-like protein (grape osmotin), a lipid-transfer protein, and a basic and an acidic chitin

41 hlight the roles of metabolite transporters, lipid-transfer proteins, and mitochondria-organelle inte

42 The lipid transfer proteins Api g 2 and Api g 6 were not rel

43 1Q) and another SNP from gene coding for the lipid transfer protein (Aradu.03ENG) showed polymorphism

44 Lipid transfer proteins are important in membrane vesicl

45 Large lipid transfer proteins are involved in lipid transporta

46 tually unifies all the RBG domain-containing lipid transfer proteins as members of an RBG protein sup

47 Finally, the lipid transfer protein ATG2 is also recruited to damaged

48 This study focuses on the role of the lipid transfer protein AtLTPI-4 in crown gall developmen

49 ated functional decline via juvenile hormone-lipid transfer protein axis and germline signaling.

50 fold difference in the major maize allergen, lipid transfer protein between nine varieties, and compl

51 Bridge-like lipid transfer proteins (BLTPs) are established to funct

52 As a model for the related plasma lipid transfer proteins, BPI illuminates a mechanism of

53 lipid composition is maintained by conserved lipid transfer proteins, but computational approaches to

54 promotes robust LC3A engagement with ATG2, a lipid transfer protein central to lysosome repair.

55 protein IncD mediates the recruitment of the lipid transfer protein CERT and the ER-resident protein

56 rane and caused a massive recruitment of the lipid transfer protein CERT that relied on the PH domain

57 mbrane contributes to the recruitment of the lipid transfer protein CERT to the inclusion.

58 sfer protein (MTP), an endoplasmic reticulum lipid transfer protein critical for apolipoprotein B (ap

59 Therefore, hepatic lipase, together with lipid transfer proteins, determines both HDL-cholesterol

60 ted to distal tissues, and this requires the lipid transfer protein, DIR1.

61 pollen-driven in Northern/Western Europe and lipid transfer protein-driven in Spain and Italy.

62 specified by the antagonistic action of the lipid transfer proteins E-Syt3 and ORP5, which transduce

63 Consistently, APCs deficient in a lysosomal lipid-transfer protein effectively present lyso-sulfatid

64 glyceride transfer protein (MTP) is a unique lipid transfer protein essential for the assembly of tri

65 ivator protein (GM2-AP) is a small lysosomal lipid transfer protein essential for the hydrolytic conv

66 BLTP1 (Bridge-Like Lipid Transfer Protein Family Member 1), previously know

67 enic acute regulatory protein (StAR)-related lipid transfer protein family.

68 asmic reticulum (ER) by FAPP2, a cytoplasmic lipid transfer protein, flipped across the ER membrane,

69 uired in Avr PeX along with the DIR1-encoded lipid transfer protein for long-distance signaling in SA

70 Vps13 is a highly conserved lipid transfer protein found at multiple interorganelle

71 LPS-binding protein, a lipid transfer protein found in serum, facilitates both

72 lipopolysaccharide-binding protein (LPB) are lipid transfer proteins found in human plasma.

73 he surface properties of LTP1, a nonspecific lipid transfer protein from barley, both in the presence

74 Non-specific lipid transfer proteins from pollen and plant foods bind

75 orage proteins, Bet v 1-like and nonspecific lipid transfer proteins from pollens and fruits, certain

76 Genomic clones of two nonspecific lipid-transfer protein genes from a drought-tolerant wil

77 affected transfer action by human glycolipid lipid transfer protein (GLTP), which is glycolipid-speci

78 Recently, a new type of bridge-like lipid transfer protein has emerged; these proteins conta

79 The allergen Pru p 3, a peach lipid transfer protein, has been well studied.

80 This study can shed more light on why large lipid transfer proteins have a well conserved alpha-heli

81 Lipid transfer proteins have important roles in cellular

82 Here, a ubiquitously expressed lipid transfer protein, human GLTPD1, named here CPTP, i

83 otein-2 (SCP-2) is an important non-specific lipid transfer protein in insects and appears to be a po

84 ation, intramitochondrial contact sites, and lipid transfer proteins in maintaining membrane homeosta

85 s) serve as phosphatidylserine (PS)-specific lipid transfer proteins in the mitochondrial intermembra

86 -TP occurs in vivo, which further implicates lipid transfer proteins in the regulation of PtdIns 3-ki

87 te that this method is suitable for assay of lipid transfer proteins including mechanistic studies of

88 Here, we show that CD1e behaves as a lipid transfer protein influencing lipid immunoediting a

89 A new approach for analyzing lipid-lipid transfer protein interactions is described.

90 P) is an endoplasmic reticulum (ER)-resident lipid transfer protein involved in the biosynthesis and

91 Of the known lipid transfer proteins, LBP is thus most able to transf

92 tarvation of yeast or overexpression of ATG2 lipid transfer protein, led to enhanced viral RNA recomb

93 that SCA isoforms have the plant nonspecific lipid transfer protein-like structure: a globular shape

94 e its discovery over 20 yr ago, is in fact a lipid-transfer protein likely operating at the ER-autoph

95 hat transcriptional co-repression of the two lipid transfer proteins, liver fatty acid-binding protei

96 nd storage proteins and members of the large lipid transfer protein (LLTP) gene family, which include

97 , and phylogenetics to investigate the large lipid transfer protein (LLTP) superfamily and ferritin-l

98 We have established that VPS13C encodes a lipid transfer protein localized to contact sites betwee

99 allergy occurs in all European populations, lipid transfer protein (LTP) allergy is considered to ma

100 uitment of the ER-plasma membrane tether and lipid transfer protein (LTP) Extended-Synaptotagmin 1 (E

101 Food allergy caused by lipid transfer protein (LTP) from peach (Pru p 3) is fre

102 and stability of the allergenic nonspecific lipid transfer protein (LTP) of peach were compared with

103 ith high cross-reactivity as observed in the lipid transfer protein (LTP) syndrome, which is characte

104 Lipid transfer protein (LTP), an abundant protein in fru

105 cids showing 87 identity with WBP1A, a wheat lipid transfer protein (LTP), but much lower homology to

106 stigma/style Cys-rich adhesin (SCA), a plant lipid transfer protein (LTP), is a small, secreted pepti

107 Of these, eight had high homology to lipid transfer protein (LTP), two were similar to glycin

108 asynchronously at different stages, but the lipid transfer protein (LTP)-encoding genes, including S

109 Here, we show that the lipid transfer protein (LTP)-like AZI1 and its closest p

110 A key component for systemic resistance, lipid transfer protein (LTP)-like AZI1, is needed for th

111 pha-amylase inhibitor (AAI) dimer, and wheat lipid transfer protein (LTP).

112 ed with hypersensitivity to the non-specific lipid transfer protein (LTP).

113 Lipid transfer protein (LTP, Pru p 3) is the major aller

114 Lipid transfer proteins (LTP) play a major role in plant

115 clones encoding Brassica napus non-specific lipid transfer proteins (LTP) were isolated and sequence

116 osin, the precursor to a family of endosomal lipid transfer proteins (LTP), exhibit specific defects

117 foods could also be due to sensitisation to Lipid Transfer Proteins (LTP).

118 profilins, pathogenesis-related (PR) 10 and lipid transfer proteins (LTP).

119 -inducible barley vegetative shoot epidermal lipid-transfer protein (LTP) family, BLT4, on the basis

120 se bands could be two isoforms of peach leaf lipid transfer proteins( LTP), so the recognition freque

121 Non-specific lipid transfer proteins (LTPs) are a family of lipid-bin

122 In the Mediterranean area, lipid transfer proteins (LTPs) are important causes of p

123 Lipid transfer proteins (LTPs) are small secretory prote

124 Lipid transfer proteins (LTPs) are thought to be involve

125 sicular transport, the latter facilitated by lipid transfer proteins (LTPs) at membrane contact sites

126 Very few lipid transfer proteins (LTPs) have been caught in the a

127 gic reactions have been implicated to maize, lipid transfer proteins (LTPs) have been identified as m

128 The characterization of lipid binding to lipid transfer proteins (LTPs) is fundamental to underst

129 of Acyl-CoA SYNTHETASE5 (ACOS5) and type III LIPID TRANSFER PROTEINs (LTPs) secreted from the anther

130 Experimental studies of barley and maize lipid transfer proteins (LTPs) show that the two protein

131 between organelles is achieved by a group of lipid transfer proteins (LTPs) that carry lipids using t

132 rtant proteins contributing to beer foam are lipid transfer proteins (LTPs), in particular LTP1 and i

133 eins such as Len c 1.0101, Len c 1.0102, and lipid transfer proteins (LTPs), indicating qualitative a

134 in HCV replication organelles (ROs) recruits lipid transfer proteins (LTPs), like oxysterol-binding p

135 mology with expansins but is a member of the lipid transfer proteins (LTPs).

136 s [mediated by both trafficking vesicles and lipid transfer proteins (LTPs)].

137 ng the localization and operation of ORP5, a lipid transfer protein maintaining PM PtdSer enrichment.

138 Lipid transfer proteins mediate nonvesicular transport o

139 expansion results from the partnership of a lipid transfer protein, moving lipids between the cytoso

140 n endosomes through the function of resident lipid transfer proteins, namely saposins.

141 odes a glycosylphosphatidylinositol-anchored lipid transfer protein, necessary for pollen exine devel

142 ective detection of Sola l 7, a non-specific lipid transfer protein (nsLTP) found in tomato seeds ass

143 Ole e 7 is a nonspecific lipid transfer protein (nsLTP) from olive pollen, one of

144 The non-specific lipid transfer proteins (nsLTP) are unique to land plant

145 s, we identified 2S albumin and non-specific lipid transfer proteins (nsLTP) as the proteins involved

146 vestigating the allergenicity of nonspecific lipid transfer proteins (nsLTPs) and seed storage protei

147 Non-specific lipid transfer proteins (nsLTPs) are cationic proteins i

148 Plant non-specific lipid transfer proteins (nsLTPs) are encoded by multigen

149 e show that cell-wall localized non-specific lipid transfer proteins (nsLTPs) facilitate VOC emission

150 e we identified eight so-called non-specific Lipid transfer proteins (nsLTPs) genes that are expresse

151 Non-specific lipid transfer proteins (nsLTPs) reported from various p

152 Nonspecific lipid transfer proteins (nsLTPs) represent a major cause

153 Sensitization to one or more non-specific lipid transfer proteins (nsLTPs), initially thought to e

154 equences classified as putative non-specific lipid transfer proteins (nsLTPs), which were classified

155 lar details and the effects of 3 nonspecific lipid transfer proteins (nsLTPs; Mal d 3 [allergenic nsL

156 Non-specific lipid-transfer proteins (nsLTPs) are a family of pan-all

157 Non-specific lipid-transfer proteins (nsLTPs) are involved in the mov

158 o perform a genomic analysis of non-specific lipid-transfer proteins (nsLTPs) in coffee.

159 Conserved lipid transfer proteins of the Ups/PRELI family regulate

160 Lipid transfer proteins of the Ups1/PRELID1 family facil

161 onarily related to the family of nonspecific lipid-transfer proteins of plants.

162 nes and are proposed to target intracellular lipid-transfer proteins of the oxysterol-binding protein

163 owed that this remodeling does not depend on lipid transfer proteins or lipases.

164 ly upon cross-reactivity between nonspecific lipid transfer proteins or thaumatin-like proteins prese

165 The data suggest that lipid transfer proteins (or other small soluble proteins

166 er show that IQSec1 forms a complex with the lipid transfer protein ORP3, and that Ca(2+) influx trig

167 Here, we show that the lipid transfer proteins ORP5 and ORP8 control LD biogene

168 that the endoplasmic reticulum (ER)-anchored lipid transfer protein PDZ domain-containing 8 (PDZD8),

169 Lipid transfer proteins play an essential role in the in

170 Phospholipid lipid transfer protein (PLTP) is ubiquitously expressed

171 Phospholipid lipid transfer protein (PLTP) mimics high-density lipopr

172 d the ER membrane proteins VAPA and VAPB and lipid transfer proteins possessing dual (ER and TGN) tar

173 stid inner envelope, TGD4 is a transmembrane lipid transfer protein present in the outer envelope.

174 CD1d is dependent on various small, soluble lipid transfer proteins present in the lysosome.

175 Sensitisation to the lipid transfer protein Pru p 3 is associated with severe

176 profilins (Phl p 12), PR-10s (Bet v 1), and lipid transfer proteins (Pru p 3).

177 A lipid transfer protein, purified from bovine brain (23.7

178 5 as a glycosylphosphatidylinositol-anchored lipid transfer protein required for normal pollen exine

179 Nonspecific lipid transfer proteins reversibly bind different types

180 in conformation (e.g., albumins, nonspecific lipid transfer proteins, saposins, nematode polyprotein

181 , encoding an endoplasmic reticulum-anchored lipid transfer protein, showed cosegregation with syndro

182 coidin C2, PH, PX), enzymes (PLA, PLC/D) and lipid-transfer proteins (START).

183 Unlike the more promiscuous lipid transfer protein, sterol carrier protein 2 (SCP2),

184 ed and recycled, assisted, in some cases, by lipid transfer proteins such as saposins.

185 Lipid transfer proteins, such as molecules of the saposi

186 that TGD4 is an integral dimeric beta-barrel lipid transfer protein that binds PtdOH with its N termi

187 G) transfer protein (MTP) is a heterodimeric lipid transfer protein that catalyzes the transport of t

188 ysaccharide (LPS) binding protein (LBP) is a lipid transfer protein that catalyzes transfer of LPS mo

189 A lipid transfer protein that facilitates the transfer of

190 GM2-activator protein (GM2-AP) is a lipid transfer protein that has the ability to stimulate

191 tasis is disrupted via depletion of ACD11, a lipid transfer protein that is specific for ceramide 1-p

192 LBP is a lipid transfer protein that moves lipopolysaccharide (LP

193 line transfer protein (PC-TP) is a cytosolic lipid transfer protein that promotes intermembrane trans

194 and glycolipid antigens, as well as a set of lipid transfer proteins that load the final version of t

195 st apply this approach to identify roles for lipid transfer proteins that traffic phosphatidylcholine

196 entiated by the LPS-binding protein (LBP), a lipid-transfer protein that binds LPS aggregates and tra

197 roove superfamily, which includes eukaryotic lipid-transfer proteins that mediate phospholipid transp

198 VAPs are known to recruit lipid transfer proteins to the ER, including oxysterol b

199 holipid scramblase, which functions with the lipid transfer protein Vps13 in MVB biogenesis.

200 expected contribution of a large bridge-like lipid transfer protein, Vps13, in this process.

201 purified from the nut while the non-specific lipid transfer protein was produced as a recombinant in

202 Lipid transfer protein was the most frequently involved

203 SCA, which shows some identity with LTP (lipid transfer protein), was localized to the transmitti

204 BLTP2/KIAA0100, a bridge-like lipid transfer protein, was reported to localize at cont

205 activator protein serves as an example of a lipid transfer protein where the ability to independentl

206 Here, we characterize spartin as a lipid transfer protein whose transfer ability is require

207 3A is an endoplasmic reticulum (ER)-anchored lipid transfer protein with a putative role in the trans

208 GM2-activator protein (GM2AP) is a lysosomal lipid transfer protein with important biological roles i