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

1 elle via the TOM complex (translocase of the outer mitochondrial membrane).

2 eins use an alternative pathway to cross the outer mitochondrial membrane.

3 osol, BAK is constitutively localized to the outer mitochondrial membrane.

4 and VDAC1 thus reducing permeability of the outer mitochondrial membrane.

5 tial but was absent in mitoplasts lacking an outer mitochondrial membrane.

6 t include the endoplasmic reticulum (ER) and outer mitochondrial membrane.

7 chondria, leading to its accumulation on the outer mitochondrial membrane.

8 ion by increasing Ca(2+) transfer across the outer mitochondrial membrane.

9 that drives the assembly of proteins in the outer mitochondrial membrane.

10 leavage product to the cytosolic face of the outer mitochondrial membrane.

11 ns (DRPs) must bind specific adaptors on the outer mitochondrial membrane.

12 s 1, 2, and 3), pore-forming proteins in the outer mitochondrial membrane.

13 d demonstrate that it is integrated into the outer mitochondrial membrane.

14 tor, Daedalus (Daed), that is located on the outer mitochondrial membrane.

15 to function as a supportive receptor for the outer mitochondrial membrane.

16 forms the protein-translocating pore in the outer mitochondrial membrane.

17 that is involved in the rearrangement of the outer mitochondrial membrane.

18 an integral membrane protein imbedded in the outer mitochondrial membrane.

19 nsmembrane helices anchor the enzymes to the outer mitochondrial membrane.

20 polyQ domains might associate early with the outer mitochondrial membrane.

21 all molecules and ions across the eukaryotic outer mitochondrial membrane.

22 urified mitochondria and associates with the outer mitochondrial membrane.

23 oapoptotic BCL-2 proteins BAX and BAK at the outer mitochondrial membrane.

24 oform enables colocalization with HK1 on the outer mitochondrial membrane.

25 ied 2Fe-2S-containing protein located in the outer mitochondrial membrane.

26 oltage-dependent anion channel (VDAC) of the outer mitochondrial membrane.

27 s a survival protein that is tethered to the outer mitochondrial membrane.

28 that erastin alters the permeability of the outer mitochondrial membrane.

29 toNEET is an integral protein present in the outer mitochondrial membrane.

30 ysiologic exchange of ATP and ADP across the outer mitochondrial membrane.

31 involving Bax's integral insertion into the outer mitochondrial membrane.

32 which assemble into fission complexes on the outer mitochondrial membrane.

33 own to be sufficient for localization to the outer mitochondrial membrane.

34 ltage-dependent anion channel present in the outer mitochondrial membrane.

35 tochondria shows that TARP is located in the outer mitochondrial membrane.

36 promote the timely loss of integrity of the outer mitochondrial membrane.

37 uitylation of subunits of the translocase of outer mitochondrial membrane.

38 atment, suggesting eNOS association with the outer mitochondrial membrane.

39 ated that huntingtin was associated with the outer mitochondrial membrane.

40 recruitment of the large GTPase Dnm1p to the outer mitochondrial membrane.

41 protein 1) and its receptor proteins on the outer mitochondrial membrane.

42 raction of mislocalized TA proteins from the outer mitochondrial membrane.

43 me biosynthesis during erythropoiesis at the outer mitochondrial membrane.

44 A), RNAs, and other signaling enzymes to the outer mitochondrial membrane.

45 l membrane protein or is integrated into the outer mitochondrial membrane.

46 rst identified Fe-S protein of the mammalian outer mitochondrial membrane.

47 tochondria by ubiquitinating proteins on the outer mitochondrial membrane.

48 nstead, Nrf2 was found to associate with the outer mitochondrial membrane.

49 of dozens of proteins on the surface of the outer mitochondrial membrane.

50 eus, and a third population localizes to the outer mitochondrial membrane.

51 ization of immune regulatory proteins on the outer mitochondrial membrane.

52 (VDAC) proteins are major components of the outer mitochondrial membrane.

53 is commitment is the permeabilization of the outer mitochondrial membrane.

54 rs permeability alterations of the inner and outer mitochondrial membranes.

55 forms at contact sites between the inner and outer mitochondrial membranes.

56 age-dependent anion channel 1 (VDAC1) at the outer mitochondrial membranes.

57 he mitochondrial translocase, translocase of outer mitochondrial membrane 22 (Tom22), steroidogenic a

58 Translocase of outer mitochondrial membrane 34 (TOMM34) orchestrates he

59 ear factor 4, alpha), TOMM34 (translocase of outer mitochondrial membrane 34) and SRC (SRC proto-onco

60 80 kDa complexes with the translocase of the outer mitochondrial membrane 40 (TOM40) import channel a

61 o studies, 449 participants), translocase of outer mitochondrial membrane 40 gene (one study, 723 par

62 e apolipoprotein E (APOE) and translocase of outer mitochondrial membrane 40 homolog (TOMM40) genotyp

63 ovel BMI associations in loci translocase of outer mitochondrial membrane 40 homolog (yeast) - apolip

64 75650, located in TOMM40 (translocase of the outer mitochondrial membrane 40 homolog)--had a genome-w

65 elated protein 6), and TOM40 (translocase of outer mitochondrial membrane 40), for which antisense ex

66 ing system 60-kD subunit, the translocase of outer mitochondrial membrane 40-kD subunit (TOM40), the

67 chondrial Rho (Miro) GTPases localize to the outer mitochondrial membrane and are essential machinery

68 -2 proteins Bax and Bak can permeabilize the outer mitochondrial membrane and commit cells to apoptos

69 l (VDAC) is the most abundant protein in the outer mitochondrial membrane and constitutes the primary

70 Fis1 in yeast localizes to the outer mitochondrial membrane and facilitates mitochondri

71 EET is a homodimeric protein anchored to the outer mitochondrial membrane and has a C-terminal [2Fe-2

72 , ceramide formation might occur both in the outer mitochondrial membrane and in the mitochondrial ma

73 nal fragment tBid, which translocates to the outer mitochondrial membrane and induces massive cytochr

74 rrier protein that has been recruited to the outer mitochondrial membrane and interacts with the inne

75 that mitochondrial MRP-1 is expressed in the outer mitochondrial membrane and is a client protein of

76 that mitochondrial MRP-1 is expressed in the outer mitochondrial membrane and is a client protein of

77 the flux of metabolites and ions across the outer mitochondrial membrane and is a key player in cell

78 nthesis that is exclusively localized to the outer mitochondrial membrane and is composed of CYB5B, M

79 strate that ABCB6 is uniquely located in the outer mitochondrial membrane and is required for mitocho

80 This is dependent upon MAO anchoring to the outer mitochondrial membrane and shuttling electrons thr

81 t phospholipase A(2) promotes rupture of the outer mitochondrial membrane and spontaneous release of

82 lls, mitofusin 2 (Mfn2), located on both the outer mitochondrial membrane and the ER surface, has bee

83 VDACs) are the most abundant proteins in the outer mitochondrial membrane and the major transport pat

84 spans from the endoplasmic reticulum to the outer mitochondrial membrane and the matrix.

85 cular weight forms, is localized to both the outer mitochondrial membrane and the plasma membrane, an

86 teins are imported by the translocase of the outer mitochondrial membrane and the presequence translo

87 e A (PKA) and other signaling enzymes at the outer mitochondrial membrane and thereby controls mitoch

88 s from the mitochondria by clustering on the outer mitochondrial membrane and thereby permeabilizing

89 totic Bcl-2 protein Bax can permeabilize the outer mitochondrial membrane and therefore commit human

90 as the crucial anti-apoptotic protein in the outer mitochondrial membrane, and additionally as a gate

91 tant for cytosolic Bax to integrate into the outer mitochondrial membrane, and c-Myc is critical for

92 APEX was targeted to the outer mitochondrial membrane, and proximity-labeled prot

93 , differential localization to the inner and outer mitochondrial membranes appears to regulate PINK1

94 localized tail-anchored (TA) proteins of the outer mitochondrial membrane are cleared by a newly iden

95 and mechanisms of their transport across the outer mitochondrial membrane are well recognized.

96 These spherular invaginations of outer mitochondrial membranes are packed with electron-d

97 hat suggest that active BAX inserts into the outer mitochondrial membrane as a monomer and then under

98 Vesicles originate from the outer mitochondrial membrane as observed by tracking Tom

99 ndrial CCP activity because Ccp1 crosses the outer mitochondrial membrane as the heme-free protein.

100 -dependent RNA polymerase interacts with the outer mitochondrial membranes as an integral membrane pr

101 Whereas outer mitochondrial membrane-associated degradation is t

102 stead employs the archaic translocase of the outer mitochondrial membrane (ATOM), a protein that show

103 rotein termed the archaic translocase of the outer mitochondrial membrane (ATOM).

104 n of dAKAP1-PKA "signaling islands" from the outer mitochondrial membrane augments progression toward

105 , however the precise mechanism by which the outer mitochondrial membrane becomes permeable to these

106 LDH is likely localized inside the outer mitochondrial membrane, but not in the mitochondri

107 flets of the Golgi complex, peroxisomes, and outer mitochondrial membrane, but only detect very low s

108 increased the content of cardiolipin in the outer mitochondrial membrane, but the distribution of ot

109 e, we report that Bbeta2 is localized to the outer mitochondrial membrane by a novel mechanism, combi

110 e, demonstrating that it associates with the outer mitochondrial membrane by binding a protein partne

111 can directly induce permeabilization of the outer mitochondrial membrane by forming a inhibitory com

112 n, Drp1 is recruited from the cytosol to the outer mitochondrial membrane by one, or several, integra

113 Localization of MRP-1 to the outer mitochondrial membrane by the chaperone protein HS

114 wild-type cells, where it is detected on the outer mitochondrial membrane by virtue of its sensitivit

115 n of a protein complex that assembles at the outer mitochondrial membrane called the transduceosome.

116 sure of VDAC leads to the opening of another outer mitochondrial membrane channel through which cytoc

117 Dissociation of the outer mitochondrial membrane compartment from that of th

118 e show that exclusive delivery of p53 to the outer mitochondrial membrane confers a significant growt

119 sol and its C-terminal TMD inserted into the outer mitochondrial membrane, consistent with a tail-anc

120 Here, we show that purified rat liver outer mitochondrial membrane contains high amidoxime red

121 ese findings support the hypothesis that the outer mitochondrial membrane contains receptors specific

122 An increase in the permeability of the outer mitochondrial membrane, controlled by BCL-2 family

123 onformational plasticity in ferric rat liver outer mitochondrial membrane cytochrome b5 (rOM b5) and

124 tochondrial permeability transition, whereas outer mitochondrial membrane damage can occur independen

125 injury during endotoxemia and that inner and outer mitochondrial membrane damage occurs through diffe

126 ay participate in lipopolysaccharide-induced outer mitochondrial membrane damage, but further investi

127 ion of Mcl-1L, which localizes mainly to the outer mitochondrial membrane, decreases significantly in

128 ic mutant stably interacts with Mdv1p on the outer mitochondrial membrane, demonstrating that assembl

129 Rerouting this inhibitor to the outer mitochondrial membrane diminishes its ability to b

130 lin B1 is required for the regulation of the outer mitochondrial membrane dynamics.

131 PINK1 that fails to accumulate at the outer mitochondrial membrane, either by mutagenesis of t

132 terparts that face the cytosolic side of the outer mitochondrial membrane/endoplasmic reticulum (ER).

133 carnitine palmitoyltransferase-1 (CPT1), an outer mitochondrial membrane enzyme that controls entry

134 ot detectably cleaved and is retained at the outer mitochondrial membrane, even though it interacts w

135 ndria in association with both the inner and outer mitochondrial membranes facing the intermembrane s

136 ay crystal structure of the first identified outer mitochondrial membrane Fe-S protein, mitoNEET.

137 dases (MAO) A and B are approximately 60-kDa outer mitochondrial membrane flavoenzymes catalyzing the

138 M7 as essential for stabilizing PINK1 on the outer mitochondrial membrane following mitochondrial dam

139 d 2 that mediate mitochondrial tethering and outer mitochondrial membrane fusion, were interrupted by

140 y regulates Mitofusin, which is required for outer mitochondrial membrane fusion.

141 The outer mitochondrial membrane GTPase mitofusin 2 (Mfn2) i

142 nd fusion machinery via interaction with the outer mitochondrial membrane GTPase proteins Miro1 and M

143 ncrease in mitofusin 2 (MFN2) expression, an outer mitochondrial membrane GTPase.

144 sion requires division of both the inner and outer mitochondrial membranes (IMM and OMM, respectively

145 ports cellular mitochondrial proteins to the outer mitochondrial membrane import receptors, and thus

146 s argue in favor of eNOS localization to the outer mitochondrial membrane in endothelial cells and id

147 late the permeability characteristics of the outer mitochondrial membrane in their nonoligomerized st

148 on, both of which are known to reside at the outer mitochondrial membrane, increases the mitochondria

149 s deposited onto the cytoplasmic face of the outer mitochondrial membrane, increasing antigenic acces

150 irus (FHV) RNA replication complexes form on outer mitochondrial membranes inside approximately 50-nm

151 d with respect to their roles in controlling outer mitochondrial membrane integrity and apoptosis.

152 Permeabilization of the outer mitochondrial membrane is an integral step in apop

153 transmembrane protein primarily found in the outer mitochondrial membrane, is evolutionarily conserve

154 The outer mitochondrial membrane isoform of mammalian cytoch

155 The outer mitochondrial membrane isoform of mammalian cytoch

156 mides can form large, stable channels in the outer mitochondrial membrane, leading to the proposal th

157 o and phosphorylation of Sab by p-JNK on the outer mitochondrial membrane leads to SHP1-dependent and

158 Tim23 tightly associates with both inner and outer mitochondrial membrane-like membranes through a hy

159 The outer mitochondrial membrane localization of MondoA sugg

160 ational boost by the MDI-Larp complex on the outer mitochondrial membrane might be essential for mtDN

161 t that the specific lipid composition of the outer mitochondrial membrane might be of crucial relevan

162 somal GPAT) and an NEM-resistant form in the outer mitochondrial membrane (mtGPAT).

163 ssion are mediated by several GTPases in the outer mitochondrial membrane, notably mitofusin-2 (Mfn-2

164 ed and identified endogenous proteins on the outer mitochondrial membrane (OMM) and endoplasmic retic

165 taVD mutants constitutively localized to the outer mitochondrial membrane (OMM) and fragmented mitoch

166 lly into the endoplasmic reticulum (ER), the outer mitochondrial membrane (OMM) and peroxisomes.

167 ontaneous Ca(2+) pacing, Ca(2+) peaks on the outer mitochondrial membrane (OMM) are much greater than

168 active caspase 8 are localized mainly on the outer mitochondrial membrane (OMM) as integral proteins.

169 been studied in their detergent-purified and outer mitochondrial membrane (OMM) bound forms using a s

170 StAR acts exclusively on the outer mitochondrial membrane (OMM) by unknown mechanisms

171 Both proteins were enriched in the IMM-outer mitochondrial membrane (OMM) contact point submito

172 lular lifespan is contingent upon preserving outer mitochondrial membrane (OMM) integrity, as permeab

173 The outer mitochondrial membrane (OMM) is the last barrier b

174 The outer mitochondrial membrane (OMM) is thought to play a

175 , but not by Bcl-2, implying that changes in outer mitochondrial membrane (OMM) permeability leading

176 However, the mechanism of outer mitochondrial membrane (OMM) permeabilization rema

177 Here, we demonstrate that Miro1, an outer mitochondrial membrane (OMM) protein crucial for t

178 ripheral-type benzodiazepine receptor, is an outer mitochondrial membrane (OMM) protein necessary for

179 Parkin-mediated polyubiquitination of outer mitochondrial membrane (OMM) proteins recruits the

180 ax and Bak spontaneously associated with the outer mitochondrial membrane (OMM) through their respect

181 StAR acts on the outer mitochondrial membrane (OMM) to facilitate movemen

182 a mitochondrial matrix protein, acts on the outer mitochondrial membrane (OMM) to facilitate the mov

183 show that IkappaBalpha also localises to the outer mitochondrial membrane (OMM) to inhibit apoptosis.

184 roapoptotic BCL-2 proteins converge upon the outer mitochondrial membrane (OMM) to promote mitochondr

185 increasing the flow of cholesterol from the outer mitochondrial membrane (OMM) to the inner membrane

186 nels (VDACs) are predominant proteins of the outer mitochondrial membrane (OMM) where they contribute

187 ansferase 1 (CPT1), which is anchored in the outer mitochondrial membrane (OMM), controls the rate-li

188 chondrion-associated membranes (MAMs) to the outer mitochondrial membrane (OMM), where it robustly in

189 oscopy showed that Tom22 is localized at the outer mitochondrial membrane (OMM), while 3betaHSD2 is l

190 Ubiquitin- and proteasome-dependent outer mitochondrial membrane (OMM)-associated degradatio

191 ome system in the regulation and turnover of outer mitochondrial membrane (OMM)-associated proteins.

192 and degrades TA proteins mistargeted to the outer mitochondrial membrane (OMM).

193 inhibit Bax-mediated permeabilization of the outer mitochondrial membrane (OMM).

194 effects in both the mitochondrial matrix and outer mitochondrial membrane (OMM).

195 tosolic and mitochondrial factors across the outer mitochondrial membrane (OMM).

196 m the ER to mitochondria and clusters at the outer mitochondrial membrane (OMM).

197 Because outer-mitochondrial membrane (OMM) constituents insert d

198 Here, we report that mitoNEET regulates the outer-mitochondrial membrane (OMM) protein voltage-depen

199 Transmembrane beta-barrels of eukaryotic outer mitochondrial membranes (OMMs) are major channels

200 abolism in yeast by re-directing Psd1 to the outer mitochondrial membrane or the endomembrane system

201 KC isoforms that were tethered either to the outer mitochondrial membrane or to the PM.

202 SFV was not significantly different from the outer mitochondrial membrane (P < 0.05).

203 robustly induced by PINK1 expression on the outer mitochondrial membrane, Parkin recruitment to mito

204 Loss of Bax/Bak reduced outer mitochondrial membrane permeability and conductanc

205 n vitro models of lipotoxicity, we show that outer mitochondrial membrane permeability is altered and

206 ell death that is not initiated by increased outer mitochondrial membrane permeability or translocati

207 the BH1,2,3 effector protein Bak, leading to outer mitochondrial membrane permeabilization (OMMP) wit

208 SK3-mediated phosphorylation status controls outer mitochondrial membrane permeabilization in hepatos

209 e as Bax coalescence on the mitochondria and outer mitochondrial membrane permeabilization, and it ma

210 proapoptotic factors and thereby regulating outer mitochondrial membrane permeabilization.

211 regulator) can commit cells to apoptosis via outer mitochondrial membrane permeabilization.

212 The tail-anchor of an outer mitochondrial membrane protein also labels autopha

213 MitoNEET is an outer mitochondrial membrane protein essential for sensi

214 of mitochondria prior to engulfment, and the outer mitochondrial membrane protein FUNDC1 interacts wi

215 iazepine receptor (PBR), is a crucial 18-kDa outer mitochondrial membrane protein involved in numerou

216 likely by influencing protein levels of the outer mitochondrial membrane protein Miro that anchors m

217 nt of kinesin-1 to mitochondria involves the outer mitochondrial membrane protein mitochondrial Rho G

218 The outer mitochondrial membrane protein mitochondrial Rho G

219 The outer mitochondrial membrane protein mitoNEET was discov

220 pioglitazone led to the discovery of a novel outer mitochondrial membrane protein of unknown function

221 Miro is an outer mitochondrial membrane protein that anchors mitoch

222 MitoNEET is a 2Fe-2S outer mitochondrial membrane protein that was initially

223 MitoNEET is an outer mitochondrial membrane protein that, upon overexpr

224 The outer mitochondrial membrane protein voltage-dependent a

225 gosomes and is sufficient to deliver another outer mitochondrial membrane protein, Fis1, to autophago

226 ong form of B-cell lymphoma-x (Bcl-x(L)), an outer mitochondrial membrane protein, has been proposed

227 Here we show that VAPB interacts with the outer mitochondrial membrane protein, protein tyrosine p

228 we utilized a cell-permeable peptide of the outer mitochondrial membrane protein, Sab (SH3BP5), as a

229 The outer mitochondrial membrane protein, the voltage-depend

230 its recently identified paralog mitoNEET, an outer mitochondrial membrane protein.

231 h is inhibited by yeast Fis1, a pore-forming outer mitochondrial membrane protein.

232 -dependent anion channel (VDAC), an abundant outer mitochondrial membrane protein.

233 Miro; encoded by YAL048C) is a tail-anchored outer mitochondrial membrane protein.

234 Mitofusins (Mfn1 and Mfn2) are outer mitochondrial membrane proteins involved in regula

235 hich is, in turn, known to interact with the outer mitochondrial membrane proteins Miro1/2, linking m

236 Then, Parkin ubiquitinates outer mitochondrial membrane proteins to trigger selecti

237 ligase activity is required to ubiquitinate outer mitochondrial membrane proteins, allowing optineur

238 olarized mitochondria where it ubiquitinates outer mitochondrial membrane proteins, initiating lysoso

239 o not regulate PTP activity through TSPO, 3) outer mitochondrial membrane regulation of PTP activity

240 /killer (Bak) undergo oligomerization in the outer mitochondrial membrane resulting in the release of

241 A damage-induced p53/Bcl2 interaction at the outer mitochondrial membrane results in a Bcl2 conformat

242 f these and other signaling molecules to the outer mitochondrial membrane results in the rapid induct

243 otein A recruits FHV RNA specifically to the outer mitochondrial membrane sites of RNA replication co

244 copy imaging method to observe the inner and outer mitochondrial membrane structures and selectively

245 Its localization to the outer mitochondrial membrane suggests an important yet u

246 tes histidine-tagged peptides to a simulated outer mitochondrial membrane surface.

247 MitoNEET (mNT) is an outer mitochondrial membrane target of the thiazolidined

248 2-associated X apoptosis regulator (BAX), an outer mitochondrial membrane-targeting pro-apoptotic pro

249 mbles into large multimeric complexes on the outer mitochondrial membrane that are visualized as punc

250 ndent proteins take another route across the outer mitochondrial membrane that involves Tom40 in a fo

251 e formation of a multivalent scaffold in the outer mitochondrial membrane that mediates the effect of

252 A and B (MAO-A and MAO-B) are enzymes of the outer mitochondrial membrane that metabolize biogenic am

253 dase A (MAO-A) is an important enzyme on the outer mitochondrial membrane that participates in the ce

254 een Bcl2 and c-Myc in the nucleus and on the outer mitochondrial membrane that significantly enhances

255 el 1 (VDAC-1) is an important protein of the outer mitochondrial membrane that transports energy meta

256 ppress tumor formation by permeabilizing the outer mitochondrial membrane, thereby releasing pro-apop

257 ne protein that forms an aqueous pore in the outer mitochondrial membrane, through which metabolites

258 AKAP1 recruits protein kinase A (PKA) to the outer mitochondrial membrane to phospho-inhibit DRP1.

259 eroidogenesis by moving cholesterol from the outer mitochondrial membrane to the inner mitochondrial

260 litates the movement of cholesterol from the outer mitochondrial membrane to the inner mitochondrial

261 However, an abnormal permeability of outer mitochondrial membranes to cytochrome c was observ

262 Self-interacting BAX proteins permeabilize outer mitochondrial membranes to trigger apoptotic cell

263 Although the translocase of the outer mitochondrial membrane (TOM) complex proteins Tom2

264 a central component of the translocon of the outer mitochondrial membrane (TOM) complex, is essential

265 The preprotein translocase of the outer mitochondrial membrane (TOM) functions as the main

266 rmore, Tim29 contacts the Translocase of the Outer Mitochondrial Membrane, TOM complex, enabling a me

267 The translocase of outer mitochondrial membrane (TOMM) complex is the entry

268 ing the interaction of MAM proteins with the outer mitochondrial membrane translocase, Tom22, to acti

269 ropose that 3betaHSD2 associates with IMM or outer mitochondrial membrane translocases facing the int

270 omolecular signaling complex composed of the outer mitochondrial membrane translocator protein (TSPO)

271 s suggests that GSK inhibitors are acting on outer mitochondrial membrane transport.

272 Targeting Rab35 to the outer mitochondrial membrane triggered actin recruitment

273 annels: voltage-dependent anion channel from outer mitochondrial membrane VDAC, bacterial porin OmpC

274 K II) that is overexpressed and bound to the outer mitochondrial membrane via the porin-like protein

275 ter and the mean distance between SR and the outer mitochondrial membrane vs. CD hearts.

276 ix, and formation of vesicles and tubules of outer mitochondrial membrane, was also observed in both

277 StAR acts on the outer mitochondrial membrane where each molecule stimula

278 ependent monooxygenase and is located in the outer mitochondrial membrane where it converts l-kynuren

279 -Ras off of the plasma membrane and onto the outer mitochondrial membrane where it induces cell death

280 punctate structures that are targeted to the outer mitochondrial membrane where they mediate mitochon

281 ia an N-terminal transmembrane domain to the outer mitochondrial membrane, where FHV RNA replication

282 cumulates as a 63-kD full-length form on the outer mitochondrial membrane, where it can recruit Parki

283 mic BAX is activated and translocates to the outer mitochondrial membrane, where it forms an oligomer

284 BNip3 localizes to the outer mitochondrial membrane, where it functions in mito

285 Mammalian Bcl-x(L) protein localizes to the outer mitochondrial membrane, where it inhibits apoptosi

286 ine phosphoprotein (FAST) is tethered to the outer mitochondrial membrane, where it interacts with BC

287 l MRP-1 is glycosylated and localized to the outer mitochondrial membrane, where it is coexpressed wi

288 rved eukaryotic AAA+ ATPase localized to the outer mitochondrial membrane, where it is thought to ext

289 nserved, ubiquitous protein localized in the outer mitochondrial membrane, where it is thought to pla

290 T-treated BL-3 cells revealed lesions in the outer mitochondrial membrane, which are larger than prev

291 ized by the rapid accumulation of BIM on the outer mitochondrial membrane, which could be functionall

292 monstrate that its apoptotic activity at the outer mitochondrial membrane, which involves conformatio

293 we showed that internalized LKT binds to the outer mitochondrial membrane, which results in the relea

294 rgeting induced ceramide accumulation on the outer mitochondrial membrane, which then directly bound

295 ia demonstrated that ABCB6 is present in the outer mitochondrial membrane, while back-titration assay

296 ed inside a 30- to 90-nm invagination of the outer mitochondrial membrane, whose necked aperture to t

297 nctional E3 ubiquitin ligase anchored in the outer mitochondrial membrane with its RING finger domain

298 ng in dissociation of hexokinase II from the outer mitochondrial membrane with subsequent mitochondri

299 modimeric iron-sulfur protein located in the outer mitochondrial membrane with unknown function, but

300 state, MondoA:Mlx complexes localize to the outer mitochondrial membrane, yet shuttle between the mi