ライフサイエンスコーパス: inner membrane

1 bunit on the intermembrane space side of the inner membrane.

2 med during insertion of the protein into the inner membrane.

3 lex) inserts multispanning proteins into the inner membrane.

4 rm protein, docking protein 4 (DOK4), on the inner membrane.

5 nit prohibitin-2 (PHB2) at the mitochondrial inner membrane.

6 is in the cytoplasm and secretion across the inner membrane.

7 obic carrier proteins into the mitochondrial inner membrane.

8 esequence either into the matrix or into the inner membrane.

9 rochemical gradient (DeltamuH(+)) across the inner membrane.

10 teins exert torque on a rotor that spans the inner membrane.

11 on and self-association within the bacterial inner membrane.

12 he PG layer approximately 90 A away from the inner membrane.

13 unctional and correctly shaped mitochondrial inner membrane.

14 nt protein accumulation in the mitochondrial inner membrane.

15 th the correct topology in the mitochondrial inner membrane.

16 distribution of respiratory complexes in the inner membrane.

17 their translocation across the mitochondrial inner membrane.

18 st thylakoid membrane, and the mitochondrial inner membrane.

19 otein complex formation in the mitochondrial inner membrane.

20 was localized to the cytoplasmic side of the inner membrane.

21 nusual interaction with the Escherichia coli inner membrane.

22 the space between the bulk nucleoid and the inner membrane.

23 ch as dipicolinic acid (DPA) and the spore's inner membrane.

24 iated with an ABC transporter complex in the inner membrane.

25 E domain-containing proteins localise to the inner membrane.

26 mbrane proteins can be concentrated near the inner membrane.

27 rial matrix, where it is associated with the inner membrane.

28 e permeability transition pore (PTP), in the inner membrane.

29 across the energy-transducing mitochondrial inner membrane.

30 ace, allowing formation of PE by Psd1 in the inner membrane.

31 xchange ADP for ATP across the mitochondrial inner membrane, an activity that is essential for oxidat

32 a T2SS nanomachines requires the assembly of inner membrane-anchored fibres called pseudopili.

33 Inner membrane-anchored long OPA1 (L-OPA1) undergoes pro

34 We present genetic evidence that a putative inner membrane-anchored protein with a large periplasmic

35 swelling of the organelle, disruption of the inner membrane and ATP synthesis, and cell death.

36 is is subtly maintained on the mitochondrial inner membrane and can be derailed by the misfolding of

37 value might ensure correct attachment of the inner membrane and cell wall needed for cell wall biosyn

38 outer membrane, and the motor complex in the inner membrane and cytoplasm.

39 AA+ enzyme that controls proteostasis at the inner membrane and intermembrane space of mitochondria.

40 wn to have defects linked to the exchange of inner membrane and matrix components.

41 ds cardiolipin glycerophospholipids near the inner membrane and promotes their PhoPQ-regulated traffi

42 ysaccharide from the external leaflet of the inner membrane and propels it along a filament that exte

43 UCP2 is located in the mitochondrial inner membrane and regulates production of reactive oxyg

44 ills E. coli by permeabilizing the bacterial inner membrane and subsequently binds the outer membrane

45 ylcholine (PC) in protein transport into the inner membrane and the matrix is unknown.

46 on density region, composed of the outer and inner membranes and the cristae cluster, which enclosed

47 hat connects the two membrane proteins CusA (inner membrane) and CusC (outer membrane).

48 exchanges ADP/ATP through the mitochondrial inner membrane, and Ant2 is the predominant isoform expr

49 swelling of the organelle, disruption of the inner membrane, and ATP synthesis, followed by cell deat

50 psin (ASR), prepared in the Escherichia coli inner membrane, and compare it to that in a bilayer form

51 tions, namely the outer membrane, periplasm, inner membrane, and cytoplasm, and we observed the indiv

52 tribution of bioactives in pomegranate peel, inner membrane, and edible aril portion was investigated

53 abolites discriminated the pomegranate peel, inner membrane, and edible aril portion, as well as the

54 units and was localized in the mitochondrial inner membrane, and its depletion resulted in reduced CI

55 l protein, is localized in the mitochondrial inner membrane, and its import into mitochondria depends

56 One arm lies in the inner membrane, and the other extends about 100 A into t

57 he secondary transporter AcrB located in the inner membrane, and the periplasmic AcrA, which bridges

58 tion of polytopic membrane proteins into the inner membrane, and Tim22 constitutes its central insert

59 for establishing and maintaining the proper inner membrane architecture and contacts with the outer

60 This establishes a clear link between inner membrane architecture and functional decline.

61 t is cotranslationally translocated into the inner membrane are generally less highly translated than

62 on of how the densely packed proteins of the inner membrane are organized to optimize structure and f

63 roteins, threaded through the channel in the inner membrane, are handed over to the import motor at t

64 haride alginate, which is synthesized at the inner membrane as a homopolymer of 1-4-linked beta-D-man

65 present on the outer surface of the spore's inner membrane, as SpoVAEa was accessible to an external

66 substrates that are laterally sorted to the inner membrane, as well as the mitochondrial matrix.

67 re common mitochondrial lipids, and abundant inner-membrane associated proteins concentrated in the b

68 urthermore, we discovered that silencing the inner membrane-associated dynamin optic atrophy 1 (OPA1)

69 The IM30 (inner membrane-associated protein of 30 kDa), also known

70 transport into the cytoplasm via the cognate inner membrane ATP-binding cassette proteins.

71 SLC25A24 encodes a mitochondrial inner membrane ATP-Mg/Pi carrier.

72 T3SSs, such as relative disposition of their inner membrane-attached export platform, C-ring/pods and

73 s of cps-6 delays breakdown of mitochondrial inner membranes, autophagosome enclosure of paternal mit

74 of the central domain of colicin D with the inner membrane before the FtsH-dependent proteolytic pro

75 proteins into the periplasm by cleaving the inner membrane-bound leader.

76 an either withdraw from or extend toward the inner membrane-bound PBP1A through peptidoglycan gaps an

77 e that Oma1 genetically interacts with other inner membrane-bound quality control proteases.

78 LPS molecule at the periplasmic face of the inner membrane, but its topology and mechanism of action

79 mic metal sensor domain is anchored into the inner membrane by two N-terminal helices.

80 -covalently attached and are anchored to the inner membrane by virtue of the membrane-embedded beta s

81 drial Ca(2+) uniporter complex (uniplex), an inner membrane Ca(2+) transporter and major pathway of m

82 e divisome regulates the invagination of the inner membrane, cell wall synthesis, and inward growth o

83 The PTP is an inner membrane channel that forms from F-ATPase, possess

84 tion of the permeability transition pore, an inner membrane channel whose opening requires matrix Ca(

85 ds on several unique structures including an inner membrane complex (IMC) that lines the interior of

86 ructural scaffold of daughter parasites, the inner membrane complex (IMC), fails to form in this aggl

87 roteinaceous network, and referred to as the inner membrane complex (IMC).

88 rates of PfCDPK1, which includes proteins of Inner Membrane Complex and glideosome-actomyosin motor a

89 In the yeast Saccharomyces cerevisiae, this inner membrane complex is composed of 11 protein subunit

90 onnected by a central stalk to a substantial inner membrane complex that is dominated by a battery of

91 hic and irreversible failure to assemble the inner membrane complex, a critical subcellular organelle

92 ntral roles in invasion and cytokinesis, the inner membrane complex, a Golgi-derived double membrane

93 ed proteins localize to the cytoskeleton and inner membrane complex, a structure beneath the plasma m

94 MotA and MotB form an inner-membrane complex that does not conduct protons and

95 Both the two inner membrane complexes, the Tic110 and 1 MDa complexes

96 sted the connectivity of the cytoplasmic and inner membrane components of the type IVa pilus machiner

97 The mitochondrial inner membrane contains a large protein complex that fun

98 st, the lipopeptides readily insert into the inner membrane core, and the concomitant increased hydra

99 outer membrane, before transport across the inner membrane, could have potentially useful biological

100 the proton gradient across the mitochondrial inner membrane, create a futile cycle of nutrient oxidat

101 es complex I oxidative damage, mitochondrial inner membrane depolarization, and apoptotic neuronal de

102 acterial cell-wall precursor lipid II on the inner membrane, disrupting the proton motive force.

103 ensures correct nuclear placement toward the inner membrane domain.

104 In particular, OPA1, regulating inner membrane dynamics, cristae remodelling, oxidative

105 ondrial activity through the function of the inner membrane dynamin OPA1.

106 demonstrated significant SOCE required high inner membrane electric potential (>-70 mV) and low rest

107 The large inner membrane electrochemical driving force and restric

108 lia of approximately 50 x 0.2 mum, devoid of inner membranes embedded in a mucus layer.

109 FTSH4 is one of the inner membrane-embedded ATP-dependent metalloproteases i

110 Biochemical studies revealed that MltG is an inner membrane enzyme with endolytic transglycosylase ac

111 the functional adaptability of an essential inner-membrane enzyme.

112 of TIM22 pathway substrate proteins into the inner membrane especially when the TIM22 complex handles

113 sion sites and compensatory shrinkage of the inner membrane, eventually resulting in rupture and slow

114 the envelope-associated needle complex, the inner membrane export apparatus, and a large cytoplasmic

115 er, the arrangement of their cytoplasmic and inner membrane export apparatuses is much less clear.

116 struction revealed the highly folded cristae inner membrane, features of functionally active mitochon

117 T tubules normally contain dense protective inner membrane folds that are formed by a cardiac isofor

118 in precursor within the lipid bilayer of the inner membrane, followed by cleavage by the inner membra

119 neries called translocators in the outer and inner membranes for import into and sorting to their des

120 ndrial cytochrome c oxidase assembles in the inner membrane from subunits of dual genetic origin.

121 During envelope stress, critical inner-membrane functions are preserved by the phage-shoc

122 rial membrane and functions in mitochondrial inner membrane fusion and cristae maintenance.

123 l dynamin-like OPA1 involved in mitochondria inner membrane fusion and increased GTP-loading on OPA1.

124 mtDNA) by deletion of mitochondrial outer or inner membrane fusion proteins (Fzo1p or Mgm1p) leads to

125 Recent studies suggest that the inner membrane GerD lipoprotein plays a critical role in

126 18-amino-acid (aa) protein essential for the inner membrane hole formation that initiates lysis and t

127 ally interacts with components important for inner membrane homeostasis and thereby supports mitochon

128 of phospholipid metabolism and mitochondrial inner membrane homeostasis.

129 2, which are key components of mitochondrial inner membrane homeostasis.

130 with type 1 diabetes exhibited mitochondrial inner-membrane hyperpolarization (MHP).

131 embrane receptor Psn and TonB as well as the inner membrane (IM) ABC transporter YbtPQ, which are req

132 The inner membrane (IM) of mitochondria displays an intricat

133 negative bacteria are either retained in the inner membrane (IM) or transferred to the inner leaflet

134 e in OM biogenesis and pathogenesis, and the inner membrane (IM) protein PbgA, containing five transm

135 ing to the proton motive force (PMF) via the inner membrane (IM) protein TonB1.

136 mbrane protein Large 3 (MmpL3), an essential inner membrane (IM) protein, is implicated in MA transpo

137 sts of an OMP, designated TamA, and a single inner membrane (IM) protein, TamB.

138 ith germinant receptors (GRs) in the spores' inner membrane (IM), in which most of the lipids are imm

139 lized phospholipids (PLs) from the OM to the inner membrane (IM).

140 th the PspBC membrane stress sensors and the inner membrane (IM).

141 tigates various problems that could increase inner-membrane (IM) permeability.

142 teins that connect the cytoplasmic membrane (inner membrane, IM) and the OM.

143 rphological alterations of the mitochondrial inner-membrane (IMM) have not been clearly elucidated.

144 re ferric enterobactin from the outer to the inner membrane in Gram-negative bacteria.

145 he present study, we show that mitochondrial inner membranes in leg muscles of endurance-trained athl

146 DOK4-dependent inactivation of p-Src on the inner membrane; inactivation of mitochondrial Src inhibi

147 hat paternal mitochondria rapidly lose their inner membrane integrity.

148 to the four subcompartments: outer membrane, inner membrane, intermembrane space, or matrix.

149 Chloroplast envelope inner membrane invaginations were frequently found in cl

150 rt, translocation through the channel in the inner membrane is coupled to the ATP-dependent action of

151 ynthesized in the cytoplasmic leaflet of the inner membrane is flipped to the periplasmic leaflet by

152 Because the mitochondrial inner membrane is impermeable to pyridine nucleotides, t

153 stems, the respirasome, in the mitochondrial inner membrane is reported in this issue of Cell.

154 dient via ATP synthase located on the folded inner membrane, known as cristae.

155 dient via ATP synthase located on the folded inner membrane, known as cristae.

156 n gene A) promotes synthesis of legiobactin, inner membrane LbtB aids in export of the siderophore, a

157 the siderophore, and outer membrane LbtU and inner membrane LbtC help mediate ferrilegiobactin uptake

158 and predominantly repacks the segment in the inner membrane leaflet due to a swivel movement.

159 no longer forms pores or translocates to the inner membrane leaflet.

160 ative zinc catalytic site are exposed to the inner membrane leaflet.

161 hey form in the sphingolipid-poor cytosolic (inner) membrane leaflet is unclear.

162 in-cholesterol interactions in the outer and inner membrane leaflets.

163 mitted the subsequent complete extraction of inner membrane lipids with chloroform-methanol-water, re

164 the structure and function of SadB, a small inner membrane lipoprotein.

165 s known about how mitochondrial lipids reach inner membrane-localized metabolic enzymes for phosphati

166 ng block of the bacterial cell wall, and its inner membrane-localized transporter FtsW.

167 nt studies suggest how gliding motors in the inner membrane may transduce force to the cell surface.

168 with electron-dense inclusions and abnormal inner-membrane morphology; (2) aggregated MT-CO2, the mt

169 show that the Agl-Glt machinery contains an inner-membrane motor complex that moves intracellularly

170 nsitive proton leak across the mitochondrial inner membrane of brown adipose tissue to produce heat,

171 es clustering of germination proteins in the inner membrane of dormant spores and thus promotes the r

172 propose a mechanism of anchoring WaaG to the inner membrane of E. coli, where the central part of MIR

173 structure of ASR is largely conserved in the inner membrane of E. coli, with many of the important st

174 aaG to membrane models designed to mimic the inner membrane of E. coli.

175 ty to selectively disrupt the OM but not the inner membrane of E. coli.

176 ed overexpression of functional PfVIT in the inner membrane of Escherichia coli which, in turn, confe

177 tuCD-F, which imports vitamin B12 across the inner membrane of Escherichia coli.

178 e synthesized at the periplasmic side of the inner membrane of Gram-negative bacteria and are then ex

179 on of antimicrobial peptides (AMPs) with the inner membrane of Gram-negative bacteria is a key determ

180 The inner membrane of Gram-negative bacteria is negatively c

181 or magainin 2 to membranes representing the inner membrane of Gram-negative bacteria, comprising a m

182 Located at the inner membrane of Gram-negative bacteria, PutAs play a m

183 eled by the fluorescent protein Venus in the inner membrane of live Escherichia coli cells at observa

184 s is the bc1 protein complex embedded in the inner membrane of mitochondria and the plasma membrane o

185 Cytochrome c oxidase in the inner membrane of mitochondria and the plasma membrane o

186 at specific domains, and CLS targets to the inner membrane of mitochondria with its C terminus in th

187 first evidence that XPD is localized in the inner membrane of mitochondria, and cells under oxidativ

188 r uncoupling proteins (UCPs), located in the inner membrane of mitochondria, play a role in setting u

189 annel (NMCC) is prominently expressed in the inner membrane of nuclei isolated from flexor digitorum

190 sicles, and lipid monolayers) that mimic the inner membrane of P. aeruginosa The study demonstrated t

191 egrity of the cell envelope by depleting the inner membrane of phospholipids.

192 ith COX2 to promote translocation across the inner membrane of the COX2 C-tail that contains the apo-

193 ubtilis, germinant receptors assemble in the inner membrane of the developing spore.

194 ndance on the luminal surfaces of the ER and inner membrane of the nuclear envelope.

195 e permeability transition pore (PTP), in the inner membranes of mitochondria can be triggered by calc

196 consequence, a loss of impermeability of the inner membranes of spores, accompanied by a decrease in

197 OPH is targeted to the inner membrane ofBrevundimonas diminutain a pre-folded c

198 ceptors, resulting in arrays embedded in the inner membrane, or they can comprise soluble receptors,

199 ns a large protein complex that functions in inner membrane organization and formation of membrane co

200 bout 50% of mitochondria from old flies, the inner membrane organization breaks down.

201 hondrial contact site complex, mitochondrial inner membrane organizing system, mitochondrial organizi

202 Alternative oxidase (AOX) is a mitochondrial inner-membrane oxidase that accepts electrons directly f

203 inner membrane, followed by cleavage by the inner membrane peptidase.

204 onstriction of a tripartite cell envelope of inner membrane, peptidoglycan (PG), and outer membrane (

205 that there is a significant change in spore inner membrane permeability at commitment.

206 uptake, isolated yeast mitochondria undergo inner membrane permeabilization due to PTP opening.

207 dylethanolamine and cardiolipin, the two key inner membrane phospholipids.

208 Here, we characterize the inner membrane platform protein PilC, the cytosolic asse

209 and the absence of exogenous substrates upon inner membrane pore formation by alamethicin or Ca(2+)-i

210 olated rabbit cardiac mitochondria following inner membrane pore formation induced by either alamethi

211 bacterial cytoplasm to the periplasm via an inner-membrane pore complex (TraC and TraG) with homolog

212 In cardiac myocytes, the activation of inner membrane pores by reactive oxygen species (ROS) is

213 Oscillatory behavior of mitochondrial inner membrane potential (DeltaPsim) is commonly observe

214 by the nonuniform collapse of mitochondrial inner membrane potential (DeltaPsim), contributes to re-

215 kly with mitochondria and did not affect the inner membrane potential or the structure of the preprot

216 ompanied by a reversible loss or decrease of inner membrane potential.

217 which also anchor the pilin subunits in the inner membrane prior to pilus assembly.

218 ed cooperative and sequential actions of two inner membrane proteases, Oma1p and Yme1p.

219 orescently labeled TcpP, but not for another inner membrane protein (TatA).

220 nsporters import nutrients by coupling to an inner membrane protein complex called the Ton complex.

221 of outer membrane, periplasmic adaptor, and inner membrane protein components.

222 Recently, a mitochondrial inner membrane protein EMRE was identified as a uniporte

223 radyrhizobium japonicum MbfA (Blr7895) is an inner membrane protein expressed in cells specifically u

224 J (also known as DnaJC15) is a mitochondrial inner membrane protein identified as an endogenous inhib

225 tide translocase 1 (Ant1) is a mitochondrial inner membrane protein involved in ATP/ADP exchange.

226 In Escherichia coli, the essential inner membrane protein MurJ is the lipid II flippase.

227 Their results show that the inner membrane protein NicD is a DGC that controls dispe

228 TolR is a 15-kDa inner membrane protein subunit of the Tol-Pal complex in

229 production, Alg44 has been identified as an inner membrane protein whose bis-(3',5')-cyclic dimeric

230 pstream of cyaY and which encodes a putative inner membrane protein, dramatically enhances the hydrog

231 analyses demonstrate MPV17L2 is an integral inner membrane protein, like MPV17.

232 ationally recognizes the nascent chain of an inner membrane protein, RodZ, with high affinity and spe

233 Smt1p is an intrinsic inner membrane protein, which, based on its sedimentatio

234 mplex organelle we have identified Aim24, an inner membrane protein.

235 ilitates an interaction between BtuB and the inner-membrane protein TonB.

236 equencing revealed that degradation rates of inner-membrane-protein mRNAs are on average greater that

237 s and that this selective destabilization of inner-membrane-protein mRNAs is abolished by dissociatin

238 matrix proteins and a considerable number of inner membrane proteins carry a positively charged, N-te

239 gs identify a new route for the targeting of inner membrane proteins in bacteria and highlight the di

240 FtsB and FtsL, which, like FtsQ, are bitopic inner membrane proteins with a large periplasmic domain

241 actors, including periplasmic chaperones and inner membrane proteins, have also recently been implica

242 spatial organization of RNA: mRNAs encoding inner-membrane proteins are enriched at the membrane, wh

243 ted in the bacterial cell, mRNAs that encode inner-membrane proteins can be concentrated near the inn

244 s an unusual transcription step: the bitopic inner-membrane proteins TcpP and ToxR activate toxT tran

245 Most inner-membrane proteins were cotranslationally targeted

246 sistance mutations all disrupt expression of inner-membrane proteins, suggesting that these proteins

247 sual step: transcription is activated by two inner-membrane proteins.

248 which functionally exhibited an increase of inner membrane proton leak.

249 translocation across the energy-transducing inner membrane, providing electrons for respiration and

250 omplex, which requires the activation of the inner membrane pump CusA, is poorly understood.

251 inor coat protein named pIII and a bacterial inner-membrane receptor, TolA, which is part of the cons

252 iplasm, the N-terminal domains bind specific inner-membrane receptors for subsequent translocation in

253 ct interactions between PilA and PilS in the inner membrane reduce pilA transcription when PilA level

254 itochondrial membrane and interacts with the inner membrane remodeling protein mitofilin (Fcj1).

255 mplex II (site IIf); (b) pore opening in the inner membrane resulting in rapid efflux of succinate/fu

256 -particle cryo-electron microscopy, with the inner-membrane-ring and outer-membrane-ring oligomers de

257 ers transport protons from the mitochondrial inner membrane space into the mitochondrial matrix indep

258 he release of protons into the mitochondrial inner membrane space to promote ATP production through A

259 rm a correlated mesh-like network within the inner membrane space, only in the vicinity of native lip

260 er irradiation occurred in the mitochondrial inner membrane space.

261 levels of cardiolipin (CL), a mitochondrial inner membrane-specific lipid.

262 ns as a primary determinant of mitochondrial inner membrane structure.

263 actin-associated proteins that laminates the inner membrane surface and attaches to the overlying lip

264 However, increasing the mitochondrial inner membrane surface comprises an alternative mechanis

265 in biochemical coupling at the mitochondrial inner membrane that enhance O2 efficiency.

266 This creates a stress in the inner membrane that progressively dissipates the mitocho

267 Although inserted into the inner membrane, the dynamic association of its intermemb

268 self-assembling GTPase that forms, below the inner membrane, the mid-cell Z-ring guiding bacterial di

269 cing proton leakage across the mitochondrial inner membrane, thereby uncoupling adenosine diphosphate

270 e essential translocase of the mitochondrial inner membrane (TIM) consisting of Tim17 in T. brucei.

271 translocons on the outer membrane (TOM) and inner membrane (TIM).

272 the mitochondrial matrix are targeted to the inner membrane Tim17/23 translocon by their presequences

273 The presequence translocase of the inner membrane (TIM23 complex) mediates the import of th

274 er the electrochemical gradient across their inner membrane to allow ATP synthesis while maintaining

275 The permeability of the mitochondrial inner membrane to HNO2, but not to NO2(-), combined with

276 zation, suggesting that lipids flow from the inner membrane to the OM in an energy-independent manner

277 esponsible for the transport of LPS from the inner membrane to the outer membrane, the mechanism for

278 ulence factors from the outer leaflet of the inner membrane to the periplasm.

279 xbD, and uses the proton motive force at the inner membrane to transduce energy to the outer membrane

280 Moreover, the inner membrane transglycosylase protein P26 could have a

281 vely, these results indicate that outer- and inner-membrane translocation steps can be uncoupled, and

282 up large amounts of calcium (Ca(2+)) via an inner membrane transporter called the uniporter.

283 omain protein MlaD is known to be part of an inner membrane transporter that is important for mainten

284 l host, with IL resistance established by an inner membrane transporter, regulated by an IL-inducible

285 analysis suggested that PEG344 serves as an inner membrane transporter.

286 ranes of the bacterium via an alpha-helical, inner membrane transporter; a periplasmic membrane fusio

287 their cognate receptors located in the spore inner membrane triggers the germination process that lea

288 nation of the proton motive force across its inner membrane under normal and acid-stress conditions.

289 Both complexes build in the mitochondrial inner membrane various supramolecular assemblies.

290 as a lipid envelope, internal lipid core, or inner membrane vesicle.

291 reconstituting them in vitro using inverted inner membrane vesicles.

292 mimic the lipid composition of the bacterial inner membrane, were performed using the MARTINI coarse-

293 t may be that they simply partition into the inner membrane where they can no longer participate in f

294 eading to its activation and transfer to the inner membrane, where it dephosphorylates P-Y419Src (act

295 WaaG is located at the cytosolic side of the inner membrane, where the enzyme catalyzes the transfer

296 a sufficient electrical potential across the inner membrane, which explains the subsequent disappeara

297 nslocator (ANT) located in the mitochondrial inner membrane, which leads to a high cytosolic ATP/ADP

298 protein is integrated into the mitochondrial inner membrane with it's C-terminus exposed to the inter

299 outer membrane rather than between wall and inner-membrane, yet still obtain nutrients from the prey

300 The A. baumannii inner membrane zinc transporter ZnuABC is required for g