ライフサイエンスコーパス: pentameric

1 amino acid [aa] residues of delta) reveals a pentameric, 145- angstrom long fiber with an N-terminal

2 of the monomers contributes unequally to the pentameric (2:1:1:1) complex of Rho dimer and Gt heterot

3 r dynamics simulations of both monomeric and pentameric Abeta, which demonstrate decreased formation

4 ate anesthetics are allosteric coagonists at pentameric alpha1beta3gamma2 GABA(A) receptors, modulati

5 xpression in Xenopus oocytes of concatenated pentameric (alpha7)5-, (alpha7)4(beta2)1-, and (alpha7)3

6 RNAs of different length capture tetrameric, pentameric and hexameric N-RNA multimers.

7 In particular, tetrameric, pentameric, and hexameric oligomeric states of MscL have

8 nge its own structure in response but remain pentameric, and then bind to pathogenic proteins deposit

9 efeldin A (BFA) that conducts to an abortive pentameric Arf1-Mg(2+)-GDP-BFA-Sec7 complex.

10 or capsid protein virus protein 1 (VP1), and pentameric arrangement of VP1 monomers results in the fo

11 Cys loop receptors are pentameric arrangements of independent subunits that ass

12 e-II PKA-AKAP18gamma complexes reveal hetero-pentameric assemblies that adopt a range of flexible tri

13 h molecular-dynamics calculations of dynamic pentameric assemblies.

14 nally identified subunit LvgA, and that this pentameric assembly binds Legionella effector proteins.

15 e external scaffolding protein D organize 12 pentameric assembly intermediates into procapsids, a rea

16 ffolding protein B mediates the formation of pentameric assembly intermediates, whereas the external

17 However, monomers are incorporated into 12 pentameric assembly intermediates, which become the caps

18 CaCC function in liposomes, is formed from a pentameric assembly of subunits.

19 The pentameric assembly presents the conserved structural sc

20 verage resolution of 4.4 angstrom, reveals a pentameric assembly that in contrast to other characteri

21 hieved by rigid body subunit rotation in the pentameric assembly.

22 ne another and assemble transiently into the pentameric Atg1 complex during starvation.

23 The pentameric B subunit of CT (CTB) contains the immunodomi

24 fined and more stable chimera comprised of a pentameric B subunit of ETEC heat-labile toxin (LTB) in

25 en linked to the simultaneous binding of the pentameric B subunit to multiple copies of glycosphingol

26 sferase PltA and the DNase CdtB, linked to a pentameric B subunit, which is alternatively made of Plt

27 ed A subunits non-covalently associated to a pentameric B subunit.

28 The pentameric B subunits of Stx types 1 and 2 (Stx1B and St

29 MSM0273 is a pentameric beta-barrel shell protein that likely plugs t

30 relevance of the dissociation of circulating pentameric C-reactive protein (pCRP) to its monomeric su

31 n, concanavalin A, and pyruvate kinase), and pentameric (C-reactive protein) complexes, ranging in si

32 hich there are 260 trimeric capsomers and 12 pentameric capsomers.

33 of a monomeric ADP-ribosylase (LTA) and its pentameric carrier B subunit (LTB).

34 Heteromeric nAChRs are pentameric cation channels, composed of combinations of

35 scL when the majority of the subunits of the pentameric channel contain the fluorescent mEos3.2 prote

36 Although the precise biological role of this pentameric channel is still unknown, this report is neve

37 For both the pentameric channel of large conductance (MscL) and the h

38 el mechanistic details of desensitization in pentameric channels.

39 n brain, mediating its actions chiefly via a pentameric chloride ion channel, the GABAA receptor.

40 iled-coil domain appended to one face of the pentameric cholera toxin B-subunit (CTB) enabled the ord

41 of imine-based pentafoil molecular knots and pentameric circular helicates despite, in practice, the

42 of an imine-based pentafoil knot and related pentameric circular helicates, each derived from a commo

43 onformation is ideal for encapsulating small pentameric clusters, either a water molecule or a fluori

44 An N-terminal pentameric coiled-coil domain is linked to a C-terminal

45 re ligand-gated ion channels that consist of pentameric combinations of alpha and beta subunits.

46 69 and genetically engineered to express CMV pentameric complex (gH/gL/pUL128/pUL130/pUL131) was deve

47 nse against HCMV glycoprotein B (gB) and the pentameric complex (PC) and the ADCC response in HCMV-se

48 GP129, which encodes a subunit of the GPCMV pentameric complex (PC) believed to govern viral entry i

49 ion of the genome encoding components of the pentameric complex (PC), in particular homologs of human

50 r neutralizing antibodies (nAbs) against CMV pentameric complex (PC)-mediated epithelial cell entry d

51 ressed and purified soluble gH/gL/pUL128-131 pentameric complex and gH/gL from Chinese hamster ovary

52 lasmic reticulum, is a membrane-bound hetero-pentameric complex consisting of Gpi8, Gpi16, Gaa1, Gpi1

53 -strain-like strains of CMV, which display a pentameric complex consisting of the viral glycoproteins

54 he necessity to monitor the integrity of the pentameric complex during the vaccine manufacturing proc

55 photocycle, the question arises whether the pentameric complex formed in the membrane via specific c

56 efective human cytomegalovirus with restored pentameric complex glycoprotein H (gH)/gL/pUL128-131 for

57 The pentameric complex has a molecular mass of 160 kDa, a st

58 light the importance of the gH/gL/pUL128-131 pentameric complex in HCMV vaccine design and emphasize

59 accine candidate but the glycoprotein H (gH) pentameric complex is now recognized as the major target

60 A 5-subunit pentameric complex is uniquely required for endothelial

61 Thus, inclusion of epitopes derived from the pentameric complex may provide enhanced efficacy by indu

62 The gH/gL/pUL128-131 pentameric complex mediates HCMV entry into endothelial

63 the dominant virus-neutralizing antigen-the pentameric complex of glycoprotein H (gH), gL, and pUL12

64 and together with the gH/gL/UL128/130/131 a pentameric complex permits infection of epithelial, endo

65 ct with the epitopes of the gH/gL/pUL128-131 pentameric complex resulting in viral neutralization, we

66 The soluble pentameric complex, but not gH/gL, adsorbs 76% of neutra

67 Functionally, the soluble pentameric complex, but not gH/gL, blocks viral entry to

68 eplication-defective virus with the restored pentameric complex, rhesus macaques can develop broadly

69 domain of Arno can also associate to form a pentameric complex, which suggests that the uncompetitiv

70 cking epithelial infection are unique to the pentameric complex.

71 completely abolished, in the absence of the pentameric complex.

72 e dissociation rate concurs to stabilize the pentameric complex.

73 t complexes representing parts or all of the pentameric complex.

74 RhgH with the other 4 RhCMV subunits of the pentameric complex.

75 ogenic sites of a dominant viral antigen-the pentameric complex.

76 targeting multiple immunogenic sites of the pentameric complex.

77 truct models of both the tail domain and the pentameric complex.

78 in a sequential manner, with tetrameric and pentameric complexes forming as intermediate states lead

79 Six of these hetero-pentameric complexes may assemble into a 1.6-MDa hexamer

80 ated ion channel family, neuronal nAChRs are pentameric, composed of various permutations of alpha (a

81 We have used a pentameric concatemer approach to express defined and co

82 s of alpha4 and beta2 subunits and establish pentameric concatemers as a means to delineate interacti

83 p16 of varphi29 was previously reported as a pentameric configuration by cryo-electron microscopy (cr

84 eta2 subunits expressed with free alpha5 and pentameric constructs incorporating a single copy of alp

85 mmon mechanism characterized by formation of pentameric contacts early in the transition.

86 The pentameric core domain, a doughnut-like structure with a

87 solution structure reveals a DotLMNYZ hetero-pentameric core from which the flexible IcmSW module pro

88 Circulating pentameric CRP (pCRP) localizes to damaged tissue where

89 tro exposure of normal neutrophils to native pentameric CRP led to a dose- and time-dependent loss of

90 FHR-1 did not bind to native, pentameric CRP, but it bound strongly to monomeric CRP v

91 e case of a 2,4-dimethoxybenzylamine-derived pentameric cyclic helicate, X-ray crystallography.

92 We report on the synthesis of 11 pentameric cyclic helicates formed by imine condensation

93 Using certain chiral amines, pentameric cyclic helices of single handedness could be

94 the activation, blockade, and regulation of pentameric Cys-loop ion channels at the atomic level.

95 xamine the role of the NCKAP1 subunit of the pentameric cytoskeletal SCAR/WAVE complex, a major downs

96 Pentameric DdrB was found to assemble into higher-order

97 using a trimeric protein (TriEst) to a small pentameric de novo-designed coiled coil domain, separate

98 A series of three pentameric derivatives of 2-methoxy-5-(2'-ethylhexyloxy)

99 The pentameric domain assists nucleosome assembly and forms

100 ral pH, bm-Calpha-PNA 1 forms a higher order pentameric double duplex of a triplex composed of two bm

101 could select Mg(2+) over Ca(2+), a bilayered pentameric filter lined with a ring of amides and a ring

102 Although both tetrameric and pentameric filters with pores that can accommodate hexah

103 f intact FMDV particles (146 S; 8200 kDa) or pentameric FMDV coat protein aggregates (12 S; 282 kDa)

104 hotoinduced conformational transition of the pentameric foldamer 105 is reflected in distinct spectra

105 Crystal structures of delta revealed novel pentameric folding repeats, which we term beta-bracelets

106 e show that monomeric CRP (mCRP) but not the pentameric form (pCRP) upregulates IL-8 and CCL2 levels

107 Another pentameric form of CRP, which exists at acidic pH, displ

108 We conclude that the pentameric form of PLN interacts with M3 of SERCA and th

109 oluene an equilibrium between tetrameric and pentameric forms exists.

110 370 microg/g in fresh leaves, assembled into pentameric forms, and bound to GM1 receptors.

111 Pentameric GABA(A) receptors mediate a large share of CN

112 On the other hand, pentameric GABAA receptors require multiple receptor sub

113 tly, potent neutralizing mAbs reacted to the pentameric gH complex but not to gB.

114 Thus, the pentameric gH complex is the primary target for antivira

115 vaccine virus in which the expression of the pentameric gH complex was restored.

116 upport a unique vaccine concept based on the pentameric gH complex, we established a panel of 45 mono

117 as dependent on high-level expression of the pentameric gH/gL/gpUL128-131A complex, a feature of WT b

118 A human cytomegalovirus (HCMV) pentameric glycoprotein complex (PC), gH-gL-UL128-UL130-

119 addition, we eliminated subunits of a viral pentameric glycoprotein complex thus limiting cell tropi

120 For example, the determination of pentameric GlyR structures bound to glycine and strychni

121 ELISA-based ligand binding assays, purified pentameric H2O2-treated CRP bound to a number of immobil

122 Here, we demonstrate for the pentameric, heptahelical membrane protein green proteorh

123 PNTs based on pentameric, hexameric, and heptameric alpha-helical barr

124 Nucleoplasmin (NP) is a pentameric histone chaperone that regulates the condensa

125 The reconstituted pentameric human stalk complex had higher affinity for R

126 ution structures of dimeric, tetrameric, and pentameric IgA-Fc linked by the joining chain (JC) and i

127 FcR specific for pentameric IgM (FCMR) is expressed at high levels by B c

128 A glycosylated model of pentameric IgM exhibits different accessibility of the g

129 suggest that OLPVRII might be a light-gated pentameric ion channel analogous to pentameric ligand-ga

130 y of, the wild-type alpha7nAChR ligand-gated pentameric ion channel, the findings point to the existe

131 r determinant of ion conductance in the GLIC pentameric ion channel.

132 ranslocated across cellular membranes by the pentameric ion channel/transporter FocA that, together w

133 Nicotinic acetylcholine receptors are pentameric ion channels that mediate fast chemical neuro

134 Pentameric ligand gated ion channels (pLGICs) mediate si

135 c acetylcholine (ACh) receptors (nAChRs) are pentameric ligand-gated cation channels that include at

136 d desensitization remain unavailable for the pentameric ligand-gated channel family.

137 GABAA receptors are pentameric ligand-gated channels mediating inhibitory ne

138 allosteric mechanisms for the superfamily of pentameric ligand-gated channels.

139 The glycine receptor (GlyR) is a pentameric ligand-gated ion channel (pLGIC) mediating in

140 omopentameric cation-selective member of the pentameric ligand-gated ion channel (pLGIC) superfamily.

141 The 5-HT(3) receptor, a pentameric ligand-gated ion channel (pLGIC), is an impor

142 ELIC, the pentameric ligand-gated ion channel from Erwinia chrysan

143 -electron microscopy Torpedo model; the only pentameric ligand-gated ion channel imaged in a native l

144 omains might be incorporated into functional pentameric ligand-gated ion channel receptors.

145 ype A receptors (GABAARs) are members of the pentameric ligand-gated ion channel superfamily.

146 agree with the structure of the prototypical pentameric ligand-gated ion channel the Torpedo nicotini

147 The nicotinic acetylcholine receptor, a pentameric ligand-gated ion channel, converts the free e

148 The homologous prokaryotic pentameric ligand-gated ion channel, Gloebacter ligand-g

149 domain of the serotonin type 3A receptor, a pentameric ligand-gated ion channel, is crucial for regu

150 d-points of the gating mechanism in the same pentameric ligand-gated ion channel.

151 Pentameric ligand-gated ion channels (LGICs) play an imp

152 Pentameric ligand-gated ion channels (pLGICs) are allost

153 Pentameric ligand-gated ion channels (pLGICs) are essent

154 Pentameric ligand-gated ion channels (pLGICs) are neurot

155 Pentameric ligand-gated ion channels (pLGICs) are target

156 -derived structure of full-length eukaryotic pentameric ligand-gated ion channels (pLGICs) is still l

157 itter-gated ion channels, the superfamily of pentameric ligand-gated ion channels (pLGICs) is unique

158 Pentameric ligand-gated ion channels (pLGICs) mediate fa

159 Pentameric ligand-gated ion channels (pLGICs) mediate fa

160 Pentameric ligand-gated ion channels (pLGICs) mediate nu

161 Pentameric ligand-gated ion channels (pLGICs) mediate si

162 Pentameric ligand-gated ion channels (pLGICs) or Cys-loo

163 Pentameric ligand-gated ion channels (pLGICs) play a cen

164 Ketamine inhibits pentameric ligand-gated ion channels (pLGICs), including

165 Pentameric ligand-gated ion channels (pLGICs), such as n

166 ulating the activity of anionic and cationic pentameric ligand-gated ion channels (pLGICs).

167 lycine receptors (GlyRs) are anion-permeable pentameric ligand-gated ion channels (pLGICs).

168 itability by modulating agonist responses of pentameric ligand-gated ion channels (pLGICs).

169 explore structure-based ligand discovery for pentameric ligand-gated ion channels (pLGICs).

170 study the structure-function relationship of pentameric ligand-gated ion channels (pLGICs).

171 binding to and modulating membrane-embedded pentameric ligand-gated ion channels (pLGICs).

172 w insights into the signalling mechanisms of pentameric ligand-gated ion channels and enhance current

173 ne receptor (nAChR) belongs to the family of pentameric ligand-gated ion channels and is involved in

174 e receptors (nAChRs) belong to the family of pentameric ligand-gated ion channels and mediate fast ex

175 ma-aminobutyric acid (GABA(A)) receptors are pentameric ligand-gated ion channels and the main driver

176 r this loop, which is vestigial in bacterial pentameric ligand-gated ion channels and was largely rem

177 Allosteric modulators of pentameric ligand-gated ion channels are thought to act

178 Pentameric ligand-gated ion channels control synaptic ne

179 igand binding at the extracellular domain of pentameric ligand-gated ion channels initiates a relay o

180 GABA(A) receptors are pentameric ligand-gated ion channels involved in fast in

181 receptor (nAChR) belongs to a superfamily of pentameric ligand-gated ion channels involved in many ph

182 Pentameric ligand-gated ion channels mediate fast chemic

183 he M3-M4 linker but also the M1-M2 linker of pentameric ligand-gated ion channels modulates function

184 Pentameric ligand-gated ion channels or Cys-loop recepto

185 Desensitization in pentameric ligand-gated ion channels plays an important

186 ways for activation, as illustrated here for pentameric ligand-gated ion channels that are principal

187 obutyric acid type A (GABA(A)) receptors are pentameric ligand-gated ion channels that mediate fast i

188 GABA(A) receptors (GABA(A)Rs) are pentameric ligand-gated ion channels that mediate synapt

189 5-HT(3) receptors are pentameric ligand-gated ion channels that regulate synap

190 ns with M1/M3 to reduce the sensitivities of pentameric ligand-gated ion channels to their surroundin

191 Inhibitory glycine receptors are pentameric ligand-gated ion channels with a definitive a

192 with other members of the Cys-loop family of pentameric ligand-gated ion channels, 5-hydroxytryptamin

193 e maturation and function of the prokaryotic pentameric ligand-gated ion channels, GLIC and ELIC, was

194 ht-gated pentameric ion channel analogous to pentameric ligand-gated ion channels, however, future pa

195 teroids potently and allosterically modulate pentameric ligand-gated ion channels, including GABA(A)

196 They belong to the family of pentameric ligand-gated ion channels, sharing a highly c

197 Although numerous studies have focused on pentameric ligand-gated ion channels, the details of ane

198 stem by acting on ion channels, most notably pentameric ligand-gated ion channels.

199 known divalent cation binding site in other pentameric ligand-gated ion channels.

200 cotinic acetylcholine receptors (nAChRs) are pentameric ligand-gated ion channels.

201 e Caenorhabditis elegans glutamate-activated pentameric ligand-gated ion channels.

202 d open a general pathway to photosensitizing pentameric ligand-gated ion channels.

203 n that is critical for channel gating in all pentameric ligand-gated ion channels.

204 Proteorhodopsin (PR) is a highly abundant, pentameric, light-driven proton pump.

205 lore the unusual host-guest chemistry of the pentameric macrocycle [{P(mu-N(t) Bu}(2) NH](5) with a r

206 NirC is a pentameric member of the formate/nitrite transporter fam

207 -nitrite transporters) form a superfamily of pentameric membrane channels that translocate monovalent

208 ome the founding father of a broad family of pentameric membrane receptors, paving the way for their

209 They are composed of a 1.4-MDa pentameric membrane translocator (TcA) and a 250-kDa coc

210 However, this pentameric model is structurally incompatible with the m

211 be bound, recognition of the canonical AUUUA pentameric motif is possible by binding to two registers

212 We predict that the tetrameric and pentameric MscL symmetries observed in previous structur

213 Npm contains a pentameric N-terminal core domain and an intrinsically d

214 in is a histone chaperone that consists of a pentameric N-terminal domain and an unstructured C-termi

215 Acetylcholine-activating pentameric nicotinic receptors (nAChRs) are an essential

216 receptor subunit, an "accessory" subunit of pentameric nicotinic receptors, that has been shown to p

217 The N-terminal domain had a pentameric nucleoplasmin-fold; making this the first rep

218 pose a new family of proteins that share the pentameric nucleoplasmin-like NPL domain and are found i

219 he acetylcholine binding protein (AChBP) are pentameric oligomers in which binding sites for nicotini

220 hesis of an azide functionalized fluorescent pentameric oligothiophene that can be utilized as a liga

221 molecules are SH3(5) (S) and PRM(5) (P), two pentameric, oppositely charged protein constructs; hepar

222 omeric right-handed four-helix bundle, and a pentameric parallel left-handed five-helix bundle.

223 tcomes correlate with the requirement of the pentameric penton base to simultaneously bind several in

224 denine recognition and ATP hydrolysis in the pentameric phage T4 large "terminase" (gp17) motor.

225 If the pentameric phenylenevinylene carries only two of these S

226 attached, regardless of their position, the pentameric phenylenevinylenes are well water-soluble.

227 aluation of three novel aldehyde-substituted pentameric phenylenevinylenes carrying branched oligo(et

228 endogenous 14-3-3 coimmunoprecipitated with pentameric PLN from cardiac membranes.

229 Mechanistically, pentameric PLN was polyubiquitinylated at the K3 residue

230 ng this model into a cryo-EM map generated a pentameric pRNA structure; five helices projecting from

231 The crown pentameric procyanidin was absent in Gewurztraminer.

232 In Chardonnay and Sauvignon Blanc, the pentameric procyanidin was present only in the cyclic fo

233 ructures of tetrameric (cinnamtannin A2) and pentameric procyanidins (cinnamtannin A3) were elucidate

234 he isolation and semisynthesis of dimeric to pentameric procyanidins from T. cacao by countercurrent

235 meric B2 and B5, trimeric C1, tetrameric and pentameric procyanidins, were isolated from unroasted co

236 the spatial arrangement of the hexameric and pentameric protein capsomers in the growing shell during

237 al Ssb, encoded by the gene ssb, and a novel pentameric protein encoded by the gene ddrB.

238 roteins and to establish the identity of the pentameric protein forming the fivefold vertices.

239 born is the center of a stargate, which is a pentameric protein oligomer.

240 C-reactive protein (CRP) is a cyclic pentameric protein whose major binding specificity, at p

241 Hillocks capped by different pentameric proteins spontaneously appear on the emerging

242 housands of subunits including hexameric and pentameric proteins that form a shell to encapsulate the

243 ype I restriction enzymes (REases) are large pentameric proteins with separate restriction (R), methy

244 of the amino acid sequence of AgSF1 reveals pentameric QPGSG iterations that are similar to conserve

245 residues line the permeation pathway of the pentameric receptor channel.

246 esolution structures of other members of the pentameric receptor superfamily provide touchstones for

247 l five pore-lining threonine residues of the pentameric receptor.

248 ans an interface between two subunits of the pentameric receptor.

249 However, the vast majority of pentameric receptors (called Cys-loop receptors in eukar

250 and beta subunits, and further assemble into pentameric receptors.

251 assembly of individual subunits into mature pentameric receptors.

252 Composed of a pentameric repeating unit of mannose, glucose, and rhamn

253 Comprised of multiple pentameric repeats, elastin-like polypeptides (ELPs) are

254 -referential contigs predominantly contained pentameric repeats, especially two motifs: AATGG and GTG

255 e with the receptor by forming an asymmetric pentameric ring around a region of the receptor carboxy-

256 catemer recognized by TerS, assembles into a pentameric ring motor on the prohead's portal vertex and

257 eriophage varphi29 is a viral genome-encoded pentameric ring of RNA (prohead RNA [pRNA]).

258 Polzeta displays a pentameric ring-like architecture, with catalytic Rev3,

259 ediated by toxin B subunits sharing a unique pentameric ring-like assembly.

260 in of the capsid protein forms hexameric and pentameric rings, while C-terminal domain homodimers con

261 e of the D76N beta2-m fibril was coated with pentameric SAP.

262 LFC) consists of the inactive Rag dimer, the pentameric scaffold Ragulator, and the FLCN:FNIP2 (FLCN-

263 engrafting the V1V2 domain into trimeric and pentameric scaffolds in structurally constrained conform

264 I-MS data, which showed mass peaks up to the pentameric self-assembly, even in the gas phase.

265 quence consisting of inverted repeats of the pentameric sequence nGAAn, known as heat shock elements

266 This collapse was most noticeable for pentameric serum amyloid P (SAP) which contains a large

267 The pentameric serum IgMs are critical to immune defense and

268 uracy of this approach by characterising the pentameric state of phospholamban, a key player in the r

269 iation' state into a catalytically competent pentameric state, is accompanied by substantial domain r

270 2+)-bound tetrameric state and a Ca(2+)-free pentameric state.

271 d beta2 subunits assemble in two predominant pentameric stoichiometries, which differ in their sensit

272 CRP, in its non-native pentameric structural conformation, binds to a variety o

273 CRP, in its native pentameric structural conformation, binds to cells and m

274 0, P1, and P2 proteins, which associate in a pentameric structure (P1(2)-P0-P2(2)).

275 these receptors do not form their functional pentameric structure in cell lines, and mechanisms that

276 ma by determining which residues support the pentameric structure in the presence or absence of Mg(2+

277 sembled from either homomeric or heteromeric pentameric subunit combinations.

278 ially expressed VLP that appear to clamp the pentameric subunits together.

279 -fold homodecamer of two head-to-head facing pentameric subunits, harboring 10 active sites at the in

280 ay dead end or at best served for storage of pentameric subunits, which was later shown to be unlikel

281 ed to dimeric, trimeric, and, in some cases, pentameric subunits.

282 s a structural change without disrupting the pentameric symmetry (pCRP*).

283 the procapsid conclusively demonstrates the pentameric symmetry of the pRNA and illuminates the rela

284 by mass spectrometry revealed that a hetero-pentameric tau3-delta-delta' Bacillus subtilis clamp-loa

285 AD-box ATPase Sub2 as assisted by the hetero-pentameric THO complex.

286 f different proteins that form hexameric and pentameric tiles, which interact to allow the formation

287 As a model, we investigated the pentameric TOG array of a Drosophila melanogaster XMAP21

288 Our data reveal that full-length pentameric TSP-4, but neither TSP-5/COMP of the pentamer

289 ture that has 42 turret-like projections: 12 pentameric turrets positioned on the icosahedral 5-fold

290 shape consistent with an arrangement of two pentameric units connected by an interstitial dimer.

291 and functional assays suggest that it forms pentameric units resembling viral capsomeres that assemb

292 e of these positions could reliably generate pentameric variants of AaLS.

293 with the capsid protein gp23 at the special pentameric vertex.

294 jacent capsomers affect the positions of the pentameric vertices, resulting in different triangulatio

295 minant SIMs in a SIM cluster often contain a pentameric VIDLT ((V/I/L/F/Y)(V/I)DLT) core sequence tha

296 Recent findings have shown that a pentameric virion complex formed by the glycoproteins gH

297 VLPs consist of 72 pentameric VP1 subunits held together by a terminal clam

298 ecific binding of the peptide to the pore of pentameric VP1.

299 We identify the formation of pentameric water clusters at pressures lower than 3 Torr

300 juni cap complex, which reveals that FliD is pentameric, with the N-terminal region of the protomer f