ライフサイエンスコーパス: pentamer

1 oligomeric states, KcsA (tetramer) and CorA (pentamer).

2 tramer formation, as an E120A mutant forms a pentamer.

3 r C) relative to the first nucleotide of the pentamer.

4 on when compared with the isolated terminase pentamer.

5 ognition in the context of the phospholamban pentamer.

6 GFP or red autofluorescent protein and a GFP pentamer.

7 ins recapitulate the structure of the native pentamer.

8 elly-roll core) associate with a neighboring pentamer.

9 n base involving clockwise untwisting of the pentamer.

10 In solution, the protein functions as a pentamer.

11 he gH/gL/UL128/UL130/UL131 (gH/gL/UL128-131) pentamer.

12 sts at least one alpha1-alpha1 interface per pentamer.

13 erized soluble forms of gH/gL, gH/gL/gO, and Pentamer.

14 351 in gH/gL/gO and with UL128-Cys162 in the Pentamer.

15 the same as well as additional sites on the pentamer.

16 suggest that it functions as a tetramer or a pentamer.

17 lpha-helix form salt bridges in hexamers and pentamers.

18 assembled in vitro from bacterially produced pentamers.

19 otide, and multiple additions of GUCCA>p RNA pentamers.

20 is closed by incorporating 12 capsid-protein pentamers.

21 14S particles have long been presumed to be pentamers.

22 teraction sites along the interfaces between pentamers.

23 S particles are 488 kDa, confirming they are pentamers.

24 ly asymmetric structure made of hexamers and pentamers.

25 terminal domains of Npm2 and Np form similar pentamers.

26 served residues in the interface between two pentamers.

27 f replication by binding repeating G(A/G)GGC pentamers.

28 ectrostatic switch that favors hexamers over pentamers.

29 ctrostatic switch that favours hexamers over pentamers.

30 two GTPCH feedback regulatory protein (GFRP) pentamers.

31 -equivalent interactions within hexamers and pentamers.

32 te monomers, dimers, trimers, tetramers, and pentamers.

33 se that L1 protein is present in the form of pentamers.

34 orts of possible ion conductance through PLN pentamers.

35 capsid proteins are exclusively organised in pentamers.

36 intrinsic signals to segregate into distinct pentamers.

37 ilt of 36.1-36.6 degrees between consecutive pentamers.

38 oups, with lower accumulation of trimers and pentamers.

39 The regioregular pentamer (2) displayed the most resolution between signa

40 The more regioregular pentamers (2 and 3) possessed a new, red-shifted shoulde

41 e chemical environments than the regiorandom pentamers (3 and 4).

42 A binding sequence is split into overlapping pentamers (5 base pairs) for calculating transcription f

43 As the arms of the stargate grow from the pentamer, a rough disk the diameter of a capsid thickens

44 Our new fragment-based pentamer algorithm and simplified energy function improv

45 In this paper, we present an efficient pentamer algorithm by splitting DNA binding sequences in

46 ow that the Z-alpha1AT trimer, tetramer, and pentamer all form ring-like structures in strong support

47 e minor capsid protein L2 associates with L1 pentamers, although it is not known if each L1 pentamer

48 by a 216S peak that was observed to contain pentamers among lipid debris in negatively stained grids

49 architectural element of the CA hexamer and pentamer and as a mechanistic element for generating lat

50 ce running along the 'top' surface of a DdrB pentamer and continuing down between two individual subu

51 We examined the polymorphic pentamer and fibril seeds of Abeta42 and its mutants and

52 ric organization of P1-P2 in the human stalk pentamer and functional non-equivalence of the individua

53 Microarrays with isoenergetic pentamer and hexamer 2'-O-methyl oligonucleotide probes

54 Quasi-equivalent generation of both the pentamer and hexamer components of the HIV-1 viral CA is

55 lic interhelix contact in helix pairs of the pentamer and hexamer systems.

56 and tetramer, and to a triplet biradical for pentamer and hexamer.

57 ates in intersubunit interactions in the CRP pentamer and is buried, to Gln resulted in a CRP mutant

58 g a change in quaternary conformation of PLB pentamer and SERCA-PLB regulatory complex.

59 l structure of Gemin2 bound to SmD1/D2/F/E/G pentamer and SMN's Gemin2-binding domain, a key assembly

60 omposed of 12 pentamers, and the other of 12 pentamers and 20 hexamers.

61 rms diverse quaternary structures, including pentamers and 60-subunit dodecahedral capsids.

62 cella spp. (BLS) is a highly stable dimer of pentamers and a scaffold with enormous plasticity on whi

63 hysiological partner locked Npm-N in ordered pentamers and counteracted the effects of phosphorylatio

64 inds SAP in its physiological conformations, pentamers and decamers.

65 roteins, which are known to oligomerize into pentamers and decamers.

66 nd assembles correctly into heterooligomers (pentamers and hexamers).

67 ractions govern the differential assembly of pentamers and hexamers.

68 stable gH/gL/gO trimers and gH/gL/UL128-131 pentamers and little, if any, unbound gH/gL.

69 d, AIM is stabilized by association with IgM pentamers and maintains its high circulating levels.

70 the relative quantities of monomers, dimers, pentamers and octamers in the C-S-H structure are measur

71 T = 1 icosahedral particles comprised of 12 pentamers and one RNA molecule.

72 Concatameric pentamers and pentamers formed from combinations of trim

73 cently determined structure of the human IgM pentamer, and how this interaction could affect parasite

74 isulfide) with two subunits in a neighboring pentamer, and reinserts into the pentamer from which it

75 active site of SubA is not occluded by the B-pentamer, and the B-pentamer does not enhance or inhibit

76 t does not bind Ca(2+) at low pH and forms a pentamer, and the transition from tetramer to pentamer i

77 The VLPs were dissociated to VP1 pentamers, and the contaminating DNA and proteins were r

78 osahedrally symmetric: one is composed of 12 pentamers, and the other of 12 pentamers and 20 hexamers

79 ipate in contacts between protomers, between pentamers, and with the viral RNA.

80 at both Kmer-Sum and PWM stacking in the new pentamer approach along with a simplified integrative en

81 The UV spectra of the tetra- and pentamer are superimposable but differ significantly fro

82 stantiate the fullerene conjecture, show how pentamers are accommodated at vertices, support the infe

83 GABAA receptor (GABAAR) pentamers are assembled from a pool of 19 subunits, and

84 a capsid varying according to how the twelve pentamers are distributed and its size depending on the

85 imers are important early intermediates, and pentamers are metastable within clusters.

86 Over a range of coverages, pentamers are the building blocks of larger arrays that

87 lexes gH/gL/gO and gH/gL/UL128/UL130/UL131A (Pentamer) are key targets of the human humoral response

88 The purified alpha7nAChR not only forms pentamers as imaged by negative-stain electron microscop

89 These effects were mediated by alpha6alpha4* pentamers, as alpha6(L9'S) mice lacking alpha4 subunits

90 the periplasmic space of E. coli as soluble pentamers, as confirmed by multiangle light scattering a

91 he resulting receptors functionally resemble pentamers assembled with two copies of alpha4 and three

92 Structures of disulfide-linked hexamer and pentamer assemblies, as well as structures of the isolat

93 nicotine was present during, but not after, pentamer assembly and was caused by increased stability

94 We also show that a model of the hexamer/pentamer assembly can be readily generated with a single

95 The folding and pentamer assembly of the simian virus 40 (SV40) major ca

96 sidues lining the 5-fold pore did not affect pentamer assembly or prevent association with the VP2 mi

97 ion in which higher-order assemblies of DdrB pentamers assist in the pairing of complementary ssDNA u

98 to solve the X-ray structure of the HIV-1 CA pentamer at 2.5 A resolution.

99 en compared to a series of related RNAs, the pentamer binds to rCUG repeats with 4.4- to >200-fold sp

100 The most avid binder, a pentamer, binds the rCUG repeat hairpin with a K(d) of 1

101 ures of two relevant complexes: a THO hetero-pentamer bound to Sub2 at 6.0 A resolution; and Sub2 ass

102 amined the polymerization efficiencies of 20 pentamer building blocks each containing one of five dif

103 , the asymmetrical hexamer would appear as a pentamer by cryo-EM, a technology that acquires the aver

104 ng the human cytomegalovirus (HCMV) envelope pentamer complex (PC) are thought to be important for pr

105 zing antibodies (NAb) targeting the envelope pentamer complex (PC) composed of the subunits gH, gL, U

106 protomers have been assembled into the full pentamer complex embedded within the lipid bilayer.

107 he gH/gL/gO or the gH/gL/UL128/UL130/UL131A (Pentamer) complex has been found to fulfill this role, a

108 ll types, while the gH/gL/UL128/130/131a (gH-pentamer) complex imparts specificity in infecting epith

109 veals that the mAbs bind to gH-trimer and gH-pentamer complexes and identify the antibodies' epitope

110 The gH/gL/gO and gH/gL/UL128/UL130/UL131 (Pentamer) complexes play a key role in HCMV cell entry a

111 SLTs are pentamers composed of a single A and five B subunits.

112 ulum (ER) and traffic to the cell surface as pentamers composed of alpha and beta subunits.

113 e further assembled into a pentamer, with 12 pentamers comprising a single HCV virion.

114 An I40A mutation of PLB did not alter pentamer conformation but increased the concentration of

115 ed to coat-coat protein interactions between pentamers, constitute the primary lattice-forming contac

116 experimental support for the hypothesis that pentamers containing a central helical bundle, observed

117 Bacterial expression of VP1 pentamers containing substitutions to residues lining th

118 ntamers, although it is not known if each L1 pentamer contains a single L2 protein.

119 py and image reconstruction revealed altered pentamer coordination, possibly as a result of electrost

120 the tetramer crystallized at neutral pH, the pentamer crystallized at low pH, suggesting that prefere

121 the well-studied raft marker cholera toxin B pentamer (CTxB) that binds up to five GM1 glycosphingoli

122 ization with epithelial cell-tropic DB or gH pentamer-deficient DB preparations, (v) UV-inactivated r

123 The recent NMR structure of a PLN pentamer depicts cytoplasmic helices extending normal to

124 nges of a short repeat, [VPGVG]5, an alanine pentamer, desmosine, and isodesmosine sites with and wit

125 the synthesis of the butadiyne-linked cyclic pentamer, despite the fact that the radii of their N5 do

126 We have identified two pentamer DNA sequences containing 6-methylisoxanthopteri

127 We observed that highly flexible pentamers do not share structural similarities with fibr

128 is not occluded by the B-pentamer, and the B-pentamer does not enhance or inhibit the activity of Sub

129 e densities are crucial for the formation of pentamers, driven by cyclic hydrogen bonding between car

130 ave been able to directly visualize SV40 VP1 pentamers encapsidating short RNA molecules (500mers).

131 The monomer-pentamer equilibrium is modulated by posttranslational m

132 lations show that hIAPP forms from trimer to pentamer exhibit high structural stability with well-pre

133 in cells compared to a BTA monomer, with the pentamer exhibiting a 65-fold improvement in efficacy co

134 omer at its alpha-helical conformation and a pentamer fibril fragment of Abeta(42) peptide with or wi

135 transient low oligomeric states of receptor pentamers, followed by partial unfolding of helical part

136 , but not P2 CTD reduced the affinity of the pentamer for RTA.

137 l strategy to obtain soluble CA hexamers and pentamers for crystallization.

138 Portal, a dodecamer, and motor, a pentamer, form two concentric rings at the special five-

139 Concatameric pentamers and pentamers formed from combinations of trimers, dimers, a

140 These data are consistent with gH/gL/gO and Pentamer forming mutually exclusive cell entry complexes

141 chaperones bind H2A-H2B dimers with a single pentamer forming the central hub.

142 ily of histone chaperones is identified by a pentamer-forming domain and multiple acidic tracts that

143 Immunization of mice with the pentamer formulated with different adjuvants elicited HC

144 mid sequences, based on their distinguishing pentamer frequencies.

145 relate extremely well with the corresponding pentamer from crystal structures of mature BEV.

146 neighboring pentamer, and reinserts into the pentamer from which it emanates.

147 namics and conductance properties of the PLN pentamers from all-atom (AA) and coarse-grained (CG) mol

148 fied CyPs facilitated the dissociation of L1 pentamers from recombinant HPV11 L1/L2 complexes in a pH

149 ally similar and unite into mirror-symmetric pentamers (G-R-B-R-G) by adhesion.

150 ingle polycistronic vector encoding the five pentamer genes separated by "self-cleaving" 2A peptides

151 Notably, Pentamer harboring the UL128-Cys162Ser/gL-Cys144Ser muta

152 planar and tubular arrays, but the predicted pentamers have not been observed.

153 ing in the cytoplasmic domain stabilizes the pentamer in a closed conformation.

154 results reveal a regulatory role of the PLN pentamer in calcium homeostasis, going beyond the previo

155 entamer, suggesting a potential role for the pentamer in promoting fibroblast fusion.

156 rom a Ca(2+)-bound tetramer to a Ca(2+)-free pentamer in response to changes in pH.

157 re-fibrillar tetramer form and the fibrillar pentamer in the Abeta40 aggregation landscape disappears

158 or understanding the important role of the B-pentamer in the assembly and the intracellular trafficki

159 This is consistent with models of the PLB pentamer in which cytoplasmic domains fan out from the c

160 constructed in total nine different receptor pentamers in at least two different ways and expressed t

161 long with increased alpha2beta1gamma1 GABAAR pentamers in hippocampal slices using cell-surface cross

162 tein products, and assembly of protomers and pentamers in infected M1-D macrophages did not differ fr

163 contacts between the hill-like hexamers and pentamers in precursor proheads.

164 recise sequence of the region containing the pentamers in replication.

165 n type 3A (5-HT3A) ICD assembles into stable pentamers in solution in the absence of the other two do

166 ing complex consists primarily of a dimer of pentamers in solution.

167 e NPL fold and form pentamers, or a dimer of pentamers in the case of HD2.

168 One of the compounds links two toxin B-pentamers in the crystal structure, which may yield impr

169 en followed to synthesize a second series of pentamers in which the Tz group is used as a pi-conjugat

170 ion, Gemin2 wraps around the crescent-shaped pentamer, interacting with all five Sm proteins, and gri

171 pairs) for calculating transcription factor-pentamer interaction energy.

172 ivated catalytic site and confirmed that the pentamer interactions are essential for productive catal

173 t the calcium ion serves as a trigger at the pentamer interface, which switches on capsid disassembly

174 u15(SR)13 model features a cyclic [Au(I)-SR] pentamer interlocked with one staple trimer motif protec

175 ex vivo used human leukocyte antigen class I pentamers, intracellular cytokine staining, and fine map

176 ade of elongation reactions in which one VP1 pentamer is added at a time, with a rate of approximatel

177 ilt angle difference between the monomer and pentamer is approximately 13 degrees , showing that intr

178 amily; (iv) a molecular docking model of the pentamer is compatible with the location of the identifi

179 l surface antigen, would ensure that the IgM pentamer is oriented on the cell membrane with its C1q b

180 nfection of fibroblasts, and the gHgLpUL128L pentamer is required for infection of endothelial, epith

181 entamer, and the transition from tetramer to pentamer is reversible with pH.

182 We find that when Mg(2+) is present, the pentamer is stabilized by the putative gating sites (M1/

183 but whether the pRNA ring is a hexamer or a pentamer is under debate.

184 tentials of mean force indicate that the PLN pentamer is unlikely to function as an ion channel.

185 The stability of pentamers is analyzed from experiments on an isomer and

186 A is also demonstrated, and the formation of pentamers is shown to be highly sensitive to local curva

187 e of beta and alpha subunits (two copies per pentamer) is consistent with a GABA(A)R homology model b

188 ns and restoration of gH/gL/UL128-UL131A (gH pentamer), (iv) equivalent neutralizing antibody titers

189 ggested an alternative structure for the PLN pentamer, known as the pinwheel model, which features a

190 ts core, the CCD of human strain ST3 forms a pentamer lacking the bound Ca(2+) despite the residues (

191 Interestingly, the Npm2 pentamer lacks a prototypical A1-acidic tract in each of

192 ed by side chain regioregularity even at the pentamer level.

193 tamer interactions for a subset of the virus pentamers, likely because some of these residues form in

194 r-tetramer-hexamer or a monomer-dimer-trimer-pentamer model.

195 Within each pentamer most of the contacts between S100A4 dimers occu

196 p)UL128, pUL130, and pUL131 (the gHgLpUL128L pentamer) neutralized HCMV infection with high potency.

197 subunits occupy specific positions in nAChR pentamers, observed FRET efficiencies from (alpha4)(3)(b

198 The phage T4 motor, a pentamer of 70-kDa large terminase, gp17, is the fastest

199 e, three-fourths-complete capsid lacking one pentamer of capsomers and a free, stable pentamer were o

200 ds missing one capsomer, capsids missing one pentamer of capsomers, and free pentamers of capsomers)

201 sults reveal a stoichiometry consisting of a pentamer of ExbB, a dimer of ExbD, and at least one TonB

202 revealed a ca. 800 kDa decamer composed as a pentamer of five homodimers.

203 ugh it is generally accepted that eIF2B is a pentamer of five non-identical subunits (alpha-epsilon),

204 astest and most powerful packaging motors, a pentamer of gp17 that translocates DNA at a rate of up t

205 The holotoxins are composed of a pentamer of identical subunits (B subunit) responsible f

206 matically active A subunit associated with a pentamer of receptor binding B subunits.

207 he primary binding sites identified in theB5 pentamer of Stx1 are also functional in Stx2a.

208 a disaccharide analog of Gb3 bound to the B5 pentamer of Stx2a holotoxin.

209 The bacteriophage T4 motor, a pentamer of the large terminase protein (gp17) assembled

210 ascent Shigella T3SA needle is topped with a pentamer of the needle tip protein invasion plasmid anti

211 Chiral pentamers of all-trans-retinoic acid molecules have been

212 amer that sandwiches DNA between two helical pentamers of ATP-associated AAA+ domains, sharply bendin

213 quentially added to the growing capsid, with pentamers of building blocks and incomplete capsids miss

214 onjecture, they are composed of hexamers and pentamers of capsid protein (CA), with the shape of a ca

215 missing one pentamer of capsomers, and free pentamers of capsomers) had been predicted in theoretica

216 round the icosahedral fivefold axes, forming pentamers of dimers that are thought to be assembly inte

217 atalytic large subunits (LSu) assembled into pentamers of dimers, (L2)5, and differs from Rubiscos fr

218 The calcium bridge between the pentamers of polyoma viruses maintains capsid metastabil

219 formed by approximately 250 hexamers and 12 pentamers of the CA protein is delivered to the cytoplas

220 symmetry formed via the interaction among 72 pentamers of the major capsid protein, L1.

221 mors, have compact capsids assembled from 72 pentamers of the protein L1.

222 of approximately 250 hexamers and exactly 12 pentamers of the viral CA protein.

223 omposed of approximately 250 hexamers and 12 pentamers of the viral CA protein.

224 of approximately 250 hexamers and exactly 12 pentamers of the viral CA protein.

225 iruses with capsids composed primarily of 72 pentamers of the viral VP1 protein, which forms the oute

226 tegration at genomic attP landing sites, two pentamers of UAS, the hsp70 core promoter, a multiple cl

227 d bilayer membrane, PLN monomers form stable pentamers of unknown biological function.

228 ent decamer in solution, consistent with the pentamer-of-dimers assembly seen crystallographically.

229 l-atom models for the hexamer-of-hexamer and pentamer-of-hexamer elements as well as for the entire c

230 ed stable complexes of crenezumab with Abeta pentamer (oligomer model) and 16-mer (fibril model).

231 cages from a previously favored trimer to a pentamer or hexamer, and another from a trimer to a much

232 dimer and, depending upon pH, an equilibrium pentamer or hexamer.

233 ific salt bridge determines the formation of pentamers or hexamers.

234 cerevisiae Fpr4, share the NPL fold and form pentamers, or a dimer of pentamers in the case of HD2.

235 c strength or temperature to form 5.8-MDa 12-pentamer particles, indistinguishable from native empty

236 sidues 69-71 and 193-197 of VP3 spanning the pentamer-pentamer interface, and another region incorpor

237 ow how the hydrophobic patch on top of the B-pentamer plays a dominant role in binding the A-subunit.

238 observed that polymerization of tetramer and pentamer PNA building blocks with a single lysine-based

239 structure observed in the four copies of the pentamer present in the asymmetric unit has been used to

240 iometry to low sensitivity (alpha4)3(beta2)2 pentamers primarily through this interaction in the endo

241 Papillomavirus capsids are composed of 72 pentamers reinforced through inter- and intrapentameric

242 nd are arranged in the capsid in consecutive pentamers related by a translation along the main viral

243 ssembly of the quasi-equivalent hexamers and pentamers requires remarkably subtle rearrangements in s

244 Incorporation of pentamers results in closer trimer contacts and induces

245 The X-ray crystal structure of an Ns1tbe pentamer revealed an all-cis PPI helix, and the CD curve

246 nformational heterogeneity of the tetra- and pentamer, revealed from their IR spectra.

247 Interestingly, alpha2 was crystallized as a pentamer, revealing the intersubunit interactions in a w

248 MscL, a compact pentamer, reversibly opens a gigantic 30-A pore at near-

249 To combine the results from overlapping pentamer scores, we developed two methods, Kmer-Sum and

250 through a novel RNA motif consisting of the pentamer sequence AGCCC with sequence restrictions at po

251 H(R)-CH2-NH-CO- residue in a model oligourea pentamer sequence was replaced by guest units bearing va

252 of CD3/CD8/PD-1/Tim-3, HSV-1, CD8(+) T cell pentamer (specific for a peptide derived from residues 4

253 e overall location of gH/gL-, gH/gL/gO-, and Pentamer-specific neutralizing antibody binding sites.

254 eptides and by HLA-A2-restricted core(18-27) pentamer staining and CD8(+) IFN-gamma enzyme-linked imm

255 CS) (CD107a, IFN-gamma, TNF-alpha and IL-2), pentamer staining and T-cell phenotyping were used to di

256 ted during tumor development, as revealed by pentamer staining in the skin and draining LNs.

257 epitope of the P1A antigen (LPYLGWLVF) using pentamer staining.

258 (V49A) had particularly large effects on PLB pentamer structure and PLB-SERCA regulatory complex conf

259 time frame, gamma peptides derived from the pentamer subunits are produced and are organized in a ve

260 Concatameric pentamers such as beta3-alpha6-beta2-alpha4-beta2 have b

261 to gB or gH/gL but also by antibodies to the pentamer, suggesting a potential role for the pentamer i

262 e, the first structural view of gH/gL/gO and Pentamer supporting the development of vaccines and anti

263 involves kinetically trapped dislocations of pentamer-templated proteins with hexameric organization.

264 utively secreting high levels of recombinant pentamer that displayed the functional antigenic sites t

265 KpBest is a pentamer that forms a five-helix transmembrane pore, clo

266 Notably, a water pentamer that interacts extensively with the reactive gr

267 esent ideas on the possible positions in the pentamer that may be occupied by the alpha5 subunit, and

268 it that induces cellular dysfunction and a B-pentamer that recognizes host glycans.

269 In membranes, PLN forms pentamers that have been proposed to function either as

270 llection of oligomers, including trimers and pentamers, that ultimately matures into amorphous aggreg

271 On both trimers and pentamers, the effect of Tz orientation on the conjugati

272 xperiments, we then demonstrate that, in the pentamer, three anaesthetic-sensitive rho1 subunits are

273 forming LS from Aquifex aeolicus (AaLS) into pentamers through a small number of rationally designed

274 c lattice containing a variable number of CA pentamers, thus allowing for closure of tubular or conic

275 states ranging from a highly ordered, folded pentamer to a highly disordered monomer.

276 Higher-order oligomeric models (ranging from pentamer to octamer), built by incremental addition of p

277 connects the hexamers while the latter links pentamers to hexamers.

278 and rIAPP polymorphic forms from monomer to pentamer using molecular dynamics simulations.

279 a homology-based structural model of the IgM pentamer using the recently obtained crystallographic st

280 ce of a ligand, galectin-3 polymerizes up to pentamers utilizing its N-terminal domain.

281 Sera from mice immunized with the pentamer vaccine neutralized infection of both epithelia

282 that the rate of association of RTA with the pentamer was higher than with either trimer.

283 y the binding portion of the toxin, the B(5) pentamer, was also observed.

284 TM protein structures ranging from dimers to pentamers, we show that our method predicts structures t

285 A series of lower homologues of this pentamer were crystallized and studied (single crystal X

286 one pentamer of capsomers and a free, stable pentamer were obtained.

287 ncluding glycoprotein B (gB), gH/gL, and the pentamer, were evaluated for their effects on viral entr

288 asmic loop is vital for the integrity of the pentamer when Mg(2+) is absent from the M1/M2 sites.

289 red over its prefibrillar counterpart in the pentamer where an interconversion bottleneck appears.

290 50) values, the most potent inhibitor is the pentamer, which also inhibits the formation of rCAG repe

291 Furthermore, we identify the pentamer, which is essential for infection of epithelial

292 They are probably formed through trimers of pentamers, which are stabilised by the interaction of tw

293 forms highly unusual cyclic hydrogen-bonded pentamers, which combine with simultaneously formed FcCO

294 eals a diagonally bound receptor on each SAP pentamer with both D1 and D2 domains of the receptor con

295 These proteins assemble as a pentamer with identical ACh binding sites at the subunit

296 etry showed that nicotine favors assembly of pentamers with (alpha3)2(beta4)3 stoichiometry; these ar

297 Pentamers with distinct subunit compositions localize di

298 The structure consists of stacked pentamers with largely alpha helical subunits containing

299 Combining these pentamers with the hexamers previously elucidated gives

300 mer of E1/E2 may be further assembled into a pentamer, with 12 pentamers comprising a single HCV viri