ライフサイエンスコーパス: transport protein

1 t of serum albumin, the extracellular Cu(2+) transport protein.

2 ansporter G family member40, encoding an ABA transport protein.

3 e and one lacking the relevant SbmA membrane transport protein.

4 Stard7, an intracellular phosphatidylcholine transport protein.

5 stulate that STM2200 functions as a specific transport protein.

6 s/cholesterol moieties onto this large lipid transport protein.

7 of the SLC25A40 inner mitochondrial membrane transport protein.

8 e inhibitors to access Fe(3+) from a primary transport protein.

9 test whether hyperforin interacts with this transport protein.

10 t nonbiphasic high-affinity nitrate-specific transport protein.

11 ds able to restore function to faulty copper transport proteins.

12 modifying, intracellular trafficking and RNA transport proteins.

13 lacenta richly expresses nonheme and heme Fe transport proteins.

14 G nucleoporins induced by the cargo-carrying transport proteins.

15 lular localization of PIN-FORMED (PIN) auxin transport proteins.

16 ted highlight novel candidate substrates for transport proteins.

17 ort facilitated by plasma membrane-localized transport proteins.

18 isite to understand the function of membrane transport proteins.

19 ase require vesicular and/or plasma membrane transport proteins.

20 sequence of CAII, a region that binds other transport proteins.

21 the combined actions of a range of membrane transport proteins.

22 ENV nonstructural protein 5 and host nuclear transport proteins.

23 pathway constitutes a unique mechanism among transport proteins.

24 l of CP110 and recruitment of intraflagellar transport proteins.

25 s found within the subunits of many membrane transport proteins.

26 F-hand mitochondrial SCaMCs buffering/solute transport proteins.

27 so is limited evidence for a role of glucose transport proteins.

28 munication in this important family of Cl(-) transport proteins.

29 enzymes, transcription factors, and membrane transport proteins.

30 g of various transmembrane receptors and ion-transport proteins.

31 steroidogenesis in the absence of additional transport proteins.

32 preferred substrate for Cu chaperones and Cu-transport proteins.

33 ll as their permeability with respect to the transport proteins.

34 al residues of different classes of specific transport proteins.

35 the host importin (IMP) alpha/beta1 nuclear transport proteins.

36 manner that depends on FA type and cellular transport proteins.

37 used to measure expression levels of key ion transport proteins.

38 n heme binding and release in bacterial heme transport proteins.

39 ulin stimulates the translocation fatty acid transport protein 1 (FATP1) to plasma membrane, and thus

40 ts the erythrocyte sugar transporter glucose transport protein 1 (GLUT1) and examines the transporter

41 spho-EPRS binds SLC27A1 (that is, fatty acid transport protein 1, FATP1), inducing its translocation

42 protein 1, and SLC27A1, encoding fatty acid transport protein 1.

43 of two types of accessory proteins, receptor transporting protein 1 short and odorant binding protein

44 We found that receptor transporting protein 1 short enhanced the membrane expre

45 in WDR35, encoding retrograde intraflagellar transport protein 121 (IFT121), in three families with a

46 of (99m)Tc-mebrofenin through organic anion transport protein 1a and 1b (Oatp1a/1b) and multidrug re

47 g and Ag(+), expression levels of the Copper Transport Protein 2 (CTR2) indicated that Ag biouptake c

48 Fatty acid transport protein 2 (FATP2) is highly expressed in the l

49 PMN-MDSCs exclusively upregulate fatty acid transport protein 2 (FATP2).

50 Sodium-glucose transport protein 2 (SGLT2) inhibitors are a class of an

51 lu (u) Finally, EAAT2 (excitatory amino acid transport protein 2) immunoreactivity was reduced next t

52 ere, we provide evidence that intraflagellar transport protein 20 (IFT20) interacts with E3 ubiquitin

53 We showed previously that the intraflagellar transport protein 20 (IFT20), a component of the intrafl

54 eation, Golgi distribution of intraflagellar transport protein 20 homologue, and ciliogenesis.

55 rane proteins, including sodium-phosphate co-transport protein 2A (NPT2A) at the plasma membrane.

56 Fatty acid transport protein 4 (FATP4) is an acyl-CoA synthetase th

57 Fatty acid transport protein 4 (FATP4) is one of a family of six tr

58 Fatty acid transport protein 4 (FATP4), a transmembrane protein in

59 n fatty acids-like 1 (ELOVL1) and fatty acid transport protein 4 (FATP4), which each have very long-c

60 1; and the fatty acid transporter fatty acid transport protein 4 have all been linked to AD.

61 variant observed in the gene Intraflagellar Transport Protein 43 (IFT43) was studied by heterologous

62 ntly inhibited mRNA expression of fatty acid transport protein 5 in the presence of DGLA, which was i

63 terolemia induced an important change in HDL-transported proteins (576 spots in HL-HDL vs. 621 spots

64 at SDCCAG3 interacts with the intraflagellar transport protein 88 (IFT88), a crucial component of cil

65 kinesin family member 3a and intraflagellar transport protein 88, proteins that are essential for ci

66 osphodiesterase-6 (PDE6), and intraflagellar transport protein-88 (IFT88).

67 rogressive synaptic, cytoskeletal and axonal transport protein abnormalities that may accompany the d

68 A. baumannii encodes for the transport protein AceI, which confers resistance to chlo

69 s uses the Type VII ESX secretion systems to transport proteins across its complex cell wall.

70 ystem is the primary method cells utilize to transport proteins across membranes.

71 s placed small vesicles as the sole means to transport proteins across stable distinct compartments o

72 y little is known about the translocons that transport proteins across the two membranes that surroun

73 bacteria have developed secretion systems to transport proteins across their cell wall, a process tha

74 ponent of the bacterial Sec machinery, which transports proteins across the cytoplasmic membrane.

75 are common substrates for the PACE family of transport proteins, adding to their broad significance a

76 nergic neurons and asked how inactivation of transport proteins affected iron homeostasis in vivo in

77 ture; IFT, in contrast, might be required to transport proteins against cellular concentration gradie

78 ells employ to correctly fold, assemble, and transport proteins along the exocytic pathway.

79 ated that hepcidin is complexed to the blood transport protein, alpha2-macroglobulin (alpha2M).

80 , these data position FABP1 as a hepatic THC transport protein and a critical mediator of cannabinoid

81 taken up by animal cells with the help of a transport protein and a membrane receptor.

82 nexpected molecular link between a vesicular transport protein and a syndrome of autoimmunity manifes

83 include the demonstration of intraflagellar transport protein and hedgehog contributions to the immu

84 Similar to LbtU, LbtP is a siderophore transport protein and is required for robust growth unde

85 Simultaneously, Cu-transport proteins and Cu chaperones sustain Cu(I) suppl

86 aled increased levels of carbon fixation and transport proteins and decreased levels of ammonia oxida

87 18), were analysed for lipase and fatty acid transport proteins and fatty acid and triglyceride conte

88 on, higher expression of ammonia and nitrite transport proteins and key metabolic enzymes mainly in t

89 Vesicular carriers transport proteins and lipids from one organelle to anot

90 e for many commonly studied water and solute transport proteins and metabolic enzymes matched expecta

91 T)-A, IFT-B, and the BBSome], which together transport proteins and other molecules along the cilium.

92 Assigning function to orphan membrane transport proteins and prioritizing candidates for detai

93 icate outside pathogens and thus express few transport proteins and thus few surface epitopes for hos

94 SCRT (endosomal sorting complex required for transport) proteins and found that ESCRT II and IV signi

95 Owing to the ubiquitous presence of ion transport-proteins and cell-cell heterogeneity in biolog

96 ormation of axonal varicosities sequestering transported proteins and progressive neuronal cell death

97 Despite the promise, the feasibility of transporting proteins and peptides into systemic circula

98 ole in intercellular signaling in mammals by transporting proteins and small RNAs.

99 ng, localization of PIN-FORMED1 (PIN1) auxin transport proteins, and in situ hybridization of leaf de

100 ractions with regulators of gene expression, transport proteins, and metabolic pathways.

101 We show here that the ROS-regulated Ca(2+) transport protein Annexin 1 in Arabidopsis thaliana (AtA

102 Here we uncover a novel role of Cu transport protein Antioxidant-1 (Atox1), which is origin

103 mount and the localization of these membrane transport proteins appears as a way to drive their activ

104 Plasma membrane-localized transport proteins are internalized through endocytosis

105 Plasma membrane-located transport proteins are key adaptations for obligate intr

106 t in B. subtilis and that the other putative transport proteins are likely to be utilized for more-sp

107 Among the smallest known transport proteins are members of the small multidrug re

108 dramatically decreased whereas other copper transport proteins are not altered.

109 r, the mechanisms regulating the location of transport proteins are still largely unknown.

110 he genes encoding sodium-dependent vitamin C transport proteins are strongly associated with plasma a

111 0 members, the solute carrier (SLC) membrane transport proteins are the largest family of transporter

112 Membrane transport proteins are therefore of upmost importance as

113 Major facilitator superfamily (MFS) transport proteins are ubiquitous in the membranes of al

114 sCOPT1, which encodes a high-affinity copper transport protein, as well as other copper-deficiency ma

115 , a member of the importin family of nuclear transport proteins, as an intracellular binding partner

116 H7 has been shown to express heme uptake and transport proteins, as well as use heme as an iron sourc

117 Transthyretin (TTR) is a homotetrameric transport protein, assembled from monomers that each con

118 lectrical contacts are made between electron transport proteins associated with the outer membranes o

119 of the regulation of water, urea, and sodium transport proteins; (b) better resolution of the anatomi

120 nd approximately 25% of prokaryotic membrane transport proteins belong to this superfamily.

121 has significant homology with several yeast transport proteins belonging to the major facilitator su

122 ntroduces variation in the activities of ion-transport proteins between cells.

123 cid (SA) and its Cu(2+) complex with a model transport protein, bovine serum albumin (BSA), have been

124 However, in the Escherichia coli OM B(12) transport protein, BtuB, the double labeling of many cys

125 Broad-spectrum inhibitors of ABC transport proteins can be of great use in cancers that s

126 zation of FG nucleoporin assemblies with the transport proteins can be understood within a first prin

127 motor expressed in inner ear hair cells that transports protein cargos within developing mechanosenso

128 paradigm for the largest family of membrane transport proteins, catalyzes the coupled translocation

129 paradigm for the largest family of membrane transport proteins, catalyzes the coupled translocation

130 intracellular distribution of the fatty acid transport protein, CD36, altering fatty acid metabolism.

131 mide phosphoribosyl transferase or in the NR transport protein, CD73.

132 By exploiting the ability of a natural heme transport protein, ChuA, to promiscuously import heme de

133 TCDB is the only transport protein classification database adopted by the

134 structures are synthesized by intraflagellar transport protein complexes, IFT-B and IFT-A, which medi

135 rotein (BCRP, ABCG2) are the three major ABC transport proteins conferring resistance to many structu

136 s, we suggest that related cases of membrane transport proteins containing similar motifs are widespr

137 Solute carrier (SLC) membrane transport proteins control essential physiological funct

138 nipulating thylakoid ion and proton flux via transport proteins could improve photosynthesis.

139 alled PCSK9 and Sec24A, a well known protein-transport protein, could lead to the development of nove

140 Moreover, knockdown copper transport protein, Ctr1, also inhibited CoCl2-induced EM

141 osides upon reconstitution with the electron transport proteins cytochrome b5 and NADH-cytochrome b5

142 inding protein (NikE), periplasmic dipeptide transport protein (DppA), and outer membrane protein A (

143 tic Sec61 translocon was able to efficiently transport proteins entirely composed of intrinsically di

144 quaporin 1 (AQP1) is a plasma membrane water-transporting protein expressed strongly in tumor microva

145 igned to analyze the distinctive features of transport proteins, extending its usefulness.

146 Baseline stromal-specific retinoid transport protein (FABP5, CRABP2) expression may be pred

147 Fatty acid transport protein (FATP) 4 is one of a family of six FAT

148 We hypothesized that placental FA transport proteins (FATP) and FA binding proteins (FABP)

149 2, beta enolase and glycogen phosphorylase), transport proteins (fatty acid-binding protein, myoglobi

150 round the crystal structure of this membrane transport protein, followed by atomistic simulations.

151 inding protein 4 (RBP4) is the sole specific transport protein for retinol in the blood, but it is al

152 rmed samt-1, coding for a candidate membrane transport protein for the presumptive donor substrate of

153 etic mechanisms may generally denote primary transport proteins for bacteria.

154 cell populations, and require intraflagellar transport proteins for their formation.

155 r binding sites on transthyretin (TTR), a T4 transport protein found in plasma and cerebrospinal flui

156 y is directed by cargo-bearing vesicles that transport proteins from one compartment to another.

157 s, because it provides a mechanism to remove transport proteins from the membrane.

158 tion of BBS proteins in photoreceptors is to transport proteins from the OS to the cell body or to pr

159 nt of coat protein complex II (COPII), which transports proteins from the endoplasmic reticulum (ER)

160 a hereditary or acquired deficiency of iron-transporting protein function that diminishes transmembr

161 cently, we established that these two sodium transport proteins functionally interact in the second p

162 e propose that COPT2, a high-affinity copper transport protein, functions under copper and iron defic

163 The human blood-brain barrier glucose transport protein (GLUT1) forms homodimers and homotetra

164 re it interacts with the ER-localised sterol transport protein Gramd1b to regulate cholesterol egress

165 A complex network of zinc import and transport proteins has evolved to control zinc concentra

166 endipitous discovery the CLC family of Cl(-) transporting proteins has been a never ending source of

167 Genes encoding Mbn biosynthetic and transport proteins have been identified in a wide variet

168 Amino acid transport proteins have been shown to be upregulated in

169 None of these mutations occurred in transport protein homologues; instead, they affected hou

170 ions in solution, using testosterone and its transport proteins human serum albumin (HSA) and sex hor

171 Intraflagellar transport proteins (IFT) are required for hedgehog (Hh)

172 o required for recruiting the intraflagellar transport proteins Ift88 and Ift52 to the mother centrio

173 e role of alpha-synuclein and other cellular transport proteins implicated in PD and how their aberra

174 We previously identified a peroxisomal transport protein in Arabidopsis (Arabidopsis thaliana)

175 olar to millimolar) for an integral membrane transport protein in both detergent-solubilised micelles

176 loride cotransporter, NCC, is the major NaCl transport protein in the distal convoluted tubule (DCT).

177 tive abundance of key mitochondrial electron transport proteins in 263K-infected animals relative to

178 membrane localization of multiple bile salt transport proteins in central hepatocytes and may act as

179 All lipid transport proteins in eukaryotes are thought to shuttle

180 eased placental expression of FA binding and transport proteins in late gestation, with fetal plasma

181 as an ion exchanger through manipulation of transport proteins in the cell membrane.

182 The crowded electron transport proteins in the periplasm of the organism cons

183 ignificant changes in other water- or sodium-transporting proteins in the gene-modified mice.

184 ce and phosphorylation of other renal sodium-transporting proteins, including NaPi-IIa, NKCC2, and EN

185 evidence has suggested that these two sodium transport proteins interact.

186 ated with contrasting cellular phenotype, to transport proteins into the mitochondria.

187 While the ensemble of ion transport proteins involved in cell volume regulation is

188 to riboswitches and to different classes of transport proteins involved in potassium uptake and expo

189 , notably in SLC genes that include membrane transport proteins involved in the transport of endogeno

190 d the uptake through a high-affinity uranium transport protein involving the modification of the uran

191 This transport protein is a major target to overcome multidru

192 irment of nuclear HR23 and nucleocytoplasmic transport proteins is an outcome of, and a contributor t

193 rs, it has been shown that a subset of these transport proteins is regulated by magnesium-responsive

194 Transferrin, an iron transport protein, is a clinically important biomarker i

195 erved, along with accumulation of the axonal transport proteins JNK-interacting protein 1 and amyloid

196 , the largest family of ion-coupled membrane transport proteins known at present.

197 is an archaeal homolog of mammalian membrane transport proteins-known as excitatory amino acid transp

198 Iron-bound legiobactin is imported by the transport protein LbtU.

199 expression of the ATP-binding cassette (ABC) transport proteins, like ABCG2, triggering active efflux

200 entified a highly conserved family of sterol transport proteins (Ltc/Lam) localized at diverse MCSs.

201 ipid-synthesizing, lipid-flippase, and lipid-transport proteins (LTPs) collaborate to control lipid b

202 amin E for common binding sites within lipid transport proteins may alter the traffic of lipid mediat

203 Defects in biliary transport proteins, MDR3 in humans and Mdr2 in mice, can

204 Here, we elucidated which transport proteins mediate the hepatic uptake of conjuga

205 nregulated, and Ca2+-dependent mitochondrial transport proteins MIRO1 and KIF5C were reduced.

206 lone protein, but together with the electron transport proteins NADH-cytochrome b5 reductase (CYB5R)

207 Such a dual use of transport proteins not only enables efficient substrate

208 EVs are diverse, nano-sized vesicles, which transport proteins, nucleic acids, and lipids between ce

209 a gene reporter, based on the organic anion transporting protein Oatp1a1, which mediates uptake of a

210 Organic anion transport proteins (OATPs) on the basolateral surface of

211 tochondrial ADP/ATP carrier (AAC) is a major transport protein of the inner mitochondrial membrane.

212 er Mhp1 is a sodium-coupled secondary active transport protein of the nucleobase-cation-symport famil

213 comprehensive genetic analysis of 35 orphan transport proteins of Plasmodium berghei during its life

214 studies show that inhibition of the hepatic transport proteins organic anion-transporting polypeptid

215 The TRAnsport Protein Particle (TRAPP) complex controls mult

216 appc11gene, which encodes a component of the transport protein particle (TRAPP) complex.trappc11mutan

217 The transport protein particle (TRAPP) complexes activate Ra

218 Originally identified in yeast, transport protein particle (TRAPP) complexes are Rab GTP

219 The conserved transport protein particle (TRAPP) complexes regulate ke

220 The large multisubunit transport protein particle (TRAPP) II complex has been p

221 The oligomeric complex transport protein particle I (TRAPPI) mediates nucleotid

222 Transport Protein Particle II (TRAPPII) is essential for

223 Here we show that transport protein particle III (TRAPPIII), a conserved a

224 Transport protein particles (TRAPPs) are multi-protein c

225 as well as the major facilitator superfamily transport protein PcaK.

226 enase (HemO) along with the cytoplasmic heme transport protein PhuS control heme flux into the cell.

227 amyloplasts and relocalization of the auxin transport protein, PIN3.

228 a novel role that MOG1, a nucleocytoplasmic transport protein, plays in cardiac physiology and devel

229 a to the gut lumen depends on the epithelial transport protein, polymeric immunoglobulin receptor (pI

230 underpin the importance of the thylakoid ion transport proteins potassium cation efflux antiporter KE

231 Compiling a molecular inventory of lipid transport proteins present at these sites is a premise t

232 Transport proteins previously described in maturation am

233 sduction, starch and sucrose metabolism, RNA transport, protein processing in endoplasmic reticulum,

234 of MUC1-ED with both NEU1 and its chaperone/transport protein, protective protein/cathepsin A.

235 genes were enriched for genes functioning in transport, protein quality control, and DNA metabolism,

236 Consistent with the association with vesicle transport proteins, re-distribution of TgDrpC to the IMC

237 idney require an overlapping set of membrane transport proteins regulated by the forkhead transcripti

238 Because other iron-transport proteins remain active, labile iron gradients

239 (MDR) mediated by ATP-binding cassette (ABC) transport proteins remains a major problem in the chemot

240 TrkH belongs to a superfamily of K(+) transport proteins required for growth of bacteria in lo

241 s a freely accessible reference database for transport protein research, which provides structural, f

242 abase serves as a common reference point for transport protein research.

243 TCDB) serves as a common reference point for transport protein research.

244 e attributed to alterations in the vitamin A-transport proteins retinol-binding protein 4 (RBP4) and

245 complex with SatPC and specific phospholipid transport protein(s) to initiate trafficking of SatPC fr

246 oincident with reduced levels of the protein transport protein Sec31A in CRT-deficient cells.

247 l proteomics to identify Sec61alpha (protein transport protein Sec61 subunit alpha isoform 1), the po

248 nslation of the mRNA coding for the selenium transport protein, selenoprotein P (SELENOP), which in v

249 t disruption is not due to nucleocytoplasmic transport protein sequestration, nor blockade of the phe

250 ce enhancement upon selective binding to the transport protein serum albumin in PBS buffer at ambient

251 han those of the protein chromophores) using transport proteins (serum albumins and alpha1-acid glyco

252 p foci is reduced in the absence of the mRNA-transport protein She3, suggesting that unphosphorylated

253 biting KRAS proximity to the SNARE vesicular transport proteins SNAP23, SNAP29, and VAMP3.

254 ransporter, B( degrees (,+))-type amino acid transport protein, sodium-dependent neutral amino acid t

255 A soluble sterol transport protein, STARD4, accounts for approximately 25

256 trieval is mediated by the activity of sugar transport proteins (STPs).

257 he method of MD, we use a number of membrane transport proteins studied in our laboratory as examples

258 ved in metabolic functions, stress response, transport, protein synthesis, and DNA repair.

259 er, to date no report exists on any specific transport protein that facilitates Cam uptake.

260 (NPF) 6.3 is a dual-affinity plasma membrane transport protein that has both high- and low-affinity f

261 zyme IIC (EIIC) is a membrane-embedded sugar transport protein that is part of the phosphoenolpyruvat

262 MlaA represents a lipid transport protein that selectively removes outer leaflet

263 Membrane transport proteins that catalyse arsenic uptake by roots

264 timicrobial compound efflux (PACE) family of transport proteins that confer resistance to a range of

265 A) transport across the ciliary body and the transport proteins that may contribute.

266 n homeostasis is maintained by iron and heme transport proteins that work in concert with ferrireduct

267 Seven LPS transport proteins (that is, LptA-LptG) form a trans-env

268 such, understanding how the two main sodium transport proteins, the thiazide-sensitive sodium chlori

269 a involves the coupling of an outer membrane transport protein to the transperiplasmic protein TonB.

270 close proximity of sterol esterification and transport proteins to each other combined with their res

271 This cellular exchange of sugars requires transport proteins to mediate uptake or release from cel

272 lar biofilms were enriched in outer membrane transport proteins to scavenge the extracellular milieu

273 s a nucleus and the machinery to express and transport proteins to subcellular locations.

274 RT (endosomal sorting complexes required for transport) proteins to induce the formation of vesicle (

275 w details are revealed about the system that transports proteins to the tip of flagella during growth

276 he 776C-->G polymorphism of the vitamin B-12 transport protein transcobalamin gene (TCN2) (rs1801198;

277 e proteins, including, for nonheme iron, the transport protein transferrin and the intracellular iron

278 We show that the iron transport protein transferrin is engaged in ancient and

279 defense mechanism mediated by conserved iron-transporting proteins transferrins.

280 proximal tubule functions (sodium and water transport, protein transport, metabolic functions, endoc

281 The tetrameric thyroxine transport protein transthyretin (TTR) forms amyloid fibr

282 reductants, and binding to human tocopherol transport protein (TTP).

283 overexpression of the mitochondrial membrane transport protein UCP2 in cancer cells is sufficient to

284 c acid treatment or by ablation of the lipid transport protein Ups1, both leading to an increase of m

285 n be found in many tyrosine kinase-regulated transport proteins using modified search programs, we su

286 an ~160-kD N-terminal fragment of the lipid transport protein VPS13 reveals an ~160- angstrom long c

287 r activity or binding to the thyroid hormone transport protein was found.

288 A transport protein was immunolocalized to the symbiosomal

289 of the kinesin family member 1B, an Mbp mRNA transport protein, was reduced in CC1+ cells in the mTOR

290 In addition, cytoskeleton and membrane transport proteins were considerably altered during rege

291 and protein abundance of nonheme and heme Fe transport proteins were evaluated in placental tissue fr

292 otonin transporter (SERT) is a transmembrane transport protein which re-uptakes excessive 5-hydroxytr

293 he major facilitator superfamily of membrane transport proteins, which contain two domains of six tra

294 regulated by the mechanical stability of the transported protein, which determines both active nuclea

295 Human serum albumin is an endogenous ligand transport protein whose long circulatory half-life is fa

296 We show that Subdued is also a moonlighting transport protein with both CAN and CaPLSase activities.

297 , we summarize the known literature of liver transport proteins with a clear emphasis on functional a

298 G protein-coupled receptors (GPCRs) and ion transport proteins with the membrane-cytoskeleton adapte

299 Hemoglobin functions as a tetrameric oxygen transport protein, with each subunit containing a heme c

300 Mutations in the zinc efflux transport protein ZnT8 have been linked with both type 1