ライフサイエンスコーパス: membrane-associated protein

1 s and 45.5% cytosol proteins (including 8.6% membrane-associated proteins).

2 tein light chain 3 (LC3), the autophagosomal membrane-associated protein.

3 One PNKD isoform is a membrane-associated protein.

4 ed that the XAP-1 antigen is a photoreceptor membrane-associated protein.

5 retromer complex and Hrs, an early endosomal membrane-associated protein.

6 elongated into a tube encased in a sheath of membrane-associated protein.

7 g of the gl14 gene, which encodes a putative membrane-associated protein.

8 lla, and demonstrate that Mig-14 is an inner membrane-associated protein.

9 of vaccinia virus was predicted to encode a membrane-associated protein.

10 elivered by Escherichia coli as a lipidated, membrane-associated protein.

11 rt the partitioning of additional well known membrane associated proteins.

12 sidues, near the protein termini, and within membrane associated proteins.

13 OMP component BamA along with several outer membrane associated proteins.

14 ment for a large number of transmembrane and membrane-associated proteins.

15 acterization of lateral interactions between membrane-associated proteins.

16 ing a role for Arp2/3 in the distribution of membrane-associated proteins.

17 sion studies revealed that CidA and LrgA are membrane-associated proteins.

18 membrane curvature, and its interaction with membrane-associated proteins.

19 d BBS proteins, and reduced ciliary entry of membrane-associated proteins.

20 e processes and as a barrier to diffusion of membrane-associated proteins.

21 ified CT049 and CT050 as potential inclusion membrane-associated proteins.

22 so affected the transport of soluble but not membrane-associated proteins.

23 ot aggregate and did not bind to 5,300 human membrane-associated proteins.

24 sinica, as a model for NMR investigations of membrane-associated proteins.

25 he endocytic process, along with a number of membrane-associated proteins.

26 ethodology facilitates the reconstitution of membrane-associated proteins.

27 ted to be outer membrane, inner membrane, or membrane-associated proteins.

28 n for a class of linkers of lipid-activated, membrane-associated proteins.

29 Slit/Robo, cell-polarity proteins, and other membrane-associated proteins.

30 ne surfaces where it may interact with other membrane-associated proteins.

31 cytosolic and nuclear proteins, but also in membrane-associated proteins.

32 igned as known integral membrane proteins or membrane-associated proteins.

33 and extracts, whereas Alb-23 and Alb-69 were membrane-associated proteins.

34 omplex derived from the peripheral stalk and membrane-associated proteins.

35 ll as numerous conserved-hypothetical and/or membrane-associated proteins.

36 ng factors, RNA-binding proteins, and plasma membrane-associated proteins.

37 ted with assaying for interactions involving membrane-associated proteins.

38 owed that Erg26p, Erg27p, and Erg28p are all membrane-associated proteins.

39 s linking spectrin-actin complexes to plasma membrane-associated proteins.

40 been identified, including both nuclear and membrane-associated proteins.

41 or that is involved in trafficking of plasma membrane-associated proteins.

42 phages derived from mice deficient for these membrane-associated proteins.

43 rves as a prototype to model large, dynamic, membrane-associated proteins.

44 arge that in turn modulate interactions with membrane-associated proteins.

45 ted that EGRs target cytoskeleton and plasma membrane-associated proteins.

46 he membrane on the structure and dynamics of membrane-associated proteins.

47 s are responsible for ectodomain shedding of membrane-associated proteins.

48 density fractions at the buoyant density of membrane-associated proteins.

49 s of membrane lipids and integral as well as membrane-associated proteins.

50 the activity of many ion channels and other membrane-associated proteins.

51 e composition, shape and the organization of membrane-associated proteins.

52 s of membrane lipids and integral as well as membrane-associated proteins.

53 ed with a diverse population of integral and membrane-associated proteins.

54 ntified, including 379 integral membrane and membrane-associated proteins.

55 ounts of perforin, granzyme B, and lysosomal membrane-associated protein 1 (CD107a) in their cytotoxi

56 ated within single-membrane acidic lysosomal membrane-associated protein 1-positive inclusions, where

57 fs, 12 lipoproteins, 9 secreted proteins, 22 membrane-associated proteins, 1 bacteriophage-associated

58 Integral membrane-associated protein-1 (Itmap1) is a CUB (complem

59 RPE65 is a membrane-associated protein abundantly expressed in the

60 n is mislocalized in this mutant, as are the membrane-associated proteins, actin and beta-catenin, th

61 ps Cdc42 to undergo the transition between a membrane-associated protein and a soluble (cytosolic) sp

62 ClipR-59 is a membrane-associated protein and has been implicated in m

63 rea denaturation process of an alpha-helical membrane-associated protein and its completely unfolded

64 mutant strains were associated only with the membrane-associated protein and not with the cytoplasmic

65 h in yeast with both a selection to identify membrane-associated proteins and a selection to identify

66 y-modulated, processive interactions between membrane-associated proteins and elongating filament end

67 Ezrin provides a linkage between membrane-associated proteins and F-actin, oscillating be

68 nt micelles, methods are outlined for larger membrane-associated proteins and for use of other solubi

69 In contrast, other membrane-associated proteins and non-CME endocytic prote

70 -level-resolution structures and dynamics of membrane-associated proteins and peptides.

71 biosynthesis as well as other cell wall and membrane-associated proteins and ROS scavenging enzymes.

72 We determined that HfaB and HfaD are membrane-associated proteins and that HfaB is a lipoprot

73 appears to provide regulated linkage between membrane-associated proteins and the actin cytoskeleton

74 proteins provide a regulated linkage between membrane-associated proteins and the actin cytoskeleton.

75 ly required for thorough characterization of membrane-associated proteins and were facilitated by the

76 ifiable MOMP either in purified form or as a membrane-associated protein, and so facilitate the inves

77 The variants include STEP(61), a membrane-associated protein, and STEP(46), a cytosolic p

78 Genes coding for putative membrane and membrane-associated proteins are among the largest class

79 cific probes to show that most or all plasma membrane-associated proteins are clustered in cholestero

80 sive properties of the RGM-related family of membrane-associated proteins are compatible with specifi

81 t regulators and conserved rickettsial outer membrane-associated proteins are critical to mediate ser

82 This suggests that membrane-associated proteins are important for the coexi

83 Several membrane-associated proteins are known to modulate the a

84 Accordingly, several receptors and other membrane-associated proteins are organized and functiona

85 rans-Golgi lumina were spanned by asymmetric membrane-associated protein arrays that had approximatel

86 Increased expression of the membrane-associated protein At14a-like1 (AFL1) led to in

87 Two membrane-associated proteins, bacteriorhodopsin and ApoA

88 one Sox2-replacing antibody antagonizes the membrane-associated protein Basp1, thereby de-repressing

89 F-BAR proteins are membrane-associated proteins believed to link the plasma

90 product of a cDNA encoding a multifunctional membrane-associated protein binds the seco-steroid 1,25(

91 51 proteins, including periplasmic and outer membrane-associated proteins, but also many determinants

92 more, TUDCA promoted the degradation of cone membrane-associated proteins by enhancing the ER-associa

93 Removal of membrane-associated proteins by proteases decreases the

94 Expression of a thylakoid membrane-associated protein called IdiA (iron-deficiency

95 mor suppressor gene encodes an intracellular membrane-associated protein, called merlin, which belong

96 Ubiquitination of membrane-associated proteins can direct their proteasome

97 Reciprocally, many membrane-associated proteins can modulate the shape, lip

98 nstrated that the membrane alone, or through membrane-associated proteins, can effect dynamic changes

99 Human ferrochelatase, a mitochondrial membrane-associated protein, catalyzes the terminal step

100 ndent increase in membrane colocalization of membrane-associated protein CD14.

101 d and colocalized with MAP17, a small 17-kDa membrane-associated protein; cMOAT, an organic anion tra

102 MyoA is part of a membrane-associated protein complex called the glideosom

103 king that intersectin is present in ECs in a membrane-associated protein complex containing dynamin a

104 Sarcoglycan is a membrane-associated protein complex found at the plasma

105 reby initiates the formation of ESCRT-III, a membrane-associated protein complex that functions immed

106 EF) activity and characterized it as a large membrane-associated protein complex that localizes to th

107 proteins encoded by the operon form an inner-membrane-associated protein complex that may interact wi

108 The dystrophin complex is a multimolecular membrane-associated protein complex whose defects underl

109 ir main function is to provide scaffolds for membrane-associated protein complexes by binding to the

110 verse range of known and novel cytosolic and membrane-associated protein complexes.

111 etergents to isolate the PSD and release its membrane-associated proteins complicates studies of thes

112 ctor (NHERF) homologous adaptors 1 and 2 are membrane-associated proteins composed of two amino (N)-t

113 mon mitochondrial lipids, and abundant inner-membrane associated proteins concentrated in the bottom-

114 p12(I) is a conserved, membrane-associated protein containing four SH3-binding

115 How these membrane-associated proteins cope with the hydrophilic c

116 ctron microscopy, using antisera against the membrane-associated protein CTRP and the soluble WARP, s

117 ficking necessarily involves both lipids and membrane-associated proteins, current mechanistic views

118 The adsorption of membrane-associated protein cytochrome c to anionic lipi

119 cific cysteine protease (ESCP) was the first membrane-associated protein described to be part of the

120 identified and shown to encode two potential membrane-associated proteins, designated LrgA and LrgB,

121 There are several examples of membrane-associated protein domains that target curved m

122 rvival in Opn1sw(-/-)Lrat(-) (/-) mice, cone membrane-associated proteins (e.g. Galphat2, GRK1 and GC

123 PSMA1-GFP copurifies with several acrosomal membrane-associated proteins (e.g., lactadherin/milk fat

124 ne-rich repeats and forms a complex with the membrane-associated protein ERBB2IP.

125 our laboratories and applied to the study of membrane-associated proteins, especially GPCRs.

126 ed previously in rat cerebellum, is a plasma membrane-associated protein expressed at the RNA level i

127 Here we demonstrate that the membrane-associated proteins FCHo and SGIP1 convert AP2

128 oteins FeoA and FeoC and a large cytoplasmic-membrane-associated protein FeoB, which has an N-termina

129 Moreover, GacJ, a small membrane-associated protein, formed a complex with GacI

130 hared with mammalian junctophilins and other membrane-associated proteins found within excitable cell

131 ithin the cell as part of the soluble and/or membrane-associated protein fraction.

132 platelet activation (APMAP [adipocyte plasma membrane-associated protein], GPLD1 [phosphate inositol-

133 The shedding of membrane-associated proteins has been recognized as a re

134 egulates cilia disassembly, ciliary entry of membrane-associated protein, Hedgehog signaling, and emb

135 inositol (GPI) linkage found in many natural membrane-associated proteins; however, the synthetic met

136 Notch1 is the first membrane-associated protein identified with either O-lin

137 Out of 1736 soluble proteins and 2187 membrane-associated proteins identified, 288 and 56, res

138 his study, we report the identification of a membrane-associated protein, Ig-like transcript 4 (ILT4)

139 We found that (i) MTMR13 is a predominantly membrane-associated protein; (ii) MTMR2 and MTMR13 cofra

140 However, immunoblots of membrane-associated proteins, immunoelectron microscopy

141 MAL is a detergent-resistant membrane-associated protein implicated in apical sorting

142 Dysferlin is a membrane-associated protein implicated in membrane resea

143 Dysferlin is a membrane-associated protein implicated in muscular dystr

144 Myoferlin is a membrane-associated protein important for muscle develop

145 In this study, we demonstrate that TcdC is a membrane-associated protein in C. difficile.

146 ptide recognizes an approximately 58-kDa egg membrane-associated protein in eggs of S. purpuratus as

147 tinoid isomerase in this pathway is Rpe65, a membrane-associated protein in the retinal pigment epith

148 to 2 s, and similarly high turnover rates of membrane-associated proteins in CME.

149 ting proteins such as ion channels and other membrane-associated proteins in defined areas of the pla

150 croscopy was used to study redistribution of membrane-associated proteins in naive T cells from young

151 yeast genetics to identify 211 ubiquitinated membrane-associated proteins in Saccharomyces cerevisiae

152 tegral membrane proteins for drug design and membrane-associated proteins in the regulation cellular

153 ated lysosomal hydrolytic enzymes and plasma membrane-associated proteins in the supernatant of Tat-e

154 ubiquitin-modifying enzymes, which act upon membrane-associated proteins in transit.

155 R may have primarily a structural role, as a membrane-associated protein, in milk fat droplet secreti

156 The mistrafficking of cone membrane-associated proteins including cone opsins (M- a

157 the phage display of representative types of membrane-associated proteins including plasma, nuclear,

158 After SPB insertion, membrane-associated proteins including the conserved Ndc

159 However, a rapidly growing number of membrane-associated proteins (including cytoskeletal pro

160 mbrane cholesterol regulates the activity of membrane-associated proteins, including BK channels.

161 eria and causes mislocalization of essential membrane-associated proteins, including MinD and FtsA.

162 r examine the interaction of PorB with outer membrane-associated proteins, including PorA and RmpM.

163 Several cytosolic and membrane-associated proteins, including the Rab family m

164 Recent studies have implicated a number of membrane-associated proteins, including the signaling pa

165 The membrane-associated proteins initiate signaling that act

166 te the applicability of TurboID in capturing membrane-associated protein interactomes using Lotus jap

167 ion, CEP-290 prevents inappropriate entry of membrane-associated proteins into cilia and keeps ARL-13

168 Dysferlin is a membrane associated protein involved in vesicle traffick

169 member of a newly recognized superfamily of membrane-associated proteins involved in eicosanoid and

170 her structures of proteins within the MAPEG (Membrane-Associated Proteins involved in Eicosanoid and

171 Caveolin-1 (CAV1), a highly conserved membrane-associated protein, is a putative regulator of

172 omal prostaglandin E synthase-1 (mPGES-1), a membrane-associated protein, is critically involved in t

173 CTRP5, a secretory and membrane-associated protein, is localized to the lateral

174 immune response of mice and Lyme patients to membrane-associated proteins isolated from Borrelia burg

175 Three membrane-associated proteins, Kibra, Merlin, and Expande

176 Sulfolobus solfataricus contains a membrane-associated protein kinase activity that display

177 c archaeon Sulfolobus solfataricus harbors a membrane-associated protein kinase activity.

178 The activity of membrane-associated protein kinase C (PKC) is tightly co

179 that the glucose sensors are coupled to the membrane-associated protein kinase casein kinase I (Yck1

180 A novel murine membrane-associated protein kinase, PKK (protein kinase

181 Two paralogous plasma membrane-associated protein kinases, Pkh1 and Pkh2 (orth

182 Additionally, the nuclear-membrane-associated proteins, lamin A/C and emerin, were

183 By contrast, alpha-helical membrane-associated proteins largely evade such approach

184 PHB2 binds the autophagosomal membrane-associated protein LC3 through an LC3-interacti

185 Mutations that alter the expression of these membrane-associated proteins lead to muscular dystrophy

186 Transcription of membrane-associated proteins leads to localized hypersup

187 n-glycoprotein complex is a large complex of membrane-associated proteins linking the cytoskeleton to

188 lize to the cell midpoint, assembling into a membrane-associated protein machine that forms the divis

189 , we identified an accessory protein, 17 kDa membrane-associated protein (MAP17), that increased SGLT

190 t the proportions of proteomes consisting of membrane-associated proteins may be currently underestim

191 IRE1alpha, an ER membrane-associated protein mediating unfolded protein r

192 structure and dynamics of the alpha-helical membrane-associated protein Mistic as well as its intera

193 lts have been reported as to whether the two membrane-associated proteins MreC and MreD are essential

194 We show that a gut-membrane-associated protein, named Mesh, plays an import

195 ay facilitate the identification of cellular membrane-associated proteins necessary for induction of

196 scribed role of SGK-1 in phosphorylating the membrane-associated protein Nedd4-2 and the integral mem

197 and peripheral nervous system (PNS), where a membrane-associated protein, Numb, is asymmetrically loc

198 The IM30 (inner membrane-associated protein of 30 kDa), also known as th

199 photoaffinity analog specifically labeled a membrane-associated protein of approximately 170 kDa.

200 We conclude that FAM65B is a plasma membrane-associated protein of hair cell stereocilia tha

201 furthermore demonstrate that RPE65, a major membrane-associated protein of the RPE, is a RBP.

202 tein annexin A5 (ANXA5) is the most abundant membrane-associated protein of ~P23 mouse vestibular hai

203 e it readily applicable to the study of many membrane-associated proteins of biochemical and pharmaco

204 Such signals include membrane-associated proteins of the oligodendrocyte plas

205 09 differentially phosphorylated residues of membrane-associated proteins on activation of the intrac

206 rotocol was found to detect ~65% more unique membrane-associated protein (p < 0.001, n = 6) based on

207 Phase separation of membrane-associated proteins participates in various tra

208 eta(2) by lipid rafts and by the presence of membrane-associated protein partners.

209 Receptor-cargo docking occurs at the membrane-associated protein Pex14.

210 ilayers and the membrane-proximal regions of membrane-associated proteins play important roles in reg

211 r results suggest that major cytoplasmic and membrane-associated protein precursors of the presynapti

212 DANGER is a membrane-associated protein predicted to contain a parti

213 RPE65, a membrane-associated protein predominantly expressed in t

214 odr-2 encodes a membrane-associated protein related to the Ly-6 superfam

215 Endophilin is a membrane-associated protein required for endocytosis of

216 FTS_1680-encoded protein was identified as a membrane-associated protein required for full cytopathog

217 FLOTILLIN4 (FLOT4), another punctate plasma membrane-associated protein required for infection.

218 A broadly conserved membrane-associated protein required for the functional

219 Spectrins represent a family of membrane-associated proteins responsible for membrane fl

220 antibodies (against agrin, adipocyte plasma membrane-associated protein, Rho GDP-dissociation inhibi

221 he identification of 231 proteins present in membrane-associated protein samples, of which a subset o

222 SIM and the Smad-binding domain (SBD) of the membrane-associated protein SARA (Smad anchor for recept

223 cted for immunoblotting against B. miyamotoi membrane-associated proteins separated by 2-dimensional

224 Pkn8 is a membrane-associated protein Ser/Thr kinase (PSTK) of Myx

225 One of the glycoproteins comigrated with the membrane-associated protein-serine/threonine kinase from

226 Membrane associated proteins SNAREs (soluble N-ethylmale

227 udies indicated that a subset of immunogenic membrane-associated proteins (some new and some previous

228 bidopsis (Arabidopsis thaliana), is a plasma membrane-associated protein specifically involved in neg

229 DIAN1 [CIR1], and SPFH/PHB DOMAIN-CONTAINING MEMBRANE-ASSOCIATED PROTEIN [SPFH]) that are mis-spliced

230 ins such as the cannabinoid CB1 receptor and membrane-associated proteins such as FAAH.

231 of the tubulin homolog FtsZ as well as other membrane-associated proteins such as FtsA, a homolog of

232 teractions, we established that heterologous membrane-associated proteins such as MinD can be targete

233 eractions with positively charged regions of membrane-associated proteins such as myristoylated alani

234 plicates trans-synaptic interactions between membrane-associated proteins such as neurexins and neuro

235 ase cascade, in turn, is regulated by apical membrane-associated proteins such as the FERM domain pro

236 studies show that upon cell contact, various membrane-associated proteins, such as Ras-family protein

237 n the cell surface distribution of polytopic membrane-associated proteins, suggesting that the mutati

238 , and did not bind to any of the 5,300 human membrane-associated proteins tested.

239 Bacteriophage 29 protein p1 is a membrane-associated protein that forms large protofilame

240 al analyses, we demonstrate that DRAG-1 is a membrane-associated protein that functions at the ligand

241 SNX1 is a membrane-associated protein that functions in lysosomal

242 enuating Notch signaling by inducing Numb, a membrane-associated protein that inhibits Notch signalin

243 Polycystin-1 is a large membrane-associated protein that interacts with polycyst

244 We recently identified Vema as a novel membrane-associated protein that is expressed at the ven

245 DAP12 is a cell membrane-associated protein that is expressed in myeloid

246 ow that TG1 is an endoplasmic reticulum (ER) membrane-associated protein that is trafficked through t

247 glo-3 encodes a predicted membrane-associated protein that lacks obvious sequence

248 indicate that BBA74 is a periplasmic, outer membrane-associated protein that lacks properties typica

249 Aer is a membrane-associated protein that mediates aerotactic res

250 Syntabulin is a peripheral membrane-associated protein that targets to mitochondria

251 resulting in the identification of T. cruzi membrane-associated proteins that are potential vaccine

252 t junction is comprised of transmembrane and membrane-associated proteins that are thought to assembl

253 matrix relies on adhesion sites, clusters of membrane-associated proteins that communicate forces gen

254 nments, placing cPLA2delta into the class of membrane-associated proteins that contain a tandem pair

255 Examining membrane-associated proteins that copurified with GOA-1

256 ing proteins (Csps) are J-domain-containing, membrane-associated proteins that have been functionally

257 analysis enabled the identification of novel membrane-associated proteins that may serve as new diagn

258 genes encode a novel class of extracellular, membrane-associated proteins that notably play an import

259 and characterization of recently identified membrane-associated proteins that regulate replication a

260 (PLSCRs) constitute a family of cytoplasmic membrane-associated proteins that were identified based

261 Dystrophin binds a set of membrane-associated proteins (the dystrophin-glycoprotei

262 Extracellular and membrane-associated proteins-the products of 40% of all

263 ver, by mediating interactions with numerous membrane-associated proteins, they are key components in

264 or normal endosomal recycling of soluble and membrane-associated proteins through the ERC and propose

265 Transforming growth factor-beta membrane associated protein (TIMAP) is an endothelial ce

266 cing the ability of BAX to transition from a membrane-associated protein to a membrane-integral prote

267 r ciliogenesis require it to localize select membrane-associated proteins to the cilium, including Ar

268 , including vacuole biogenesis, targeting of membrane-associated proteins to the vacuole, and secreti

269 that requires A-type lamin, an inner nuclear membrane-associated protein, to accelerated aging observ

270 A thiol-reactive membrane-associated protein (TRAP) binds covalently to t

271 , gK, and gM, the membrane protein UL20, and membrane-associated protein UL11 play important roles in

272 c envelopment, in a protein complex with the membrane-associated protein UL20 (UL20mp).

273 The highly membrane-associated proteins UL20p and glycoprotein K (g

274 it is in close proximity to a thiol-reactive membrane-associated protein under basal and insulin-stim

275 he targeted degradation of extracellular and membrane-associated proteins using conjugates that bind

276 We previously showed that the novel membrane-associated protein Vema is localized to the flo

277 Aberrant localization of these membrane-associated proteins was evident at postnatal da

278 MURC, a plasma membrane-associated protein, was found to be more abunda

279 a previously uncharacterized gene encoding a membrane-associated protein, was sensitive to acid and f

280 Membrane associated proteins were extracted from cells w

281 Moreover, the majority of these immunogenic membrane-associated proteins were recognized by sera fro

282 f X. nematophila and is produced as an outer membrane-associated protein when expressed in Escherichi

283 C2 domains are found in a variety of membrane-associated proteins where they have been implic

284 RP2 is a ubiquitous 350 amino acid plasma membrane-associated protein, which shares homology with

285 n), is a member of the protein 4.1 family of membrane-associated proteins, which also includes ezrin,

286 Both cytoplasmic- and membrane-associated proteins, which are normally restric

287 age-gated calcium channels are extracellular membrane-associated proteins, which are post-translation

288 of changes in sarcomeric, nonsarcomeric, and membrane-associated proteins, which could have important

289 enzyme from C. crescentus is a homodimeric, membrane-associated protein while the enzyme from M. tub

290 es during maturation of cysteine-containing, membrane-associated proteins while ignoring the same cys

291 bly, gCfull was expressed predominantly as a membrane-associated protein, while both gC104 and gC145

292 ionship is regulated in part by a cytosolic, membrane-associated protein with a unique structural fol

293 Each gene encodes a predicted membrane-associated protein with diguanylate cyclase act

294 Caveolin 1 (Cav-1) is a plasma membrane-associated protein with the capacity to modulat

295 lic-nucleotide 3'-phosphodiesterase (CNP), a membrane-associated protein with unknown function in mam

296 Although podocin and MEC-2 are membrane-associated proteins with a predicted hairpin-li

297 ochondria and in submitochondrial particles, membrane-associated proteins with apparent molecular mas

298 -dependent colocalization of these and other membrane-associated proteins with crosslinked receptors

299 ifunctional Golgi-endoplasmic reticulum (ER) membrane-associated protein, with roles in enhancing vir

300 ol critical biological processes by cleaving membrane-associated proteins within a transmembrane segm