ライフサイエンスコーパス: pentameric

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

2 The pentameric acetylcholine-binding protein (AChBP) is a so

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

4 m a contiguous network that interconnects 12 pentameric and 30 hexameric CP capsomers.

5 metry with the capsid protein organized into pentameric and hexameric clusters that interact via prom

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 mutation increases the stability of the PLN pentameric assembly via disulfide bridge formation, prev

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

22 lorperazine (PCP) complex exhibits a similar pentameric assembly.

23 Like wild-type CRP, E42Q CRP remained pentameric at acidic pH.

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

25 The pentameric ATPase motor gp16 packages double-stranded DN

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

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 ich is composed of a cytotoxic A subunit and pentameric B subunits that bind globotriaosylceramide on

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

31 econstructions, supporting the presence of a pentameric, but not hexameric, pRNA ring in the context

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

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

34 The pentameric capsomers consist of five single jelly-roll p

35 the genome by displacing one or more of the pentameric capsomers may be the result of a low-pH envir

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

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

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

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

40 s isoflurane and propofol of the prokaryotic pentameric channel GLIC is investigated by molecular sim

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

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

43 el mechanistic details of desensitization in pentameric channels.

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

45 ing DNA clamps, which are loaded onto DNA by pentameric clamp loader complexes belonging to the AAA+

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 It exists in a stable pentameric complex, which is regulated at multiple level

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

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

71 e dissociation rate concurs to stabilize the pentameric complex.

72 ogenic sites of a dominant viral antigen-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 targeting multiple immunogenic sites of the pentameric complex.

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

77 cking epithelial infection are unique to the pentameric complex.

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

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

80 ially affected a specific GABA binding site, pentameric concatamers were used.

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 Circulating pentameric CRP (pCRP) localizes to damaged tissue where

88 At physiological pH, native pentameric CRP exhibits calcium-dependent binding specif

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 d by acidic pH-induced structural changes in pentameric CRP.

92 is similar to that of homologues with known pentameric crystal structures.

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

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

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

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

97 The alpha-subunit of these pentameric Cys-loop neurotransmitter-gated ion channels

98 Pentameric DdrB was found to assemble into higher-order

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

100 The pentameric Escherichia coli enzyme 2-hydroxypentadienoic

101 Using a homology model of the pentameric extracellular domain of alpha1beta2 channel,

102 tilage oligomeric matrix protein (COMP) is a pentameric extracellular protein expressed in cartilage

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

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

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

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

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

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

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

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

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

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

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

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

117 artilage oligomeric matrix protein (COMP), a pentameric glycoprotein found in cartilage, tendon, liga

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

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

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

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

122 olecular assembly binds multivalently to the pentameric human C-reactive protein, a biomolecule impli

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

124 We also present a pentameric humanoid nAChR extracellular domain with the

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

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

127 The hypothesized pentameric intermediate, the 12S particle, contains 16 p

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

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

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

131 three components: dodecameric portal (gp20), pentameric large terminase motor (gp17), and 11- or 12-m

132 ype A receptor (GABA(A)R) is a member of the pentameric ligand gated ion channel (pLGIC) family that

133 ay in several closely related members of the pentameric ligand gated ion channel family.

134 Pentameric ligand gated ion channels (pLGICs) mediate si

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

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

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

138 nding to the bacterial Gloeobacter violaceus pentameric ligand-gated ion channel (GLIC), a structural

139 tures of the bacterial Gloeobacter violaceus pentameric ligand-gated ion channel (GLIC), which is sen

140 IC), a proton-gated prokaryotic homologue of pentameric ligand-gated ion channel (LGIC) from G. viola

141 ructure of GLIC, a prokaryotic member of the pentameric ligand-gated ion channel (pLGIC) family, prov

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

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

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

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

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

147 GlyRs are members of the pentameric ligand-gated ion channel superfamily (pLGIC)

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

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

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 neurot

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

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

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

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

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

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

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

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

161 Rapid opening and closing of pentameric ligand-gated ion channels (pLGICs) regulate i

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

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

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

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

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

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

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

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

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

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

172 tational approaches, we show that eukaryotic pentameric ligand-gated ion channels are characterized b

173 Pentameric ligand-gated ion channels are targets of gene

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

175 Pentameric ligand-gated ion channels control synaptic ne

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

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

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

179 Pentameric ligand-gated ion channels mediate fast chemic

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

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

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

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

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

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

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

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

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

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

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

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

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

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

194 bition of GLIC and possibly other homologous pentameric ligand-gated ion channels.

195 ng and closing of the ion-conducting pore in pentameric ligand-gated ion channels.

196 tate the allosteric mechanisms of eukaryotic pentameric ligand-gated ion channels.

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

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

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

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

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

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

203 Herein, we propose that the pentameric model of SH protein presented is a physiologi

204 r crystal structure at 3.5 A resolution of a pentameric MscL from Mycobacterium tuberculosis represen

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

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

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

208 cotinic acetylcholine receptors (nAChRs) are pentameric, neurotransmitter-gated ion channels responsi

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

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

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

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

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

214 2) had a high propensity to form paranuclei (pentameric or hexameric) structures that could self-asso

215 ng platform for RTA on the ribosome and that pentameric organization of the stalk accelerates recruit

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

217 olding protein mediate the association of 12 pentameric particles into procapsids.

218 eractions between the trimeric fiber and the pentameric penton base are mediated by a hydrophobic rin

219 structure and its mode of attachment to the pentameric penton base by using an integrative approach

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

221 he trimeric fiber attaches to its underlying pentameric penton base.

222 hat a maximum of four integrins fit over the pentameric penton base.

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

224 If the pentameric phenylenevinylene carries only two of these S

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

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

227 Here, we report the T-state structure of pentameric PLN solved by a hybrid solution and solid-sta

228 Mechanistically, pentameric PLN was polyubiquitinylated at the K3 residue

229 The pentameric pRNA ring anchors itself directly to the phag

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

246 assembly of individual subunits into mature pentameric receptors.

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

248 binding behavior and substrate affinity to a pentameric recognition protein (C-reactive protein, CRP)

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

250 arly, the central thymine nucleotide of both pentameric repeats was essential for efficient toxT acti

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

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

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

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

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

256 position relative to two tau protomers in a pentameric ring.

257 (2+)-S100A4/TFP dimers into a tightly packed pentameric ring.

258 The NTD forms either hexameric or pentameric rings, whereas the CTD forms symmetric homodi

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

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

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

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

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

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

265 The pentameric serum IgMs are critical to immune defense and

266 ompared the interaction of RTA with the full pentameric stalk complex containing two pairs of P1/P2 p

267 specificity of CRP in its acidic pH-induced pentameric state has implications for toxic conditions i

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 acidosis or other possible modifiers of the pentameric structure of CRP at the sites of inflammation

278 c pH did not monomerize CRP but modified the pentameric structure, as determined by gel filtration, 1

279 sembled from either homomeric or heteromeric pentameric subunit combinations.

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

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

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

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

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

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

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

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

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

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

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

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

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 2-subunit portal situated beneath one of the pentameric vertices, thus removing uncertainty over the

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

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

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

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

300 ia formation within a 400-kilodalton, hetero-pentameric WAVE regulatory complex (WRC).