ライフサイエンスコーパス: crystal form

1 nterface and results in a CYP126A1 monomeric crystal form.

2 te transition to be observed within a single crystal form.

3 eaker thermoelectric response than in single crystal form.

4 lyl)-N-hydroxy-2-propenamide (APHA) in a new crystal form.

5 ture determination of the enzyme in a second crystal form.

6 ation and determined this structure in a new crystal form.

7 tical to the wild-type structure in the same crystal form.

8 ructure determination required finding a new crystal form.

9 potential if they were available in a single crystal form.

10 -free protein have been obtained in the same crystal form.

11 lids that frequently exhibit polymorphism of crystal form.

12 e, but intercalation occurs only in the I222 crystal form.

13 from a bicellar solution, yielding a new bR crystal form.

14 replacement to 1.9 A using the orthorhombic crystal form.

15 75 in complex with full-length Rtt109 in two crystal forms.

16 (NNRTIs), including effects of mutation and crystal forms.

17 on interfaces across a majority of available crystal forms.

18 distinct from the asymmetric units of their crystal forms.

19 ous to helices seen previously in other Vps4 crystal forms.

20 has been determined in two related hexagonal crystal forms.

21 le and largely disordered in the other three crystal forms.

22 which is functionally unclassified, in three crystal forms.

23 s reported for the same protein in different crystal forms.

24 ined for the full-length protein in multiple crystal forms.

25 crystal structure of Gam from two different crystal forms.

26 occurrence of the interface across different crystal forms.

27 li PL to delipidated LacY leads to different crystal forms.

28 ure of active BoNT/F catalytic domain in two crystal forms.

29 en and closed conformations in two different crystal forms.

30 rt here ligand transition structures in both crystal forms.

31 tates have been determined in a total of six crystal forms.

32 yt c2 were co-crystallized in two monoclinic crystal forms.

33 action as well as the lattice changes of the crystal forms.

34 re of glycogenin was solved in two different crystal forms.

35 mer ring subunits that are related to the 2D crystal forms.

36 lizes, although screened extensively for new crystal forms.

37 4b in complex with PDEdelta in two different crystal forms.

38 rigid-body motion of a protein in different crystal forms.

39 of the APOBEC3B catalytic domain in multiple crystal forms.

40 oquadratum walsbyi (HwBR), was solved in two crystal forms.

41 ons of mouse P-gp derived from two different crystal forms.

42 /epsilon inhibitor PF670462 in two different crystal forms.

43 states are also observed in different IgE-Fc crystal forms.

44 solved structures of BamB in three different crystal forms.

45 e rate of nucleation, and the quality of the crystal formed.

46 refinement at 2.2A resolution revealed that crystal form 1 (a=95.76A, b=70.53A, c=103.41A, beta=96.8

47 X-ray structures of two crystal forms (1.5 and 1.9 A) of a complex between cathe

48 The 2.6A resolution structure of crystal form 2 (a=118.60A, b=109.10A, c=120.80A and beta

49 In crystal form 2, a calcium ion is bound closely to a beta

50 In crystal forms 3 and 4, a sulfate ion or a phosphate anio

51 m CH(2)Cl(2)/hexanes yields a mixture of two crystal forms, 4.4CH(2)Cl(2).H(2)O (4a) and 4.6CH(2)Cl(2

52 s with a subset of these, MOF-801-SC (single crystal form), -802, -805, -806, -808, -812, and -841 re

53 ng shells by displaying an alternate CaCO(3) crystal form, a cross-linked organic matrix, and an elev

54 In one crystal form, a molecule of Mes [2-(N-morpholino)ethane

55 four tRNA-binding sites were occupied in the crystal form, a question was raised regarding whether th

56 In every crystal form, a residue inserts between tryptophan resid

57 receptor Slr1694 have been determined in two crystal forms, a monoclinic form at 1.8 A resolution and

58 Crystals formed after a month and were characterized.

59 The availability of different crystal forms allowed us to investigate the effect of th

60 These two crystal forms allowed, for the first time, modeling of t

61 enated lamprey hemoglobin in an orthorhombic crystal form along with the structure of these crystals

62 Analysis of both crystal forms, along with data from HbI mutants, suggest

63 e lack of ligand binding to the orthorhombic crystal form also obtained at pH 7.5.

64 er pH 6.5 or pH 8.5), and a second hexagonal crystal form (analyzed at 100 K), all reveal the shift o

65 s first solved to 3.4 A using the tetragonal crystal form and a three-wavelength Se-Met multi-wavelen

66 y cases, it is challenging to produce a pure crystal form and establish a sensitive detection method

67 ese results draw attention to the effects of crystal form and refinement procedure on experimental AD

68 e structure of wt-PHM in the Met(314)Ile-PHM crystal form and showed that it does not differ from the

69 revealed by x-ray diffraction studies of the crystal form and thus provide a complete and better unde

70 2 is relatively stable in crystal form and when neutralized to SNCEE (2a) in aqueo

71 the two proteins were found to have the same crystal forms and almost identical X-ray structures.

72 We determined FKBP26 structures from four crystal forms and analyzed chaperone domains in light of

73 rminal MA3 (cMA3) domain of Pdcd4 in several crystal forms and demonstrated its similarity to the MA3

74 imulated by conformational variability among crystal forms and evidence suggesting that the functiona

75 lyses of 10 independent molecules in various crystal forms and from comparisons with mitochondrial co

76 gomer of the cyclic peptide is found in both crystal forms and indicates that under appropriate condi

77 e of FtsZ structures determined in different crystal forms and nucleotide states, and in the presence

78 We also crystallized M in two crystal forms and show that it assembles into equivalent

79 We show that CPE forms a trimer in both crystal forms and that this trimer is likely to be biolo

80 conformational flexibility within the three crystal forms and the NMR ensemble, with no evidence of

81 The described crystal forms and the observations of different defined

82 ome c from Shewanella oneidensis MR-1 in two crystal forms and two redox states.

83 Why these crystals form and how they contribute to joint damage in

84 New information on how crystals form and how they exert their biologic effects

85 were calculated to 8.5 A from two different crystal forms, and show a single reaction centre surroun

86 hairpin region is ordered in only one of the crystal forms, and that may suggest open and closed stat

87 A novel feature of this crystal form appears to be a shared hydrogen between the

88 at an interface is biological if two or more crystal forms are available.

89 Both crystal forms are dimers, which are also observed in sol

90 The refined structures from the two crystal forms are nearly identical with no significant d

91 Surprisingly, the first calcite crystals formed are perfect rhombohedra, and the soluble

92 In one crystal form, arginine was bound adventitiously to the e

93 The structure, characterized in a novel crystal form as an R(6) zinc hexamer at 2.3 A resolution

94 alpha-14 giardin determined in two different crystal forms as well as the Ca(2+)-bound crystal struct

95 arge differences in position between the two crystal forms, as have residues 86-96 in the hatch domai

96 red bat/Guatemala/164/2009 (GU09-164) in two crystal forms at 1.95 A and 2.5 A resolution and A/littl

97 d N-terminal domain of ClpA in two different crystal forms at 2.3- and 3.3-A resolution.

98 mplex with the mbtA-mbtB operator DNA in two crystal forms at 2.4 A and 2.6 A, the highest resolution

99 , and with the product NADP in two different crystal forms at 2.45 A and 2.0 A resolution, respective

100 (9004G) and the Cn2 toxin, determined in two crystal forms at 2.5 and 1.9 A resolution.

101 1 determined from orthorhombic and hexagonal crystal forms at 3.0- and 3.5-A resolution, respectively

102 bstrate analogue, nicotinic acid, from three crystal forms at resolutions of 1.7 A, 1.8 A and 2.4 A,

103 ecA protein has been determined in three new crystal forms at resolutions of 1.9 A, 2.0 A, and 2.6 A.

104 Diastereomeric interactions in 2D crystals formed at solid surfaces serve as excellent mod

105 atory syndrome coronavirus (SARS-CoV) in two crystal forms, at 1.17 A (monoclinic) and at 1.85 A (cub

106 the catalytic core domain of hPus1 from two crystal forms, at 1.8A resolution.

107 In order to classify the crystal form based on the quantitative morphological pro

108 ture of the wild-type, proenzyme CT from two crystal forms, both of which exhibit (i) better geometry

109 ces or compliant crystals on droplets, these crystals formed branched, ribbon-like domains with large

110 eport the organization of cholesteric liquid crystal formed by nanorods in spherical droplets.

111 ry strategy based on a supramolecular liquid crystal formed by peptide amphiphiles (PAs) that encapsu

112 alter and control crystal habits of a 3D DNA crystal formed by self-assembly of a DNA 13-mer.

113 structure of the soluble form of CPE in two crystal forms by X-ray crystallography, to a resolution

114 Purple membranes (PM) are two-dimensional crystals formed by bacteriorhodopsin and a variety of li

115 e of the crystals from meteorite ALH84001 to crystals formed by certain terrestrial bacteria has been

116 measurements carried out with isomorphic co-crystals formed by halogen-bonding (XB) between tritylac

117 cattering at room temperature in 2D phononic crystals formed by the introduction of air holes in a si

118 Analysis of crystals formed by the monomeric protein reveals that th

119 Amyloid-like fibrous crystals formed by the peptide KFFEAAAKKFFE have been pr

120 The high degree of spatial uniformity of the crystals, formed by a soft nanoimprint technique, provid

121 or lack of common interfaces across multiple crystal forms can be used to predict whether a protein i

122 howed that the matrix protein is specific to crystal-forming cells.

123 eterodimeric interfaces observed in multiple crystal forms (CFs).

124 t in identifying interfaces observed in many crystal forms compared with the PDB and the European Bio

125 d the FtsZ/tubulin superfamily fold, and one crystal form contained sheets of protofilaments, suggest

126 ntee that two crystals are actually the same crystal form, containing similar relative orientations a

127 The second crystal form contains PGH only in one subunit and the ac

128 Using this novel approach, 3 wt % of one crystal form could be detected in mixtures of the two po

129 Enamel crystals form de novo in a rich extracellular environmen

130 TD revealed by the analysis of the different crystal forms delineates possible interfaces that could

131 imilar to the two described earlier, the new crystal form demonstrates extensive hinge movement betwe

132 t became apparent that the reactivity of the crystal forms depends exclusively on the molecular arran

133 he best crystals of native rhodopsin in this crystal form diffracted X-rays from a microfocused synch

134 ubunits in the two asymmetric units of these crystal forms display three distinct tertiary structures

135 While trying to visualize uric acid crystals formed during EPEC and STEC infections, we noti

136 ructure, reducing the size and number of fat crystals formed during storage; furthermore they present

137 In one crystal form, each subunit contains PGH, which is coordi

138 richia coli PabB determined in two different crystal forms, each at 2.0 A resolution.

139 ution) and S. aureus (SaMDD, in two distinct crystal forms, each diffracting to 2.3 A resolution) hav

140 with TMC278 at 1.8 A resolution, using an RT crystal form engineered by systematic RT mutagenesis.

141 in the octameric RNA assembly include a new crystal form, evidence of multiple conformations and str

142 Because the two crystal forms exhibit mostly unrelated packing interacti

143 ly 3 degrees), based on analysis of distinct crystal forms for ligated and unligated molecules.

144 Two crystal forms for NreA were obtained, with either bound

145 ations, the interactions result in different crystal forms for the two protein forms.

146 utative active site of the enzyme in the new crystal form (Form II) after exposure to the inhibitor.

147 f clopidogrel bisulfate were prepared in two crystal forms (Form I and Form II).

148 endent dimers are observed in three distinct crystal forms, formed via pleomorphic coordination of Zn

149 We have analyzed 9596 unique protein crystal forms from the August 2003 PDB and have found a

150 Our observations indicate that the CuAu-I crystals form from CsCl parent crystals by a diffusionle

151 Dithionite-reduced crystals or crystals formed from dithionite-reduced enzyme revealed

152 anipulation of a wide variety of ion Coulomb crystals formed from small numbers of ions.

153 n determined to a resolution of 1.3 A from a crystal form grown in the presence of ethylene glycol.

154 One crystal form has two tetramers bound to form an octamer,

155 1,4-benzenedicarboxylate), with well-defined crystal form have been investigated during CO2 uptake at

156 Six new crystal forms have been characterized.

157 Both crystal forms have four normal H-bonds; the enol has two

158 Crystal form I reveals structural details of farnesylate

159 d-methylated KRAS4b binding to PDEdelta, and crystal form II suggests the potential binding mode of g

160 In crystal form II, we see the full-length structure of far

161 e detection method for the identification of crystal form in a mixture of polymorphs.

162 1.9 A resolution, which was solved in a new crystal form in the absence of DNA.

163 diffraction from a highly hydrated triclinic crystal form in which the asymmetric unit contains two i

164 le manifestation of three dimensional Wigner crystal formed in InSb by light electrons and heavy hole

165 Hemozoin (HZ) is an insoluble crystal formed in the food vacuole of malaria parasites.

166 The mutant enzyme, however, grows in two crystal forms in the presence of saturating AMP.

167 New crystal forms in the presence of two different Fabs to M

168 why and how calcium pyrophosphate dihydrate crystals form in articular cartilage has been hampered b

169 A 1.6 A OmpF structure, obtained from crystals formed in 1 M Mg2+, has one Mg2+ bound in the s

170 onfirmed by functional studies; however, the crystals formed in ATD5 cells were basic calcium phospha

171 For both conditions, crystals formed in related space and plane groups with s

172 d cryoelectron microscopy of two-dimensional crystals formed in the presence of decavanadate and dete

173 ion to hydroxyapatite (HA), while aligned HA crystals formed in the presence of non-phosphorylated LR

174 can form two different dimers (in P1 and R32 crystal forms) in the same crystallization solution, whe

175 structures obtained in multiple independent crystal forms indicates that the mini-zipper is a stable

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

177 The hexameric assemblage in this crystal form is very similar to those observed in the pr

178 e conformation of the PTC-CCA in the two 70S crystal forms is identical to that of the 2.8 A 70S mode

179 dimeric assembly, which is seen in different crystal forms, is formed by packing of helices and a sho

180 he interactions between commonly used liquid crystal-forming molecules and phospholipid bilayers.

181 s the conformation of OMPLA in the different crystal forms (monomer versus dimer; with/without bound

182 igher-order assemblies is seen in any of the crystal forms nor does the structure vary significantly

183 The thermodynamically stable enol crystal form of barbituric acid, previously prepared as

184 ting that the dimer may only be found in the crystal form of CR2.

185 llized at pH 7.6, 8.0, and 8.4) and a second crystal form of DEBS TE.

186 The same structure and a second crystal form of FtsA reveal that FtsA forms actin-like p

187 e open state of HePTP, we identified a novel crystal form of HePTP that allowed the closed-state-to-o

188 In addition, the metastable crystal form of indomethacin (the alpha-form) also react

189 Here we report a novel orthorhombic crystal form of NK1 at 2.5 A resolution in which four NK

190 four high-resolution structures of a single crystal form of Sky1p, a constitutively active serine ki

191 In this study, we present a new crystal form of the apoenzyme in the canonical conformat

192 tric unit compared to the one present in the crystal form of the native protein.

193 The stable, guest-free crystal form of the simple molecular cavitand, Me,H,SiMe

194 We report here two crystal forms of a complex between the Grb2 SH2 domain a

195 pse of an active CT in structures from three crystal forms of a single-site A-subunit CT variant, Y30

196 We recently demonstrated that different crystal forms of chrome yellow pigments (PbCrO(4) and Pb

197 In all crystal forms of Fis, the separation between the DNA rec

198 Two monoclinic (P2(1)) crystal forms of human serum amyloid P component (SAP) i

199 Different crystal forms of ligand-free DprE1 reveal considerable l

200 Pressurization of two crystal forms of MMOH with xenon resulted in the identif

201 Analysis of four additional crystal forms of MntR.Mn(2+) reveals that the AB conform

202 in which cross-crystal averaging between two crystal forms of the 70S ribosome was used to evaluate r

203 he same dimeric structure as observed in all crystal forms of the active repressor with and without b

204 Here, we report the crystal structure in two crystal forms of the BIR1 domain of XIAP, which does not

205 We report here the structures of two crystal forms of the frameshifting RNA pseudoknot from b

206 Crystal forms of the octameric assembly formed by this s

207 nzyme has been determined from six different crystal forms of the protein.

208 C1 from different species produced different crystal forms of the RCC1/nucleosome complex consistent

209 We determined structures from several crystal forms of the RevErb-DNA complex and analyzed the

210 ClO(4)) and [Fe(OEP)NO](ClO(4)).CHCl(3) (two crystal forms of the same complex) has been established.

211 Two different crystal forms of truncated DC-SIGNR comprising two neck

212 ulti-microsecond MD simulations of different crystal forms of ubiquitin.

213 Two crystal forms of XRCC1-NTD complexed with Pol beta have

214 ive SHG microscopy enabled discrimination of crystal form on a per particle basis with 99.95% confide

215 lines of evidence indicating that most anvil crystals form on mid-tropospheric rather than boundary-l

216 ssion electron microscopy revealed that Ag2S crystals form on the surface of AgNWs within 1 h of incu

217 les containing protein signals acquired from crystals formed on the border of the MALDI sample spot,

218 , comprising bundles of small needle-like HA crystals, formed on etched surfaces that were cut perpen

219 the full-length human Ape1 enzyme in two new crystal forms, one at neutral and one at acidic pH.

220 The complexes were crystallized in two crystal forms, one of which is in a new space group for

221 ence, superposition of free HEL in different crystal forms onto bound HEL in the wild type and mutant

222 e of Bacillus subtilis PurS in two different crystal forms P2(1) and C2 at 2.5 and 2.0 A resolution,

223 A resolution and of the zinc complex in two crystal forms (P2(1)2(1)2(1) and F222) to 1.88 A and 1.7

224 ermined the structures of AaNusG also in two crystal forms, P2(1) and C222(1), and surprisingly found

225 ncentrated along the protein fibers and that crystals form preferentially on the fiber crossings.

226 thereby at least augmenting matrix-mediated crystal-forming processes in this system.

227 ally expressed protein yielded two different crystal forms (Protein Data Bank identifiers [PDB ID], 3

228 roteins, which exist as dimers only in their crystal form, provide examples of two vastly different s

229 All structures were solved in the same crystal form, providing an unusual opportunity to compar

230 E (IgE)-Fc(3-4) has been solved in three new crystal forms, providing 13 snapshots of the Fc conforma

231 n crystal structure of ToxA in two different crystal forms, providing four independent views of the p

232 One crystal form, refined to 1.85 A resolution, contains a t

233 ptimized to produce a high-resolution apo-RT crystal form, reported here at 1.85 A resolution, with a

234 etermined a structure of human SAA1.1 in two crystal forms, representing a prototypic member of the f

235 Lattice contacts in a 4.1-A resolution crystal form reveal a tetrameric (dimer-dimer) arrangeme

236 ructure of molybdopterin synthase in a novel crystal form revealed a binding pocket for the terminal

237 Six structures of NleL observed in two crystal forms revealed a large range of different positi

238 Analysis of three crystal forms revealed binding of single chain lipids an

239 In addition, a different crystal form reveals that the locally closed and open co

240 We find that the nanoparticle crystals form reversibly during heating and cooling cycl

241 Comparison of five monomers in two different crystal forms showed conformational changes in the finge

242 rved surface residue (M610R) led to a second crystal form showing a substantially different conformat

243 nding sites for two derivatives and of a new crystal form showing important domain swapping.

244 la17-HNP2 were determined in three different crystal forms, showing a well preserved beta-bulge ident

245 In the monoclinic crystal form, six SMChd molecules form two turns of a he

246 A new crystal form (space group P21/n) of the photoresponsive

247 This new orthorhombic crystal form (space group P21212) comprises two polymera

248 ructure of the H-NOX domain in two different crystal forms suggests a mechanism whereby alteration in

249 gand that binds there, comparison of the two crystal forms suggests differences in the region of the

250 p-cage is remarkably stable and afforded two crystal forms suitable for X-ray diffraction.

251 rid) complexes were crystallized in distinct crystal forms, supporting the homogeneity of the conform

252 Well-developed pseudocubic jarosite crystals formed surface coatings, and in some instances,

253 In both crystal forms, T.tenax TIM exists as a tetramer of the f

254 This material occurs in two crystal forms, tetragonal and orthorhombic, both with a

255 tional structure containing zinc in the same crystal form that allows direct comparison with the zinc

256 The inability to obtain a crystal form that has previously been prepared is indeed

257 x-ray crystal structure of Cascade in a new crystal form that provides insight into the mechanism of

258 uctures of the A3B catalytic domain in a new crystal form that show alternative, yet still closed, co

259 ared in dimeric form, yielded numerous novel crystal forms that cannot be realized by monomeric lysoz

260 We observe three different crystal forms that diffract to increasingly better resol

261 In the other crystal form the extension is largely alpha-helical.

262 In one crystal form the LH1 forms a circular ring, and in the o

263 In both crystal forms the protein is in complex with cholesterol

264 The stable crystal form (the gamma-form), however, is inert to ammo

265 In two crystal forms, the PknD sensor domain forms a rigid, six

266 In both the P2(1) and the C2 crystal forms, the quaternary structure of PurS is a tet

267 wo surfaces on the N-terminal domain in both crystal forms; the more extensive interface was shown to

268 Between two crystal forms, there are three crystallographically inde

269 bits marked conformational variability among crystal forms, these glycines consistently maintain posi

270 The frameworks remained in their single crystal form throughout.

271 The amplitude of rocking varies from one crystal form to another and is correlated with the resol

272 ed from both a hexagonal and an orthorhombic crystal form to resolutions of 2.5A and 2.3A, and refine

273 iles; factors that enable out-of-equilibrium crystal forms to be obtained.

274 e have solved the structure of NaD1 from two crystal forms to high resolution (1.4 and 1.58 A, respec

275 nt-1-deoxypentalenic acid, in four different crystal forms to up to 1.31 A resolution.

276 ymorphs (as well as the emergence of elusive crystal forms) to demonstrate the enduring relevance of

277 We report the structures of AcnR in two crystal forms together with ligand binding experiments a

278 ure of the lambda repressor CTD in three new crystal forms, under a wide variety of conditions.

279 e with the already available structures, the crystal form used in this study contains 24 independent

280 (2+), and Zn(2+)), was synthesized in single crystal form via a mild hydrothermal technique utilizing

281 nanoliter volumes, we observed that calcite crystals form via an amorphous precursor phase.

282 A new crystal form was also obtained; it displays the flexible

283 A second GABARAP crystal form was determined at 1.9 A resolution and docu

284 allizing the inhibitor complex, a new native crystal form was identified which had the homodimer 2-fo

285 Whilst, the particle shapes of the two crystal forms were all irregular, the surface of CLP II

286 In this study, unfavored noncentrosymmetric crystal forms were observed by SHG microscopy.

287 bserved by Olea et al. for Tt H-NOX P115A in crystal form, where four different heme structures were

288 common interfaces across only a minority of crystal forms, whereas higher-order structures exhibit c

289 The oxidized simulation stays true to the crystal form with a heavy atom root mean-squared deviati

290 Soaking of this crystal form with ATP and pantoate gives a fully occupie

291 und AF1665 AlaDH (AF-AlaDH) at 2.3 A in a C2 crystal form with the 70 kDa dimer in the asymmetric uni

292 ms resolution crystal structure of YajL in a crystal form with two molecules in the asymmetric unit.

293 The neurofascin dimer, captured in two crystal forms with independent packing patterns, reveals

294 in (Y100H/V102F) was solved in two different crystal forms with two other orientations of the flexibl

295 At high temperature, hexagonal Au nano-crystals form with facets along {111} and {100} likely d

296 A structure of AQP0 in two-dimensional (2D) crystals formed with Escherichia coli polar lipids (EPLs

297 Two different two-dimensional crystal forms, with p2 and p3 symmetry, were obtained us

298 Crystal structures of R163K in two different crystal forms, with six and two subunits per asymmetric

299 The crystals formed within the drying drops of solutions dur

300 One trigonal crystal form, Xe@111y(solvent), is exceptionally stable,