ライフサイエンスコーパス: mitochondrial inner membrane

1 Aifm2 associates with the outer side of the mitochondrial inner membrane.

2 essential for the proper architecture of the mitochondrial inner membrane.

3 -terminal end and predominantly localizes to mitochondrial inner membrane.

4 onmotive force by pumping protons across the mitochondrial inner membrane.

5 d complete translocation of Pink1 across the mitochondrial inner membrane.

6 enzyme, and sodium ion transport across the mitochondrial inner membrane.

7 AAC) is the most abundant transporter of the mitochondrial inner membrane.

8 the transport of small molecules across the mitochondrial inner membrane.

9 o gain insight into AC interactions with the mitochondrial inner membrane.

10 ion to the protein-conducting channel of the mitochondrial inner membrane.

11 r the surface of mitochondria but not inside mitochondrial inner membrane.

12 ghtly associated with the matrix side of the mitochondrial inner membrane.

13 contributes to UPR(mt) signaling across the mitochondrial inner membrane.

14 duction, as a proton motive force across the mitochondrial inner membrane.

15 s an anchor for FB to the matrix side of the mitochondrial inner membrane.

16 the chaperoned translocation of Tim23 to the mitochondrial inner membrane.

17 al carriers Tim23, Tim22, and Tim17 into the mitochondrial inner membrane.

18 moiety as the proton transporter across the mitochondrial inner membrane.

19 itate the exchange of ADP and ATP across the mitochondrial inner membrane.

20 iates with the i-AAA protease complex in the mitochondrial inner membrane.

21 highly similar DSPs on opposing sides of the mitochondrial inner membrane.

22 tor designated Coa1 that associates with the mitochondrial inner membrane.

23 f electrons down the cytochrome chain on the mitochondrial inner membrane.

24 catalytic core of the enzyme located in the mitochondrial inner membrane.

25 hemical driving force for protons across the mitochondrial inner membrane.

26 of the i-AAA protease complex located in the mitochondrial inner membrane.

27 10) that escorts polytopic proteins into the mitochondrial inner membrane.

28 ase (POX) is a redox enzyme localized in the mitochondrial inner membrane.

29 ltrastructural studies revealed disorganized mitochondrial inner membrane.

30 f presequence-containing proteins across the mitochondrial inner membrane.

31 of enzymes peripherally associated with the mitochondrial inner membrane.

32 contains a J domain and is localized to the mitochondrial inner membrane.

33 ies indicate Atp22p to be a component of the mitochondrial inner membrane.

34 cassette (ABC) transporter localized to the mitochondrial inner membrane.

35 btained by extensive subfractionation of the mitochondrial inner membrane.

36 -ATP synthase forms a dimeric complex in the mitochondrial inner membrane.

37 ndrial dysfunction and depolarization of the mitochondrial inner membrane.

38 ncoupling proteins at the matrix side of the mitochondrial inner membrane.

39 at they occur at the cytoplasmic side of the mitochondrial inner membrane.

40 absence of a permeability transition at the mitochondrial inner membrane.

41 tes insertion of polytopic proteins into the mitochondrial inner membrane.

42 oA to carnitine for translocation across the mitochondrial inner membrane.

43 an essential import component located in the mitochondrial inner membrane.

44 a proton electrochemical gradient across the mitochondrial inner membrane.

45 protected from proteolytic digestion by the mitochondrial inner membrane.

46 drive protons across the energy-transducing mitochondrial inner membrane.

47 g complex subunit prohibitin-2 (PHB2) at the mitochondrial inner membrane.

48 ort of hydrophobic carrier proteins into the mitochondrial inner membrane.

49 tely build a functional and correctly shaped mitochondrial inner membrane.

50 eads to aberrant protein accumulation in the mitochondrial inner membrane.

51 be embedded with the correct topology in the mitochondrial inner membrane.

52 3 complex for their translocation across the mitochondrial inner membrane.

53 the chloroplast thylakoid membrane, and the mitochondrial inner membrane.

54 fusion and protein complex formation in the mitochondrial inner membrane.

55 ainst the electrostatic potential across the mitochondrial inner membrane.

56 duction, as a proton motive force across the mitochondrial inner membrane.

57 Upon entry, they are embedded into the mitochondrial inner membrane.

58 mitochondrial protein that localizes to the mitochondrial inner membrane.

59 in (CL) is the signature phospholipid of the mitochondrial inner membrane.

60 d cells, Mfrn2 is an iron transporter in the mitochondrial inner membrane.

61 d GTPase Mgm1 is required to tether and fuse mitochondrial inner membranes.

62 P synthase dimers are a conserved feature of mitochondrial inner membranes.

63 ase (HD), associates with the translocase of mitochondrial inner membrane 23 (TIM23) complex, resulti

64 n deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a) and loss o

65 n deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a).

66 ntified was MDL1, which like ATM1, encodes a mitochondrial inner membrane ABC transporter.

67 nonselective ion channels are present in the mitochondrial inner membrane, along with several known c

68 (ANT) family exchange ADP for ATP across the mitochondrial inner membrane, an activity that is essent

69 ) reduction of the proton conductance of the mitochondrial inner membrane and (ii) inhibition of the

70 esicles (SUVs) with the lipid composition of mitochondrial inner membrane and analyze its oligomeric

71 , inorganic ions, and nucleotides across the mitochondrial inner membrane and are crucial for many ce

72 that Mtg2p is peripherally localized to the mitochondrial inner membrane and associates with the 54S

73 tein homeostasis is subtly maintained on the mitochondrial inner membrane and can be derailed by the

74 tes the import of membrane proteins into the mitochondrial inner membrane and consists of two interme

75 We showed that it is located in the mitochondrial inner membrane and forms a approximately 3

76 MICU1 is associated with the mitochondrial inner membrane and has two canonical EF ha

77 -ATP synthase forms dimeric complexes in the mitochondrial inner membrane and in a manner that is sup

78 : in the transport of ADP and ATP across the mitochondrial inner membrane and in the formation of the

79 Atp23p is associated with the mitochondrial inner membrane and is conserved from yeast

80 C-mitochondrial erythroid), localizes to the mitochondrial inner membrane and is expressed at particu

81 ncoupling proteins (UCPs) are located in the mitochondrial inner membrane and partially dissipate the

82 ucing ubiquinone to drive protons across the mitochondrial inner membrane and power oxidative phospho

83 UCP2 is located in the mitochondrial inner membrane and regulates production of

84 dentify KCNJ1(ROMK) in purified bovine heart mitochondrial inner membrane and ROMK mRNA was confirmed

85 release does not affect the integrity of the mitochondrial inner membrane and that, in the absence of

86 ional Ang II type 2 receptors are present on mitochondrial inner membranes and are colocalized with e

87 nslocase (ANT) exchanges ADP/ATP through the mitochondrial inner membrane, and Ant2 is the predominan

88 ion of proteins from the cytosol, across the mitochondrial inner membrane, and into the matrix.

89 nd core CI subunits and was localized in the mitochondrial inner membrane, and its depletion resulted

90 bTim62, a novel protein, is localized in the mitochondrial inner membrane, and its import into mitoch

91 2p) is synthesized on the matrix side of the mitochondrial inner membrane, and its N- and C-terminal

92 The mitochondrial inner membrane anion channel (IMAC) carrie

93 tential (AP) through a mechanism involving a mitochondrial inner membrane anion channel (IMAC) modula

94 The model includes the mitochondrial inner membrane anion channel (IMAC), the c

95 d: PsiM oscillations involving ROS-sensitive mitochondrial inner membrane anion channels (IMAC), and

96 lear encoded gene (COX4) associated with the mitochondrial inner membrane are not present when PGS1 e

97 ltapsi(m)), increases in currents across the mitochondrial inner membrane as detected by direct patch

98 rotein revealed that it is part of a soluble mitochondrial inner-membrane-associated, RNase-sensitive

99 Abcb10, a mitochondrial inner membrane ATP-binding cassette transp

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

101 family AAA-Domain containing protein 3) is a mitochondrial inner membrane ATPase with unknown but vit

102 Loss of cps-6 delays breakdown of mitochondrial inner membranes, autophagosome enclosure o

103 ies observed are a consequence of defects in mitochondrial inner membrane biogenesis.

104 and directed to its final destination in the mitochondrial inner membrane by a bipartite, cleaved, am

105 the mitochondrion, Cox17 was tethered to the mitochondrial inner membrane by a fusion to the transmem

106 Cox11 is tethered to the mitochondrial inner membrane by a single transmembrane h

107 est that during cell stress, Bif-1 regulates mitochondrial inner membrane by interacting with prohibi

108 ly event in import of preproteins across the mitochondrial inner membrane by the TIM23 complex.

109 re, we unravel the sequence of events in the mitochondrial inner membrane by which cytochrome b is he

110 - properties that differentiate it from the mitochondrial inner membrane carnitine/acylcarnitine exc

111 of permeability transition (PT) pores in the mitochondrial inner membrane causes the mitochondrial pe

112 Atp10p was identified as a mitochondrial inner membrane component necessary for the

113 its association with pure lipid vesicles of mitochondrial inner membrane composition.

114 iling identified a FUNDC1 interactome at the mitochondrial inner membrane, comprising the AAA+ protea

115 The mitochondrial inner membrane consists of the inner bound

116 d molecular dynamics model of a patch of the mitochondrial inner membrane containing a transmembrane

117 The mitochondrial inner membrane contains a large protein co

118 The mitochondrial inner membrane contains two separate trans

119 tion of imported polytopic proteins into the mitochondrial inner membrane, contains the nonessential

120 which reduce the proton gradient across the mitochondrial inner membrane, create a futile cycle of n

121 that although mgm1 mutants display aberrant mitochondrial inner membrane cristae, mgm1 dnm1 double m

122 rge hetero-oligomeric protein complex in the mitochondrial inner membrane, crucial for the maintenanc

123 thane treatment induced hyperpolarization of mitochondrial inner membrane, decreased cellular ATP lev

124 activity causes complex I oxidative damage, mitochondrial inner membrane depolarization, and apoptot

125 ith the translocon on the matrix side of the mitochondrial inner membrane, drives translocation of pr

126 eta-cells associated with dissipation of the mitochondrial inner membrane electrochemical gradient, D

127 FS/DGS) and encodes proline oxidase (POX), a mitochondrial inner-membrane enzyme that catalyzes the f

128 xamine these processes in ABCB10 (ABC-me), a mitochondrial inner membrane erythroid transporter invol

129 Structural damage to the mitochondrial inner membrane, evidenced by a decrease in

130 charomyces cerevisiae, Cmc2 localizes to the mitochondrial inner membrane facing the intermembrane sp

131 haromyces cerevisiae, Cmc1p localizes to the mitochondrial inner membrane facing the intermembrane sp

132 e protein is an extrinsic constituent of the mitochondrial inner membrane facing the matrix.

133 ine exposure, particularly the inhibition of mitochondrial inner membrane functions related to oxidat

134 f the solute carrier family localized in the mitochondrial inner membrane, functions as an essential

135 nner mitochondrial membrane and functions in mitochondrial inner membrane fusion and cristae maintena

136 The mammalian mitochondrial inner membrane fusion protein OPA1 is cont

137 significant changes in the expression of the mitochondrial inner membrane fusion protein optic atroph

138 tion system, we describe a mechanism for how mitochondrial inner-membrane fusion is regulated by the

139 th components of phospholipid metabolism and mitochondrial inner membrane homeostasis.

140 , Phb1 and Phb2, which are key components of mitochondrial inner membrane homeostasis.

141 ABCB10 indicates that ABCB10 embedded in the mitochondrial inner membrane homodimerizes and homo-olig

142 from patients with type 1 diabetes exhibited mitochondrial inner-membrane hyperpolarization (MHP).

143 the ISR via a distinct mechanism related to mitochondrial inner-membrane hyperpolarization.

144 nd Mgr3 are known to associate with the Yme1 mitochondrial inner membrane i-AAA protease and to parti

145 ney mitochondria from the matrix side of the mitochondrial inner membrane: (i) Exogenous superoxide i

146 ic pathways in eukaryotes, one occurs in the mitochondrial inner membrane (IM) and is executed by pho

147 port of polytopic membrane proteins into the mitochondrial inner membrane (IM) is facilitated by Tim9

148 ix domain-containing protein 3 (ChChd3) is a mitochondrial inner membrane (IM) protein facing toward

149 The mitochondrial inner membrane (IM) serves as the site for

150 se upon oxidation of cardiolipin (CL) in the mitochondrial inner membrane (IM) under oxidative stress

151 fatty acid chains, is located mainly in the mitochondrial inner membrane (IM).

152 l division, morphological alterations of the mitochondrial inner-membrane (IMM) have not been clearly

153 he properties of Sco1p, a constituent of the mitochondrial inner membrane implicated in copper transf

154 e caused by decreased levels of Tim23 in the mitochondrial inner membrane in affected tissues.

155 orientation and are expressed highly in the mitochondrial inner membrane in several tissues includin

156 In the present study, we show that mitochondrial inner membranes in leg muscles of enduranc

157 Ion channels on the mitochondrial inner membrane influence cell function in

158 els relevant to cytoprotection may be on the mitochondrial inner membrane instead of on the sarcolemm

159 rylation, reactive oxygen species (ROS), and mitochondrial inner membrane ion channels.

160 Facilitated pyruvate transport across the mitochondrial inner membrane is a critical step in carbo

161 ubiquinone oxidoreductase (complex I) of the mitochondrial inner membrane is a multi-subunit protein

162 Detachment of cytochrome c from the mitochondrial inner membrane is a necessary first step f

163 Translocation of proteins across the mitochondrial inner membrane is an essential process req

164 The biogenesis of the mitochondrial inner membrane is dependent on two distinc

165 tion of proteins from the cytosol across the mitochondrial inner membrane is driven by action of the

166 tion of proteins from the cytosol across the mitochondrial inner membrane is driven by the action of

167 The mitochondrial inner membrane is impermeable to NAD (nico

168 Because the mitochondrial inner membrane is impermeable to pyridine

169 Protein translocation across the mitochondrial inner membrane is mediated by the TIM23 co

170 cate enzyme systems, the respirasome, in the mitochondrial inner membrane is reported in this issue o

171 ipin (CL), the characteristic lipid from the mitochondrial inner membrane, is another nonlamellar lip

172 plex, crucial for proper architecture of the mitochondrial inner membrane, is localized primarily at

173 , an ATP-dependent protease localized in the mitochondrial inner membrane, is required for the growth

174 Atm1p is an ABC transporter localized in the mitochondrial inner membrane; it functions to export an

175 e find neurons of the Fmr1(-/y) mouse have a mitochondrial inner membrane leak contributing to a "lea

176 identify dramatic decreases in the critical mitochondrial inner membrane lipid, cardiolipin, in diab

177 se (Ant) is the most abundant protein on the mitochondrial inner membrane (MIM) primarily involved in

178 surface membrane (sK(ATP)) and others in the mitochondrial inner membrane (mitoK(ATP)).

179 alcium-activated K+ channel was found on the mitochondrial inner membrane (mitoKCa) of guinea pig ven

180 We observed changes in mitochondrial inner membrane morphology and a reduction

181 n the plasma membrane (Alr1 and Alr2) or the mitochondrial inner membrane (Mrs2 and Lpe10).

182 nucleotide-sensitive proton leak across the mitochondrial inner membrane of brown adipose tissue to

183 tein-1 (UCP1) is abundantly expressed in the mitochondrial inner membrane of brown adipose tissues an

184 lycerol are synthesized and localized in the mitochondrial inner membrane of eukaryotes.

185 py revealed both proteins to localize to the mitochondrial inner membrane of human T cells.

186 We localized the Letm1 protein to the mitochondrial inner membrane of mammalian cells, where i

187 tions and the proton motive force across the mitochondrial inner membrane or prokaryotic cytoplasmic

188 veal new insight into the composition of the mitochondrial inner membrane organizing machinery.

189 The mitochondrial inner membrane organizing system (MINOS) i

190 The mitochondrial inner membrane organizing system (MINOS) i

191 amed the mitochondrial contact site complex, mitochondrial inner membrane organizing system, mitochon

192 , no apoptosis-associated alterations in the mitochondrial inner membrane, outer membrane, or matrix

193 We performed time-lapse imaging of the mitochondrial inner membrane over 50 min (3.9 s per fram

194 Alternative oxidase (AOX) is a mitochondrial inner-membrane oxidase that accepts electr

195 One such enzyme, the mitochondrial inner membrane peptidase, has two catalyti

196 chondrial permeability transition, inhibited mitochondrial inner membrane permeabilization and depola

197 This was followed by mitochondrial inner membrane permeabilization, depolariz

198 mitochondrial ROS are critical in initiating mitochondrial inner membrane permeabilization, which lea

199 id PGE(2), which promotes protection against mitochondrial inner membrane perturbation and necrosis.

200 MCU forms oligomers in the mitochondrial inner membrane, physically interacts with

201 al stress testing, confocal live imaging for mitochondrial inner membrane polarity, and immunohistoch

202 Coupling factor B (FB) is a mitochondrial inner membrane polypeptide that facilitate

203 ion, caspase-3 activation and dissipation of mitochondrial inner membrane potential (Delta(Psi)(m)).

204 sis of caspase activation and dissipation of mitochondrial inner membrane potential (DeltaPsi(m) loss

205 Recovery of the mitochondrial inner membrane potential (DeltaPsi(m)) is

206 ndria, thus preventing the disruption of the mitochondrial inner membrane potential (DeltaPsi(m)), ca

207 sed to assess the effect of Mn on astrocytic mitochondrial inner membrane potential (DeltaPsi(m)).

208 ing rhodamine 123 (R123) was used to monitor mitochondrial inner membrane potential (deltapsi(m)).

209 Ca2+ overload can trigger depolarization of mitochondrial inner membrane potential (DeltaPsim) and c

210 Oscillatory behavior of mitochondrial inner membrane potential (DeltaPsim) is co

211 An indicator dye for mitochondrial inner membrane potential (DeltaPsim) revea

212 sinks, caused by the nonuniform collapse of mitochondrial inner membrane potential (DeltaPsim), cont

213 n pore (mPTP) opening and dissipation of the mitochondrial inner membrane potential (DeltaPsim).

214 els and rescues mitochondrial functionality (mitochondrial inner membrane potential and expression of

215 etal muscle fibers display localized loss of mitochondrial inner membrane potential in fiber segments

216 emarkably prevented the catastrophic loss of mitochondrial inner membrane potential induced by H2O2,

217 in mitochondria, both of which contribute to mitochondrial inner membrane potential loss, were dramat

218 Surprisingly, a high mitochondrial inner membrane potential was maintained in

219 tochondrial-Nix cells, showed dissipation of mitochondrial inner membrane potential, Deltapsi(m), and

220 oad in SNc DaNs is counterbalanced by a high mitochondrial inner membrane potential, even under condi

221 Treatment of sensitive cells caused loss of mitochondrial inner membrane potential, G(2)/M arrest, a

222 fects of MeHg treatment on oxidative injury, mitochondrial inner membrane potential, glutamine uptake

223 menon through a large-scale fluctuation of a mitochondrial inner membrane potential.

224 in [Ca(2+)]i and exaggerated instability in mitochondrial inner membrane potential.

225 d with an increase rather than a decrease in mitochondrial inner-membrane potential, as monitored by

226 A mitochondrial inner-membrane protease, PARL, removes an

227 Recently, a mitochondrial inner membrane protein EMRE was identified

228 cation and characterization of a novel human mitochondrial inner membrane protein homologous to the y

229 MCJ (also known as DnaJC15) is a mitochondrial inner membrane protein identified as an en

230 time the detergent-free reconstitution of a mitochondrial inner membrane protein into liposomes usin

231 Adenine nucleotide translocase 1 (Ant1) is a mitochondrial inner membrane protein involved in ATP/ADP

232 end strongly and directly interacts with the mitochondrial inner membrane protein mitofilin, which is

233 MPV17 is a mitochondrial inner membrane protein of unknown function

234 The mammalian mitochondrial inner membrane protein Oxa1L is involved i

235 In humans the mitochondrial inner membrane protein Oxa1L is involved i

236 l genome (rho(0) cell) or elimination of the mitochondrial inner membrane protein Oxa1p causes a dram

237 Additionally, loss of the mitochondrial inner membrane protein Oxa1p generates a s

238 DIC1 codes for a mitochondrial inner membrane protein that exchanges cyto

239 Uncoupling protein (UCP)2 is a mitochondrial inner membrane protein that is expressed i

240 ROS activates uncoupling protein-2 (UCP2), a mitochondrial inner membrane protein that negatively reg

241 The AEP3 gene encodes a peripheral mitochondrial inner membrane protein that stabilizes mit

242 f the ERBB2 receptor tyrosine kinase and the mitochondrial inner membrane protein UCP2 occurs frequen

243 Whether a given hydrophobic segment in a mitochondrial inner membrane protein will ultimately for

244 Atp25p is a mitochondrial inner membrane protein with a predicted ma

245 inding cassette (ABC) transporter ABCB8 is a mitochondrial inner membrane protein with an unknown fun

246 ing protein-1 (UCP1) is a brown fat-specific mitochondrial inner membrane protein with proton transpo

247 e forward reaction of NNT, a nuclear-encoded mitochondrial inner membrane protein, couples the genera

248 NOS1/MIO10 (C1orf151/YCL057C-A), a conserved mitochondrial inner membrane protein.

249 Uncoupling protein (UCP) 2 is a mitochondrial inner-membrane protein that mediates proto

250 BCS1L, a mitochondrial inner-membrane protein, is a chaperone nec

251 Mitochondrial inner membrane proteins appear to be not e

252 The two mitochondrial inner membrane proteins Cox11 and Sco1 are

253 Sorting of mitochondrial inner membrane proteins is a complex proce

254 ve roles for the translocation and import of mitochondrial inner membrane proteins, little is known a

255 or alternatively as a chaperone for selected mitochondrial inner membrane proteins.

256 A protease and are defective for turnover of mitochondrial inner membrane proteins.

257 translocase of inner membrane)22 pathway for mitochondrial inner membrane proteins.

258 Our results demonstrate the importance of mitochondrial inner-membrane proteostasis to both mitoch

259 ative phosphorylation (OXPHOS) to generate a mitochondrial inner membrane proton gradient (DeltaP).

260 change in glucose stimulation increased the mitochondrial inner membrane proton leak, and thus signi

261 The electrical gradient across the mitochondrial inner membrane (Psi(m)) is established by

262 In Saccharomyces cerevisiae, the mitochondrial inner membrane readily allows transport of

263 dynamin superfamily, mediates fusion of the mitochondrial inner membranes, regulates cristae morphol

264 In this study, we report that the mitochondrial inner membrane rhomboid protease presenili

265 ndrial uncouplers transport protons from the mitochondrial inner membrane space into the mitochondria

266 n histone deacetylase HDAC7 localizes to the mitochondrial inner membrane space of prostate epithelia

267 transfer to the release of protons into the mitochondrial inner membrane space to promote ATP produc

268 drial MKP1 after irradiation occurred in the mitochondrial inner membrane space.

269 increases the levels of cardiolipin (CL), a mitochondrial inner membrane-specific lipid.

270 Moreover, we found that mitochondrial inner membrane structure is dramatically d

271 omplex functions as a primary determinant of mitochondrial inner membrane structure.

272 e protein is functional when tethered to the mitochondrial inner membrane, suggesting its functional

273 t association of the BER activities with the mitochondrial inner membrane, suggesting that CSB may pa

274 pproximately equally toward each side of the mitochondrial inner membrane, suggesting that the Q-bind

275 el: 1) The formation of cristae creates more mitochondrial inner membrane surface area and thus more

276 However, increasing the mitochondrial inner membrane surface comprises an altern

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

278 the insertion of polytopic proteins into the mitochondrial inner membrane (the Tim54p-Tim22p complex)

279 roxide and release it into both sides of the mitochondrial inner membrane: the mitochondrial matrix a

280 cells by inducing proton leakage across the mitochondrial inner membrane, thereby uncoupling adenosi

281 ater molecules from the negative side of the mitochondrial inner membrane through a water channel int

282 aracterized the essential translocase of the mitochondrial inner membrane (TIM) consisting of Tim17 i

283 PRAT proteins, such as the translocon of the mitochondrial inner membrane (TIM) proteins TIM22 and TI

284 Translocases of mitochondrial inner membrane (TIMs) are multiprotein com

285 UCP1 catalyzes proton leak across the mitochondrial inner membrane to disengage substrate oxid

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

287 gnaling after the loss of the ability of the mitochondrial inner membrane to undergo fusion and lacti

288 of cytosolic/nuclear Fe-S proteins, but the mitochondrial inner membrane transporter Atm1 is importa

289 d between the two sites by passing along the mitochondrial inner membrane using the hydrophobic natur

290 g aspartate/glutamate carriers (AGCs) of the mitochondrial inner membrane, using cross-linking and im

291 Both complexes build in the mitochondrial inner membrane various supramolecular asse

292 in the translocation of proteins across the mitochondrial inner membrane via the TIM23-PAM complex a

293 Yeast Mdm38 is localized to the mitochondrial inner membrane where it was proposed to ac

294 a distinct cochaperone that localizes at the mitochondrial inner membrane, where it interacts prefere

295 ric structure predominantly localized in the mitochondrial inner membrane, where it is closely associ

296 on for nitric oxide (NO) within cells is the mitochondrial inner membrane, where NO binds to and inhi

297 on powered by the proton gradient across the mitochondrial inner membrane, which is generated by mito

298 nucleotide translocator (ANT) located in the mitochondrial inner membrane, which leads to a high cyto

299 The protein is integrated into the mitochondrial inner membrane with it's C-terminus expose

300 otein Bcs1 translocate substrates across the mitochondrial inner membrane without previous unfolding.