ライフサイエンスコーパス: transmembrane protein

1 RFC is a multipass transmembrane protein.

2 in and AP-1 control the sorting of an apical transmembrane protein.

3 y inhibited by the anti-sigma factor RsiV, a transmembrane protein.

4 e formation and is mastered by p24, a type I transmembrane protein.

5 ve capacities, and cwr-2 encodes a predicted transmembrane protein.

6 to trigger budding, is synthesized as an ER transmembrane protein.

7 containing 7A (THSD7A), a podocyte-expressed transmembrane protein.

8 s amyloid protein precursor and other type I transmembrane proteins.

9 integrin ligands, lectins, and other type-1 transmembrane proteins.

10 otein Tom40 and four auxiliary alpha-helical transmembrane proteins.

11 S protein-driven entry by interferon-induced transmembrane proteins.

12 f CASP12 domains, and works just as well for transmembrane proteins.

13 r understanding clustering of other synaptic transmembrane proteins.

14 inked to retromer's role in the recycling of transmembrane proteins.

15 preference for acetylating N termini of the transmembrane proteins.

16 function of ion channels and other polytopic transmembrane proteins.

17 e further research on alloherpesvirus virion transmembrane proteins.

18 okines), extracellular matrix molecules, and transmembrane proteins.

19 improving detection of actively secreted and transmembrane proteins.

20 rse clients, from tail-anchored to polytopic transmembrane proteins.

21 internal vesicular transport of cortex-bound transmembrane proteins.

22 (Cn symmetry) found in most homo-oligomeric transmembrane proteins.

23 t themselves from potentially toxic aberrant transmembrane proteins.

24 the plasma membrane is interferon-inducible transmembrane protein 1 (IFITM1).

25 Transmembrane protein 107 (TMEM107) is localized in the

26 Transmembrane protein 16 (TMEM16) family members play nu

27 ation markers in vivo (e.g., aquaporin-5 and transmembrane protein 16).

28 +)/Ca(2+)/Mn(2+) exchanger known as TMEM165 (transmembrane protein 165) participates in normal milk p

29 n the gene encoding the human Golgi TMEM165 (transmembrane protein 165), belonging to UPF0016 (unchar

30 Transmembrane protein 16A (TMEM16A), also called anoctam

31 -) channel, anoctamin 1 (Ano1, also known as transmembrane protein 16A) contributes to intestinal pac

32 Transmembrane protein 16F (TMEM16F) is an enigmatic Ca(2

33 induced phosphatidylserine exposure through transmembrane protein 16F, a calcium-dependent phospholi

34 ease from macrophages and monocytes, whereas transmembrane protein 173-dependent TANK-binding kinase

35 Transmembrane protein 175 (TMEM175) is a K(+)-selective

36 Transmembrane protein 175 (TMEM175), the lysosomal K(+)

37 Here, we show that disruption of transmembrane protein 176B (TMEM176B) contributes to CD8

38 The present work identifies this gene as transmembrane protein 189 (TMEM189).

39 Fat storage-inducing transmembrane protein 2 (FIT2) aids in partitioning of c

40 Fat storage-inducing transmembrane protein 2 (FIT2) is less abundant in type

41 we determined that fibronectin leucine-rich transmembrane protein 2 (FLRT2), a repulsive ligand of t

42 Mutation of proline-rich transmembrane protein 2 (PRRT2), a regulator of neurotra

43 fied the cell-surface hyaluronidase (HAase), Transmembrane Protein 2 (TMEM2), as a potent modulator o

44 We also identified transmembrane protein 208 (TMEM208), a putative componen

45 uolar protein sorting 37 homolog A (VPS37A), transmembrane protein 251 (TMEM251), amyotrophic lateral

46 the antiviral restriction factor IFN-induced transmembrane protein 3 (IFITM3) are associated with sus

47 Here we identify interferon-induced transmembrane protein 3 (IFITM3) as a gamma-secretase mo

48 Interferon-induced transmembrane protein 3 (IFITM3) has previously been ide

49 The antiviral restriction factor IFN-induced transmembrane protein 3 (IFITM3) inhibits cell entry of

50 Interferon-induced transmembrane protein 3 (IFITM3) is a cellular endosome-

51 egulation and function of interferon-induced transmembrane protein 3 (IFITM3), an antiviral immune ef

52 Transmembrane protein 30A (TMEM30A) maintains the asymme

53 Here we show that transmembrane protein 33 (TMEM33) interacts with the ion

54 Here we show that transmembrane protein 33 (tmem33), which has no known fu

55 , and TMEM64 (VTT) domain-containing protein transmembrane protein 41B (TMEM41B) for infection by SAR

56 C5), caused by a p.S358L mutation in TMEM43 (transmembrane protein 43).

57 Transmembrane protein 67 (TMEM67) is mutated in Meckel G

58 Here, we report that transmembrane protein 74 (TMEM74), which contains two pu

59 re, coexpression of the viral reticulon-like transmembrane protein A17 and the capsid-like scaffold p

60 Two type-I transmembrane proteins, Ac45 and (pro)renin receptor, al

61 data, revealed an unanticipated strategy for transmembrane protein acylation with catalysis occurring

62 t droplets can harbor functional soluble and transmembrane proteins, allowing for the colocalization

63 ionic proteins, can alter the disposition of transmembrane proteins and causes the local accumulation

64 diated ER translocation to include multipass transmembrane proteins and suggest that TRPC6 N-glycosyl

65 ncrease stability and ion conductance of the transmembrane protein, and lysosomal localization was no

66 MEGF8, a transmembrane protein, and MGRN1, a RING superfamily E3

67 eases are involved in ectodomain cleavage of transmembrane proteins, and ADAM17 is known to cleave Ne

68 The large isoform of the transmembrane protein angiomotin (AMOT130) controls cell

69 viral restriction factor interferon-induced transmembrane protein are markedly higher in the prefron

70 Both of these single-pass transmembrane proteins are enriched in hair cells and un

71 Roughly 10% of eukaryotic transmembrane proteins are found on the nuclear membrane

72 at almost the entire populations of all four transmembrane proteins are immobilized by either the inc

73 ABSTRACT: Small transmembrane proteins are important for regulation of c

74 Transmembrane proteins are membrane-anchored proteins wh

75 ntified TMEM79/MATTRIN, an orphan multi-span transmembrane protein, as a specific inhibitor of Wnt/FZ

76 spectrometry to identify vezatin, a two-pass transmembrane protein, as an acetylcholine receptor (ACh

77 that most of these genes encode single-pass transmembrane proteins, as seen in another resistance re

78 Accessory and transmembrane proteins assemble in signaling complexes t

79 LINC complexes are transmembrane protein assemblies that physically connect

80 iruses translate their genomes as multi-pass transmembrane proteins at the endoplasmic reticulum (ER)

81 t determination of extracellular segments of transmembrane proteins based on the identification of su

82 tif alone is insufficient to induce RAT of a transmembrane protein because TM4SF4, a relative of TM4S

83 keleton via its N-terminal half and with the transmembrane protein beta-dystroglycan via its C-termin

84 This transmembrane protein binds to the transmembrane domain

85 ighlight how flaviviruses hijack the EMC for transmembrane protein biogenesis to achieve optimal expr

86 n, implying a role for RPLP1/2 in multi-pass transmembrane protein biogenesis.

87 e presence of IgE autoantibodies against the transmembrane protein BP antigen 2 (BP180, type XVII col

88 R as the Vgamma9Vdelta2 T cell Ag-presenting transmembrane protein butyrophilin 3A1, providing inform

89 , and RAT leads to an inverted topology of a transmembrane protein by altering the direction of its t

90 a method to interrogate the organization of transmembrane proteins by measuring their mobilities wit

91 hese properties enable regulation of certain transmembrane proteins by regulated intramembrane proteo

92 process in all photosynthetic organisms is a transmembrane protein called the reaction center.

93 reviously reported that ceramide regulates a transmembrane protein called TM4SF20 (transmembrane 4 L

94 inclusion, which is enriched with bacterial transmembrane proteins called Incs.

95 s to a poorly understood family of four-pass transmembrane proteins called tetraspanins.

96 nct S-acylated domains in the same polytopic transmembrane protein can be regulated by different acyl

97 nsgene mRNA, and show that intracellular and transmembrane proteins can be expressed.

98 Exosomes expressing the transmembrane protein CD63 were isolated by size-exclusi

99 ermeability via modulating expression of the transmembrane protein claudin-8, we used cultured mouse

100 ed by the first extracellular loop of the TJ transmembrane protein CLDN1.

101 endocytosis (CME) is key to maintaining the transmembrane protein composition of cells' limiting mem

102 ction in insulin SG number, changes in their transmembrane protein composition, and defects in granul

103 ow that most short homopolymeric polyleucine transmembrane proteins containing single amino acid subs

104 Tetraspanin (TSPAN) transmembrane proteins control Ca(2+) handling, and thus

105 or both Mpp5a and Rab11a operate through the transmembrane protein Crumbs.

106 The transmembrane protein Cx43 has key roles in fibrogenic p

107 Dendritic cell-specific transmembrane protein (DC-STAMP) plays a key role in the

108 s TRAP, Cathepsin K, dendritic cell-specific transmembrane protein (DCSTAMP), nuclear factor of activ

109 y be applied to other forms of NCL caused by transmembrane protein deficiencies in the future.

110 l that peptidisc peptides can arrange around transmembrane proteins differently, thus revealing the s

111 role for the EMC in stabilizing challenging transmembrane proteins during synthesis.

112 The recently-discovered single-span transmembrane proteins endoregulin (ELN), dwarf open rea

113 ntegrin and metalloprotease 10 (ADAM10) is a transmembrane protein essential for embryonic developmen

114 purified components FtsZ, FtsA and truncated transmembrane proteins essential for cell division.

115 revealed that the vast majority of all four transmembrane proteins exhibit very restricted movement

116 Ninety-five percent of all transmembrane proteins exist in kinetically trapped aggr

117 Transferrin receptor 2 (TFR2) is a transmembrane protein expressed mainly in hepatocytes an

118 or expressed on myeloid cells 2 (TREM2) is a transmembrane protein expressed on microglia within the

119 lar ligands: fibronectin leucine-rich repeat transmembrane proteins (FLRTs) and teneurins.

120 tion, which reveals a previously undescribed transmembrane protein fold.

121 Specifically, the seven-pass transmembrane protein Frizzled and the cytoplasmic prote

122 NT*-transmembrane protein fusions yield up to eight times mo

123 onsisting of ER targeted proteins, including transmembrane proteins, glycoproteins, and proteins with

124 The cell-surface and ER transmembrane protein gp78/AMFR, a receptor for the prom

125 by Wnt7a and Wnt7b in cooperation with the 7-transmembrane protein Gpr124.

126 d heteromeric receptor consisting of three 7-transmembrane proteins Gr22, Gr23, and Gr24.

127 ree recent studies find that the single-pass transmembrane protein HAP2 mediates gamete fusion and is

128 The sperm-restricted single-pass transmembrane protein HAP2-GCS1 has been postulated to f

129 ting the brain for NCLs caused by defects in transmembrane proteins has been more challenging and onl

130 Bacteriorhodopsin (bR), a representative transmembrane protein, has demonstrated exceptional opto

131 Nevertheless, some multispan helical transmembrane proteins have been proposed to partition i

132 ent revolutions in the structural biology of transmembrane proteins have, for the first time, yielded

133 CD7 is a transmembrane protein highly expressed in acute T-cell l

134 in type III domain containing 5 (Fndc5) is a transmembrane protein highly expressed in the skeletal m

135 y the actin cortex, whereas freely diffusing transmembrane proteins hinder swimming.

136 hically solved structures of homo-oligomeric transmembrane proteins (HoTPs) and find that ~97% are Cn

137 mprising 10(10) variants targeting the multi-transmembrane protein human CD20 (hCD20).

138 plex with proteins of the interferon-induced transmembrane protein (IFITM) family.

139 The interferon-induced transmembrane proteins (IFITMs) are a family of highly r

140 Interferon-induced transmembrane proteins (IFITMs) are innate effector prot

141 The IFN-induced transmembrane proteins (IFITMs) inhibit virus infections

142 Interferon-induced transmembrane proteins (IFITMs) restrict infections by m

143 sts or mouse cells, we show that IFN-induced transmembrane proteins (IFITMs), a family of restriction

144 tiviral function is the interferon-inducible transmembrane proteins (IFITMs), of which IFITM3 has bee

145 cell-intrinsic factors (interferon-inducible transmembrane proteins, IFITMs), on the pH regulation in

146 gs were: (i) the FL strain encodes 16 virion transmembrane proteins; (ii) eight of these proteins are

147 Fatty acid transport protein 4 (FATP4), a transmembrane protein in the endoplasmic reticulum (ER),

148 mice deficient in NRROS, a myeloid-expressed transmembrane protein in the endoplasmic reticulum, deve

149 ne fusion is triggered by synaptotagmin-1, a transmembrane protein in the vesicle membrane (VM), but

150 HIV-1 particles incorporate various host transmembrane proteins in addition to viral Env glycopro

151 heterodimers in metazoans and single subunit transmembrane proteins in apicomplexans such as TRAP in

152 scopy for the analysis of oligomerization of transmembrane proteins in cell-derived lipid membranes.

153 Thylakoid transmembrane proteins in the stroma can interact with C

154 e outer membrane leaflet, interacts with the transmembrane protein integrin beta1 and activates focal

155 d single molecule binding assays to discover transmembrane protein interactions in cells.

156 Megalin is a transmembrane protein involved in clathrin-mediated endo

157 e that ODZ1 (also known as TENM1), a type II transmembrane protein involved in fetal brain developmen

158 egrin and Metalloproteinase-15 (ADAM15) is a transmembrane protein involved in protein ectodomain she

159 Intramembrane cleavage of transmembrane proteins is a fundamental cellular process

160 The influence of the membrane on transmembrane proteins is central to a number of biologi

161 e identification of transmembrane helices in transmembrane proteins is crucial, not only to understan

162 Endocytic recycling of internalized transmembrane proteins is essential for many important p

163 Endocytosis of transmembrane proteins is orchestrated by the AP2 clathr

164 /H(+) exchanger type I (chNHE1), a multispan transmembrane protein, is a cellular receptor of the sub

165 port here that TMEM203, a conserved putative transmembrane protein, is an intracellular regulator of

166 Caveolin (Cav)1, a widely expressed transmembrane protein, is involved in the regulation of

167 riguingly, there was also association with a transmembrane protein kinase that may function as a rece

168 dentified the leucine-rich repeat-containing transmembrane protein known as Fish-lips (Fili) as a nov

169 We show that LRP4, a conserved transmembrane protein known for its postsynaptic roles,

170 In transmembrane proteins like the aquaporin and M2 channel

171 vel research suggests that disruption to the transmembrane protein linkage between the cytoskeleton a

172 Disruption to the transmembrane protein linkage between the cytoskeleton a

173 ur model consists of a molecular paddling by transmembrane proteins linked to and advected by the act

174 Full length TANGO1 is a transmembrane protein localised at endoplasmic reticulum

175 We discovered that Shisa7, a single-passing transmembrane protein, localizes at GABAergic inhibitory

176 we term "megacyte," is defined by a specific transmembrane protein marker (TM7318) and high expressio

177 Although similar transmembrane proteins mediate self/nonself recognition

178 MDR is typically associated with transmembrane proteins mediating efflux of administered

179 lic end-products is facilitated by polytopic transmembrane proteins mediating secondary active or pas

180 VE-cadherin, occludin and interferon-induced transmembrane protein mRNAs compared to both "low inflam

181 a membrane upon triggered phosphorylation of transmembrane protein nephrin.

182 affic, including the poorly understood small transmembrane proteins neural-specific gene 1 and 2 (Nsg

183 e-wide haploid genetic screen identified the transmembrane protein neuropilin 2 (NRP2) and tetraspani

184 hy with subcortical cysts 1 (Mlc1), an eight-transmembrane protein normally expressed in perivascular

185 ve triple response 1 (CTR1); an ER-localized transmembrane protein of unknown biochemical activity, c

186 biquitin ligase WWP2 and a tumor-suppressing transmembrane protein of unknown biochemical function, T

187 We use this method to study MFSD12, a transmembrane protein of unknown molecular function that

188 Tetraspanins are four-span transmembrane proteins of host cells that facilitate inf

189 4) domain of Sun proteins [5-7], a family of transmembrane proteins of the inner nuclear membrane (IN

190 r a number of backbone hydrogen bonds in the transmembrane protein OmpW.

191 Syntaxin, a transmembrane protein on the plasma membrane, has been o

192 effective means for studying the effects of transmembrane proteins on lipid distribution in both sym

193 Polycystin-1 (PC1) is a transmembrane protein originally identified in autosomal

194 alpha) expressed on myeloid cells to CD47, a transmembrane protein overexpressed on cancer cells, act

195 Hedgehog binds the transmembrane protein Patched, which in turn regulates S

196 is a common solubilizing agent used to study transmembrane proteins/peptides in biological and synthe

197 Unlike most transmembrane proteins, phospholipids can migrate from o

198 een the helical membrane-spanning domains of transmembrane proteins play central roles in the proper

199 Transmembrane proteins play crucial role in signaling, i

200 ch on alloherpesvirus VTPs.IMPORTANCE Virion transmembrane proteins play key roles in the biology of

201 igh throughput RNA sequencing identified the transmembrane protein Pmepa1 as a differentially express

202 CLEC-2 is activated by the transmembrane protein podoplanin, which is found outside

203 kidney disease (ADPKD), encode the multipass transmembrane proteins polycystin-1 (PC1) and polycystin

204 Mutations in PKD1 and PKD2, which encode the transmembrane proteins polycystin-1 and polycystin-2, re

205 , the de novo design of stable, well-defined transmembrane protein pores that are capable of conducti

206 Chloroplasts integrate nearly all thylakoid transmembrane proteins posttranslationally, but mechanis

207 Here we show that VCAM1, a transmembrane protein previously found in quiescent adul

208 The translocator protein (TSPO), an 18-kDa transmembrane protein primarily found in the outer mitoc

209 domains to interact with Rab7-GTP and the ER transmembrane protein Protrudin and together these compo

210 ms, such as the excluded volume of polytopic transmembrane proteins, proximity FRET, and rotational d

211 Notably, uropod transmembrane proteins PSGL-1 and CD43 cocluster specifi

212 The transmembrane protein Raw is cell autonomously required

213 a new regulator of axonal degeneration: the transmembrane protein Raw.

214 to the classical pathway of secretion, some transmembrane proteins reach the plasma membrane through

215 -14 homologs may also function in regulating transmembrane protein recycling and BMP signaling.

216 ue to mutations in the NPC1 gene, encoding a transmembrane protein related to the Sonic hedgehog (Shh

217 t to date, there are no solved structures of transmembrane proteins representing these attractive the

218 ABCD1 encodes a peroxisomal transmembrane protein required for very long chain fatty

219 Both the lipid molecules and the transmembrane proteins reside on the plasma membranes of

220 aperone that improves trafficking of several transmembrane proteins, restored Abeta-induced impaired

221 We find that the transmembrane protein semaphorin 6A (Sema6A) is required

222 In addition, the ER transmembrane proteins SERCA and calnexin were not detec

223 Analysis of transmembrane proteins shows several sequence-based char

224 The lysosomal transmembrane protein, SLC38A9, is required for mTORC1 a

225 At the same time, the transmembrane protein Smoothened (SMO) is released of it

226 r-like receptor Patched1 regulates the seven-transmembrane protein Smoothened remains mysterious, par

227 the ubiquitin hydrolase that deubiquitinates transmembrane proteins sorted as cargoes into ILVs.

228 After tagging individual ciliary transmembrane proteins, specifically Smoothened, with si

229 termini of NPHP4 and NPHP5 interact with the transmembrane protein SSTR3 and thus spatially map to th

230 localize to distal cell ends, the four-pass transmembrane protein Strabismus and the cytoplasmic pro

231 We found that the integral transmembrane proteins SUN1/UNC84A and SUN2/UNC84B are p

232 canonical Hh signaling through smoothened, a transmembrane protein targeted by small-molecule Hh inhi

233 t CUB domain-containing protein 1 (CDCP1), a transmembrane protein that acts as a substrate for SRC f

234 DEC205 is a transmembrane protein that bound mtDNA and contributed t

235 ession of the mRNA encoding ferroportin 1, a transmembrane protein that cooperates with CP and HEPH t

236 how that NRG3, like CRD-NRG1, is a dual-pass transmembrane protein that harbors a second transmembran

237 PIK3IP1, also known as TrIP, is a transmembrane protein that has been shown to inhibit PI3

238 The only known ligand, 4-1BBL, is a trimeric transmembrane protein that has no costimulatory activity

239 The interleukin 3 receptor (CD123) is a transmembrane protein that is absent or hardly expressed

240 The calcium pump SERCA is a transmembrane protein that is critical for calcium trans

241 how that PINCH-1 interacts with myoferlin, a transmembrane protein that is critical for cancer progre

242 ceptor is an evolutionarily highly conserved transmembrane protein that is essential to a wide spectr

243 gered by mutations in NPC1, a multi-spanning transmembrane protein that is trafficked through the exo

244 LINGO1 is a transmembrane protein that is up-regulated in the cerebe

245 Dysferlin is a large transmembrane protein that plays a key role in cell memb

246 Neuropilin 1 (Nrp1) is a type I transmembrane protein that plays important roles in axon

247 The regulated trafficking of Sanpodo, a transmembrane protein that potentiates receptor activity

248 BST-2/CD317/tetherin is a host transmembrane protein that potently inhibits human immun

249 as TMEM97, an endoplasmic reticulum-resident transmembrane protein that regulates the sterol transpor

250 rt that Selenoprotein N (SEPN1) is a type II transmembrane protein that senses ER calcium fluctuation

251 and stabilizes Smoothened (Smo), the 7-pass transmembrane protein that transduces the Hh signal.

252 AtUPS5 (Arabidopsis UREIDE PERMEASE 5) is a transmembrane protein that transports allantoin with hig

253 Cytochrome c oxidase (CcO) is a transmembrane protein that uses the free energy of O2 re

254 contact sites composed of clustered connexin transmembrane proteins that act in dual capacities as ch

255 KEY POINTS: Ion channels are transmembrane proteins that are synthesized within the c

256 ry of a family of endoplasmic reticulum (ER) transmembrane proteins that associate with and modulate

257 uclear membrane is functionalized by diverse transmembrane proteins that associate with nuclear lamin

258 They are heterodimeric transmembrane proteins that bind extracellular matrix (E

259 ture virions, were severely deficient in the transmembrane proteins that comprise the entry fusion co

260 Voltage-gated sodium channels (VGSC) are transmembrane proteins that generate an action potential

261 A subset of eSTKs are single-pass transmembrane proteins that have extracellular penicilli

262 ensions in studying GABA(A)Rs due to several transmembrane proteins that interact with GABA(A)Rs and

263 Cadherins constitute a family of transmembrane proteins that mediate calcium-dependent ce

264 Transporters are transmembrane proteins that mediate the selective transl

265 ted sodium (Na(V)) channels are pore-forming transmembrane proteins that play essential roles in exci

266 Tetraspanins are a unique family of 4-pass transmembrane proteins that play important roles in a va

267 PATs are multi-pass transmembrane proteins that possess a catalytic Asp-His-

268 findings identify the PCDHGs as pro-survival transmembrane proteins that select inhibitory interneuro

269 enes that encode Polycystin 1 and 2 (PC1/2), transmembrane proteins that translocate to the cilium.

270 We identify myristoylation on a transmembrane protein, the microneme protein 7 (MIC7), w

271 naling network largely initiated by three ER transmembrane proteins, the UPR constantly surveils prot

272 gy-related gene 9 (Atg9) encodes a multipass transmembrane protein thought to act as a membrane carri

273 We found that the lysosomal transmembrane protein TMEM55B recruits JIP4 to the lysos

274 This led to prioritization of transmembrane protein Tmem63c as a novel potential targe

275 ected by mutations in the genes encoding the transmembrane proteins TMHS, TMIE, TMC1 and TMC2.

276 nation state of embedded charged residues in transmembrane proteins (TMPs) can control the onset of p

277 includes the APMS, the phospholipid bilayer, transmembrane proteins (TMPs), and integral monotopic pr

278 tropic system requiring only a retinal-bound transmembrane protein to convert photons of light to an

279 Adopting a proper topology is crucial for transmembrane proteins to perform their functions.

280 ct cargo-selecting module for a large set of transmembrane proteins transiting the endosome, in addit

281 Starting with an unbiased screen of ~ 1,500 transmembrane proteins using the purified GluN1-NTD prot

282 ion translocation by Ca(2+)-regulated TMEM16 transmembrane proteins utilizes a membrane-exposed hydro

283 -binding Proteins (SMP) domain-containing ER transmembrane protein, utilizes distinct domains to inte

284 Here, we found that the V. dahliae tetraspan transmembrane protein VdSho1, a homolog of the Saccharom

285 A hexameric assembly of a large viral transmembrane protein was found to form the core of the

286 Interestingly, other transmembrane proteins were mislocalized upon emc1 deple

287 ABCG4 is an ATP-binding cassette transmembrane protein which has been shown, in vitro, to

288 TNF is synthesized as a transmembrane protein, which is further matured via prot

289 Cytochrome bo (3) ubiquinol oxidase is a transmembrane protein, which oxidizes ubiquinone and red

290 The TMC genes encode a set of homologous transmembrane proteins whose functions are not well unde

291 Lu/BCAM is a type I transmembrane protein with a cytoplasmic domain of 59 (L

292 und that OIG-8, a previously uncharacterized transmembrane protein with a single immunoglobulin (Ig)

293 In the present study, we found that USH2A, a transmembrane protein with a very large extracellular do

294 Wdp is a single-pass transmembrane protein with leucin-rich repeat (LRR) moti

295 n as integrin-associated protein (IAP), is a transmembrane protein with multiple biological functions

296 ntributions when designing drugs that target transmembrane proteins with improved efficacy and safety

297 Plexins are single-pass transmembrane proteins with multiple domains in both the

298 Choanoflagellate semaphorins are transmembrane proteins with multiple fibronectin type II

299 iors.SIGNIFICANCE STATEMENT Ion channels are transmembrane proteins with selective permeability to sp

300 re we report that modification of several ER transmembrane proteins with the photosensitive degron (p