ライフサイエンスコーパス: asymmetric unit

1 d to gp55 and gp58 (each with two copies per asymmetric unit).

2 tion, and two tetramers were observed in the asymmetric unit.

3 crystals of GCRho have only a monomer in an asymmetric unit.

4 metry space group with four molecules in the asymmetric unit.

5 nly an alpha- domain are present in the same asymmetric unit.

6 ce between the two Shp(180) molecules in the asymmetric unit.

7 demonstrative structural differences in the asymmetric unit.

8 cture (1.95 A resolution) has two dimers per asymmetric unit.

9 There are two molecules of DnaK-ATP in the asymmetric unit.

10 e six subunits (1(1)/(2) holoenzymes) in the asymmetric unit.

11 rystallographic trimeric architecture in the asymmetric unit.

12 5, 1,3-propanediamine, C(3)H(10)N(2)) in the asymmetric unit.

13 xists as an octamer with two monomers in the asymmetric unit.

14 interfaces between identical domains in the asymmetric unit.

15 heterotrimeric complexes, dI(2)dIII, in the asymmetric unit.

16 llographic symmetry-related molecules in the asymmetric unit.

17 in a crystal form with two molecules in the asymmetric unit.

18 one protein monomer in the crystallographic asymmetric unit.

19 tions among the four unique complexes in the asymmetric unit.

20 group (triclinic) with six molecules in the asymmetric unit.

21 in space group P2(1) with three monomers per asymmetric unit.

22 and 15-phenyl rings in both molecules of the asymmetric unit.

23 e P3(2)21 space group with a tetramer in the asymmetric unit.

24 up I222 and contain a single molecule in the asymmetric unit.

25 graphically independent Fab fragments in the asymmetric unit.

26 r the metal site 1 in all eight subunits per asymmetric unit.

27 d lateral segregation within the icosahedral asymmetric unit.

28 with the (alpha1alpha2) dimer comprising the asymmetric unit.

29 p P3(2)12, containing a single strand in the asymmetric unit.

30 m a "trimer of dimers" packing motif in each asymmetric unit.

31 d in space group P2, with one monomer in the asymmetric unit.

32 20.6% (R(free)=23.6%) with two molecules per asymmetric unit.

33 = 30.26 A and two independent strands in the asymmetric unit.

34 osed to the previously observed dimer in the asymmetric unit.

35 nces among the three molecular copies in the asymmetric unit.

36 domain assembles as a trimer in the crystal asymmetric unit.

37 , there are two independent molecules in the asymmetric unit.

38 c=55.9 A, beta=113.58 degrees and a dimeric asymmetric unit.

39 ) has three molecules of indomethacin in the asymmetric unit.

40 There are two monomers in the asymmetric unit.

41 ers are packed in two distinct dimers in the asymmetric unit.

42 ological hexamer within the crystallographic asymmetric unit.

43 ndependent molecules in the crystallographic asymmetric unit.

44 tical complexes of the same crystallographic asymmetric unit.

45 and crystallizes with an intact dimer in an asymmetric unit.

46 5.7 A, accommodating one enzyme molecule per asymmetric unit.

47 mer with one subunit in the crystallographic asymmetric unit.

48 crystal containing 88 selenium sites in the asymmetric unit.

49 d 117.6 A, respectively, and one subunit per asymmetric unit.

50 rent conformation in the two subunits of the asymmetric unit.

51 4(1)22 with two independent molecules in the asymmetric unit.

52 with 222 noncrystallographic symmetry in the asymmetric unit.

53 and a half tetramers in the crystallographic asymmetric unit.

54 oclinic space group C2 with one dimer in the asymmetric unit.

55 gamma = 120 degrees, with one duplex in the asymmetric unit.

56 inactive mutant both have two molecules per asymmetric unit.

57 ((-)FTC-TP) with four ternary complexes per asymmetric unit.

58 pace group P4(1)2(1)2, with one molecule per asymmetric unit.

59 l domain are found to be well defined in the asymmetric unit.

60 ic space group P1, with two molecules in the asymmetric unit.

61 ntains one duplex and 77 water molecules per asymmetric unit.

62 olution and crystallizes with a dimer in the asymmetric unit.

63 group P3221 with one monomer of CV-N in each asymmetric unit.

64 dimer, the active form of the enzyme, in the asymmetric unit.

65 90.2 A, and c = 47.5 A and one protomer per asymmetric unit.

66 comprise a tetramer in the crystallographic asymmetric unit.

67 rees with a pseudodyad related duplex in the asymmetric unit.

68 beta = 90.58 degrees ), with two dimers per asymmetric unit.

69 type and the other with two molecules in the asymmetric unit.

70 quasi-equivalent subunits in the icosahedral asymmetric unit.

71 a dimer of dimers arrangement in the crystal asymmetric unit.

72 y in space group C2221 with one molecule per asymmetric unit.

73 of the two molecules in the crystallographic asymmetric unit.

74 n monomers are found in the crystallographic asymmetric unit.

75 that contains three intact tetramers in the asymmetric unit.

76 contains an octamer in the crystallographic asymmetric unit.

77 domain trapped in the same crystallographic asymmetric unit.

78 ur and one-third VP6 trimers per icosahedral asymmetric unit.

79 ide in three of the four active sites in the asymmetric unit.

80 There are two ArsD molecules in the asymmetric unit.

81 pace group P2(1) with four homodimers in the asymmetric unit.

82 ntains two tensegrity triangle molecules per asymmetric unit.

83 ymerase/DNA complexes present in the crystal asymmetric unit.

84 the two active sites of the crystallographic asymmetric unit.

85 cal reelin-N domains in one crystallographic asymmetric unit.

86 to a dimer of dimers in the crystallographic asymmetric unit.

87 he 25 trimeric CIV capsomers per icosahedral asymmetric unit.

88 symmetric assembly composed of 60 identical asymmetric units.

89 from methanogenic archaea from only 320,000 asymmetric units.

90 is a T=1 capsid with 60 heterodimers as the asymmetric units.

91 ), showed only four proteins per icosahedral asymmetric unit: a dimer of the major capsid protein, on

92 tructure contains two domain I dimers in the asymmetric unit (AB and CD); the dimers are intimately a

93 =95.16 degrees ) showed ten sub-units in the asymmetric unit, all with two bound calcium ions and lig

94 crystal structure has three molecules in the asymmetric unit, an R-factor of 22.0%, and an R(free) of

95 The analyses of three molecules in the asymmetric unit and comparison with RF2 revealed the pre

96 tors and salts with a single molecule in the asymmetric unit and devoid of significant packing intera

97 onolayers with more than one molecule in the asymmetric unit and displayed multiple packing patterns.

98 oth independent copies of the complex in the asymmetric unit and does not appear to be influenced by

99 MsAcT is an octamer in the asymmetric unit and forms a tightly associated aggregate

100 graphic model there are two molecules in the asymmetric unit and from size-exclusion chromatography,

101 consists of an alpha2 beta2 tetramer in the asymmetric unit and has been refined to a R-factor of 0.

102 ntains two 40-kDa/20-kDa heterodimers in the asymmetric unit and has structural features comparable w

103 d symmetry operator on three subunits in the asymmetric unit and held together by extensive ionic int

104 l-length enzyme contain two molecules in the asymmetric unit and in both molecules the N-terminal dom

105 in three of the four chains constituting the asymmetric unit and is accompanied by a backbone rearran

106 with four molecules in the crystallographic asymmetric unit and its crystal structure was determined

107 the P1 space group with one tetramer in the asymmetric unit and provided a view of the entire biolog

108 ith 4,7-DOSA (PDB code ) shows one dimer per asymmetric unit and reveals that the inhibitor forms two

109 apo SOD1 crystallizes with two dimers in the asymmetric unit and shows changes in the metal-binding s

110 the observation of multiple molecules in the asymmetric unit and stabilization of pseudopolymorphs we

111 tion can prevent large rearrangements of the asymmetric units and a loss of symmetry of the unit cell

112 biological units (BUs) often differ from the asymmetric units and it is usually preferable to model f

113 (space group P2(1)2(1)2(1); three molecules/asymmetric unit) and its structure determined to 2.0 A r

114 or sulfinic acid in the two molecules in the asymmetric unit, and a mechanism for this oxidation is p

115 erify phase purity, specify one molecule per asymmetric unit, and provide an initial structural model

116 .2 A resolution, four or fewer copies in the asymmetric unit, and the availability of structures of h

117 inding region is present as a monomer in the asymmetric unit, and the structure reveals novel feature

118 contains two independent quadruplexes in the asymmetric unit, and the trigonal form contains one.

119 r amongst the eight molecules of the crystal asymmetric unit appears to correlate with alternative po

120 (1) described here, the four monomers in the asymmetric unit are arranged as a dimer of dimers.

121 differences between the two molecules in the asymmetric unit are correlated with changes in accessibi

122 , the two complexes making up the KPC-2-BLIP asymmetric unit are distinct, and in one structure, the

123 s of the four structural models found in the asymmetric unit are in an alternate orientation to that

124 The two C-terminal domains in the asymmetric unit are organized about a slightly distorted

125 stinct shifts for different molecules in the asymmetric unit are seen, and all differ substantially f

126 ystals contained a pentamer of dimers in the asymmetric unit arranged in an improper non-crystallogra

127 T1 that has two copies of the complex in the asymmetric unit arranged to form an intimate domain-swap

128 C2 crystal form with the 70 kDa dimer in the asymmetric unit, as the first structural representative

129 ndent D scaffolding proteins per icosahedral asymmetric unit, as well as their interaction with the F

130 est specimen and obtained a map from 210,000 asymmetric units at a resolution better than 5 A.

131 alculate low-frequency modes on one or a few asymmetric units (AUs) and generate exact modes of a who

132 For HICA-G41A, two of 12 chains in the asymmetric unit bind bicarbonate ion exclusively at the

133 group P2(1)/n, contains two radicals in the asymmetric unit, both of which adopt slipped pi-stack st

134 wo subunits are almost fully resolved in the asymmetric unit, but they are not related by any 2-fold

135 The asymmetric unit cell contains a new type of antiparallel

136 h only one of the three p53 protomers in the asymmetric unit cell is specifically bound to DNA.

137 tion, intermolecular contacts in the crystal asymmetric unit cell suggest a likely surface for protei

138 pendent duplexes (molecules I and II) in the asymmetric unit cell, a = 24.95, b = 45.25 and c = 73.67

139 ounds with known numbers of molecules in the asymmetric unit cell, and show that 19F spin diffusion i

140 oiety had three distinct conformations in an asymmetric unit cell.

141 oup symmetry and contain six monomers in the asymmetric unit cell.

142 f these structures have two molecules in the asymmetric unit compared to the one present in the cryst

143 hown to be a quasi-crystalline array with an asymmetric unit composed of a filament with 14 actin-scr

144 The four molecules in the asymmetric unit comprise two MIP-1beta-like dimers.

145 denylic acid [c(dAp)3] indicates for each an asymmetric unit consisting of two conformationally simil

146 sly reported examples in space group P1; the asymmetric unit consists of a hydrated head-to-head host

147 The asymmetric unit consists of one DNA duplex containing an

148 Both duplexes in the asymmetric unit contain 1,2-intrastrand cross-links in w

149 The asymmetric unit contained eight molecules of VH9 and fou

150 ved within the same crystal lattice, with an asymmetric unit containing one molecule of apoNPC2 and t

151 eals that the filaments are bipolar, with an asymmetric unit containing two subunits of ICP8 that con

152 One specific capsomer in each asymmetric unit contains a fiber-like protrusion.

153 The asymmetric unit contains a homotetramer with substrate/p

154 The crystallographic asymmetric unit contains a PqsD dimer.

155 The asymmetric unit contains a single molecule whose seconda

156 The asymmetric unit contains four CheY** molecules, two with

157 Each of the eight subunits within the asymmetric unit contains MgIIoxalate as a bidentate comp

158 Although the asymmetric unit contains only a single monomer, crystal

159 The crystal asymmetric unit contains three back-back vancomycin dime

160 The crystallographic asymmetric unit contains three dimers of Der p 5 that ar

161 The crystallographic asymmetric unit contains three independent molecules of

162 hydrated triclinic crystal form in which the asymmetric unit contains two independent methotrexate mo

163 The asymmetric unit contains two P(46) monomers and the func

164 The crystallographic asymmetric unit contains two sigma3 subunits, tightly as

165 The asymmetric unit contains two such double-dimer complexes

166 .25 A, ten mono- and divalent metal ions per asymmetric unit could be identified, giving insight into

167 echnical problems because of the size of the asymmetric unit, crystal variability and sensitivity to

168 ies of VP2 and thus 2 copies per icosahedral asymmetric unit, designated VP2A and VP2B.

169 he conformations of the two molecules in the asymmetric unit differ both in the linker and the stem p

170 Each structure has two molecules in the asymmetric unit, differing in the conformation of the NA

171 The two Pdx1/DNA complexes in the asymmetric unit display conformational differences: in t

172 arm of CoA bound to one protomer within the asymmetric unit displays the dPCoA-like conformation wit

173 The three E monomers per icosahedral asymmetric unit do not have quasiequivalent symmetric en

174 th structures show that two dimers occupy an asymmetric unit; each subunit has a alpha/beta mononucle

175 at least two copies of the clamp protein per asymmetric unit, FAKV's clamp protein bound at only one

176 The two molecules in the asymmetric unit form contacts along the entire length of

177 Each of the four strands in the asymmetric unit forms a parallel tetraplex with symmetry

178 g, Xis crystals contain five subunits in the asymmetric unit, four of which align into a Xis filament

179 space group P6(5) with two molecules in the asymmetric unit from perfectly merohedrally twinned crys

180 P)-L30 fusion protein with two copies in the asymmetric unit has been determined.

181 e four copies of the pentamer present in the asymmetric unit has been used to analyze the intrinsic f

182 dimer contained within one crystallographic asymmetric unit has one molecule of the inhibitor 1-hexa

183 nd CsA, with eight independent copies in the asymmetric unit, has been determined at a resolution of

184 ing furan, all four molecules in the crystal asymmetric unit have DNA in the polymerase active site,

185 t capsid protein residues in the icosahedral asymmetric unit (IAU) using azimuthal polar orthographic

186 r filament by helical diffraction, since the asymmetric unit in a bipolar filament would be twice the

187 22, and P2(1)2(1)2(1), with one molecule per asymmetric unit in each case.

188 contains three independent molecules in the asymmetric unit in P2(1) (4) (Z = 6).

189 ld-type has a single PfCyP19/CsA complex per asymmetric unit in space group P1 and refined to an R-wo

190 There are two alphabeta heterodimers to the asymmetric unit in space group P4(1)2(1)2.

191 molecule crystallizes with one duplex in the asymmetric unit in space group R3 and unit cell dimensio

192 The asymmetric unit in the crystal is the active dimer, and

193 t the C terminus, presents two complexes per asymmetric unit in the orthorhombic space group P2(1)2(1

194 ature factors seen for the six chains of the asymmetric unit in the zone around the interruption poin

195 PXR crystallizes as a homodimer in the asymmetric unit in this structure and possesses a novel

196 rst generated based on the limited number of asymmetric units in a unit cell as well as limited commo

197 four copies of GRHPR in the crystallographic asymmetric unit: in each homodimer, one subunit forms a

198 e interactions, because two molecules in the asymmetric unit interact by the binding of one molecule

199 ng adopts two different conformations in the asymmetric unit interacting with residues in the beta4-b

200 ructure exhibits P12(1) symmetry, having two asymmetric units inverted with respect to one another in

201 The asymmetric unit is a homodimer of (alpha/beta)8 barrels

202 The asymmetric unit is composed of two identical subunits th

203 d for HPPD from other bacterial sources, the asymmetric unit is composed of two weakly associated pro

204 -ZSM-5 containing one Bronsted acid site per asymmetric unit is deliberately chosen to host pyridine,

205 The asymmetric unit is different from PDB and/or Protein Qua

206 mers that are formed between monomers in the asymmetric unit is distinct from both hBD2 and other mam

207 The trimer of dimers found in the asymmetric unit is essentially identical to complexes se

208 The asymmetric unit is the single B15D beta-sandwich molecul

209 tains 1,914 nonhydrogen protein atoms in the asymmetric unit, is the largest determined ab initio wit

210 eighboring glycoproteins in each icosahedral asymmetric unit, leaving the third Asn67 residue vacant.

211 heme iron-ligated GAF(DosT) monomers in the asymmetric unit may result from crystal lattice limitati

212 ticles that form two-dimensional crystals of asymmetric unit membrane (AUM) covering >90 % of the api

213 igen that assembled into detergent-resistant asymmetric unit membrane particles.

214 cells formed junctional complexes and had an asymmetric unit membrane, a hallmark of terminal differe

215 nally differentiated, superficial urothelial asymmetric unit membrane.

216 es packed hexagonally to form 2D crystals of asymmetric unit membranes (AUM) that contribute to the r

217 In one of the two protein monomers in an asymmetric unit, O(2) binds as a second axial ligand to

218 sity, and varying number of molecules in the asymmetric unit occurring within a very narrow free ener

219 ndent purple CuA azurin molecules are in the asymmetric unit of a new P21 crystal, and they have near

220 longated molecules of CusB were found in the asymmetric unit of a single crystal, which suggests the

221 Similarly, the three subunits in the asymmetric unit of both structures exhibit differing rel

222 The asymmetric unit of each crystal form is a dimer.

223 between the two independent molecules in the asymmetric unit of each structure, has provided new mole

224 of the complex in form I and one copy in the asymmetric unit of forms II and III.

225 SSZ-58 possesses 12 tetrahedral atoms in the asymmetric unit of its highest topological symmetry, and

226 One of the monomers in the asymmetric unit of the A264H crystals was in a novel con

227 otide ligands in each of the subunits in the asymmetric unit of the beta,gamma-methyleneadenosine-5'-

228 ure of each of the 14 actin protomers in the asymmetric unit of the bundle filament was assumed to be

229 There are four molecules in the asymmetric unit of the C2 cell, and in one of the molecu

230 imeric and two monomeric zip proteins in one asymmetric unit of the CIV capsid.

231 The asymmetric unit of the crystal contains two SH3 domains

232 ur independent copies of the aglycon in each asymmetric unit of the crystal exhibit a high degree of

233 The asymmetric unit of the crystal lattice contains a dimer

234 (outer diameter approximately 700 A) in the asymmetric unit of the P2(1)2(1)2(1) unit cell of dimens

235 r similar to the tetramer in the icosahedral asymmetric unit of the procapsid.

236 The asymmetric unit of the RT fragment-DNA-netropsin crystal

237 two of the four molecules of Sec4-GDP in the asymmetric unit of the Sec4-GDP crystals, the switch II

238 The asymmetric unit of the unit cell contains two independen

239 ly two of the three protein molecules in the asymmetric unit of this complex, the structure of the th

240 n the presence of multiple homodimers in the asymmetric unit of this structure.

241 Individual monomers within the tetrameric asymmetric unit of TM0322 exhibit high root mean square

242 rystal structures, but are distinct from the asymmetric units of their crystal forms.

243 Twenty total subunits in the two asymmetric units of these crystal forms display three di

244 salt (400 mm KCl) shows two molecules in the asymmetric unit, one of which assumes an unprecedented c

245 There are two distinct sites in the asymmetric unit: one containing four in-plane waters wit

246 sembled with multiple parallel copies of the asymmetric unit or multiple twisted protofilaments.

247 ndary conditions defined with respect to the asymmetric unit or the primitive unit cell as well as us

248 tudy contains 24 independent subunits in the asymmetric unit permitting comparison between them.

249 ach subunit of the tetramer contained in the asymmetric unit plus a total of 327 solvent molecules.

250 PDB Entries contain only the contents of the asymmetric unit rather than the biological unit, some ke

251 p P3(1), with two molecules of rhodopsin per asymmetric unit, related by a non-crystallographic 2-fol

252 he first T=1 capsid with a heterodimer as an asymmetric unit reported to date and follows the archite

253 The four molecules in the RpiB asymmetric unit represent a dimer of dimers.

254 lls, such that the observed crystallographic asymmetric unit represents one repeat averaged over six

255 s two different ligand-free structures in an asymmetric unit (resolution 2.1 A) and two co-crystal st

256 A with one and two domain-swapped dimers per asymmetric unit, respectively.

257 independent positions within an icosahedral asymmetric unit, resulting in 120 binding sites on the v

258 of another C4 scFv:HTT(1-17) complex in the asymmetric unit, resulting in a beta-sheet interface wit

259 es for the three sites for Gd/Y atoms in the asymmetric unit reveal a partially ordered arrangement o

260 The two tetraubiquitin complexes in the asymmetric unit show the complete connectivity of the ch

261 First, similarities in space group, asymmetric unit size, and cell dimensions and angles (wi

262 mages to achieve the same number of averaged asymmetric units; structural variability will increase t

263 sordered in two of the eight monomers in the asymmetric unit suggesting that they function as a lid c

264 rder varies in the four Lys-169 loops in the asymmetric unit, suggesting that the mutation has led to

265 the three molecules in the crystallographic asymmetric unit, sulfate is coordinated to Mn2 in a mono

266 The chains feature the combination of two asymmetric units [Ta(2)S(11)] and [AsS(3)] and exhibit s

267 The two CheY** molecules in the asymmetric unit that are bound to FliM16 adopt a conform

268 R state contains two catalytic chains in the asymmetric unit that are different.

269 ree Link_TSG6 contains five molecules in the asymmetric unit that are highly similar to the NMR struc

270 tals contain two Rossmann domains within the asymmetric unit that are unconstrained by the crystal la

271 o space group P4(1)2(1)2 with a dimer in the asymmetric unit that closely resembles asymmetric dimers

272 ndependent molecules, A, B, C, and D, in the asymmetric unit that exists as A-B and C-D units of two

273 orhombic crystals contained a monomer in the asymmetric unit that is arranged about a 2-fold crystall

274 R structures, containing two subunits in the asymmetric unit (the so-called A and B subunits) but for

275 p (monoclinic) with a single molecule in the asymmetric unit, the beta form appeared as thin fibers a

276 In the three molecules that populate the asymmetric unit, the Mg(2+) ion that normally coordinate

277 oup I23 (a=118.2 A), with one subunit in the asymmetric unit.The medium of crystallization, 1.8 M SO(

278 , and c = 144.28 A) with two subunits in the asymmetric unit; the HGPRT tetramer is completed by the

279 group I23 (a=228.6 A) with a tetramer in the asymmetric unit; the structure has been refined with dat

280 In the other two molecules in the asymmetric unit, these interactions do not take place.

281 ent for the two independent molecules in the asymmetric unit; these findings are attributed to the co

282 Two molecules of IGFRK-0P are seen in the asymmetric unit; they are associated as a dimer with the

283 P2(1) with three quadruplex molecules in the asymmetric unit, two associating together as a head-to-h

284 In the asymmetric unit, two scFv735 molecules associate with on

285 erent complexes were captured in the crystal asymmetric unit: two have DNA in the polymerase active s

286 aining four subunits in the crystallographic asymmetric unit, were re-refined to have the same subuni

287 1.85 A resolution, contains a trimer in the asymmetric unit, whereas another contains an antiparalle

288 otein crystallizes with two molecules in the asymmetric unit which we propose to resemble the dimer w

289 rystallized with two distinct species in the asymmetric unit, which closely resemble the autoinhibite

290 ansmembrane "anchor" protein per icosahedral asymmetric unit, which extends from beneath one of the c

291 aining 16 silicon and 32 oxygen atoms in its asymmetric unit, which would be very difficult to solve

292 es 3'-3' stacking of two quadruplexes in the asymmetric unit, while the bulged nucleotide mediates cr

293 a=96.80 degrees) contained a pentamer in the asymmetric unit with a structure very similar to that of

294 VC.actin 1:1 complex shows two actins in the asymmetric unit with extensive actin-actin contacts.

295 ucture (2.35 A resolution) has one dimer per asymmetric unit with nitrate bound in an open active sit

296 Two dimers are present in the asymmetric unit with one monomer of each pair exhibiting

297 ic trimer (alpha(3)) in the crystallographic asymmetric unit with similar arrangement of neighboring

298 cted by the presence of two molecules in the asymmetric unit with the dimeric interface formed by ant

299 al bundle) and it packs as a tetramer in the asymmetric unit with the insertions forming part of the

300 There are three molecules in the asymmetric unit with unique crystal-packing environments