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 naling by liberating EGFR ligands from their membrane anchor.

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

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

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

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

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

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

9 ique N-terminal alpha-helix that serves as a membrane anchor.

10 phatidylinositol 3-phosphate (PI3P)-specific membrane anchor.

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

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

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

14 al proteins that use hydrophobic residues as membrane anchors.

15 binding constant of soluble proteins without membrane anchors.

16 hile the nonspecific interactions are mainly membrane-anchored.

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

18 GARP has been assumed to require membrane anchoring.

19 oteins that regulate its activity and plasma membrane anchoring.

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

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

22 Strikingly, membrane-anchored Abeta42 robustly accelerated Abeta dep

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

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

25 tion product, which is cleaved into a 57-kDa membrane-anchored active form.

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 e molecular entity that serves as the plasma membrane anchor and the possible mechanism of regulated

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

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

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

35 Myristoylation of BBLF1 both facilitates its membrane anchoring and stabilizes it.

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

37 is an unusual membrane glycoprotein with two membrane anchors and an extended coiled-coil ectodomain.

38 FtsH is the only membrane-anchored and essential ATP-dependent protease i

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

40 They are important for pore formation, membrane anchoring, and enzyme activity.

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

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

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

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

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

46 ociated ubiquitin-conjugating enzyme and its membrane anchor are both mutated, suggesting that matrix

47 The membrane-anchored atlastin GTPase couples nucleotide hyd

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

49 csA is the catalytically active subunit, the membrane-anchored BcsB subunit is essential for catalysi

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

51 The current view is that membrane-anchored beta(2a) immobilizes the channel inact

52 linked glycans, glycosylphosphatidylinositol membrane anchors, beta1,3- and beta1,6-linked glucans, a

53 tial for the association of the full-length, membrane-anchored beta3 subunit with itself.

54 337-Gly340, Thr343, and Thr345) could act as membrane anchor, binding interface for a second rhodopsi

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

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

57 membrane proteins do not merely function as membrane anchors but play active roles in many important

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

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

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

61 ne fusion protein (or adaptor); and an outer-membrane-anchored channel.

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

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

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

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

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

67 regulated by the proteolytic activity of the membrane-anchored collagenases, MT1-, MT2-, and MT3-matr

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

69 lex glycolipid, lipid A, which serves as the membrane anchor component of lipopolysaccharide (LPS) an

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

71 f of concept, the mechanism of action of the membrane-anchored cytochrome P450 reductase (POR) is stu

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

73 dophilin B2-plectin 1 complex functions as a membrane-anchoring device organizing and stabilizing the

74 tein engineering technology called MAD-TRAP (membrane-anchored display for Tat-based recognition of a

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

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

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

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

79 nits within the dimer creates an amphiphilic membrane-anchor domain structure.

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

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

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

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

84 on occurs at cysteine residues juxtaposed to membrane-anchoring domains such as transmembrane helices

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

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

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

88 oupled receptors, going beyond their role as membrane anchoring elements.

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

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

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

92 Membrane-anchored Eph receptors and ephrins represent a

93 Membrane-anchored ephrinB2 and its receptor EphB4 are in

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

95 arbohydrate-carbohydrate interaction between membrane-anchored epitopes derived from the marine spong

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

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

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

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

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

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

102 rminal hydrophobic region serves as a stable membrane anchor for proper enzyme functionality.

103 embrane-binding domain, making SepF a unique membrane anchor for the FtsZ ring.

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

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

106 id-alpha1-diacylglycerol), which function as membrane anchors for LM-A and LM-B, respectively.

107 The TM segments do not serve as mere membrane anchors for the cytosolic domain but rather med

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

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

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

111 ectodomain should allow reengineering of the membrane anchoring from a native N-terminal to an artifi

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

113 cherichia coli; (ii) in vitro AC assays with membrane-anchored full-length human AC and recombinant B

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

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

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

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

118 nsertion of peripheral proteins by using the membrane anchor (gamma-carboxyglutamic-acid-rich domain;

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

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

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

122 udies have revealed that nicastrin, a type I membrane-anchored glycoprotein, plays a role in gamma-se

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

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

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

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

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

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

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

130 -energy profile for the position of the syb2 membrane anchor in the membrane was determined using umb

131 To probe further the function of membrane anchoring in alpha(2)delta subunits, we have no

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

133 the signal peptide of Gp3 does not act as a membrane anchor, indicating that it is completely transl

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

135 The glycosyl-phosphatidylinositol (GPI) membrane anchor is also not absolutely required for LON-

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

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

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

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

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

141 Membrane-anchored lipoproteins have a broad range of fun

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

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

144 ain reveals a beta-prism fold, a hydrophobic membrane-anchoring loop, and an electropositive phosphoi

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

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

147 , including the glycosylphosphatidylinositol membrane-anchored major surface protease (MSP).

148 Membrane-anchored mammalian small GTPase Rap1 is known t

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

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

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

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

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

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

155 codes a protein with two distinct domains: a membrane-anchored metal ion permease and a diphtheria to

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

157 The membrane-anchored metalloproteinase a disintegrin and me

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

159 demonstrate that conditional deletion of the membrane-anchored metalloproteinase MT1-MMP (Mmp14) in m

160 ntegrin and metalloproteinase 17 (ADAM17), a membrane-anchored metalloproteinase that regulates epide

161 Thus, membrane-anchored Mff differentially regulates various D

162 olution impairs functional interactions with membrane-anchored Mff.

163 of recombinant protein variants lacking the membrane-anchored MHYT domain support NbdA being an acti

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

165 8, MMP-2, MMP-9, or MT1-MMP, we identify the membrane-anchored MMP, MT1-MMP, as the dominant collagen

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

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

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

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

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

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

172 neuronal gangliosides is due to the C18 acyl membrane anchor of CerS1-derived precursor ceramides.

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

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

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

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

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

178 decyl phosphocholine micelles to solvate the membrane anchor of the protein and the hydrophobic tail

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

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

181 uestions, we developed a system to mimic the membrane anchoring of Rho GTPases by creating liposomes

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

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

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

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

186 established when the palmitoylation-mediated membrane-anchor of the STREX insert was removed by eithe

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

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

189 nation is within the cell envelope as either membrane-anchored or cell wall-anchored proteins, wherea

190 ed two novel mouse models, expressing either membrane-anchored or nonanchored versions of the human A

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 ic enzymes that catalyze depalmitoylation of membrane-anchored, palmitoylated H-Ras and growth-associ

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

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 ne-integrated catalytic BcsA subunit and the membrane-anchored, periplasmic BcsB protein.

200 ity and liberation of the YtgR domain from a membrane-anchored permease in C. trachomatis could repre

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

202 ha(0) are required for selective cleavage of membrane-anchored portions of the HCV polyprotein and fo

203 le's syndrome are irreversibly stimulated by membrane-anchored proteases (MAPs) and furin-like conver

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

205 Hyaluronidase (HYAL) 2 is a membrane-anchored protein that is proposed to hydrolyze

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

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

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

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

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

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

212 How a membrane-anchored proteinase with an extracellular catal

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

214 e approach enables isolation of integral and membrane anchored proteins and is also applicable follow

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

216 Transmembrane adaptor proteins are membrane-anchored proteins consisting of a short extrace

217 The membrane-anchored proteins of enveloped viruses form lab

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

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

220 bunits of voltage-gated calcium channels are membrane-anchored proteins, which are highly glycosylate

221 otail interact in the context of full-length membrane-anchored proteins.

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

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

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

225 atypical G protein beta subunit Gbeta5 and a membrane anchor, R7BP.

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

227 risingly, we identified here dimerization of membrane anchored Ras by combining attenuated total refl

228 as evaluated by the spatial distribution of membrane-anchored Ras isoforms.

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

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

231 We have investigated the binding of membrane-anchored receptor and ligand proteins with mole

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

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

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

235 Membrane-anchored receptors are essential cellular signa

236 igned a membrane 'staple', which consists of membrane-anchored repeats of the trans-aggregating FM do

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

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

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

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

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

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

243 YpeB lacking its putative membrane anchoring sequence (YpeB(M)) or its N- and C-te

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

245 Matriptase is a membrane-anchored serine protease encoded by Suppression

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

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

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

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

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

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

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

253 Membrane-anchored serine proteases (MASPs) play critical

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

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

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

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

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

259 r chemically controlling cell adhesion using membrane-anchored single-stranded DNA oligonucleotides.

260 ull-length complexin-I binds more tightly to membrane-anchored SNARE complex than Cpx26-83, and it is

261 elix and an inhibitory helix (Cpx26-83) from membrane-anchored SNARE complex under equilibrium condit

262 ing the synaptotagmin-1 C2 domains (C2AB) to membrane-anchored SNARE complex.

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

264 Membrane anchoring strongly affects the morphology of co

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

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

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

268 ation enabling association with Sdh2 and the membrane anchor subunits.

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

270 Using variants of membrane-anchored synaptotagmin in which the Ca(2+)-bind

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

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

273 mbrane via its physical interaction with the membrane-anchored TgSUB1.

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

275 ane fusion and provides a direct view of the membrane anchor that initiates fusion.

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

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

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

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

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

281 red in the crystal structure, functions as a membrane anchor to increase the effective EIIA(Glc) conc

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

283 of a protein, releasing the active form of a membrane-anchored transcription factor (MTF) or a membra

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

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

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

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

288 ly two MMPs-one secreted type (Mmp1) and one membrane-anchored type (Mmp2)-to study the function and

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

290 nce its discovery in the mid-1980s, the cell membrane-anchored urokinase-type plasminogen activator r

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

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

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

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

295 These peripherally membrane-anchored virulence factors mediate niche-specif

296 e, Rv3645, as a reporter enzyme in which the membrane anchor was substituted by the Escherichia coli

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

298 The Psd1 beta-subunit (Psd1beta) forms the membrane anchor, which binds the intermembrane space-loc

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