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1 ng, recruits the other COPII proteins to the endoplasmic reticulum membrane.
2 equired for its translocation to the nuclear/endoplasmic reticulum membrane.
3 cognition particle-dependent transfer to the endoplasmic reticulum membrane.
4 y interacts with the hydrophobic core of the endoplasmic reticulum membrane.
5 characterized by solving its topology in the endoplasmic reticulum membrane.
6 phosphatase complex localized in the nuclear/endoplasmic reticulum membrane.
7 ptor (IP(3)R) Ca(2+) release channels in the endoplasmic reticulum membrane.
8 sponsible for lipid synthesis at the nuclear/endoplasmic reticulum membrane.
9 Sec61 translocon prior to insertion into the endoplasmic reticulum membrane.
10 xpansion, without proliferating the cortical endoplasmic reticulum membrane.
11 s that are organized in a complex within the endoplasmic reticulum membrane.
12 sufficient information for targeting to the endoplasmic reticulum membrane.
13 es synthesizing presecretory proteins to the endoplasmic reticulum membrane.
14 ghly enriched in the mitochondria-associated endoplasmic reticulum membrane.
15 the potential to affect interactions at the endoplasmic reticulum membrane.
16 quence of KvAP S4 can be inserted across the endoplasmic reticulum membrane.
17 omplex during their translocation across the endoplasmic reticulum membrane.
18 chaperones and enzymes on both sides of the endoplasmic reticulum membrane.
19 roper protein folding and/or assembly in the endoplasmic reticulum membrane.
20 e boundary between a bud and the surrounding endoplasmic reticulum membrane.
21 talytic sites relative to the surface of the endoplasmic reticulum membrane.
22 binding and peptide translocation across the endoplasmic reticulum membrane.
23 ing the translocation and integration at the endoplasmic reticulum membrane.
24 predicted to be on the cytosolic side of the endoplasmic reticulum membrane.
25 equired for peptide translocation across the endoplasmic reticulum membrane.
26 its (Ost3p and Stt3p) in a subcomplex in the endoplasmic reticulum membrane.
27 f the nascent lipoprotein particles from the endoplasmic reticulum membrane.
28 -translational insertion through or into the endoplasmic reticulum membrane.
29 ufficient to prevent ribosome binding to the endoplasmic reticulum membrane.
30 in targeting to and translocation across the endoplasmic reticulum membrane.
31 of single type 1 InsP(3)R channels in native endoplasmic reticulum membrane.
32 easomes following their dislocation from the endoplasmic reticulum membrane.
33 anslational protein translocation across the endoplasmic reticulum membrane.
34 before precursor protein transfer across the endoplasmic reticulum membrane.
35 vement of misfolded polypeptides through the endoplasmic reticulum membrane.
36 ytoplasm, where some are associated with the endoplasmic reticulum membrane.
37 in the translocation of proteins across the endoplasmic reticulum membrane.
38 cretory proteins are translocated across the endoplasmic reticulum membrane.
39 wo alternate transmembrane structures at the endoplasmic reticulum membrane.
40 tionally to the Sec61 complex present in the endoplasmic reticulum membrane.
41 probably exists on the cytosolic face of the endoplasmic reticulum membrane.
42 component of the VKOR enzyme complex in the endoplasmic reticulum membrane.
43 te targeting to and translocation across the endoplasmic reticulum membrane.
44 f the protein translocation apparatus of the endoplasmic reticulum membrane.
45 osome-nascent chain complex, the SRP and the endoplasmic reticulum membrane.
46 e E1 proteins most likely takes place in the endoplasmic reticulum membrane.
47 at viperin, LS, and SM form a complex at the endoplasmic reticulum membrane.
48 al rather than integral association with the endoplasmic reticulum membrane.
49 with a bias towards the lumenal side of the endoplasmic reticulum membrane.
50 n of phosphatidylinositol-4-phosphate at the endoplasmic reticulum membrane.
51 ronment to transfer an acyl chain across the endoplasmic reticulum membrane.
52 es and thereby activates Pah1 at the nuclear/endoplasmic reticulum membrane.
53 the adaptor protein STING on the surface of endoplasmic reticulum membrane.
54 main are segregated on opposite sides of the endoplasmic reticulum membrane.
55 eins to the Sec61 protein translocase in the endoplasmic reticulum membrane.
56 is and Asp residues on opposite sides of the endoplasmic reticulum membrane.
57 n nuclear deformation and a proliferation of endoplasmic reticulum membrane.
58 al cytoplasmic membrane or to the eukaryotic endoplasmic reticulum membrane.
59 tial lipid transporter that localizes to the endoplasmic reticulum membrane.
60 ting a phase transition in the lipids of the endoplasmic reticulum membrane.
61 protein, transfer it, and insert it into the endoplasmic reticulum membrane.
62 endoplasmic reticulum or is retained in the endoplasmic reticulum membrane.
63 membrane-domain-docking site embedded in the endoplasmic-reticulum membrane.
64 cytochrome P450 reductase (CPR) in mammalian endoplasmic reticulum membranes.
65 a membrane fraction with characteristics of endoplasmic reticulum membranes.
66 ouse MCs and is localized to the nuclear and endoplasmic reticulum membranes.
67 trol of the permeability of mitochondria and endoplasmic reticulum membranes.
68 proteins on cisternal and protein body rough endoplasmic reticulum membranes.
69 mmunication between events in the plasma and endoplasmic reticulum membranes.
70 tar is located in the nuclear and contiguous endoplasmic reticulum membranes.
71 hin cells, possibly by binding components in endoplasmic reticulum membranes.
72 o the outer mitochondrial, outer nuclear and endoplasmic reticulum membranes.
73 g in vitro insertion of fusion proteins into endoplasmic reticulum membranes.
74 the cell cycle progression and the fusion of endoplasmic reticulum membranes.
75 e distribution of IP(3)R type 1 (IP(3)R1) in endoplasmic reticulum membranes.
76 hreshold previously found for PFO binding to endoplasmic reticulum membranes.
77 rather attaches the protein peripherally to endoplasmic reticulum membranes.
78 d, 26 S proteasome-mediated degradation from endoplasmic reticulum membranes, a reaction that slows a
79 ding proteins (SREBPs) are released from the endoplasmic reticulum membrane, allowing them to translo
80 ls are low, the SREBPs are released from the endoplasmic reticulum membrane, allowing them to translo
81 proteins with the translocon complex of the endoplasmic reticulum membrane and are cleaved off durin
82 secretory vesicles, Golgi, mitochondria, and endoplasmic reticulum membrane and associates with the m
83 ining genes by tethering Opi1 to the nuclear/endoplasmic reticulum membrane and controlling its trans
84 PM8), which is localized in the keratinocyte endoplasmic reticulum membrane and controls mitochondria
85 of integral membrane proteins located in the endoplasmic reticulum membrane and includes the gamma-ca
87 nt-shaped membranes were continuous with the endoplasmic reticulum membrane and oriented with the con
88 ures Ca2+ release from discrete sites in the endoplasmic reticulum membrane and random spatial distri
89 importin-alpha-16 after integration into the endoplasmic reticulum membrane and release from the tran
90 ocation of class I MHC heavy chains from the endoplasmic reticulum membrane and target them for prote
91 uggest that Nrf1 is normally targeted to the endoplasmic reticulum membrane and that endoplasmic reti
93 antibodies that faithfully recognized rough endoplasmic reticulum membranes and amyloid fibrils, the
95 Like MP:GFP, TAD5:GFP interacted with the endoplasmic reticulum membranes and colocalized with its
96 signal recognition particle was bound to the endoplasmic reticulum membranes and less was in the free
97 lular localizations, with rsec22 residing on endoplasmic reticulum membranes and rbet1 found on Golgi
99 polypeptide being synthesized, binds to the endoplasmic reticulum membrane, and even nonsecretory pr
100 ptides, transport of the peptides across the endoplasmic reticulum membrane, and expression of the MH
101 ane-bound ribosomes, translocated across the endoplasmic reticulum membrane, and GPI-anchored by GPI
102 ane phospholipids, the growth of the nuclear/endoplasmic reticulum membrane, and the formation of lip
103 al domain not shared by M87, may insert into endoplasmic reticulum membrane, and together with reticu
104 n to cause extensive remodeling of Golgi and endoplasmic reticulum membranes, and a number of the hos
105 stribution from cytosol to mitochondrial and endoplasmic reticulum membranes, and caspase-independent
106 1a accumulation, localization to perinuclear endoplasmic reticulum membranes, and recruitment of 2a(p
107 le Bcl-2 is located in the mitochondrial and endoplasmic reticulum membranes as well as the nuclear e
108 opose that this NPL4 function extends to all endoplasmic reticulum-membrane-associated targets of the
109 ngle-domain b5 and b5R proteins localized on endoplasmic reticulum membrane, b5+b5R also has binding
110 is thought to contact the lipid core of the endoplasmic reticulum membrane based on antibody epitope
111 pro-alpha-factor (ppalphaF) across the yeast endoplasmic reticulum membrane begins with the binding o
112 very high levels in developing endosperm in endoplasmic reticulum membrane-bound protein bodies.
113 o target the proteasome to the ubiquitinated endoplasmic reticulum membrane-bound proteins Mga2p and
115 ol regulatory element binding protein, is an endoplasmic reticulum membrane-bound transcription facto
116 o synthesize N-glycan precursors) across the endoplasmic reticulum membrane, but subsequent studies s
117 , are inserted post-translationally into the endoplasmic reticulum membrane by a dedicated protein-ta
118 Cytochromes P450 (P450) are anchored to the endoplasmic reticulum membrane by an N-terminal transmem
121 complex that directs ribosomes to the rough endoplasmic reticulum membrane by binding to targeting s
122 ne-bound protein that was removable from the endoplasmic reticulum membrane by chaotropic salt wash,
124 us, are post-translationally targeted to the endoplasmic reticulum membrane by the guided entry of TA
125 -binding proteins (SREBPs) are released from endoplasmic reticulum membranes by proteases whose activ
126 terminal domains of SREBPs are released from endoplasmic reticulum membranes by two sequential cleava
128 ol 1,4,5-trisphosphate (IP(3)) receptors are endoplasmic reticulum membrane calcium channels that, up
130 Although particle assembly takes place on endoplasmic reticulum membranes, capsid localizes in nuc
131 -dependent carboxylase, a constituent of the endoplasmic reticulum membrane, catalyzes the conversion
134 cells and in cells depleted for adaptin-3 or endoplasmic reticulum membrane complex subunits, also id
137 ge PM clusters that represent specialized PM:endoplasmic reticulum membrane contact sites (PM:ER MCS)
138 of a number of proteins from the plasma and endoplasmic reticulum membranes control SOCE to replenis
141 this fusion protein gives rise to a type of endoplasmic reticulum membrane domain in which adjacent
143 receptor (InsP(3)R) targeting to specialized endoplasmic reticulum membrane domains are unknown.
145 clathrin-mediated endocytosis, vimentin, the endoplasmic reticulum, membrane dynamics, and Natural Ki
146 O-mannosyltransferases (PMTs) are conserved endoplasmic reticulum membrane-embedded enzymes responsi
147 is the core structural component of a large endoplasmic reticulum membrane-embedded protein complex
148 lin-induced gene 1 (Insig-1) and Insig-2 are endoplasmic reticulum membrane-embedded sterol sensors t
149 the NE in both these circumstances involves endoplasmic reticulum membranes enveloping the chromatin
150 n the outer mitochondrial membrane (OMM) and endoplasmic reticulum membrane (ERM) of living human fib
151 es, such as temperature sensitivity, nuclear/endoplasmic reticulum membrane expansion, decreased tria
152 sensitivity, respiratory deficiency, nuclear/endoplasmic reticulum membrane expansion, derepression o
153 h1Delta mutant did not result in the nuclear/endoplasmic reticulum membrane expansion, which occurs i
155 equired for protein translocation across the endoplasmic reticulum membrane following translation.
156 lved in the transport of peptides across the endoplasmic reticulum membrane for antigen presentation,
157 transporters, transports peptides across the endoplasmic reticulum membrane for assembly of major his
158 rokaryotic plasma membrane or the eukaryotic endoplasmic reticulum membrane for secretion or membrane
159 ah1 phosphatidate phosphatase at the nuclear-endoplasmic reticulum membrane for the synthesis of tria
162 suppression of SREBP activation, we isolated endoplasmic reticulum membrane fractions from long-term
164 se Atlastin has recently been shown to drive endoplasmic reticulum membrane fusion and three-way junc
165 e ABCF3-OAS1B complex to the virus-remodeled endoplasmic reticulum membrane has been shown before.
168 AP translocates cellular peptides across the endoplasmic reticulum membrane in an ATP hydrolysis-depe
170 eceptor to the protein-conducting channel on endoplasmic reticulum membrane in eukaryotes or plasma m
172 We assessed N tail translocation across the endoplasmic reticulum membrane in the presence and absen
175 labeling at the cytosolic side of the rough endoplasmic reticulum membranes, in the nucleus, occasio
176 er immobilization through association to the endoplasmic reticulum membrane, initial proximity betwee
177 t chain complexes to the SRP receptor in the endoplasmic reticulum membrane, initiating translocation
178 ral domains from the late proteins supported endoplasmic reticulum membrane insertion as transmembran
179 f cholera toxin retrotranslocates across the endoplasmic reticulum membrane into the cytosol, where i
180 ional targeting of secretory proteins to the endoplasmic reticulum membrane involves the recognition
181 tween ribosomes and the pore proteins at the endoplasmic reticulum membrane is important to co-transl
182 protein in that its translocation across the endoplasmic reticulum membrane is inefficient, resulting
183 Anchoring of this protein segment to the endoplasmic reticulum membrane is likely to bring the me
185 Ralpha, suggesting that dislocation from the endoplasmic reticulum membrane is the rate-limiting step
186 The topography of the PS molecule in the endoplasmic reticulum membrane is widely accepted as exh
188 ed that ECA1p was associated mainly with the endoplasmic reticulum membranes isolated from Arabidopsi
189 protein phosphatase required for the nuclear/endoplasmic reticulum membrane localization of Pah1, a p
190 Stromal Interaction Molecule1 (STIM1) is an endoplasmic reticulum membrane-localized calcium (Ca(2+)
191 ATPase SERCA2b transports Ca(2+) across the endoplasmic reticulum membrane maintaining a vital Ca(2+
192 nel 2 (VDAC2) at the mitochondria-associated endoplasmic reticulum membrane (MAM) prior to its transl
193 e and dynamics, with mitochondria-associated endoplasmic reticulum membranes (MAMs) serving as the pl
195 ses fluorescently tagged nuclear envelope or endoplasmic reticulum membrane marker proteins to precis
196 ated in the plant cytoplasm, associated with endoplasmic reticulum membranes; medicarpin biosynthetic
197 thylmaleimide (NEM)-sensitive isoform in the endoplasmic reticulum membrane (microsomal GPAT) and an
198 uding chromosome, cytoplasmic, cytoskeleton, endoplasmic reticulum, membrane, mitochondrion, and nucl
199 id droplet formation, maintenance of nuclear/endoplasmic reticulum membrane morphology, and cell grow
200 ah1Delta effects on lipid synthesis, nuclear/endoplasmic reticulum membrane morphology, and lipid dro
201 synthesis, lipid droplet formation, nuclear/endoplasmic reticulum membrane morphology, vacuole fusio
202 ns is prevented by chaperones present in the endoplasmic reticulum membrane; now the first experiment
203 on of SRP-dependent targeting of RNCs to the endoplasmic reticulum membrane observed with long nascen
205 -helical membrane proteins directly into the endoplasmic reticulum membrane of eukaryotes or into the
207 anslational protein translocation across the endoplasmic reticulum membrane of yeast requires a seven
208 IP(3)) receptors form tetrameric channels in endoplasmic reticulum membranes of mammalian cells and m
209 osophila RyR and GFP-Drosophila RyR-C on the endoplasmic reticulum membranes of transfected cells.
210 provide essential lipid modifications in the endoplasmic reticulum membrane or function as molecular
211 ation of many proteins across the eukaryotic endoplasmic reticulum membrane or the prokaryotic plasma
212 complete translocation across the eukaryotic endoplasmic reticulum membrane or the prokaryotic plasma
213 n-conducting Sec61 channel in the eukaryotic endoplasmic reticulum membrane or the SecY channel in th
214 For its catalytic function on the nuclear/endoplasmic reticulum membrane, Pah1 translocates to the
215 d fatty acids at concentrations that lead to endoplasmic reticulum membrane phospholipid remodeling i
216 osphatidate to produce diacylglycerol at the endoplasmic reticulum membrane, plays a major role in co
217 elix of GTP-bound Sar1 stably penetrates the endoplasmic reticulum membrane, promoting local membrane
219 2 bound with Ca(V)beta(3) to a chaperone-the endoplasmic reticulum membrane protein complex (EMC)(8,9
220 These proteins are components of the human endoplasmic reticulum membrane protein complex (EMC), wh
221 oorly characterized secreted protein, EMC10 (endoplasmic reticulum membrane protein complex subunit 1
222 A mutation in the largest subunit of the endoplasmic reticulum membrane protein complex, emc1 was
223 own as seipin) is a lipodystrophy-associated endoplasmic reticulum membrane protein essential for whi
224 own as Emopamil-Binding Protein (EBP), is an endoplasmic reticulum membrane protein involved in chole
225 tion indicated that MoPhzF recruits both the endoplasmic reticulum membrane protein MoEmc2 and the re
227 processing is Ste24p/Afc1p, a multispanning endoplasmic reticulum membrane protein that contains an
228 s previously determined interaction with the endoplasmic reticulum membrane protein VAP-A (vesicle-as
234 ween co-translational and post-translational endoplasmic-reticulum membrane protein targeting and ins
236 nding of the membrane domain of reductase to endoplasmic reticulum membrane proteins called Insig-1 a
238 epresent a conserved family of multispanning endoplasmic reticulum membrane proteins involved in glyc
239 he founding member of a homologous family of endoplasmic reticulum membrane proteins present in all e
241 (IP(3)Rs) are large, ubiquitously expressed, endoplasmic reticulum membrane proteins that form tetram
243 identified Lam/GramD1 proteins, a family of endoplasmic reticulum membrane proteins with sterol-bind
245 inal proteolytic fragments of two homologous endoplasmic reticulum membrane proteins, Spt23p and Mga2
249 ping and helicase-like domains, localizes to endoplasmic reticulum membranes, recruits BMV 2a polymer
250 otypes, such as the expansion of the nuclear/endoplasmic reticulum membrane, reduced lipid droplet fo
251 onsible, with the major pool of STIM1 in the endoplasmic reticulum membrane regulating CRAC channel a
253 It is proposed that formation of VKOR in the endoplasmic reticulum membrane resembles formation of th
254 veal that DEGS1 is a mitochondria-associated endoplasmic reticulum membrane-resident (MAM-resident) e
255 tly hydroxylated to benzyl salicylate by the endoplasmic reticulum membrane-resident cytochrome P450
256 -dependent gamma-carboxylation system in the endoplasmic reticulum membrane responsible for gamma-car
257 unexpected link between perturbation of the endoplasmic reticulum membrane's lipid phase, induction
258 doplasmic reticulum, and sitosterol-enriched endoplasmic reticulum membranes show evidence of membran
259 x that dephosphorylates Pah1p at the nuclear/endoplasmic reticulum membrane, stabilized Pah1p abundan
264 controls an aspect of MPD orientation in the endoplasmic reticulum membrane that is crucial for its a
265 fied a region integrally associated with the endoplasmic reticulum membrane that is likely to interac
266 ex forms a protein-conducting channel in the endoplasmic reticulum membrane that is required for secr
267 SEC63 encodes a resident protein in the endoplasmic reticulum membrane that, when mutated, cause
268 thesizing machinery associates with modified endoplasmic reticulum membranes that are transformed int
269 ors form tetrameric, IP(3)-gated channels in endoplasmic reticulum membranes that govern the release
270 ght protein translocation defects across the endoplasmic reticulum membrane, the principal role of th
272 ain interactions in translocation across the endoplasmic reticulum membrane, the translocation of wil
273 al integration of a nascent protein into the endoplasmic reticulum membrane, the transmembrane (TM) s
274 rotein substrates are transported across the endoplasmic reticulum membrane through a translocation c
275 eins is established cotranslationally at the endoplasmic reticulum membrane through the action of alt
276 ts are properly targeted and oriented in the endoplasmic reticulum membrane, thus making them amenabl
277 olic enzyme that associates with the nuclear/endoplasmic reticulum membrane to catalyze the dephospho
278 des in the cytoplasm and translocates to the endoplasmic reticulum membrane to catalyze the phosphati
279 ulum where they retro-translocate across the endoplasmic reticulum membrane to enter the cytoplasm.
280 CP)/p97 extracts misfolded subunits from the endoplasmic reticulum membrane to the cytosolic proteaso
281 transduction of the ethylene signal from the endoplasmic reticulum membrane to the nucleus, where its
283 the vehicles of protein transport across the endoplasmic reticulum membrane), transmembrane segments,
285 cytosolic organelles that protrude from the endoplasmic reticulum membrane under energy-rich conditi
286 ide, a fraction of GRP94 associated with the endoplasmic reticulum membrane undergoes specific proteo
287 rminants that direct protein topology at the endoplasmic reticulum membrane usually function with hig
288 and is anchored to the cytosolic face of the endoplasmic reticulum membrane via a hydrophobic C-termi
291 toplasm apart from its substrate or with the endoplasmic reticulum membrane where its enzyme reaction
292 protein phosphatase Nem1-Spo7 at the nuclear/endoplasmic reticulum membrane where the PA phosphatase
293 ls emphasize the role of STIM located in the endoplasmic reticulum membrane, where a Ca2+-binding EF-
294 ons can be similar to those found within the endoplasmic reticulum membrane, where phase separation a
295 for activity on the cytoplasmic side of the endoplasmic reticulum membrane, whereas the analogous se
296 , and His-176 reside on the same side of the endoplasmic reticulum membrane, which is supported by th
298 es with the coating of specific areas of the endoplasmic reticulum membrane with Sar1-GTP and the Sec
299 We show that maMYB is associated with the endoplasmic reticulum membrane with the transcription fa
300 ytes resulted in an interspersion of nuclear/endoplasmic reticulum membranes with the chromatin.