ライフサイエンスコーパス: membrane anchor

1 igh potency and wash resistance (an index of membrane anchoring).

2 -Bbp1 complex is the central unit of the SPB membrane anchor.

3 rate that in C. crescentus, FzlC is one such membrane anchor.

4 naling by liberating EGFR ligands from their membrane anchor.

5 rane domain, an ectodomain, and a C-terminal membrane anchor.

6 hat provides a cytosolic domain and a plasma membrane anchor.

7 n carried out largely on atlastins lacking a membrane anchor.

8 e role of this substructure as a hydrophobic membrane anchor.

9 ytoplasmic tail of the Heart of glass (HEG1) membrane anchor.

10 as the expression level and geometry of the membrane anchor.

11 ows us to estimate the area density of these membrane anchors.

12 e with barriers for membrane exit due to the membrane anchors.

13 hile the nonspecific interactions are mainly membrane-anchored.

14 d the Sec17 apolar loop has functions beyond membrane anchoring.

15 f the gammaCA domain subunit composition and membrane anchoring.

16 ng; and (iii) mutation R252E, affecting nsP1 membrane anchoring.

17 single-point mutations of PhCCD1 to improve membrane anchoring.

18 AspH is an endoplasmic reticulum (ER) membrane-anchored 2-oxoglutarate oxygenase whose C-termi

19 ential for localization and interacting with membrane-anchored A-Kinase-Anchoring Proteins (AKAPs).

20 The human YME1L protease is a membrane-anchored AAA+ enzyme that controls proteostasis

21 FtsH, a bacterial membrane-anchored AAA+ protease, plays a vital role in m

22 Here, we identify Msp1, a conserved, membrane-anchored AAA-ATPase (ATPase associated with a v

23 the C-terminal cytosolic tail of RHD3 has a membrane anchoring ability that is required for efficien

24 single-residue substitution that alters the membrane-anchoring ability of Ail significantly contribu

25 identical 6TM design and obtained an active, membrane-anchored AC.

26 This constitutes a new mechanism for membrane anchoring among the beta-subunit family that al

27 N-terminal helical segment having a role of membrane anchor, an unstructured C-terminal region that

28 brane-associated NTD, which serves as both a membrane anchor and an allosteric activator.

29 ive amino acids N-terminal to the C-terminal membrane anchor and at a gamma-like site in the middle o

30 RIAM, a membrane anchor and small GTPase RAP1 effector, is known

31 Photolysis releases the bioagent from its membrane anchor and thereby renders it biologically acti

32 s confirm that the combined functionality of membrane anchoring and microtubule tip affinity is in pr

33 residues resulted in significant loss of PLB membrane anchoring and mislocalization to the cytoplasm

34 Here, we show that selective membrane anchoring and the compartmentalization of the e

35 150 different proteins to facilitate proper membrane anchoring and trafficking to lipid rafts.

36 terium tuberculosis, lack the canonical FtsZ-membrane anchors and Z-ring regulators described for E.

37 CRAF activation requires binding to membrane-anchored and active GTP-bound RAS.

38 r the identification and characterization of membrane-anchored and extracellular proteins that bind h

39 d cognate ligand for CX3CR1, signals both in membrane-anchored and soluble forms.

40 terplay between motor pulling forces, cortex-membrane anchoring, and network connectivity.

41 ged residues, which is strictly required for membrane anchoring, and when transferred to the cytoplas

42 ifications are able to act as more than just membrane anchors, and dynamic S-acylation in particular

43 alcium signaling of the B cell upon cellular membrane anchors anti-E. coli O157:H7 IgM.

44 The motor of the membrane-anchored archaeal motility structure, the archa

45 A plethora of examples show these membrane anchors are not merely anchors but can multimer

46 d II is polymerized, nascent polymers remain membrane-anchored at one end, and the other end becomes

47 The membrane-anchored atlastin GTPase couples nucleotide hyd

48 In this study, we used membrane-anchored atlastins in assays that separate teth

49 utocatalysis severs the protein into a large membrane-anchored beta subunit that noncovalently associ

50 337-Gly340, Thr343, and Thr345) could act as membrane anchor, binding interface for a second rhodopsi

51 n from the membrane-anchored transducer, and membrane-anchored biotin displayed on the surface of a s

52 We have thus generated membrane-anchored bursicon constructs that can activate

53 hic helix of the monomers not only acts as a membrane anchor but also generates significant positive

54 ocation channel as a weakly self-interacting membrane anchor but establishes a heteromeric TM-TM heli

55 ontain a beta barrel domain that serves as a membrane anchor, but the assembly and quality control of

56 FAT signalling whereas the dominant negative membrane-anchored C-terminal fragment (PC1-MAT) increase

57 acellular juxtamembrane region, generating a membrane-anchored C-terminal fragment.

58 on of Ca(2+) influx by the dominant negative membrane-anchored C-terminal tail fragment of PC1 elevat

59 The FtsZ GTPase domain is separated from its membrane-anchoring C-terminal conserved (CTC) peptide by

60 oluble forms of the protein lacking both the membrane-anchoring C-terminal tail and the intrinsically

61 gulation in Magnetospirillum gryphiswaldense Membrane-anchored CcfM localizes in a filamentous patter

62 gosaccharide chain attached to a hydrophobic membrane anchor, ceramide.

63 nteractions between their fusion protein and membrane-anchored chaperone protein.

64 Placing membrane-anchoring cholesterol at the tail of the arrow

65 recruitment of the Cryptochrome CRY2 to its membrane-anchored CIBN partner.

66 t that connects the alpha3beta3 head and the membrane-anchored cn ring.

67 tissue injury by physical separation of the membrane-anchored cofactor tissue factor (TF) from inact

68 ucleate actin filaments colocalize in plasma membrane-anchored complexes called nodes in the constric

69 Ras is the only membrane-anchored component in the EGFR-ERK signaling ax

70 euronal loss were significantly reduced when membrane-anchored CX3CL1 C-terminal fragment (CX3CL1-ct)

71 The membrane-anchored CX3CL1 is best known to exert its sign

72 Cell membrane-anchored Decay Accelerating Factor (DAF, a.k.a.

73 erminal calpain protease is regulated by the membrane-anchored DEK1 MEM, which is connected to the ca

74 Mutations that affect membrane anchoring, disrupt heme and/or substrate bindin

75 most relevant avenues and accomplishments of membrane-anchored DNA nanostructures for investigating,

76 SpoIIIE is a membrane-anchored DNA translocase that localizes to the

77 by a 'glycan', which is preassembled onto a membrane-anchored dolichol molecule embedded within the

78 region (amino acids 1-135) and a C-terminal membrane-anchoring domain (amino acids 135-164).

79 sPom121 lacks the nuclear membrane-anchoring domain and thus does not localize to

80 uence located between its Bcl-2 homology and membrane anchor domains and blocks homo- and heteromeric

81 budding virions on the cell surface with its membrane anchor domains.

82 in response to low oxygen requires the Golgi membrane-anchored Dsc E3 ligase complex.

83 ith Bag1 then shifts hERG degradation to the membrane-anchored E3 ligase TRC8 and its E2-conjugating

84 VSV vectors (N4CT1-EBOVGP1), which expresses membrane-anchored EBOV GP from the first position in the

85 plant secretory system, KORRIGAN1 (KOR1), a membrane-anchored endo-beta-1,4-glucanase involved in ce

86 KOR1 is a membrane-anchored endo-beta1,4-glucanase and contains ei

87 rify key molecular-level differences between membrane-anchored Env and soluble gp140.

88 Here we show that exogenous membrane-anchored Envs, which can be produced in large q

89 Membrane-anchored Eph receptors and ephrins represent a

90 ver, more recent work has suggested that the membrane-anchored epithelial cell serine protease matrip

91 subtilis grows without FtsA or the putative membrane anchor EzrA and why bacteria lacking FtsA conta

92 hondrial surface, and involves mitochondrial membrane-anchored factors.

93 and the membrane; in the active state, with membrane-anchored farnesyl and unrestrained HVR, the cat

94 nanomachines requires the assembly of inner membrane-anchored fibres called pseudopili.

95 in has a globular head that is attached to a membrane-anchored flexible stalk of approximately 80 res

96 actions were investigated using Laurdan as a membrane-anchored fluorescent dye.

97 They reveal a novel membrane-anchoring fold that plays a significant role in

98 esent evidence that type I myosin is the key membrane anchor for endocytic actin assembly factors in

99 Our characterization of FzlC as a novel membrane anchor for FtsZ expands our understanding of Ft

100 ) are functionally important glycolipids and membrane anchors for cell wall lipoglycans in the Coryne

101 ing membrane proteins are commonly viewed as membrane anchors for functional domains.

102 fluenza virus type 1 (rHPIV1) expressing the membrane-anchored form of EBOV glycoprotein GP, as an in

103 Herein a membrane-anchored form of GIFT4 was constructed by fusin

104 mor surveillance functions when expressed in membrane-anchored form on activated immune effector cell

105 f FtsZ regulators and establishes a role for membrane-anchored FtsZ in the regulation of cell wall hy

106 uctural information on full-length, natively membrane-anchored fusogens is scarce.

107 e show that WNT5A stimulates dimerization of membrane-anchored FZD4 CRDs and oligomerization of full-

108 ure neuronal GIRK2 activity as a function of membrane-anchored G protein concentration.

109 in 2 to a GPR27V2 chimera in the presence of membrane-anchored G protein-coupled receptor kinase-2.

110 Through local injection, the membrane anchored GC-PEG-PpIX enables strong physical as

111 By developing conditional, membrane-anchored GCaMP3 mice, we found that microdomain

112 We reconstituted "membrane-anchored" gliding motility assays using truncat

113 he binding of vaccine-elicited antibodies to membrane-anchored gp160.

114 membranes, we redesigned it by introducing a membrane anchor group based on negatively charged sulfon

115 nditions in the absence of other activators, membrane-anchored GTP-Rab5A provides strong, virtually b

116 se activity and PI3P production triggered by membrane-anchored GTP-Rab5A.

117 n of the human enzyme lacking its N-terminal membrane anchor has allowed for physical and biochemical

118 ies require membrane attachment of FtsZ, few membrane anchors have been characterized.

119 scattering to produce full-length models of membrane-anchored Hck.

120 YME1L is an inner membrane-anchored hexameric protease with distinct N-ter

121 HO isoforms contain a C-terminal hydrophobic membrane anchor; however, their sequences diverge.

122 screening, these antibodies are expressed as membrane-anchored IgM (mIgM) in 293F indicator cells.

123 inct mechanisms: classic signaling using the membrane-anchored IL-6 receptor and trans-signaling usin

124 used to a glycosylphosphatidylinositol (GPI) membrane anchor, immobilizing it on the extracellular su

125 ns, two amphipathic helices, and an in-plane membrane anchor in IL-26, which are structural features

126 revealed that it contains a redox-sensitive membrane anchor in its C terminus.

127 lts provide new evidence for the role of the membrane anchor in PrP-lipid interactions, highlighting

128 he view that SNARE TMDs serve as nonspecific membrane anchors in vacuole fusion.

129 etypical DNA nanotube inserted via a ring of membrane anchors into a phospholipid bilayer.

130 Only membrane-anchored isoforms of PMEPA1 interacted with R-S

131 Its cytoplasmic components are the membrane-anchored Kar1, the yeast centrin Cdc31, and the

132 scopy, and determined distinct structures of membrane-anchored KRAS dimers in the active GTP- and ina

133 consensus model for authentically processed, membrane-anchored KRAS.

134 in vivo delivery of a corresponding soluble membrane anchored ligand, we generated lipidated analogs

135 Alternatively, membrane-anchored ligands (t-toxins, DARTs) target endog

136 which leads to multivalent interactions with membrane-anchored ligands and very high binding affiniti

137 A beta loop and a C-terminal membrane-anchoring linker occlude the active-site cavity

138 NlpA is an inner-membrane-anchored lipoprotein that has a minor role in m

139 Membrane-anchored lipoproteins have a broad range of fun

140 single-layered PG is also regulated by outer membrane-anchored lipoproteins.

141 s and hydrolases require activation by outer-membrane-anchored lipoproteins.

142 In contrast, the membrane-anchored lipoteichoic acids (LTAs) do not show

143 OPA1 exists as membrane-anchored long form (L-OPA1) and short form (S-O

144 Inner membrane-anchored long forms of OPA1 (l-OPA1) are proteo

145 Inner membrane-anchored long OPA1 (L-OPA1) undergoes proteolyt

146 However, nonsense mutations caused membrane anchor loss in three clades: human/bonobo/chimp

147 LpoA structures helped explain how an outer membrane-anchored LpoA can either withdraw from or exten

148 Membrane-anchored mammalian small GTPase Rap1 is known t

149 The membrane-anchored matrix metalloprotease MT1-MMP is a po

150 thought to depend on the mobilization of the membrane-anchored matrix metalloproteinases MMP14 (MT1-M

151 elaxed lipid density; therefore this type of membrane anchor may assist in keeping the Z ring positio

152 e test the hypothesis that the length of the membrane anchor may impact the outcome by comparing sing

153 Although Fis1 is dispensable for fission, membrane-anchored Mdv1, Mff, or MiDs paired individually

154 We demonstrate here that EphA2 and membrane-anchored membrane type-1 matrix metalloproteina

155 te tethered to a genetically targeted-plasma membrane anchor (membrane anchored Photoswitchable Ortho

156 have attached mucus as they did not shed the membrane-anchored meprin beta into the luminal mucus.

157 ntegrin And Metalloprotease (ADAM) family of membrane-anchored metalloproteases are synthesized as pr

158 The membrane-anchored metalloproteinase a disintegrin and me

159 ial regulator of cell-cell interactions, the membrane-anchored metalloproteinase ADAM17, in endochond

160 lpha)-converting enzyme (TACE) are prominent membrane-anchored metalloproteinases that regulate the t

161 Thus, membrane-anchored Mff differentially regulates various D

162 olution impairs functional interactions with membrane-anchored Mff.

163 RSV G is expressed as membrane-anchored (mG) and -secreted (sG) forms, both co

164 sults are consistent with a model in which a membrane anchored MinC/MinD complex is targeted to the Z

165 of Dn-MIP to other putative cell-surface and membrane-anchored MIP virulence factors.

166 irectly to lipid bilayers and identified its membrane anchoring moiety, consisting of a hydrophobic l

167 We reason that the transport efficiency of membrane-anchored motors is reduced because of their sli

168 However, the collective transport by membrane-anchored motors, that is, motors attached to a

169 s (MMPs) are a family of secreted soluble or membrane-anchored multimodular peptidases regularly foun

170 ively, these findings indicate that MyoB are membrane-anchored myosin receptors that define a distinc

171 In contrast, using a membrane-anchored nanobody to trap Dpp, the other study

172 spectroscopic study of HCV NS5B lacking its membrane anchor (NS5BDelta21).

173 transmembrane helices and together form the membrane anchor of complex II.

174 In contrast, the membrane anchor of HO1 did not influence its dynamics.

175 its role in the biosynthesis of lipid A, the membrane anchor of lipopolysaccharide (LPS), has not bee

176 ents of the bacteria, including lipid A, the membrane anchor of lipopolysaccharide, could affect any

177 constitutively add palmitate to lipid A, the membrane anchor of lipopolysaccharide.

178 ectra such as those produced by lipid A, the membrane anchor of lipopolysaccharide.

179 The diffusivity, majorly influenced by the membrane anchor of the component, and the repulsed abili

180 a model system we used the lipidated minimal membrane anchor of the GTPase, N-Ras (tN-Ras).

181 eurofascin-186 enrichment in turn reinforces membrane anchoring of Ankyrin-G and subsequent recruitme

182 Membrane anchoring of farnesylated KRAS is critical for

183 hai3 on cell membranes and that constitutive membrane anchoring of GIV in yeast cells or rapid membra

184 In this study, we simulated the membrane anchoring of human immunodeficiency virus-1 myr

185 pecifically induce BPL cell apoptosis due to membrane anchoring of sTRAIL and simultaneous activation

186 Glycosylphosphatidylinositol (GPI) membrane anchoring of the prion protein (PrP(C)) directs

187 CaaX motif (class B), which is important for membrane anchoring of the protein; the presence of such

188 Interchanging the membrane anchors of Bax and Bak reverses their subcellul

189 ting the dynamics and thermodynamics of this membrane anchor on a POPC bilayer using all-atom, explic

190 ion atomistic model for the huntingtin Htt17 membrane anchor on a POPC bilayer.

191 virtue of its interaction with the wild-type-membrane-anchored ORF67.

192 sion of the K2 C terminus as an extension of membrane-anchored P-selectin glycoprotein ligand-1 (PSGL

193 Ectopic expression of membrane-anchored Pak1 overrides this spatial specificat

194 ECAM) is a approximately 180-kDa multidomain membrane-anchored pan-peptidase inhibitor, which is clea

195 Fibroblast activation protein (FAP), a membrane-anchored peptidase, is highly expressed in canc

196 This compound provides a prototype membrane-anchored peptide for the treatment of inflammat

197 nyl-MurNAc-pentapeptide (lipid I), the first membrane-anchored peptidoglycan precursor.

198 entirely dependent on CD4 anchoring, not on membrane anchoring per se, and required optimal Ab geome

199 ividing cells expand their PG layer by using membrane-anchored PG synthases, which are guided by dyna

200 genetically targeted-plasma membrane anchor (membrane anchored Photoswitchable Orthogonal Remotely Te

201 Sequence analysis identified similar membrane-anchored PMMs, encoded in conserved coaBC-dut-a

202 oblasts had not previously been screened for membrane anchored proteases that could contribute to cel

203 NTNG2 encodes netrin-G2, a membrane-anchored protein implicated in the molecular or

204 Semaphorin7A (SEMA7A) is a membrane-anchored protein involved in immune and inflamm

205 Semaphorin 7a is a glycophosphatidylinositol membrane-anchored protein that promotes attachment and s

206 esent genetic evidence that a putative inner membrane-anchored protein with a large periplasmic domai

207 ied in the cytoplasmic N-terminal end of the membrane-anchored protein YfgM of Escherichia coli.

208 ble activity, BGLC3 (At5g04885) is usually a membrane-anchored protein.

209 ional, extra-mitochondrial functions of this membrane-anchored protein.

210 Surprisingly, binding of the membrane-anchoring protein FzlC disrupts DeltaCTL bundli

211 fectors, Bcl-2 family members, and organelle membrane anchor proteins.

212 Cleavage of membrane-anchored proteins by ADAM (a disintegrin and me

213 are used as a zip code to guide a subset of membrane-anchored proteins through the secretory pathway

214 Transmembrane proteins are membrane-anchored proteins whose topologies are importan

215 Adam10), a member of the ADAM family of cell membrane-anchored proteins, has been linked to the regul

216 This proteome is enriched in membrane-anchored proteins, including multiple regulator

217 e membrane-associated, involving a myriad of membrane-anchored proteins, proteomic efforts to better

218 many signalling pathways is the shedding of membrane-anchored proteins.

219 in ligase mediates the polyubiquitylation of membrane-anchored proteins.

220 All membrane-anchored, proximally located, oncogenic Ras iso

221 Membrane-anchored PrP(C) and neural cell adhesion molecu

222 ings and webs are the first demonstration of membrane-anchored PrP(Sc) amyloids.

223 thered to the outer segment membranes by its membrane anchor, R9AP.

224 much less capable of phosphorylating plasma membrane-anchored Rab10 than soluble LRRK2.

225 e cells, which facilitates binding of OPG to membrane-anchored RANKL.

226 d by the IL1RL1 gene, is expressed as both a membrane-anchored receptor (ST2L) activated by IL33 and

227 d sensitively on the binding constant of the membrane-anchored receptor and ligand proteins that medi

228 ful route to compute the binding constant of membrane-anchored receptor and ligand proteins.

229 The membrane-anchored receptor cluster of differentiation 14

230 f acrosome-reacted sperm, and the egg plasma-membrane-anchored receptor Juno [1,2].

231 des in this network are myosins XI and their membrane-anchored receptors (MyoB) that, together, drive

232 Membrane-anchored receptors are essential cellular signa

233 ore dynamic than truncated forms lacking the membrane-anchoring region, despite sharing the same stea

234 Furthermore, Pex15, the membrane anchor required for Pex1/Pex6 recruitment to pe

235 clearly show the interactions of interfacial membrane-anchoring residues with the lipids.

236 ized by the fusion of ribbon precursors with membrane-anchored ribbons that also appear to fuse with

237 ll as plasma membrane proteins with putative membrane-anchoring roles.

238 vaccine that encodes a prefusion stabilized, membrane-anchored SARS-CoV-2 full-length spike protein.

239 binding domain; or BNT162b2, which encodes a membrane-anchored SARS-CoV-2 full-length spike, stabiliz

240 Syntrophins are a family of proteins forming membrane-anchored scaffolds and serving as adaptors for

241 We identified the membrane-anchored SdhF as a subunit of the complex.

242 and refine the NMR measurements on the Htt17 membrane anchor segment of huntingtin that is of fundame

243 their hydrophobic N-terminal polymerization/membrane anchor segment with the major pilins but are mu

244 both the hydrophobic signal sequence and the membrane anchor sequence promoting translocation of the

245 The membrane-anchored serine prostasin (CAP1/PRSS8) is essen

246 Matriptase is a membrane-anchored serine protease encoded by suppression

247 emical analyses, matriptase, a member of the membrane-anchored serine protease family, is found to pl

248 TMPRSS2 is an important membrane-anchored serine protease involved in human pros

249 The membrane-anchored serine protease prostasin (CAP1/PRSS8)

250 Matriptase is an epithelia-specific membrane-anchored serine protease that has received cons

251 Matriptase-2 (MT2), encoded by TMPRSS6, is a membrane-anchored serine protease that plays a key role

252 In this study, we show how the membrane-anchored serine protease TMPRSS2 stimulates a p

253 Prostasin, a membrane-anchored serine protease with trypsin-like subs

254 The membrane-anchored serine protease, matriptase, is consis

255 d by a non-enzymatic activity of this unique membrane-anchored serine protease.

256 Membrane-anchored serine proteases (MASPs) play critical

257 ur knowledge of non-proteolytic functions of membrane-anchored serine proteases and provides unexpect

258 biochemical observations regarding these two membrane-anchored serine proteases and their downstream

259 The membrane-anchored serine proteases prostasin (PRSS8) and

260 n, however, has focused on the potential for membrane-anchored serine proteases to regulate PAR activ

261 evidence for an interplay between PAR-2 and membrane-anchored serine proteases, which may co-conspir

262 quamous cell carcinoma (HAT/DESC) cluster of membrane-anchored serine proteases.

263 e showed that BACE1 can effectively shed the membrane-anchored signaling molecule Jagged 1 (Jag1).Wea

264 on its own interferes with the zippering of membrane-anchored SNARE complexes midway through the zip

265 Syntaxins are a family of membrane-anchored SNARE proteins that are essential comp

266 and-binding activity in both its soluble and membrane-anchored states.

267 mino acid-induced cleavage of this synthetic membrane-anchored substrate occurs in a Deltatether stra

268 ydrogenase that lacks a typical cytochrome b membrane anchor subunit, which transfers electrons to th

269 ains unclear if R7BP serves exclusively as a membrane anchoring subunit or further modulates RGS prot

270 rt that RGS7 is selectively modulated by its membrane anchoring subunit R7BP, which sets the dynamic

271 eared to be secreted and Mmp2 appeared to be membrane-anchored, suggesting that protein localization

272 CpaB is a membrane-anchored T2SS chaperone that interacts with Cpa

273 with testisin in solution but also with cell membrane-anchored testisin on U937 cells.

274 Membrane-anchored TF directly interacts with substrates

275 gand recognition by this enigmatic family of membrane-anchored TGF-beta family signaling regulators a

276 geted to the plasma membrane by a C-terminal membrane anchor that comprises a farnesyl-cysteine-methy

277 ChE is anchored at the TSC by a proline-rich membrane anchor, the small transmembrane protein anchor

278 As for most known membrane anchors, the C-terminal peptide of FtsZ is requ

279 e followed by assembly toward the C-terminal membrane anchors, thus initiating membrane fusion.

280 e results indicate that being more than just membrane anchors, TM helices could play an important rol

281 rast, low pH did not affect the formation of membrane-anchored TNFR1-containing signaling complex (co

282 is of fundamental importance: it serves as a membrane anchor to control the localization of huntingti

283 Further experiments with membrane-anchored TR3 variants and the native cytokine c

284 K2-in which both protease recruitment to the membrane-anchored transcription factor and LOV domain op

285 t, which together produce translocation of a membrane-anchored transcription factor to the nucleus to

286 ity is read out via proteolytic release of a membrane-anchored transcription factor, and we temporall

287 iotin, did not displace the protein from the membrane-anchored transducer, and membrane-anchored biot

288 ssing virus-like particles (VLPs) displaying membrane-anchored trimeric Env.

289 cated form of the Rieske protein lacking the membrane anchor (trunc-TtRp) to investigate redox-state-

290 genicity 15 protein (ST15)], which encodes a membrane-anchored tumor suppressor glycoprotein.

291 Here we report that the prenylated membrane-anchored ubiquitin-fold protein (MUB) is an ear

292 er, the FATC domain of ATM may function as a membrane-anchoring unit for other biomolecules.

293 f membrane mimetics and may thereby act as a membrane-anchoring unit.

294 omposed of cytosolic V1-sector and lysosomal membrane-anchored V0-sector, regulates lysosomal acidifi

295 le CX3CL1 isoform, suggesting that it is the membrane-anchored version of CX3CL1 that regulates micro

296 ht to determine the relative contribution on membrane-anchored versus soluble CX3CL1 in regulating th

297 eltaCR_PrP), were equipped with a C-terminal membrane anchor via a semisynthesis strategy.

298 ntly, structure and orientation of the Htt17 membrane anchor were determined using a combined solutio

299 ny bacterial and most eukaryotic ACs possess membrane anchors with six transmembrane spans.

300 scherichia coli interaction of FtsZ with its membrane anchors, ZipA and FtsA, as well as the spatial