ライフサイエンスコーパス: space group

1 R51A/R239A heterodimers and belong to the C2 space group.

2 tallizes in a structure with the Pmcm (Pmma) space group.

3 ells, is best described by a tetragonal P4mm space group.

4 superstructural ordering in a lower symmetry space group.

5 e, with a = 4.0611(7) A, defined in the Pm3m space group.

6 ucture crystallizing in an orthorhombic Pnma space group.

7 sing with 52 Se-Met sites in an orthorhombic space group.

8 tional changes resulted in conversion of the space group.

9 obtained from crystals belonging to the same space group.

10 bed in the centrosymmetric orthorhombic Pnma space group.

11 ntly single mutants and belong to the P42212 space group.

12 xylene had a monoclinic phase with the Cc(9) space group.

13 om monoclinic P21/n into orthorhombic P21212 space groups.

14 d indicators of band topology in all the 230 space groups.

15 lso crystallize in one of the lower symmetry space groups.

16 ogically distinct band-structures for all 3D space groups.

17 145C crystallizes as a hetero-octamer in two space groups.

18 izing in high-symmetry trigonal or hexagonal space groups.

19 tively, by one of the 17 plane groups or 230 space groups.

20 to obtain the filling conditions for all 230 space groups.

21 e re-exposure 48 hr later, compared with the spaced group.

22 ces (isostructural with the compound AlB(2); space group 191, P6/mmm) of large nanocrystals occupying

23 The pure compounds crystallize in different space groups ([2]2B, P1, Z = 2; [2]2Be, P2(1)/c, Z = 4)

24 t3BuN(+)Br(-)) crystallizes in the cubic Ia3 space group (a = 22.573(5) A, V = 11502(4) A(3)), with t

25 tropic form crystallizes in the orthorhombic space group Aba2 with a = 19.082(2) A, b = 9.551(1) A, c

26 This tetragonal phase in P4/mcc space group, along with the defect structure Fe(0.74)Sn(

27 The orthorhombic Amm2 space group also provides an adequate description, sugge

28 provided a protein structure in a different space group and at a higher resolution than the structur

29 e new crystal structures, each in a distinct space group and lattice packing arrangement, together wi

30 Both proteins crystallize in the same space group and lattice.

31 stallized the poliovirus polymerase in a new space group and solved the complete structure of the pro

32 ssed, purified and crystallized in the P6(3) space group and two different data sets were obtained at

33 Space-group and chemical-composition information are not

34 le in protein crystals (one protein for each space group) and on another set of 83 ultra-high-resolut

35 ent molecules, and overall crystal symmetry (space group) and represents an important caveat to worke

36 allized at a pH ranging from 2 to 9 in three space groups, and four structures have been determined b

37 The structures, which are in different space groups, are almost identical to each other but dif

38 n (+)-catechin 4.5-hydrate and establish the space group as C2.

39 k are arranged in different highly symmetric space groups as a function of a variety of anions (cubic

40 We prepared nanocrystals of both space groups as well as fibril samples that reproducibly

41 First, similarities in space group, asymmetric unit size, and cell dimensions a

42 ound to the ALDH site were determined in two space groups at 1.7-1.9 A resolution.

43 nted in each state from two crystallographic space groups at 1.8 and 2 A resolution.

44 to an orthorhombic phase (Phase II with Pmm2 space group) at approximately 50 GPa and 1400 K.

45 The performance of PIM was tested on all 65 space groups available in protein crystals (one protein

46 h also crystallizes in an axial (tetragonal) space group but which now is recognized to consist of a

47 The beta-form crystallizes in the monoclinic space group C2 with a = 9.5948(7) A, b = 8.3608(6) A, c

48 rystal structure of the biological tetramer (space group C2) demonstrates that all protomers bear a c

49 Compound 3 crystallizes in the space group C2/c (Z = 4) with a = 41.2238 (2) A, b = 11.

50 The diradical crystallizes in the monoclinic space group C2/c with cell parameters a = 21.1411(8) A,

51 tallizes as semiconducting black-red plates (space group C2/c, a = 12.633(5) A, b = 21.770(8) A, c =

52 )O)(4) crystallizes as bright yellow plates (space group C2/c, a = 12.7337(7) A, b = 22.1309(16) A, c

53 formula C(72)H(112)Au(2)F(12)N(4)P(2)Sb(2), space group C2/c, a = 21.388 (4), b = 19.679 (4), c = 19

54 The 6H-BaIrO(3) polytype is monoclinic, space group C2/c, with a = 5.7483(2) A, b = 9.9390(3) A,

55 rystallize in the centrosymmetric monoclinic space group C2/c.

56 ully determined and both were found to be in space group C2/c.

57 rystallize isostructurally in the monoclinic space group C2/m (no.12) and adopt the MnSb(2)Se(4) stru

58 -RbBi(3)Se(5) crystallizes in the monoclinic space group C2/m with a = 36.779(4) A, b = 4.1480(5) A,

59 The compound crystallizes in the monoclinic space group C2/m with a = 51.9205(8) A, b = 4.4025(1) A,

60 icance is the base-centred monoclinic phase (space group C2/m) of Ca2C, a quasi-two-dimensional metal

61 Cu2IrO3 has the same monoclinic space group (C2/c) as Na2IrO3 with a layered honeycomb s

62 4)T(3)G(4)) crystallized in the orthorhombic space group C222 and has a structure very similar to the

63 The heptamer crystallized in the space group C222 with a unit cell of a = 25.74, b = 106.

64 The enzyme crystallizes in the orthorhombic space group C222(1) with cell dimensions a=41.02A, b=86.

65 es of Aquifex aeolicus dihydroorotase in two space groups, C222(1) and C2, were determined at a resol

66 r to the one that was captured previously in space group C2221 with one molecule per asymmetric unit.

67 The crystal belongs to the space group C2221 with unit cell dimensions a = 132.162

68 at although the crystals belong to different space groups, CA monomers are packed with the same P6 he

69 and upon reduction of NQO2-CQ crystals, the space group changed from P2(1)2(1)2(1) to P2(1), with 1-

70 lizes in the noncentrosymmetric orthorhombic space group Cmc21 (No. 36, Z = 4).

71 rmer adopts the CaIrO(3)-type structure with space group Cmcm, whereas the latter crystallizes in a s

72 ce group Pbam) and (Sr(x)Eu(1-x))(2)Ge(2)Pb (space group Cmmm).

73 hanges among forms, whole molecule disorder, space group diversity, and varying number of molecules i

74 been solved at 1.73A resolution in the cubic space group F23 with unit cell parameters a=b=c=240.6A.

75 t are absent in ordinary cubic (c-) diamond (space group: Fd-3m).

76 pression of the as-crystallized alpha-phase, space group Fdd2, to 3-4 GPa leads to its conversion int

77 Cubic (space group: Fmm) iridium phosphide, Ir2P, has been synt

78 The material crystallizes in space group Fmmm, where a = 27.7508(5) A, b = 25.2969(7)

79 two crystal forms, one of which is in a new space group for this enzyme and diffracts to the highest

80 XRD reflections precludes determination of a space group for this layered silicate.

81 (2) degrees , and it was refined in the C2/m space group from NPD data collected at room temperature.

82 In the low-temperature phase, a change in space group from P31c to R3c occurs, involving a triplin

83 -forming DP, 1.95 A resolution, rhombohedral space group H32)) is reported herein.

84 duced by the asymmetry of the global crystal space group has limited the search for spintronics mater

85 9 A (alpha = beta = gamma = 90 degrees ) and space group I 222.

86 b = 5.281 (5) A and c = 11.550 (6) A with a space group I 41/a (88).

87 This new zeolite crystallizes in the space group I2/m, with cell parameters a = 17.511 A, b =

88 ers, crystallizes in a monoclinic structure (space group: I2/a; a = 5.7048(1)A, b = 5.1610(1)A, c = 1

89 d-like cubic crystalline hydrocarbon K 4-CH (space group I21/3).

90 The crystals belong to the space group I222 and contain a single molecule in the as

91 Crystals from the space group I222 diffracted to 1.65-A resolution.

92 action pattern was consistent with the cubic space group I23 (a = 7.5856(1) A).

93 k of 1 is chiral and adopts the very unusual space group I23.

94 ingle-crystal X-ray diffraction: tetragonal, space group I4(1)/acd, a = 19.102(2), b = 19.102(2), c =

95 (alpha-phase) crystallizes in the tetragonal space group I4(1)cd (a = 23.5028(4) A, c = 12.4607(3) A)

96 MOSC-II-tOc-Ni/Mg/Co, all crystallize in the space group I4/m and assume a pseudo body-centered cubic

97 ulting in a tetragonal hollandite structure (space group I4/m).

98 o(2)O(4)Cl(2) is described in the tetragonal space group I4/mmm [a = 4.007(1) A, c = 22.282(1) A]; ho

99 e majority phase was found to be tetragonal (space group I4/mmm) with lattice parameters a = 3.9697(2

100 olymorph to a ten-coordinated structure with space group I4/mmm.

101 e of a protein racemate that crystallized in space group I41/a.

102 It has the crystal structure of space group I41/amd with lattice parameters of a = b = 1

103 llapsed variant of SiO(2) beta-cristobalite, space group I42d, in which the CO(4) tetrahedra are tilt

104 rtain u value (u not equal 0) for a specific space group if their crystal structures can be engineere

105 The 1/1 AC crystallizes in space group Im, a = 13.863(2) A, Z = 8, and the 2/1 AC,

106 2.2(1)In6.3(2) (e/a = 1.73), crystallizes in space group Im, with a = 15.152(2) A, Z = 8, and the 2/1

107 These phases crystallize in the cubic space group Im3m (a = 14.617(1) A, Z = 2, R(1) = 0.0155

108 ce is accompanied by a metastable structure (space group Imcm) featuring minimal octahedral rotations

109 at they have body-centered cubic structures (space group = Imm, a = 13.34, 13.30, and 13.10 A for 1a,

110 pt a structure with orthorhombic symmetry in space group Immm [a = 3.9757(5) A, b = 4.0294(5) A, and

111 This new zeolite crystallizes in the space group Immm with cell parameters a = 19.6007(8) A,

112 e donor and acceptor stacks having triclinic space group in the crystalline state.

113 Whereas the parent oligocholates (with no spacing groups in between the cholates) require at least

114 observed perfect trigonal symmetry in the P3 space group, in a narrow cone shape, and a brick-wall ty

115 hybrid which crystallizes in an orthorhombic space group, in which its three basic building blocks, i

116 We classify the F-space groups into four fundamental geometries on the bas

117 ring this transformation, and the beta-phase space group is I4(1) (a = 22.7482(3) A, c = 13.0168(3) A

118 The space group is Pnma, and the unit cell dimensions are a

119 Conversely, two crystals in different space groups may be quite similar in terms of all the in

120 peared as thick rods and crystallized in P21 space group (monoclinic) with a single molecule in the a

121 cm(2) +/- 2.8, P<.001) and were 31% (2.5-cm spacing group: multiple antenna mean area, 26.6 cm(2); 3

122 tenna mean area, 20.28 cm(2)) to 59% (3.0-cm spacing group: multiple antenna mean area, 32.2 cm(2); 3

123 ystallizes in a layered structure in the R3m space group (No.

124 Solvent-free crystals with the same space group obtained by a first-order phase transition b

125 phase transition from the P1 to the P2(1)/c space group occurs at x = 0.1, but the conductivities of

126 smox]12(OH2)3}.178H2O (2), retains the polar space group of 1 and is ferroelectric below 260 K.

127 a monoclinic structure but with a different space group of C2(5), indicating that a phase transition

128 orthorhombic-like monoclinic structure with space group of Cm (=8).

129 -centered cubic CaF(2)-type structure with a space group of Fm3m and a refined lattice parameter of 5

130 ntered cubic Mn(2)O(3)-type structure with a space group of Ia3.

131 The c axis for the trigonal space group of oxidized NAO is 485 A, and there are six

132 y stable packing structures that possess the space group of P2(1) as well as high to ultrahigh sponta

133 single crystals were successfully refined in space groups of lower symmetry than Fmm including P4/mmm

134 arcs in DSMs, using a K-theory analysis for space groups of Na3Bi and Cd3As2 Generically, the arcs d

135 A-II crystallizes in the triclinic space group P in the form of centrosymmetric dimers, {[P

136 ne B host-guest assembly are triclinic, with space group P(-)1, and two molecules per unit cell with

137 Sr(5)Co(4)O(12) crystallizes in the space group P-3c1 with lattice parameters of a = 9.4705(

138 ].0.25MeCN, both of which occur in triclinic space group P.

139 irmed the formation of rutile structure with space group (P(42)/mnm) and nanocrystalline nature of th

140 allizes in the non-centrosymmetric triclinic space group P1 (No. 1).

141 Compound 1 crystallizes in the space group P1 (Z = 2) with a = 8.262 (5) A, b = 12.264

142 analogue L(2) crystallizes in the triclinic space group P1 as two different solvates [L(2)].2DMF.5C(

143 The compounds crystallize in the triclinic space group P1 with the lattice parameters a = 7.0832(2)

144 The compound crystallizes in the triclinic space group P1.

145 , and carbon monoxide-bound bjFixLH in a new space group ( P1) and at resolutions (1.5-1.8 A) higher

146 approximately 90 K to a triclinic structure (space group: P1; a = 5.1791(5)A, b = 5.7043(6)A, c = 6.8

147 tragonal (space group P4/nmm) to monoclinic (space group P112/n) at low temperatures, and then, at ap

148 n monoclinic structure of Gd 5Si 2Ge 2-type (space group P2 1/ a) because all Ge...Ge contacts betwee

149 2, a monoclinic, U 2Mo 3Si 4-type structure (space group P2 1/ c) occurs as the majority phase.

150 All structures were solved in space group P2(1) at resolutions ranging from 1.65 A to

151 veals that it crystallizes in the monoclinic space group P2(1) with four homodimers in the asymmetric

152 Selenomethionine-labeled RF1 crystallized in space group P2(1) with three monomers per asymmetric uni

153 )(Br)UTTG(4)) crystallized in the monoclinic space group P2(1) with three quadruplex molecules in the

154 For 2: Monoclinic, space group P2(1), a = 4.2222(6), b = 6.9057(9), c = 7.3

155 3MeOH (SOF-1) crystallizes in the monoclinic space group P2(1)/c and forms a 3D stable supramolecular

156 und crystallized in a monoclinic system with space group P2(1)/c and unit cell dimensions a = 12.2575

157 e B host-guest assembly are monoclinic, with space group P2(1)/c, and four molecules per unit cell wi

158 The beta-phase, space group P2(1)/c, consists of cross-braced pi-stacked

159 (5) and isostructural CsBi(3)Se(5) adopt the space group P2(1)/m with a = 13.537(2) A, b = 4.1431(6)

160 y 1.4 eV), K(4)P(8)Te(4) crystallizes in the space group P2(1)/m, with a = 6.946(1) A, b = 6.555(1) A

161 Crystal data: monoclinic, space group P2(1)/n (No.

162 The alpha-phase, space group P2(1)/n, contains two radicals in the asymme

163 The compound is noncentrosymmetric with space group P2(1)2(1)2(1) and exhibits second-harmonic a

164 ve crystallized murine Golgi mannosidase IA (space group P2(1)2(1)2(1)), and the structure was solved

165 nment of the polar phase to the orthorhombic space group P2(1)ma, although peak broadenings in the di

166 nd uncomplexed plasmepsin II crystallized in space group P2, with one monomer in the asymmetric unit.

167 radicals and the room temperature structure (space group P2/c) together with the conductivity of sigm

168 ystallized in the monoclinic system with the space groups P2(1)/c, C2/c, and P2(1)/c, respectively, r

169 BamB crystallized in space groups P2(1)3, I222, and P2(1)2(1)2(1), with one m

170 A dAGGG(TTAGGG)(3), Tel22, determined in two space groups, P2(1)2(1)2 and P6, at 1.65 and 2.15 A reso

171 m atoms, and the primitive monoclinic phase (space group P21/c) of CaC with zigzag C4 groups.

172 torted rutile type, similar to that of MoO2; space group P21/c, a = 5.6891(1), b = 4.7546(1), c = 5.5

173 structural and crystallize in the monoclinic space group P21/c.

174 A new crystal form (space group P21/n) of the photoresponsive azo-dye Disper

175 This new orthorhombic crystal form (space group P21212) comprises two polymerases molecules

176 We find a particular space group P212121 (#19) that is conducive to the Dirac

177 omalous X-ray diffraction (AXRD) in a chiral space group P212121 using Cu-irradiation resulting in a

178 nal crystals of the domain, belonging to the space group p22(1)2(1).

179 ution using untwinned native crystals in the space group P3(1), by molecular replacement from the 2.8

180 The crystals belong to the trigonal space group P3(1), with two molecules of rhodopsin per a

181 ning a 2.8 A resolution crystal structure in space group P3(2) that contains three intact tetramers i

182 self-complementary oligomer crystallizes in space group P3(2)12, containing a single strand in the a

183 The crystals belong to the space group P3(2)21 and have unit cell dimensions a=b=66

184 4], crystals of which belong to the trigonal space group P3.

185 Here, we present two crystal structures, in space groups P3(2)21 and C2 at 1.35 and 1.40 A resolutio

186 fraction quality crystals with two different space groups (P3(2)21 and P4(3)2(1)2) were obtained unde

187 The enzyme crystallized in the space group P3121, and the structure was determined to a

188 = K, Rb) crystallize in the chiral trigonal space group P3121, with a = 7.2728(9) A, c = 18.872(4) A

189 Its crystal structure, in the space group, P31m, with a = 8.063(3) A, c = 8.509(4) A,

190 tate (PALA) have previously been made in the space group P321, in which the two independent r (regula

191 Complex 5 crystallizes in the enantiomorphic space group P3221.

192 re was determined at 2.8 A resolution in the space group P3221.

193 lize in a new structure type in the trigonal space group P3c1.

194 in the berndtite 4H crystallographic phase (space group P3m1).

195 the simple trigonal SrAlSiH structure type (space group P3m1, Z = 1, a = 4.22-4.56 A, c = 4.97-5.30

196 cement from the 2.8 A model (1F88) solved in space group P4(1).

197 The crystals belong to space group P4(1)2(1)2 with a dimer in the asymmetric un

198 abeta heterodimers to the asymmetric unit in space group P4(1)2(1)2.

199 liganded form at 1.35 Angstrom resolution in space group P4(1)2(1)2.

200 recovery of a Ge(0.9)Sn(0.1) solid solution (space group P4(3)2(1)2, a = 6.014 (1) A, c = 7.057 (1) A

201 ffraction data and belongs to the tetragonal space group P4/m (no.

202 These compounds crystallize in tetragonal space group P4/mnc with the Sc2Fe3Si5-type structure, ha

203 55 K, changing the symmetry from tetragonal (space group P4/nmm) to monoclinic (space group P112/n) a

204 The chiral compounds crystallize in the space groups P4(1) and P4(3), respectively, with toluene

205 -x)Te2N3 where x approximately 0.48 forms in space group P42/m (a = 8.718(3)A, c = 6.719(2)A; Z = 2)

206 presence of NADPH (2.4 A) and NADP (2.1 A) (space group P6(1)22).

207 e-packed arrangement of inverse micelles, of space group P6(3)/mmc.

208 is consistent with a single phase (hexagonal space group P6(3)mc; a = approximately 5.95 angstroms, c

209 t was solved by molecular replacement in the space group P6(5) with two molecules in the asymmetric u

210 s crystallize in a unique crystal structure (space group P6/mmm; a = 10.975(3) A (La) and 10.844(1) A

211 at 3.40 A spacing; R(merge) = 8.8% (38.5%), space group, P6(1)22; and unit cell parameters, a = b =

212 crystallizes in the achiral and nonpolar NCS space group P62m, whereas Cs9Mg6(CO3)8F5 is found in the

213 h crystallized in a hexagonal unit cell with space group P63/m.

214 is cobalt molybdenum nitride crystallizes in space group P63/mmc with lattice parameters of a = 2.851

215 Of those, space group P6522 model, a = 7.1443(4)A, c = 25.350(4)A,

216 ic structure of comparable unit cell volume (space group Pa3, a = 22.4310(15) A, V = 11286.2(13) A(3)

217 stallize in the centrosymmetric orthorhombic space group Pbam (no. 55, Z = 2), and their structures f

218 d-state compounds: (Eu(1-x)Ca(x))(2)Ge(2)Pb (space group Pbam) and (Sr(x)Eu(1-x))(2)Ge(2)Pb (space gr

219 TcBr(4) crystallizes in the orthorhombic space group Pbca (a = 6.3237(5) A, b = 12.1777(9) A, c =

220 pts a unique corrugated layered structure in space group Pbca with unit cell a = 18.901(4) A, b = 11.

221 AMH II crystallizes in space-group Pbca with 16 formula units in a unit-cell of

222 , namely, the well-known orthorhombic phase (space group Pbcm) and the current polar phase, the relat

223 Crystal data for 1: Orthorhombic, space group Pbcm, a = 9.997(2), b = 6.997(1), c = 10.332

224 e CsNaNbOF5 crystallizes in the orthorhombic space group Pbcn (No.

225 A third or gamma-phase, also space group Pbn2(1), is generated by further compression

226 al and crystallize in the polar orthorhombic space group Pca2(1).

227 by single crystal X-ray diffraction means in space group (Pearson symbol: tP10) P4/nmm, a = 6.264(1)

228 )Nay (OH)6 x H2 O crystallizes in the cubic space group Pm3m with a=10.0476(1) A.

229 y as nanowires that crystallize in the polar space group Pmc2(1), with a = 7.5357(2) A, b = 13.7783(6

230 Li2Ca3[N2]3 (space group Pmma, no. 51, a = 4.7747(1), b = 13.9792(4),

231 hat TcBr(3) crystallizes in the orthorhombic space group Pmmn (a = 11.0656(2) A, b = 5.9717(1) A, c =

232 ng agent and crystallize in the orthorhombic space group Pmmn (Z = 2, Li(14)Ce(5)[Si(11)N(19)O(5)]O(2

233 whereas Cs9Mg6(CO3)8F5 is found in the polar space group Pmn21.

234 which crystallize in the polar orthorhombic space group Pna2(1), revealed the importance of intermol

235 5 crystallizes in the orthorhombic and polar space group Pna21 (No.

236 tallizes in the centrosymmetric orthorhombic space group Pnma (No. 62, Z = 4).

237 ed mixed stack structure in the orthorhombic space group Pnma with a = 14.739(3) A, b = 10.7869(19) A

238 benzene-bridged bisdithiazolyl radical IBBO (space group Pnma) gives rise to strong ferromagnetic exc

239 ha-SnS orthorhombic herzenbergite structure (space group Pnma) with no evidence of secondary phases.

240 m belong to the orthorhombic, Gd 5Si 4-type (space group Pnma).

241 (4)Se(10) crystallizes with the orthorhombic space group Pnma, whereas Fe(0.96)Pb(3.04)Sb(4)Se(10) ad

242 skite, instead belonging to the orthorhombic space group Pnma.

243 le compound in the MgSrSi-type structure, in space group Pnma.

244 4) crystallizes in a new structure-type with space group Pnnm and dimensions of a = 11.784(1) A, b =

245 m benzene formed clathrate structures in the space group Ponemacr; with one molecular compass and two

246 nylcalix[4]arene (TBSC), crystallizes in the space group R3 and adopts pseudo face-centered cubic (fc

247 by annealing at 400-500 degrees C, occur in space group R3[overline]c (a approximately 8.6-8.9 A, c

248 re of Ras from crystals with symmetry of the space group R32 in which switch II is disordered and fou

249 Sr(6)Co(5)O(15) crystallizes in the space group R32 with lattice parameters of a = 9.5020(10

250 The compound Ca6Te3N2 crystallizes in space group R3c (a = 12.000(3)A, c = 13.147(4)A; Z = 6);

251 to an increase in unit cell volume with the space group remaining unchanged during adsorption.

252 This space group results from the four-layered stacking seque

253 taining L- and D-dimers in a centrosymmetric space group, revealed unexpected homology with bacterial

254 ipid complexes in different crystallographic space groups reveals considerable conformational variati

255 5)Mn(0.5)O(2) adopts the LiCoO(2) structure (space group Rm) and comprises separate lithium layers, t

256 on occurs from an ambient rhombohedra phase (Space group (SG): R-3m) to monoclinic phase (SG: C2/m) a

257 ructure, which was determined in a different space group, shows that the E2 domains share a conserved

258 cture, stable above 200 GPa, and LaH8 a C2/m space group structure.

259 derived from crystals belonging to different space groups, suggesting that the trimer of dimers may n

260 btained from crystals belonging to different space groups suggests that asymmetric dimers can be a co

261 six-, and eight-band crossings stabilized by space group symmetries in solid-state systems with spin-

262 All structures were crystallized in C2 space group symmetry and contain six monomers in the asy

263 Using space group symmetry arguments, we show that these resul

264 cell that doubles the c-axis and changes the space group symmetry from R3 to R3.

265 The results showed that considering space group symmetry in mode calculation is crucial for

266 The space group symmetry is lowered to Pbn2(1), and there is

267 l X-ray diffraction data, we re-evaluate the space group symmetry of the intermediate-temperature pha

268 y obtained orthorhombic forms, with apparent space group symmetry P2(1)2(1)2(1), have cell dimensions

269 bicontinuous cubic architectures with P or I space group symmetry that have been identified previousl

270 The unit cell and space group symmetry were found from the XPD data, and w

271 ances, with unit cell parameters (though not space group symmetry) provided by XRD, a comprehensive s

272 he cmm plane group and 3D packings with I4mm space group symmetry, in contrast to uncharged spherical

273 xact modes of a whole unit cell according to space group symmetry, while the translational symmetry b

274 nuous thermotropic cubic phase with the Im3m space group symmetry.

275 e of MBCD, giving a different morphology and space group than crystals grown without MBCD.

276 tallize in either tetragonal or orthorhombic space groups; their structures consist of 2D square laye

277 neutron diffraction data to retain the P213 space group, though with a cubic lattice parameter of a

278 chalcopyrite CuIn3Se5-xTex (x = 0-0.5) with space group through isoelectronic substitution of Te for

279 peared as thin fibers and crystallized in P1 space group (triclinic) with six molecules in the asymme

280 res of SAG2603 V/R sortase C1 in a different space group (type I) and that of its complex with a smal

281 agalactiae SAG2603 V/R sortase SrtC1 in two space groups (type II and type III) and that of its "lid

282 eometry optimization calculations, yield the space group, unit cell parameters, and atomic positions

283 The solid solution in the P21/n space group was found to be stable for high iron concent

284 (lambda = 0.8702 A) after the unit cell and space group were determined from tilt electron diffracti

285 d this phase is characterized by the P2(1)/c space group which involves a doubling of the unit cell a

286 red, three-dimensional crystal having the P6 space group, which has a "honeycomb-like" structure and

287 structures determined for the P2(1)2(1)2(1) space group, while these residues adopt an alpha-helix i

288 refined from XRD data in the monoclinic C2/m space group with a = 10.0046(3) A, b = 5.75362(14) A, c

289 om ammonium sulfate solutions in the P3(2)21 space group with a tetramer in the asymmetric unit.

290 gammaN308K crystals belonged to a tetragonal space group with an unusually long unit cell (a = b = 95

291 -11 giardin crystallized in a lower-symmetry space group with four molecules in the asymmetric unit.

292 allized from poly(ethylene glycol) in the P1 space group with one tetramer in the asymmetric unit and

293 s that ambuic acid crystallizes in the P2(1) space group with unit cell parameters a = 15.5047(7), b

294 und to crystallize in the monoclinic P2(1)/n space group with unit cell parameters a = 6.0936(1) A, b

295 rosymmetric structure in the tetragonal I42m space group with unit cell parameters a=6.9016(5) A and

296 from cholic acid, form crystals in the P6(1) space group with unusually wide unidimensional pores.

297 ft-handed forms crystallized in the trigonal space groups with mirror image 3-fold helical screw axes

298 218 space group) with rhenium and technetium in the 7+ oxida

299 They crystallize in the P4/nmm space group, with the ZrCuSiAs-type structure, as indica

300 iving a disordered structure in the Rm (166) space group (Z = 3).