ライフサイエンスコーパス: ABC transporter

1 wn to be the first characterized glucosamine ABC transporter.

2 first structure of an antibacterial peptide ABC transporter.

3 which are also substrates for the ChvE-MmsAB ABC transporter.

4 e I ABC transporters but never for a type II ABC transporter.

5 so shared by the archetypical type I maltose ABC transporter.

6 closely related binding site to regulate an ABC transporter.

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

8 a Drosophila multidrug resistant-associated ABC transporter.

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

10 rameter in the mechanism of this homodimeric ABC transporter.

11 arge and functionally diverse superfamily of ABC transporters.

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

13 gated the structural evolution of eukaryotic ABC transporters.

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

15 ploys a distinct mechanism relative to other ABC transporters.

16 crystal structures of evolutionarily related ABC transporters.

17 esterol flux pathways, initiated in cells by ABC transporters.

18 displays positive cooperativity in numerous ABC transporters.

19 any pathogens rely upon the ZnuABC family of ABC transporters.

20 idence suggests they are components of lipid ABC transporters.

21 e relevant to the entire class of asymmetric ABC transporters.

22 ferent folds of the transmembrane domains of ABC transporters.

23 t system and not by an ion-trap mechanism or ABC transporters.

24 in regulating cholesterol metabolism through ABC transporters.

25 investigated in a flow cytometric screen of ABC transporters.

26 gned with the current views on mechanisms of ABC transporters.

27 ed reverse cholesterol transport mediated by ABC transporters.

28 nistic divergence within the efflux class of ABC transporters.

29 unction that are not present in conventional ABC transporters.

30 iply effective inhibitors of the three major ABC transporters.

31 ry system (TCS) and an ATP-binding cassette (ABC) transporter.

32 altose transporter, an ATP-binding cassette (ABC) transporter.

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

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

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

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

37 to be often caused by ATP-binding cassette (ABC) transporters.

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

39 on gradient-driven and ATP-binding cassette (ABC) transporters.

40 g and up-regulation of ATP-binding cassette (ABC) transporters.

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

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

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

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

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

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

47 catalysts of the PIN-FORMED and B family of ABC transporter (ABCB) classes.

48 ump, such as the human ATP-binding-cassette (ABC) transporter ABCB1, coupling of drug-binding by the

49 SP cells overexpressed ATP-binding-cassette (ABC) transporters, ABCB1 and ABCB5.

50 The ABC transporter ABCC4 is recognized as an ATP-dependent

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

52 coding the peroxisomal ATP-binding cassette (ABC) transporter ABCD1 (adrenoleukodystrophy protein, AL

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

54 In this study, we measured dynamics of ABC transporter activity during formation of sea urchin

55 modulates CD33 expression nor is affected by ABC transporter activity, AMG 330 is highly promising fo

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

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

58 ctional and physical interaction between the ABC transporter and the peroxisomal long chain acyl-CoA

59 o restore complete symmetry in an asymmetric ABC transporter and to study its effects, which might be

60 f mRNA and protein levels of the peroxisomal ABC transporters and by blocking with specific antibodie

61 cussed in light of the crystal structures of ABC transporters and homology models of CFTR.

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

63 nce of a sensory complex composed of TCS and ABC transporters and provide the first functional insigh

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

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

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

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

68 ence, conjugation of the pAtC58 megaplasmid, ABC transporters, and cell envelope architecture.

69 nces similar to ethylene signaling proteins, ABC transporters, and diterpenoid hydroxylases were asso

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

71 Although crystal structures of several ABC transporters are available, a structural basis for s

72 Eukaryotes ABC transporters are classified into seven main families

73 The substrates transported by different ABC transporters are diverse, ranging from small ions to

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

75 ABC transporters are polytopic membrane proteins that ut

76 ABC transporters are predominately localized to the lume

77 ATP-binding cassette (ABC) transporters are a group of transmembrane proteins

78 ATP-binding cassette (ABC) transporters are an ancient family of transmembrane

79 all kingdoms of life, ATP binding cassette (ABC) transporters are essential to many cellular functio

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

81 ATP-binding cassette (ABC) transporters are molecular pumps that harness the c

82 In bacteria, ATP-binding cassette (ABC) transporters are vital for the uptake of nutrients

83 hese insects to repel their enemies, rely on ABC transporters as a key element.

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

85 y analyses, we identified ABCG1, encoding an ABC transporter, as a gene responsive to the pathogen-as

86 The ATP-binding cassette (ABC) transporter associated with antigen processing (TAP

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

88 ransfer analysis was used to verify specific ABC transporter B1 (ABCB1)-TWD1 interaction.

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

90 ATP-binding cassette (ABC) transporters belong to one of the largest protein s

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

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

93 ing the Escherichia coli vitamin B12 type II ABC transporter BtuCD.

94 These issues have been resolved for type I ABC transporters but never for a type II ABC transporter

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

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

97 Although other ABC transporters can be studied through various imaging

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

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

100 a plethora of genes including efflux pumps, ABC transporters, catalases and transcription factors, e

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

102 The fungal ATP-binding cassette (ABC) transporter Cdr1 protein (Cdr1p), responsible for c

103 ed glycosylation of the eukaryotic multidrug ABC transporter Cdr1p without special purification steps

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

105 g immunity, we heterologously expressed this ABC transporter complex in four different sensitive stre

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

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

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

109 dentified as the S-layer glycoprotein and an ABC transporter component.

110 he immunity complex that we identified is an ABC transporter composed of two proteins: SmbF (the ATPa

111 ABC transporters comprise a large and ubiquitous family

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

113 The functional unit of ATP-binding cassette (ABC) transporters consists of two transmembrane domains

114 narily distinct, clinically important fungal ABC transporters containing a characteristic, deviant AT

115 ATP-binding cassette (ABC) transporters couple the translocation of solutes ac

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

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

118 Activation of ABC transporter-dependent cholesterol efflux pathways in

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

120 en serotypes represent model systems for the ABC transporter-dependent synthesis of bacterial polysac

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

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

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

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

125 In this study, a putative ABC transporter encoded by the gxySBA operon is identifi

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

127 ght significant mechanistic divergence among ABC transporters, even when they share the same substrat

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

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

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

131 identifying pathogenic mechanisms regulating ABC transporter expression and function in ALS may lead

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

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

134 n processing (TAP1 and TAP2), members of the ABC transporter family that play an essential role in an

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

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

137 ubgroup members of the ATP-binding cassette (ABC) transporter family.

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

139 tem encoded by Salmonella is the siderophore ABC transporter FepBDGC.

140 with the ligand and the cytoplasmic membrane ABC transporter (FepCD), respectively.

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

142 atopoietic cell multidrug resistance protein ABC transporter (floppase), and protein-disulfide isomer

143 ABC transporters form one of the largest protein superfa

144 10 is one of the three ATP-binding cassette (ABC) transporters found in the inner membrane of mitocho

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

146 two tested multispecific vacuolar ABCC-type ABC transporters from Arabidopsis exhibit ABA-GE transpo

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

148 how that activity of CwlO is regulated by an ABC transporter, FtsEX, which is required for cell elong

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

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

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

152 ABC transporter G2 (ABCG2) was expressed in recombinants

153 pidermis characterized by the lateral marker ABC transporter G36/PLEIOTROPIC DRUG-RESISTANCE8/PENETRA

154 Mutations in the ABC transporters G5 and G8 are known to cause an accumul

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

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

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

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

159 Many ABC transporter genes were regulated in the bacteria att

160 expression of several ATP-binding cassette (ABC) transporter genes, thus affecting global drug efflu

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

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

163 ABC transporters harness the energy from ATP binding and

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

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

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

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

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

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

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

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

172 MacB represents an ABC transporter in pathogenic microorganisms with unique

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

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

175 iae), which also supports the involvement of ABC transporters in ABA-GE uptake.

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

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

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

179 The ABCC subfamily of the ABC transporters includes active drug exporters (the mul

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

181 the adenosine triphosphate-binding cassette (ABC) transporters, including adenosine triphosphate-bind

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

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

184 modulation, non-translational motility, and ABC-transporter inhibition via a calcein-AM efflux assay

185 was insensitive to the ATP-binding cassette (ABC) transporter inhibitor vanadate.

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

187 We have recently identified protein F, an ABC transporter involved in NTHi immune evasion.

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

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

190 The ChvE-MmsAB ABC transporter is involved in the utilization of a wide

191 In ALS, expression and function of ABC transporters is increased at the BBB/BSCB and their

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

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

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

195 y multiple drug efflux ATP-binding cassette (ABC) transporters, is a critical issue in the treatment

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

197 These structures indicate that ABC transporters may exist in an open-inwards conformati

198 The ABC transporter McjD exports the antibacterial peptide M

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

200 mologue Cdr2p or from cells expressing a non-ABC transporter Mdr1p.

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

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

203 cholesterol overload, ATP-binding cassette (ABC) transporters mediate cholesterol efflux from the ce

204 ATP binding cassette (ABC) transporters mediate vital transport processes in e

205 enotypes, such as high ATP binding cassette (ABC) transporter mediated efflux of Hoechst substrates (

206 We conclude that the zinc uptake ABC transporter mediates uptake of zinc in environments

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

208 The ABC transporter, MolBC-A, imports molybdate by passing s

209 in the highly dynamic ATP-binding cassette (ABC) transporter MsbA.

210 enosine triphosphate (ATP)-binding cassette (ABC) transporters, much less is known about how they sel

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

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

213 o Smb upon deletion of smbT, which makes the ABC transporter nonfunctional.

214 epithelial cells demonstrated that the zinc ABC transporter of M. catarrhalis is critical for invasi

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

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

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

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

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

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

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

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

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

224 export mediated by the ATP-binding cassette (ABC) transporter P-glycoprotein contributes to clinical

225 all kingdoms of life, ATP Binding Cassette (ABC) transporters participate in many physiological and

226 The function of BBB is modulated by multiple ABC transporters, particularly P-glycoprotein.

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

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

229 ens adenosine triphosphate-binding cassette (ABC) transporter permease.

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

231 Among other functions, ABC transporters play a key role in protecting the brain

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

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

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

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

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

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

238 n anion channel in the ATP-binding cassette (ABC) transporter protein family.

239 idation is mediated by ATP binding cassette (ABC) transporter proteins of subfamily D, which includes

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

241 Evidence is shown that the peroxisomal ABCD transporter (PXA1) plays a critical role in this br

242 istic differences between type I and type II ABC transporters raise the question whether in respect t

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

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

245 In parasites, ATP-binding cassette (ABC) transporters represent an important family of prote

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

247 ent work has also demonstrated that multiple ABC transporters share an ATPase; whether this evolved f

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

249 C frameshift insertion in a gene encoding an ABC transporter similar to that of the teichoic acid tra

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

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

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

253 of apo-ABCB10 shows a classic exporter fold ABC transporter structure, in an open-inwards conformati

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

255 Many fungal ABC transporters such as Pdr5 display an inherent asymme

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

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

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

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

260 rotein (ABCG2) is an important member of the ABC transporter superfamily, which has been suggested to

261 Regulator protein (CFTR) is a member of the ABC transporter superfamily.

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

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

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

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

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

267 We propose a dual function of the Vps/VacJ ABC transporter system in S. flexneri in both the mainte

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

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

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

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

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

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

274 e identified and characterized a zinc uptake ABC transporter that is present in all strains of M. cat

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

276 ding cassette (ABC) exporters are ubiquitous ABC transporters that extrude cytotoxic molecules across

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

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

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

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

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

282 with another disease-causing mutation in an ABC transporter, the deletion of Phe-508 (DeltaF508) in

283 many differences between type I and type II ABC transporters, the fundamental mechanism of ATP hydro

284 reducing ROS, which drives transcription of ABC transporters through activation of LXRalpha.

285 o temozolomide, which is not a substrate for ABC transporters, through IL-8 upregulation.

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

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

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

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

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

291 their transport cycle, ATP-binding cassette (ABC) transporters undergo large-scale conformational cha

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

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

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

295 e proposed communication between TCS and the ABC transporter, we characterized their interactions by

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

297 tes (pB(25)R) show overexpression of a novel ABC transporter, which was classified as ABCC2 or Leishm

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

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

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