ライフサイエンスコーパス: antiparallel

1 ed R-loops, where the two DNA strands remain antiparallel).

2 other and a lower capacitance when spins are antiparallel.

3 ical axes are oriented either in parallel or antiparallel.

4 ks run diagonally between connected pairs of antiparallel actin filaments and are oriented at an angl

5 inated by a pseudo-chain of Pt-Pt dimers and antiparallel alignment of the azide substituents, in com

6 Magnetization switching between parallel and antiparallel alignments of two magnetic layers in magnet

7 Dimerization is mediated by formation of an antiparallel alpha-helical coiled-coil involving residue

8 Two antiparallel alpha-helices form a coiled-coil domain lin

9 ociation states above this are known, as are antiparallel and mixed arrangements of the helices.

10 g of the monomer secondary structure between antiparallel and parallel beta-sheet architectures.

11 urements, very important differences between antiparallel and parallel ion pair-pi interactions are i

12 ally limited to parallel (ferroelectric) and antiparallel (antiferroelectric) collinear alignments of

13 y limited agreement with either parallel- or antiparallel-arranged dimer structures when spin labels

14 forms pairs of protofilaments that adopt an antiparallel arrangement in vitro and in vivo.

15 odel to approximate the compact parallel and antiparallel arrangement of alpha-helices and beta-stran

16 We show that mu and p prefer an antiparallel arrangement, predict that Fe-doped CaZnOS i

17 e beta-sheet is assumed to retain its native antiparallel arrangement.

18 eir middle domains to form both parallel and antiparallel arrangements in solution.

19 During cytokinesis, the antiparallel array of microtubules forming the central s

20 econdary structure with a strong increase in antiparallel beta sheet content.

21 ith a significant fraction of intermolecular antiparallel beta sheet FP structure with adjacent stran

22 rmolecular amphipathic two- or three- strand antiparallel beta sheet.

23 her proportion of intermolecular-beta-sheets+antiparallel beta sheets and lower alpha-helix had great

24 beta-sandwich topology formed by 2 sheets of antiparallel beta strands stabilized by the hallmark dis

25 28 shares a "mog1p"-fold consisting of seven antiparallel beta strands stacked between alpha helices.

26 structure shows AtDIR6 as an eight-stranded antiparallel beta-barrel that forms a trimer with spatia

27 fied fold comprised of a compact 12-stranded antiparallel beta-sandwich wrapped in two short alpha he

28 vealed a novel fold comprising a four strand antiparallel beta-sheet and two helical turns stabilized

29 eptide demonstrates that the out-of-register antiparallel beta-sheet arrangement of monomers also occ

30 ved for the NTAIL protein that folds into an antiparallel beta-sheet at the A/W interface and present

31 The reason is that NMR data strongly suggest antiparallel beta-sheet calcitonin assembly, whereas mod

32 iophage P22, but TTPA contains an additional antiparallel beta-sheet carrying a lectin-like domain th

33 he monomers in the fibril are arranged in an antiparallel beta-sheet conformation.

34 presence of hydrophobic crowders reduces the antiparallel beta-sheet content of fibrils, whereas hard

35 actin reveals an amphipathic hydrogen-bonded antiparallel beta-sheet dimer that binds chloride anions

36 were dimerized to form a large 10-stranded, antiparallel beta-sheet flanked by alpha-helices on each

37 el beta-sheet despite the co-existence of an antiparallel beta-sheet in the same structure.

38 luate pairwise amino acid interactions in an antiparallel beta-sheet motif.

39 We also propose that the antiparallel beta-sheet of teixobactin is important for

40 stabilization of the experimentally observed antiparallel beta-sheet packing.

41 orms a novel protein fold of a four-stranded antiparallel beta-sheet stabilized by a crossing-over al

42 ur-residue alpha-helix and one three-residue antiparallel beta-sheet stabilized by two disulfide bond

43 ver, it adopts the canonical triple-stranded antiparallel beta-sheet structure of WW domains when bou

44 peptide chain is sufficient to nucleate some antiparallel beta-sheet structure; addition of beta-capp

45 ular copper concentration, and the amount of antiparallel beta-sheet structures were significantly ch

46 ment that is necessary for oligomers with an antiparallel beta-sheet to propagate into fibrils that h

47 alpha-helices and a layer of three-stranded antiparallel beta-sheet with flexible N and C termini.

48 esolution of 1.79 angstrom revealed a single antiparallel beta-sheet with six conserved cysteine resi

49 cystatin-like fold composed of a 5-stranded antiparallel beta-sheet wrapped around a 5-turn alpha-he

50 protein structures lead to the formation of antiparallel beta-sheet, beta-turns, intermolecular beta

51 ovel fold organized around a central core of antiparallel beta-sheet, showing an N-terminal alpha/bet

52 intrinsic helicity, while both parallel and antiparallel beta-sheet-like structures are realized.

53 nal amyloid assembly and further reveal that antiparallel beta-sheet-rich amyloids can be functional

54 ed by residues 30-42, which arranges into an antiparallel beta-sheet.

55 a-helices and a highly curved three-stranded antiparallel beta-sheet.

56 s, provide a characteristic signature of the antiparallel beta-sheet.

57 refibrillar oligomers that consist of mainly antiparallel beta-sheets and fibrillar oligomers with on

58 Two antiparallel beta-sheets assemble with symmetric homodim

59 rin complexes require (1) an increase in PF4 antiparallel beta-sheets exceeding approximately 30% (ac

60 n core features a globular architecture with antiparallel beta-sheets forming a central beta sandwich

61 S is unique in that its amyloids are rich in antiparallel beta-sheets instead of the more common para

62 fold like architecture which consists of two antiparallel beta-sheets with 7 main strands, packing ag

63 otyrosine vs lysine, coassemble as stacks of antiparallel beta-sheets with precisely patterned charge

64 beta-sheets (recognized by antiserum OC) or antiparallel beta-sheets, beta-solenoids, beta-barrels,

65 housed within a flexible loop connecting two antiparallel beta-sheets, flanked by disordered N- and C

66 SA2 nanocarriers are built of interdigitated antiparallel beta-sheets, which bear little resemblance

67 All three WW domains display a similar three antiparallel beta-strand structure and interact with the

68 itially natively folded proteins with an all antiparallel beta-stranded structure.

69 ises four alpha-helices enwrapping a pair of antiparallel beta-strands (ribbon).

70 te that formation of hairpins connecting two antiparallel beta-strands determines overall folding.

71 allelic mutations in WDR1 affecting distinct antiparallel beta-strands of Aip1 were identified in all

72 ss a typical Ig-like fold encompassing seven antiparallel beta-strands organized in two beta-sheets,

73 rms a squashed beta-barrel consisting of six antiparallel beta-strands similar to what was observed i

74 n inhibitor cystine knot structure, with two antiparallel beta-strands stabilized by three disulfide

75 ised of two layers of beta-sheets possessing antiparallel beta-strands with each being anchored by a

76 a nine-stranded beta-barrel fold with mostly antiparallel beta-strands, and the loops extending out t

77 on a cylindrin-like shape composed of mostly antiparallel beta-strands.

78 th a simultaneous increase in the content of antiparallel-beta-sheet.

79 regates (1604cm(-1)), H-bonded parallel- and antiparallel-beta-sheets (1690cm(-1)) and H-bonded beta-

80 were positively correlated to intermolecular+antiparallel-beta-sheets and negatively with beta-turn+

81 alpha-helix and negative with intermolecular+antiparallel-beta-sheets in gluten.

82 the Notch1-DLL4 complex reveals a two-site, antiparallel binding orientation assisted by Notch1 O-li

83 also stabilized and rearranged into a novel antiparallel bundle associated with the spindle pole bod

84 spindle bipolarity requires the microtubule antiparallel bundler PRC1/Ase1 to recruit CLASP/Cls1 to

85 ified oMAP4 aligns dynamic microtubules into antiparallel bundles that withstand motor forces in vitr

86 a result, when intersecting microtubules are antiparallel, canonical transport of one microtubule alo

87 dule of the complementary subunit to form an antiparallel CBS module.

88 hat has been experimentally observed for the antiparallel CC of the dynein stalk region and the nucle

89 lain why nature has evolved the principle of antiparallel chain orientation and has not used the para

90 In our design the two antiparallel chemistries are thiol-disulfide exchange an

91 Herein we introduce the concept of antiparallel chemistries, in which the same functional g

92 embrane protein and by combining parallel or antiparallel chloride and proton gradients, we show that

93 istinct FtsX-binding sites located within an antiparallel coiled coil domain of EnvC.

94 urprisingly, this structure is a continuous, antiparallel coiled coil where GCN4-p1 pairs with myosin

95 structural outcome of adjacent parallel and antiparallel coiled coils.

96 ed by a central helical domain that forms an antiparallel coiled-coil motif and mediates the dimeriza

97 gn rationally a well-defined and hyperstable antiparallel coiled-coil tetramer (apCC-Tet).

98 The dimer core comprises an antiparallel coiled-coil with a distinctive, symmetric p

99 protocadherin-15 EC1-3 molecules forming an antiparallel complex with two cadherin-23 EC1-2 molecule

100 ysiological solutions have an intramolecular antiparallel configuration that is distinct from the int

101 ociated with a loop of either "parallel" or "antiparallel" configuration.

102 a CC interface is different for parallel and antiparallel configurations, both are characterized by a

103 nces of homodimeric CC, in both parallel and antiparallel configurations.

104 in fact, the DFNKF sequence is not stable in antiparallel conformation, suggesting that the residue f

105 beta-sheets, whereas they quickly unfold in antiparallel conformation.

106 Our NMR results show that our antiparallel cross-link performs as predicted: dramatica

107 In the collapsed R-loops, antiparallel d(TTC+).d(GAA):r(UUC) is unstable, while pa

108 The D'D3 dimer ([D'D3]2) comprises 2 antiparallel D3 monomers with flexibly attached protrusi

109 entral trimeric coiled-coil and a C-terminal antiparallel DCC.

110 magainin 2 derivative displayed a homochiral antiparallel dimer association featuring a "phenylalanin

111 P have provided evidence for formation of an antiparallel dimer at pH 5.5, stabilized by stacking of

112 Thus, myosin X functions as an antiparallel dimer in cells with a unique geometry optim

113 inimal B-repeat construct (Brpt1.5) forms an antiparallel dimer in the presence of 2-3 Zn(2+) ions.

114 A large antiparallel dimer interface formed by the first 4 extra

115 ctin is important for its bioactivity and an antiparallel dimer of teixobactin is the minimal binding

116 The fundamental units of the crystals are antiparallel dimer ribbons of SERCA, known for decades a

117 SERCA molecules are organized into identical antiparallel dimer ribbons.

118 The antiparallel dimer structure in the magainin 2 simulatio

119 asymmetric unit, whereas another contains an antiparallel dimer was refined at 2.58 A.

120 r-transmembrane helix domains folded into an antiparallel dimer, where the orientation of the two dom

121 ding it, forming an approximately 150-A-long antiparallel dimer.

122 The unusual symmetrical antiparallel dimeric architecture of Flucs demands that

123 ules that bind to the minor groove of DNA as antiparallel dimers in a specific orientation.

124 nce transporters from this family consist of antiparallel dimers that resemble the inverted repeats p

125 While Myo10 is known to form antiparallel dimers, DdMyo7 lacks a coiled-coil domain i

126 s without tail-head interaction, tail-folded antiparallel dimers, tail-folded antiparallel tetramers,

127 ngth proceeds from folded monomers to folded antiparallel dimers, tetramers, and hexamers that unfold

128 at the tripartite motif (TRIM) of KAP1 forms antiparallel dimers, which further assemble into tetrame

129 plex structures: a parallel, a hybrid and an antiparallel DNA and a parallel RNA, in the presence of

130 led angles, and the lines are represented by antiparallel DNA crossover tiles of variable lengths.

131 th conventional double stranded DNA and with antiparallel DNA double crossover molecules, it is clear

132 cation occurs semidiscontinuously due to the antiparallel DNA strands and polarity of enzymatic DNA s

133 ss of bilayer cholesterol concentration, the antiparallel double helix (ADH) conformation was observe

134 We show that Dvl DIX forms antiparallel, double-stranded oligomers in vitro, and th

135 we provide a structural perspective on known antiparallel duplex structures in which at least one str

136 idging fibre, suggesting that it consists of antiparallel dynamic microtubules.

137 We present the structure of the antiparallel EC1-4 homodimer of human PcdhgammaB3, a mem

138 on analysis, we found evidence for a similar antiparallel EC1-4 interaction in non-clustered Pcdh fam

139 Now, we have used the antiparallel EmrE crystal structure to design a cross-li

140 that they alternate and hydrogen bond in an antiparallel fashion along the fibril axis.

141 onsists of two similar domains aligned in an antiparallel fashion.

142 arized, motile comet tails that associate by antiparallel filament bundling to form bipolar, DNA-segr

143 ocess for motor motion with switches between antiparallel filaments and binding kinetics.

144 d a dense and anisotropic array of elongate, antiparallel filaments, whereas myosin II was organized

145 and hexamers that unfold and polymerize into antiparallel filaments.

146 ils to induce a conformational change in the antiparallel fold of OTABA, subsequent additions of OTA

147 ated to adopt a novel type of mixed parallel/antiparallel fold-back DNA structure, which is stabilize

148 yQ fibrils might also be a zipper layer with antiparallel four-stranded stretches as this structure s

149 longer myosin-10 segments in these parallel/antiparallel fusions are dynamic and do not fold coopera

150 ermodynamically stable species (parallel and antiparallel G-quadruplex in K+ and Na+, respectively).

151 iomers binds specifically to human telomeric antiparallel G-quadruplex.

152 eir longer counterparts form parallel and/or antiparallel G-quadruplexes (G4s).

153 quadruplex structure containing two central antiparallel G-tetrads and six i-motif C-C+ base pairs.

154 n the presence of Na(+) that consist of both antiparallel G4s and i-motifs.

155 ive microtubule sliding in both parallel and antiparallel geometries, an activity that has been sugge

156 ) binding aptamer (OTABA) that folds into an antiparallel GQ in the absence and presence of target OT

157 uence in ssDNA which forms both parallel and antiparallel GQs, dsDNA displays only parallel folding.

158 discoidal structure, which included pairs of antiparallel helices of apolipoprotein AI circumscribing

159 e are seen in the 1:1 heterotetramer with an antiparallel helix arrangement.

160 solution of 2D IR spectroscopy, parallel and antiparallel helix associations were identified by vibra

161 nserved PRMT domain architecture and form an antiparallel heterodimer that corresponds to the canonic

162 We have substituted an antiparallel heterodimeric coiled-coil motif for the bet

163 ith those present in the prototypical linear antiparallel heterotetramer as well as recently reported

164 Here, we focus on antiparallel homo- or heterodimeric small multidrug resi

165 We thus deduce that the EC1-4 antiparallel homodimer is a general interaction strategy

166 nsmembrane domain and forms a highly unusual antiparallel homodimer that is stably associated with MC

167 eterologous binding partners, BECN1 forms an antiparallel homodimer via its coiled-coil domain (CCD).

168 ork, we sought to design a set of orthogonal antiparallel homodimeric coiled coils using a computatio

169 amework to engineer sets of three orthogonal antiparallel homodimeric coiled coils.

170 fluoride channels are assembled as primitive antiparallel homodimers.

171 abilizing propeller type loops, shifting the antiparallel htel-22 into hybrid or parallel quadruplexe

172 with oligonucleotides forming mixed parallel/antiparallel hybrid-1 and hybrid-2 topologies {e.g. d[TT

173 tional form of human telomeric G-quadruplex (antiparallel, hybrid, parallel monomers or a 48 nt seque

174 N-terminal edge of the BamA catalyst has an antiparallel hydrogen-bonded interface with the C-termin

175 ped or ring-like containing parallel G4s and antiparallel i-motifs.

176 the M10:O1 complex displays a chevron-shaped antiparallel Ig-Ig architecture held together by a conse

177 The antiparallel interaction with tropomyosin contained abun

178 ts that G monomers can re-associate, through antiparallel interactions between fusion domains, into d

179 g structures, base triplets, or other 3D non-antiparallel interactions.

180 kinetic constants involving a rapidly formed antiparallel intermediate were observed with oligonucleo

181 ew solid-state NMR constraints that indicate antiparallel intermolecular alignment of beta-strands wi

182 l, kinesin-5 motors persistently slide apart antiparallel interpolar microtubules (ipMTs).

183 on of push-pull fluorophores originates from antiparallel ion pair-pi attraction to their polarized e

184 he excited state; i.e., parallel rather than antiparallel ion pair-pi interactions are preferred, des

185 l predictions, we find that parallel but not antiparallel ionpair-pi interactions afford operational

186 ization, stability, and motor composition of antiparallel ipMTs at the midzone, thereby facilitating

187 e starting peptide arrangement (parallel vs. antiparallel) is still observed on this timescale.

188 akes them more stable than putatively formed antiparallel L18W-PGLa and MG2a homodimers.

189 is expected for one of these conformations-"antiparallel" loop.

190 Therefore, "antiparallel" looping is observed in a single-molecule t

191 o occurred in a configuration similar to the antiparallel (lower) dimer.

192 e, involving fusion domains associated in an antiparallel manner to form an intermolecular beta-sheet

193 binds the tandem WW domain polypeptide in an antiparallel manner, that is, the WW1 domain binds the s

194 on nearly the same timescale as formation of antiparallel melittin dimers, about 6 to 9 ms for 0.3 mM

195 omains in the MKLP1 dimer to be suitable for antiparallel microtubule bundling.

196 alpha and beta preferentially inhibit XCTK2 antiparallel microtubule cross-linking and sliding by de

197 c, microtubule-independent enrichment of the antiparallel microtubule crosslinker Prc1 at kinetochore

198 zone bundle formation results from promoting antiparallel microtubule crosslinking, stopping microtub

199 rd the cell's apex and base with a region of antiparallel microtubule overlap at the cell's midzone.

200 The antiparallel microtubule overlap geometry may offer a pr

201 the motion of Xklp1 motors on reconstituted antiparallel microtubule overlaps demonstrated that moto

202 e enables them to cross-link and slide apart antiparallel microtubules (MTs) emanating from the oppos

203 In anaphase spindles, antiparallel microtubules associate to form tight midzon

204 Kinesin-5 slides antiparallel microtubules during spindle assembly, and r

205 Besides sliding apart antiparallel microtubules during spindle elongation, the

206 ic motor protein, can push apart overlapping antiparallel microtubules to generate a force whose magn

207 fferential is low on parallel and extreme on antiparallel microtubules where one motor domain pair be

208 rallel microtubules at the spindle poles and antiparallel microtubules within the spindle midzone to

209 ross-link and drive the extensile sliding of antiparallel microtubules.

210 with kinesin-1 driving outgrowth by sliding antiparallel microtubules.

211 rs to be more stable than the mixed parallel/antiparallel MidG4.

212 that the low level of adhesion allows rapid antiparallel migration.

213 novel CaM-binding motif, binds to CaM in an antiparallel mode with the N-terminal helix (alpha1) anc

214 Moreover, BTPA-TCNE shows an antiparallel molecular packing (i.e., centrosymmetric di

215 oms, which are only partially compensated by antiparallel moments of 1.53(14)-3.26(5) mu(B) on the 3

216 , the vertebrate neural tube is patterned by antiparallel morphogen gradients.

217 the central beta-hairpin coordinated with an antiparallel motion of the C-terminal helix, which may a

218 used here was to fix the orientation of two antiparallel MRAP molecules and then introduce inactivat

219 vestigated the contribution of the midzonal, antiparallel MT-cross-linking nonmotor MAP, Feo, to this

220 gulator of cytokinesis 1), which cross-links antiparallel MTs and is essential for the completion of

221 associated with MTs may cross-link and slide antiparallel MTs emanating from the two nuclei, whereas

222 preferentially cross-links and slides apart antiparallel MTs while the MT plus ends exhibit dynamic

223 s-end-directed motility upon binding between antiparallel MTs.

224 We reveal the solution structure of a short, antiparallel, myosin-10 coiled-coil fused to the paralle

225 c transport properties of colloidal beads in antiparallel networks of overlapping actin filaments.

226 is doubly degenerate and corresponds to two antiparallel non-zero wavevectors.

227 short loops two parallel NHR helices and an antiparallel one with the inverse sequence followed by e

228 e parallel configuration with respect to the antiparallel one, while the behaviour of the force patte

229 AtFH14 bundles actin filaments randomly into antiparallel or parallel spindle-like structures; howeve

230 etal filaments assemble into dense parallel, antiparallel, or disordered networks, providing a comple

231 te residues and the FimA core and not by the antiparallel orientation of the donor strand alone.

232 eudo-palindromic sequence, is inserted in an antiparallel orientation relative to the last beta-stran

233 with the Nte inserted in the pilus rod-like, antiparallel orientation, only depends on the identity o

234 bonding between C horizontal lineO...HN with antiparallel orientation.

235 n bond formation at the correct distance and antiparallel orientation.

236 ding to DNA over RNA and specifically in the antiparallel orientation.

237 on the EC1-EC4 domains, which interact in an antiparallel orientation.

238 oth SIM2 and SIM3 bind SUMO3 in parallel and antiparallel orientations and identified main interactio

239 variable binding of the SIMs in parallel and antiparallel orientations.

240 at several sequences are capable of adopting antiparallel orientations.

241 ties in protein aggregation diseases contain antiparallel, out-of-register beta-sheet structures and

242 Its accumulation at the central antiparallel overlap zone is key for recruitment and reg

243 of links, presumably alpha-actinin, linking antiparallel overlapping ends of the actin filaments fro

244 e, including proteins needed to generate the antiparallel overlapping interzonal MTs.

245 The length of the central antiparallel overlaps in these microtubule bundles is si

246 led-coil linear strands and their hexagonal, antiparallel packing within the crystal.

247 e of the molecular hinge in promoting myosin antiparallel packing.

248 ergo ligand-induced topology changes between antiparallel, parallel, or hybrid GQ structures.

249 We also construct an antiparallel pi-sheet, wherein terminal PPV blocks are a

250 nts and theoretical calculations point to an antiparallel pi-stacking interaction as the most stable

251 in-5 both preferentially cross-link MTs into antiparallel polarity patterns, kinesin-5 cannot substit

252 omerization reaction to give exclusively the antiparallel product.

253 rientation is more stable; both parallel and antiparallel protonated d(GA+A).d(GAA):d(TTC) triplexes

254 witch involves the conversion of alternative antiparallel quadruplex structures binding only one cati

255 s primarily remove Gh from Na(+)-coordinated antiparallel quadruplexes but not K(+)-coordinated paral

256 ructure adjoined to two stacked parallel and antiparallel quadruplexes.

257 bacteria is mediated by homology across the antiparallel recombinase-specific recognition sites pres

258 es from one to over 100 and suggest distinct antiparallel registries for interprotofibril association

259 The antiparallel self-assembled pore of the fluorinated trip

260 Antiparallel sequence-complementary oligomers generally

261 molecularly H-bonded molecules stacked in an antiparallel sheet alignment.

262 d it tends to align well across parallel and antiparallel sheets, like rungs on a ladder.

263 nt dimer is a Cu(II)-bound structure with an antiparallel side-by-side configuration.

264 otubule depolymerase, plus-end motility, and antiparallel sliding activities.

265 ipole moment, consistent with the contracted antiparallel solid-state pi-pi stacking distances of 8.6

266 oscopy, we reconstruct ParM doublets forming antiparallel spindles.

267 he condensation of electrons into pairs with antiparallel spins in a singlet state with an s-wave sym

268 ed structure at high salt is most likely the antiparallel stacked-X structure.

269 moments with spatial orientations that favor antiparallel stacking and whose structure allows the res

270 as well as electrostatic interactions in the antiparallel stacking mode were first utilized to obtain

271 d(TAGGGTTA) tetraplex to give the first such antiparallel strand assembly in which syn-guanosine is a

272 Oligonucleotides with parallel or antiparallel strand orientation incorporating 2'-fluorin

273 -stranded DNA, RNA, and DNA-RNA hybrids with antiparallel strand orientation.

274 ruplex structures with parallel, hybrid, and antiparallel strand orientations depending on the temper

275 placement at non-H-bonding positions across antiparallel strands has proven useful for achieving ful

276 of domain atrophy through deletion of 2 core antiparallel strands, resulting in the loss of an entire

277 on, resulting in the formation of remarkable antiparallel streams of cells along the tracks.

278 hanges of telomeric DNA G-quadruplexes to an antiparallel structure (as determined by circular dichro

279 of the human telomeric G-quadruplexes to an antiparallel structure and that this conformational chan

280 parallel arrangement and one of the possible antiparallel structures (with Asp(15) and Phe(19) aligne

281 own to bind preferentially to hybrid than to antiparallel structures, and L2H2-6M(2)OTD, known not to

282 emical basis for F(-) permeation and how the antiparallel subunits convene to form a F(-)-selective p

283 tail-folded antiparallel dimers, tail-folded antiparallel tetramers, unfolded bipolar tetramers, and

284 rromagnetic (WFM) components are parallel or antiparallel to each other.

285 etization (FDy) has a natural tendency to be antiparallel to Fe(3+) sublattice magnetization (FFe) wi

286 to date whether mu prefers to be parallel or antiparallel to mu.

287 nder the icosahedral 2-fold axis rather than antiparallel to the betaB strand, eliminating many intra

288 etrotransposons for the first time, oriented antiparallel to the coding strand of L1 open reading fra

289 ated Mn magnetic moment is observed which is antiparallel to the Fe magnetization.

290 The flow of electrons, parallel and antiparallel to the magnetic field, reveals a complex to

291 ore of the protease domain undergoes a major antiparallel-to-parallel conformational transition.

292 A first switch is based on a remarkable antiparallel-to-parallel conversion, taking place in a f

293 ghts about molecular factors controlling the antiparallel-to-parallel equilibrium in muPA.

294 mation of parallel strands and these adopted antiparallel topologies.

295 Antiparallel trajectory of excitons in nonparallel D-A s

296 dimers whereby the two subunits assemble in antiparallel transmembrane orientation.

297 imicrobial peptides within the unit cell: an antiparallel trimer, which we suggest might be related t

298 utions and are almost completely depleted of antiparallel triplex-forming sequences.

299 arallel-stranded homo-base paired duplex and antiparallel unimolecular hairpin in a pH-dependent mann

300 angular momentum, aligned either parallel or antiparallel with their linear momentum, labelled as lef