ライフサイエンスコーパス: ABC transporter

1 ncy antigen, ABCC4 (an ATP-binding cassette [ABC]-transporter).

2 FAS)-polyketide synthase (PKS) system and an ABC transporter.

3 sol:membrane interface, before export by the ABC transporter.

4 a Drosophila multidrug resistant-associated ABC transporter.

5 essed in trans with the mutant CBM-deficient ABC transporter.

6 rameter in the mechanism of this homodimeric ABC transporter.

7 22) and Wzt(Mx) (MXAN_4623) form the Wzm/Wzt ABC transporter.

8 t to and translocation by WzmWzt and related ABC transporters.

9 l function of extra transmembrane domains of ABC transporters.

10 ompounds through the potential inhibition of ABC transporters.

11 idence suggests they are components of lipid ABC transporters.

12 nistic divergence within the efflux class of ABC transporters.

13 unction that are not present in conventional ABC transporters.

14 iply effective inhibitors of the three major ABC transporters.

15 s and explaining the number and diversity of ABC transporters.

16 arge and functionally diverse superfamily of ABC transporters.

17 e stimulates ATP hydrolysis, the hallmark of ABC transporters.

18 gated the structural evolution of eukaryotic ABC transporters.

19 es of the solute binding proteins (SBPs) for ABC transporters.

20 ploys a distinct mechanism relative to other ABC transporters.

21 ry of the current knowledge of hepatobiliary ABC transporters.

22 a compensatory mechanism by other erythroid ABC transporters.

23 of other solute binding proteins of type II ABC transporters.

24 y to substrate-binding proteins in bacterial ABC transporters.

25 Lan, which encodes an ATP-binding cassette (ABC) transporter.

26 des (O-PS) involves an ATP-binding cassette (ABC) transporter.

27 via periplasmic-binding proteins (PBPs) and ABC-transporters.

28 minant Bacteroides that lack glycan-specific ABC-transporters.

29 cell lines was reversible upon inhibition of ABC-transporters.

30 is in part mediated by ATP-binding cassette (ABC) transporters.

31 environments by using ATP-binding cassette (ABC) transporters.

32 d ubiquitous family of ATP-binding cassette (ABC) transporters.

33 xtrusion from cells by ATP-binding cassette (ABC) transporters.

34 (SDP1) triacylglycerol lipase or PEROXISOMAL ABC TRANSPORTER 1 (PXA1), here we show that TAG is a key

35 al cells in vitro, reducing the abundance of ABC transporter A1 (ABCA1) and thus cholesterol efflux a

36 The multidrug ABC transporter, aadE, bacA, acrB, tetM, tetW, vanR and

37 ys are mediated by the ATP-binding cassette (ABC) transporters ABCA1 and ABCG1, which are membrane li

38 rch provided evidence that, along with other ABC transporters (ABCA1 and ABCA7), they might be corner

39 of adenosine triphosphate-binding cassette (ABC) transporters, ABCA1 and ABCG1.

40 ave suggested that the ATP-binding cassette (ABC) transporter, ABCC4, functions in platelet-dense gra

41 tional protein (HSD17B4) and the peroxisomal ABC transporter ABCD3 are essential in peroxisomal oxida

42 erent drug efflux capability mediated by the ABC transporter ABCG2 using the side population assay, a

43 Here, we find that inhibition of ABC transporter activity reduces migration of GSCs towar

44 utward-facing structures across evolution of ABC transporters allowed construction of a high-confiden

45 N- and C-terminal halves in many eukaryotic ABC transporters, allowing all four consensus functional

46 The O12 ABC transporter also binds its cognate O-PS via a CBM, a

47 The Znu system consists of an inner membrane ABC transporter and an outer membrane TonB-dependent rec

48 se, putative sortase substrates, lantibiotic ABC transporters and a putative siderophore biosynthetic

49 implication in the regulation of metastable ABC transporters and other plasma membrane proteins acti

50 ation in the function of these mycobacterial ABC transporters and their regulation via intracellular

51 e architecture of several medically relevant ABC transporters and their supramolecular assemblies, in

52 lute carrier (SLC) and ATP-binding cassette (ABC) transporters and drug-metabolizing enzymes, many of

53 x pathways mediated by ATP-binding cassette (ABC) transporters and HDL suppress atherosclerosis.

54 e ubiquitous family of ATP-binding cassette (ABC) transporters and is located in the canalicular memb

55 re orchestrated by the ATP-binding cassette (ABC) transporters and the organic solute carrier family

56 ges from those seen in ATP-binding cassette (ABC) transporters and thus distinguishes CFTR from other

57 issue-specific clusters of SLC transporters, ABC transporters, and DMEs.

58 yl-activating enzymes, ATP binding cassette (ABC) transporters, and central carbon metabolic proteins

59 ABCC6 (ATP binding cassette transporter C6) ABC transporter are associated with pseudoxanthoma elast

60 Many human ABC transporters are associated with disease; we highlig

61 Eukaryotes ABC transporters are classified into seven main families

62 er enzymes that use ATP as an energy source, ABC transporters are notorious for having high levels of

63 ABC transporters are polytopic membrane proteins that ut

64 ATP-binding cassette (ABC) transporters are evolutionarily conserved proteins

65 ATP-binding cassette (ABC) transporters are membrane proteins present in all k

66 ATP-binding cassette (ABC) transporters are molecular pumps ubiquitous across

67 ATP-binding cassette (ABC) transporters are the largest family of ATP-hydrolyz

68 sin gene) and piaB (permease gene of the pia ABC transporter) are currently used as the gold-standard

69 y models have been developed using bacterial ABC transporters as templates but these have low sequenc

70 and signaling network" consisting of SLC and ABC transporters, as well as DMEs and regulatory protein

71 ool in the matrix, the ATP-binding cassette (ABC) transporter ATM3 and the mitochondrial thioredoxin

72 with 2 plasma membrane ATP-binding cassette (ABC) transporters: Aus1p and Pdr11p.

73 y network orchestrates the production of the ABC transporter BceAB, the UPP phosphatase BcrC and the

74 (BceRS) working in a sensory complex with an ABC-transporter (BceAB), together acting as a flux-senso

75 rolonged ATP hydrolysis is beneficial to the ABC transporter BtuC2D2.

76 mechanism of conformational coupling in the ABC transporter BtuCD-F, which imports vitamin B12 acros

77 tivity level could be applicable to not only ABC transporters but other types of membrane transporter

78 ar L-glutamate via the GltT-GltM L-glutamate ABC transporter, but the underlying mechanism remained u

79 While a small number of plasma membrane ABC transporters can export chemotherapeutic drugs and c

80 In this key position, ABC transporters can mediate multidrug resistance in can

81 Using the energy of ATP hydrolysis, ABC transporters catalyze the trans-membrane transport o

82 ling factor (ECF)-type ATP-binding cassette (ABC) transporters catalyze membrane transport of micronu

83 ATP-binding cassette (ABC) transporters chemomechanically couple ATP binding a

84 The peroxisomal ABC transporter, Comatose (CTS), a full length transport

85 with PstS, the periplasmic component of the ABC transporter complex (PstSACB) involved in phosphate

86 otein, MlaD, forms a ring associated with an ABC transporter complex in the inner membrane.

87 and its interacting protein AtSTAR1 form an ABC transporter complex in the tonoplast.

88 he cytoplasmic portion of the larger MlaFEDB ABC transporter complex, which drives phospholipid traff

89 rithm to proteins from ATP-binding cassette (ABC) transporter complexes, and obtain accurate predicti

90 ABC transporters comprise a large and ubiquitous family

91 n modification was dependent on a functional ABC transporter, consistent with modification in the per

92 ATP-binding cassette (ABC) transporters constitute one of the largest and most

93 ATP-binding cassette (ABC) transporters constitute the largest family of prima

94 The recent availability of structures of ABC transporters containing linker regions has allowed u

95 , we show that a novel, putative ferric iron ABC transporter contributes to low iron fitness in Msmeg

96 ABC-transporter copy number, expression and activity wer

97 n, the presence of altered 3'-UTR lengths in ABC transporters could lead to functional consequences r

98 The ATP-binding cassette (ABC) transporter cystic fibrosis transmembrane conductan

99 steps of astaxanthin biosynthesis, including ABC transporters, cytochrome P450 enzymes, and an acyltr

100 In the ABC transporter-dependent biosynthesis pathway, O antige

101 Activation of ABC transporter-dependent cholesterol efflux pathways in

102 riophage-mediated O-antigen glucosylation in ABC transporter-dependent pathways.

103 g step appears to be unique to streptococcal ABC transporter-dependent RhaPS biosynthesis, whereas th

104 disaccharide motif, but its assembly uses an ABC transporter-dependent system.

105 s study focuses on the ATP-binding cassette (ABC) transporter-dependent pathway, where glycans are co

106 antigen produced in an ATP-binding cassette (ABC) transporter-dependent system.

107 uorimetry, we determined that the SBP for an ABC transporter encoded by the genome of Mycobacterium s

108 Bal6GBP) that governs the specificity of the ABC transporter encoded by the same beta-galactoside uti

109 processing (TAP) is an ATP-binding cassette (ABC) transporter essential to cellular immunity against

110 How do ABC transporters evolve to carry such diverse molecules

111 gainst closely related Bacillus strains, the ABC transporter exported the toxic Bacillunoic acids upo

112 ABCA7 is an ABC transporter expressed on the plasma membrane, and ac

113 enosine triphosphate (ATP)-binding cassette (ABC) transporter expressed at the canalicular membrane o

114 eless be controlled by ATP-binding cassette (ABC) transporters expressed at the blood-brain barrier.

115 ns synergistically (3-40 fold) downregulated ABC transporter expression, and inhibited P-glycoprotein

116 ABC transporters facilitate the movement of diverse mole

117 The seven eukaryote ABC transporter families (A to G) fell into three groups

118 ispecific "drug" transporters of the SLC and ABC transporter families.

119 ansporters (PCATs) are unique members of the ABC transporter family that proteolytically process and

120 analogous to the multidrug exporters of the ABC transporter family, which pump out structurally dive

121 distinguishes CFTR from other members of the ABC transporter family.

122 take systems, predominant among which is the ABC transporter family.

123 mechanisms may exist more broadly across the ABC transporter family.

124 brosis, belongs to the ATP-binding cassette (ABC) transporter family and works as a channel for small

125 annel evolved from the ATP-binding cassette (ABC) transporter family.

126 butyrate biosynthesis, ATP-binding cassette (ABC) transporters, flagella assembly and bacterial chemo

127 access mechanism as it applies to eukaryotic ABC transporters, focusing on type I exporters.

128 lasmic leaflet by the channel-forming WzmWzt ABC transporter for ligation to the core lipopolysacchar

129 ated across the inner membrane by the WzmWzt ABC transporter for ligation to the lipopolysaccharide c

130 ABC transporters form one of the largest protein superfa

131 Pdr5 is a plasma membrane-bound ABC transporter from Saccharomyces cerevisiae and is inv

132 BP) associated with an ATP binding cassette (ABC) transporter from the probiotic Bifidobacterium anim

133 ping efficient and specific drugs that alter ABC transporter function are hindered by a lack of in vi

134 n Ankyrin-like protein, IKI3 family protein, ABC transporter G family and pentatricopeptide repeat pr

135 ioxygenase3 involved in ABA biosynthesis and ABC transporter G family member40, encoding an ABA trans

136 accept cholesterol via ATP-binding cassette (ABC) transporter G1, an impaired ability of HDL3 to supp

137 However, a mutation in an ABC transporter gene (ABCC2) is linked to Cry1Ac resista

138 However, studies on how various ABC transporter gene structures evolved is still absent.

139 egions of high similarity with CFTR, another ABC transporter gene, which is associated with cystic fi

140 Analysis of shikimic acid accumulation, ABC-transporter gene expression, and cell death were use

141 nstrate that knockdown of two root-expressed ABC transporter genes in tomato cv. Moneymaker, ABC-C6 a

142 Many ABC transporter genes were regulated in the bacteria att

143 However, nitrate ABC transporter genes were upregulated under UV and FR l

144 ranscriptome involving ATP binding cassette (ABC) transporter genes.

145 apamil, which were initially docked into the ABC transporter, get translocated through the exporter b

146 nes were present, and genes encoding various ABC transporters, glutamate synthase and CO oxidation we

147 Forty-eight human ABC transporters have been identified in the genome, and

148 Why do some ABC transporters have connectors and others not?

149 In insects, ABC transporters have previously been implicated in inse

150 ATP-binding cassette (ABC) transporters have evolved an ATP-dependent alternat

151 ATP-binding cassette (ABC) transporters help export various substrates across

152 iffer from previous observations for similar ABC transporters, highlighting the extent of mechanistic

153 ATP binding by Type I ABC transporters (importers of amino acids, sugars, pept

154 In Type II ABC transporters (importers of trace elements, e.g. vita

155 rted an unusual case in which the loss of an ABC transporter in Candida albicans, orf19.4531 (previou

156 s, which define the crucial function of this ABC transporter in human immunity and health.

157 MacB represents an ABC transporter in pathogenic microorganisms with unique

158 e profiles indicated distinct roles for each ABC transporter in root exudation.

159 This process requires an ABC transporter in the inner envelope membrane with thre

160 Hence, the humanization of ABC transporters in mice has become a major focus in pha

161 x in macrophages have focused on the role of ABC transporters in moving cholesterol onto high-density

162 the compound, suggesting the involvement of ABC transporters in the uptake or intracellular accumula

163 terize a non-canonical ATP-binding cassette (ABC) transporter in Escherichia coli that provides energ

164 /MRP4 gene encoding an ATP-binding cassette (ABC) transporter in PEL-negative individuals.

165 enosine triphosphate (ATP)-binding cassette (ABC) transporters in the pyrethroid-resistant Puerto Ric

166 m and shuttle it to an ATP-binding cassette (ABC)-transporter in the bacterial inner membrane.

167 R implicated the potential role of MDR49, an ABC transporter, in DDT resistance, however, to date the

168 s clearly resolve characteristic features of ABC transporters, including helices in the transmembrane

169 on has been amassed on ATP-binding cassette (ABC) transporters, including hundreds of structures of i

170 y interventions upon raft cholesterol and by ABC transporter-inducing liver X receptor agonists.

171 A member 1 (NR4A1) and ATP-binding cassette (ABC) transporters, influenced the function and different

172 MDR, making it one of the three most potent ABC transporter inhibitors and reversers of ABC transpor

173 These are the first ABC transporter inhibitors shown to block ATPase activit

174 em as some of the 50 most potent multitarget ABC transporter inhibitors.

175 hat reside in the highly conserved motifs of ABC transporters, involved in ATP binding.

176 trate translocation by ATP-binding cassette (ABC) transporters involves coupling of ATP binding and h

177 o the cytoplasm by the ATP binding cassette (ABC) transporter IrtAB(4), which features an additional

178 a feature distinguishing CFTR from all other ABC transporters is the helix-loop transition in transme

179 rug efflux mediated by ATP-binding cassette (ABC) transporters is one of the major MDR mechanisms.

180 However, oligomerization of peroxisomal ABCD transporters is incompletely understood but is of p

181 Overexpression of ABC transporters like P-glycoprotein (P-gp) has been cor

182 We propose that other Type II ABC transporters likely share the fundamentals of this m

183 In this system, the ATP-binding cassette (ABC) transporter LptB(2) FGC extracts LPS from the inner

184 Instead, ABC transporters may be induced after insecticide exposu

185 es in susceptibility of ICEC0942 and THZ1 to ABC-transporters, may help guide their future clinical u

186 The ABC transporter McjD exports the antibacterial peptide M

187 lipids associated with the Escherichia coli ABC transporter McjD, which translocates the antibacteri

188 ntly proposed that the ATP-binding cassette (ABC) transporter Mdr49 functions in the embryonic mesode

189 show pharmacologically and genetically that ABC transporters mediate cAMP export.

190 and signalling hypothesis identifies SLC and ABC transporter-mediated communication between organs an

191 ABC transporter inhibitors and reversers of ABC transporters-mediated MDR.

192 , and we show that MetQ association with the ABC transporter MetNI depends on its N-terminal lipid an

193 s six Mla proteins, MlaFEDBCA, including the ABC transporter MlaFEDB, which functions via an unknown

194 nd outer membrane integrity, and includes an ABC transporter, MlaFEDB.

195 endent NRAMP family transporter MntH and the ABC transporter MntABCD.

196 osquitoes with deltamethrin, with or without ABC transporter modulators, showed that Rock and PR resp

197 role in the control of ATP-binding cassette (ABC)-transporter mRNA degradation and translation into p

198 restricted HMGCoA-reductase (Hmgcr) and the ABC transporter Multi-drug-resistant-49 (Mdr49).

199 The ATP-binding cassette (ABC) transporter multidrug resistance protein 1 (MRP1/AB

200 templates, we used structures of homologous ABC transporters, namely TM(287-288), ABC-B10, McjD, and

201 ividual maturation factors, we find that the ABC transporter NosFY and the accessory NosD protein are

202 We also establish that an ABC transporter of unknown function, YadH, together with

203 The ATP-binding cassette (ABC) transporter of mitochondria (Atm1) mediates iron ho

204 ATP-binding cassette (ABC) transporters of the cluster 9 family are ubiquitous

205 ATP binding cassette (ABC) transporters of the exporter class harness the ener

206 Bacterial ATP-binding cassette (ABC) transporters of transition metals are essential for

207 yeast oligomycin resistance 1 gene (YOR1, an ABC transporter) of Saccharomyces cerevisiae phenocopies

208 stem cell research, assesses the activity of ABC transporters on Hoechst staining in the presence and

209 the potassium transporter operon kdp and an ABC transporter operon of uncharacterized function.

210 dentified the previously identified ctrABCD (ABC transporter) operon, a lipA (kpsC)-like gene, a lipB

211 nt activity on the stability and function of ABC transporters or any other enzyme.

212 The ABC transporters P-glycoprotein (P-gp, official gene sym

213 binding and hydrolysis, protease-containing ABC transporters (PCATs) export amphipathic and hydrophi

214 We describe a mutation, A666G, in the yeast ABC transporter Pdr5 that shows greater resistance to mo

215 mponents, including the NADPH oxidase RBOHD, ABC-transporter PEN3, calcium-ATPase ACA8, noncanonical

216 res membrane-localized ATP-binding cassette (ABC) transporter PENETRATION (PEN) 3.

217 P. aeruginosa mutant defective in a putative ABC transporter permease is resistant to both streptococ

218 ions in the digestive vacuole membrane-bound ABC transporter PfMDR1 (P. falciparum multidrug resistan

219 ida adenosine triphosphate-binding cassette (ABC) transporter, PhABCG1, we demonstrate that passage o

220 lipoprotein PiuA from the piu Fe acquisition ABC transporter PiuBCDA, previously described as an Fe-h

221 Blocking ABC transporter, PLA2 or 12-Lox activity also inhibits h

222 ATP binding cassette (ABC) transporters play critical roles in maintaining ste

223 ATP-binding cassette (ABC) transporters play several critical roles in this pr

224 dicate that a highly conserved residue of an ABC transporter plays an important role in adenylate kin

225 s PENETRATION 3 (PEN3) ATP binding cassette (ABC) transporter plays a role in defense against numerou

226 ABCD3 is one of three ATP-binding cassette (ABC) transporters present in the peroxisomal membrane ca

227 investigated the expression patterns of six ABC transporters previously characterized as differentia

228 The core of the ABC transporter protein is composed of transmembrane dom

229 enzymes or proteins, including HMA, YSL1 and ABC transporter protein were involved in Cr uptake and h

230 (BCRP) is a member of ATP-binding cassette (ABC) transporter proteins whose primary function is to e

231 the adenosine triphosphate-binding cassette (ABC) transporter proteins, P-glycoprotein or breast canc

232 thway, argininosuccinate lyase-encoding, and ABC transporter-related genes as compared to the parenta

233 ATP-binding cassette (ABC) transporters represent a large group of efflux pump

234 The ATP-binding cassette (ABC) transporters represent a superfamily of proteins th

235 Solute carriers (SLC) and ABC transporters represented an important subset of DEG,

236 PEN3, encoding an atypical myrosinase and an ABC transporter, respectively, required for synthesis an

237 Deletion of either ABC transporter results in Are2p relocalization to deter

238 This study exposes the link between ABC transporters, root exudate composition, and ex plant

239 The ABC transporter Rv1747, which is important for Mycobacte

240 e we show that both an ATP-binding cassette (ABC) transporter(s) and an H(+)-antiporter(s) are involv

241 n number and domain organizations, eukaryote ABC transporters show diverse structures: the single str

242 rulence, including an l,d-transpeptidase, an ABC transporter solute-binding protein, and a methionine

243 oside hydrolase 13 family enzymes, and three ABC transporter solute-binding proteins that are abundan

244 biosynthetic enzymes (FatM and RAM2) and an ABC transporter (STR) that are required for symbiosis an

245 pment, and incorporation of two PAM-resident ABC transporters, STR and STR2, is limited.

246 xplain the wide functional diversity of this ABC transporter subfamily.

247 ATP-binding cassette (ABC) transporters such as ABCB1 (P-glycoprotein), ABCC1

248 zation is diminished upon deletion of murine ABC transporters, such as Abcg1, which itself is DRM ass

249 alterations in oxidative phosphorylation and ABC transporters, suggesting energy accumulation and inc

250 tructure and the crystal structures of other ABC transporters suggests a possible trajectory of confo

251 ng Kir6.2 potassium channel and a regulatory ABC transporter sulfonylurea receptor 1 (SUR1) regulate

252 ing the structure and mechanism of an entire ABC transporter superfamily and the many diverse functio

253 In Escherichia coli, FtsEX, a member of the ABC transporter superfamily, is involved in regulating t

254 TR) is a member of the ATP-binding cassette (ABC) transporter superfamily.

255 The ATP binding cassette (ABC) transporters superfamily is one of the largest clas

256 uman pancreatic KATP channel, containing the ABC transporter SUR1 and the inward-rectifier K(+) chann

257 This work demonstrates that the SBPs of an ABC transporter system function in the uptake of basic a

258 Substrate binding protein 2 (SBP2) of an ABC transporter system has recently been identified as a

259 ber of mutants with OM defects, including an ABC transporter system homologous to the Mla system in E

260 The Vps/VacJ ABC transporter system is proposed to function in mainta

261 The human lysosomal polypeptide ABC transporter TAPL (ABC subfamily B member 9, ABCB9) t

262 econstituted the human lysosomal polypeptide ABC transporter TAPL, expressed in Pichia pastoris, into

263 t of the two-component ATP-binding cassette (ABC) transporter TarGH, which exports WTA precursors to

264 MacB is an ABC transporter that collaborates with the MacA adaptor

265 h BcrC (a C55 -PP phosphatase) and BceAB (an ABC transporter that confers bacitracin resistance).

266 transmembrane domains of a conserved fungal ABC transporter that exports a mating pheromone and sele

267 ABCG2 is an ABC transporter that extrudes a variety of compounds fro

268 is disrupted, and these vesicles contain an ABC transporter that functions as an ecdysone pump to fi

269 FtsEX is a bacterial ABC transporter that regulates the activity of periplasm

270 ABCB5 is an ABC transporter that was shown to confer low-level multi

271 The Mce systems are complex ABC transporters that are encoded by different numbers o

272 an autocrine signaling molecule exported by ABC transporters that enhances chemotaxis in GSCs migrat

273 ve structural evolutionary path of eukaryote ABC transporters that will increase our understanding on

274 ycoprotein (Pgp) is an ATP-binding cassette (ABC) transporter that alternates between inward- and out

275 nce protein MRP1 is an ATP-binding cassette (ABC) transporter that confers resistance to many antican

276 MalFGK2 is an ATP-binding cassette (ABC) transporter that mediates the uptake of maltose/mal

277 BCG2) is a homodimeric ATP-binding cassette (ABC) transporter that not only has a key role in helping

278 regulator (CFTR) is an ATP-binding cassette (ABC) transporter that uniquely functions as an ion chann

279 the functionality of two different multidrug ABC transporters, the homodimer BmrA from Bacillus subti

280 At the example of the bacterial ABC transporter TM287/288, we show that two gadolinium-l

281 chanistic understanding of the heterodimeric ABC transporter TmrAB, a functional homolog of the trans

282 Here we report that, for the heterodimeric ABC transporter TmrAB, the extent of delipidation can be

283 responded differently, but a contribution of ABC transporters to deltamethrin toxicity is suspected.

284 he producing bacteria that utilize dedicated ABC transporters to provide self-immunity.

285 der to assess the contribution of individual ABC transporters to root exudation, we performed an LC-M

286 ATP-binding cassette (ABC) transporters translocate substrates across cell mem

287 l pathways under stressed condition, such as ABC transporters, two-component systems, and carbohydrat

288 ABC transporters undergo substantial conformational chan

289 oxantrone-resistant cell lines demonstrating ABC-transporter upregulation.

290 , such as apolipoprotein A1-based compounds, ABC-transporter upregulators, selective peroxisome proli

291 ATP-binding cassette (ABC) transporters use ATP to drive solute transport acro

292 f Escherichia coli, an ATP binding cassette (ABC) transporter, uses the energy of ATP binding and hyd

293 and with overexpression of the peptides and ABC transporters, were correlated with the levels of Com

294 uctural information on ATP binding cassette (ABC) transporters, which are expressed in the human live

295 tabolizing enzymes and ATP-binding cassette (ABC) transporters, whose overexpression in cancers and w

296 An ABC transporter with a periplasmic metallo-aminopeptidas

297 e examples of neurotransmitter receptors and ABC transporters with the dual CARC/CRAC motifs are pres

298 understanding of sterol transport driven by ABC transporters, with an emphasis on these two extensiv

299 and TonB as well as the inner membrane (IM) ABC transporter YbtPQ, which are required for Fe(3+) acq

300 ed synthesis of misfolded forms of the yeast ABC transporter Yor1.