ライフサイエンスコーパス: pentamer

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

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

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

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

5 h allowed the direct visualization of an SLN pentamer.

6 351 in gH/gL/gO and with UL128-Cys162 in the Pentamer.

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

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

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

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

11 on when compared with the isolated terminase pentamer.

12 ognition in the context of the phospholamban pentamer.

13 GFP or red autofluorescent protein and a GFP pentamer.

14 ins recapitulate the structure of the native pentamer.

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

16 o that observed following depletion with the pentamer.

17 omeric PLN and storage of PLN as an inactive pentamer.

18 intrinsic signals to segregate into distinct pentamers.

19 ilt of 36.1-36.6 degrees between consecutive pentamers.

20 oups, with lower accumulation of trimers and pentamers.

21 assembled in vitro from bacterially produced pentamers.

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

23 is closed by incorporating 12 capsid-protein pentamers.

24 14S particles have long been presumed to be pentamers.

25 teraction sites along the interfaces between pentamers.

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

27 terminal domains of Npm2 and Np form similar pentamers.

28 served residues in the interface between two pentamers.

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

30 ectrostatic switch that favors hexamers over pentamers.

31 ctrostatic switch that favours hexamers over pentamers.

32 two GTPCH feedback regulatory protein (GFRP) pentamers.

33 viral epitope at the junction between capsid pentamers.

34 lattice of capsid protein (CA) hexamers and pentamers.

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

36 ly asymmetric structure made of hexamers and pentamers.

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

38 hloroform) and a subsequent self-assembly of pentamer 1 into larger aggregates (in 80% methylcyclohex

39 synthetic protocol toward a merocyanine (MC) pentamer 1 which represents the first merocyanine oligom

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

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

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

43 n particular the noncovalent complexes up to pentamers (332 kDa) destroyed in FAIMS and not detected

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

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

46 Both IgM hexamers and pentamers adopted hexagonal, dome-shaped structures with

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

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

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

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

51 C heat-labile toxin (LTB) in lieu of the CTB pentamer and a donor strand truncation (dsc(14)) of CfaE

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

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

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

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

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

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

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

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

60 extended defect rows made from face-sharing pentamer and octamer rings.

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

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

63 mics simulations provided models for the SLN pentamer and the novel interaction between SERCA and an

64 Two tetramer and pentamer and three hexamer loops were selected to test t

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

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

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

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

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

70 ular interactions that allow CA to form both pentamers and hexamers and show how invariant pentamers

71 ns with variant single jelly-roll folds form pentamers and hexamers which assemble into a T = 43 icos

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

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

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

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

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

77 entamers and hexamers and show how invariant pentamers and structurally plastic hexamers associate to

78 oligomer they form: BMC-H (hexamer), BMC-P (pentamer), and BMC-T (trimer).

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

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

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

82 ctance for sequence-defined dimers, trimers, pentamers, and a heptamer.

83 ays that favor the rapid incorporation of CA pentamers, and leads to increased structural pleomorphis

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

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

86 Therefore, both the trimer and pentamer are important targets of NAbs.

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

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

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

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

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

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

93 gH-gL-gO trimer and gH-gL-UL128-UL130-UL131A pentamer), as well gH-gL and the fusion protein gB, whic

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

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

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

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

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

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

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

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

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

103 lex with pre-formed nucleosomes; wherein two pentamers bind to a nucleosome.

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

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

106 this vaccine did not express the gH/gL-based pentamer complex (PC) and failed to fully protect agains

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

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

109 tomegalovirus (GPCMV) encodes a glycoprotein pentamer complex (PC) for entry into non-fibroblast cell

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

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

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

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

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

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

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

117 rently known capsid cofactors, influenced by pentamer composition or curvature.

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

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

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

121 n patterns established that sequence-defined pentamers containing imidazole or pyrrole groups in spec

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

123 Each GABA(A) receptor pentamer contains two phosphatidylinositol-4,5-bisphosph

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

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

126 n several surfaces suggests that the octamer-pentamer defect motif acts as a flexible strain relief m

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

128 copies of the NFS1-ISD11-ACP-ISCU-FXN hetero-pentamer, delineates the interactions of FXN with other

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

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

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

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

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

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

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

136 The monomer-pentamer equilibrium is modulated by posttranslational m

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

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

139 rinsically disordered tail domains of two NP pentamers, facing each other through their distal face,

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

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

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

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

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

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

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

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

148 tameric TSP-4, but neither TSP-5/COMP of the pentamer-forming subgroup B nor TSP-2 of the trimer-form

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

150 mid sequences, based on their distinguishing pentamer frequencies.

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

152 ion, presumably because 14-3-3 protected PLN pentamers from dephosphorylation.

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

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

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

156 f neutralizing antibodies (NAbs) is the HCMV pentamer glycoprotein gH/gL/UL128-131.

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

158 old symmetry axis, and forming a basket-like pentamer helix bundle.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

178 In the 2D crystals, a PLN pentamer interacts with transmembrane segments M3 of SER

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

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

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

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

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

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

185 mains associated with SERCA and that the PLN pentamer is required for the regulation of cardiac contr

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

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

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

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

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

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

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

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

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

195 Here, we demonstrate that both trimer and pentamer NAbs are frequently found in human transplant p

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

197 fect and replicate, while laboratory-adapted pentamer-null strains do not.

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

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

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

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

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

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

204 consists of a dimer of MotB surrounded by a pentamer of MotA.

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

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

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

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

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

210 inated pentafoil knot, derived from a cyclic pentamer of the same building block.

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

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

216 nalysis revealed the presence from dimers to pentamers of native procyanidins.

217 rimentally tested this prediction, using the pentamers of SH3 domains and proline-rich motifs (SH3(5)

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

219 psid is an icosahedral lattice comprising 72 pentamers of the major capsid protein (L1) and the assoc

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

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

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

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

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

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

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

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

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

229 c MC subunits (in chloroform) up to the full pentamer pai-stack (in 75% methylcyclohexane/25% chlorof

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

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

232 The interaction of the pentamer places the cytoplasmic domains of PLN at the me

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

234 ial lines, in that gH/gL/UL128/UL130/UL131A (pentamer)-positive strains can infect and replicate, whi

235 8(+) epitopes were defined, with peptide-MHC pentamer-positive cells displaying the central and effec

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

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

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

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

240 Incorporation of pentamers results in closer trimer contacts and induces

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

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

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

244 The observation of octamer-pentamer rows in ice films formed on several surfaces su

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

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

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

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

249 The trimer- and pentamer-specific antibodies acted in a synergistic fash

250 It was also reported that pentamer-specific antibodies correlate with protection a

251 orrelation between the titers of trimer- and pentamer-specific NAbs and transmission of HCMV from mot

252 One problem with the studies on pentamer-specific NAbs to date has been that the studies

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

254 bilizing annulus was seen, instead the intra-pentamer stability comes from the interaction of VP4C an

255 VP4A capsid proteins and RNA, provides inter-pentamer stability.

256 ke other viruses of Picornavirales, no intra-pentamer stabilizing annulus was seen, instead the intra

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

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

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

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

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

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

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

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

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

268 rfacing array of capsid protein hexamers and pentamers that are recognized by numerous cellular prote

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 le the closed state structure is a symmetric pentamer, the open state displayed unexpected asymmetric

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

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

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

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

276 ced an antibody immune response to the viral pentamer to enhance virus neutralization on non-fibrobla

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

278 as been that the studies did not compare the pentamer to the other major form of gH/gL, the gH/gL/gO

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

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

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

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

283 and alpha1(-) subunits of the GABAA receptor pentamer was also identified.

284 The SLN pentamer was found to interact with transmembrane segmen

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

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

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

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

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

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

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

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

293 al or human sera were found to recognize the pentamer, which mediates HCMV entry into endothelial and

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

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

296 Pentamers with distinct subunit compositions localize di

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

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

299 It forms a pentamer, with a symmetrical, bottle-like central channe

300 FAME2) is caused by an expansion of an ATTTC pentamer within the first intron of STARD7.