ライフサイエンスコーパス: the structure of

1 The structures of 15 anti-protein antibodies were analys

2 The structure of 8 complexed with the CGRP receptor was

3 The structure of a 2D-COF consists of two dimensional sh

4 Here we present the structure of a CCC, the Mus musculus K(+)-Cl(-) cotr

5 Here we determine the structure of a class D GPCR, the Saccharomyces cerev

6 We determined the structure of a close BotCYP homolog and used our dat

7 The structure of a Dfg5*beta1,3-glycoside complex predic

8 into metazoan innate immunity, and determine the structure of a full-length TIR-STING fusion from the

9 However, the structure of a functional full-length CYP102A1 enzym

10 We solved the structure of a malate racemase apoprotein and used i

11 7 in the presence of detergents and obtained the structure of a narrow tetrameric channel with a stro

12 Here, we solved the structure of a newly identified TCR in complex with

13 Here we solved the structure of a non-peptide agonist, TT-OAD2, bound t

14 We present the structure of a novel solvate adduct formed by dissol

15 We determined the structure of a poplar cellulose synthase CesA homotr

16 Experimental determination of the structure of a potassium channel VSD in the intermed

17 scopy map of Tetrahymena telomerase revealed the structure of a previously uncharacterized TERT domai

18 Chemical transformations determine the structure of a product, and therefore its properties

19 This problem is of fundamental importance as the structure of a protein largely determines its functi

20 fold is achieved using pressure to modulate the structure of a recently developed 2D perovskite (HA)

21 e used cryo-electron microscopy to determine the structure of a reconstituted human 48S The structure

22 Here we present the structure of a second SM-Qa-SNARE complex, Vps45-Tlg

23 owth and earthworm bioturbation in restoring the structure of a severely compacted soil.

24 We previously determined the structure of a short motif in the disordered XPA N-t

25 riple helices have been studied extensively, the structure of a strand dimer is unknown.

26 ene viuB (vibriobactin utilization) to study the structure of a V. cholerae population over the cours

27 Here, we solve the structures of a natural AAV isolate complexed with a

28 The structures of A11 and B12A TCR are nearly identical

29 tudy was to explore the relationship between the structure of abacavir with HLA-B*57:01 binding and t

30 Investigating the structure of active ingredients, such as agrochemica

31 While the structure of ADO has been previously described, stru

32 mpacted by both the size of confinements and the structure of alkanols in the E1 pathway of dehydrati

33 The structures of all proposed mechanisms were optimized

34 al treatment (45-95 degrees C for 30 min) on the structure of almond milk proteins was assessed, as t

35 pectroscopy (AFM-IR), we were able to reveal the structure of alpha-synuclein oligomers present at di

36 The evolution of the structure of amorphous carbon (a-C) films during dep

37 e used cryo-electron microscopy to elucidate the structure of an agonist-bound activated DRD2-G(i) co

38 e lacks a canonical phospholipase A2 domain, the structure of an EDTA-treated capsid, determined to 2

39 Here we report the structure of an unliganded human Fzd5 determined by

40 The structure of any BL-BGC derived metabolites, their f

41 These structures and the structure of apo-hGGT reveal movement of amino acid

42 decades has given us important insights into the structure of ApoE and how this might impact the neur

43 with a rate constant similar to the k (cat) The structure of AsFMO complexed with FAD at 2.08- angst

44 The structures of assembled 3D clusters are verified by

45 We also demonstrated the structure of AtERF96 EDLL motif, a unique conserved

46 ID, enabling the generation of hypotheses on the structures of biological assemblies of many systems.

47 The structure of BON1 bound to Mn(2+) is also presented.

48 rid DFT/parametric method, DU8+, and revised the structures of briarellin C14-C3 epsilon-lactones to

49 X-ray crystallography revealed the structure of Bs164, the first known structure of a G

50 Importantly, for the first time, we report the structure of BTNL2 as determined by solution NMR spe

51 -guanosine number influences fate, we probed the structures of capped HIV-1 leader RNAs by deuterium-

52 he fused tags at the termini probably affect the structure of CENH3 and reduce its interaction with o

53 enantiopure carbohydrate polymer inspired by the structure of chitosan.

54 The structure of chromatin impacts gene expression.

55 egulatory sequences that physically organize the structure of chromatin, including promoters, enhance

56 of the first known CntA inhibitors and solve the structure of CntA in complex with the inhibitor, dem

57 ppearance and generates new hypotheses about the structure of color space.

58 Knowing the structure of conserved structural RNAs is important

59 nation of this puzzling observation based on the structure of contact networks.

60 , and discuss implications for understanding the structure of cortical functional architecture.

61 fluence the Tombusviridae viral life cycles, the structures of cucumber leaf spot virus (CLSV; genus

62 ls to fingerprint the multifunctionality and the structure of cutin in planta.

63 V-DDB may be the first responder in altering the structure of damage containing-nucleosomes, allowing

64 We refined the structure of DDM and evaluated the activity of novel

65 We solved the structure of Dfg5 from a filamentous fungus and used

66 Here we determined the structure of dimeric human DGAT1, a member of the me

67 e of the bovine dimer also demonstrates that the structures of dimeric ATP synthases in a tetrameric

68 Selective chemistry that modifies the structure of DNA and RNA is essential to understandi

69 Here we report the structure of DNA-bound Mfd, which reveals large DNA-

70 The structure of DslA reveals a modified lysozyme superf

71 The structure of each antenna is optimized to act both a

72 ructural basis of this phenomenon, we solved the structures of ELIC embedded in palmitoyl-oleoyl-phos

73 ing the feasibility of viral genome studies, the structure of encapsidated MS2 RNA was exclusively de

74 gands and high surface area), it was used in the structure of fabricated nano-adsorbent.

75 The structure of final products depended on the nature o

76 The structure of full-length M1, and how it oligomerizes

77 Here, we report the structure of full-length PrgA, which shows that PrgA

78 The structure of fungal oxyluciferin (light emitter) was

79 Understanding the structure of gamma-Al(2)O(3) is essential to tuning

80 Herein, we unravel the structure of glycosyl cations involved in remote par

81 Controlling the structure of graphene and graphene oxide (GO) phases

82 The structure of GTUB5 was characterized using single cr

83 The structure of H767A PlGoxA revealed a previously unde

84 t these two tryptophan residues do not alter the structure of HC/B or the interactions with its recep

85 We determined the structure of HhaI in complex with cognate DNA at an

86 electron microscopy (cryo-EM), we determined the structure of human cohesin bound to its loader NIPBL

87 gammaTuRC-mediated nucleation by determining the structure of human gammaTuRC and performing quantita

88 Here, we report the structure of human RFC bound to PCNA by cryogenic el

89 Here, we report the structure of human SOAT1 (hSOAT1) determined by cryo

90 Here we report the structures of human B3GNT2 in complex with UDP:Mg(2+

91 Here, using cryo-EM, we determine the structures of human SERINC5 and its orthologue from

92 Using the reported methods we solved the structures of (i) Pseudorabies virus (PRV) RNA G-qua

93 The structure of individual CA chains, their arrangement

94 The structure of intact IgE and the impact of IgE-target

95 To characterize and compare the structure of interfaces between cell types or of int

96 We investigate the structure of interfacial turbulence and its relation

97 lecules throughout the visual pathway and in the structure of interneurons in the primary visual cort

98 This work provides insight into the structure of IRBP, displaying an elongated, flexible

99 physicochemical properties of pea flour and the structure of isolated pea starch.

100 positioned for further optimization based on the structure of its complex with Keap1 and synthetic ac

101 PscK from Pseudomonas aeruginosa, as well as the structure of its interacting partner, the cytoplasmi

102 by ab initio calculations are used to solve the structures of K(5)[Mo(3)O(4)F(9)].3H(2)O (1), K(5)[M

103 re we use cryo-electron microscopy to reveal the structure of KBP and of a KBP-kinesin motor domain c

104 still struggle to accurately predict de novo the structures of large proteins, membrane proteins, or

105 Last, we inspected the structures of LBDs from nonplant species and generat

106 exhibit structural plasticity when comparing the structures of lethal and edema toxins.

107 The structure of lincomycin A consists of the unusual ei

108 As the structure of lipid A (endotoxin) determines the inna

109 he mass transfer coefficients by fragmenting the structure of low-molecular-weight neutral organics i

110 M1 within intact virus particles, as well as the structure of M1 oligomers reconstituted in vitro.

111 sm of this dynamic translocon, we determined the structure of mammalian Sec61 inhibited by the Mycoba

112 elf-)propelled agents and a key component in the structuring of many biological systems.

113 Here, we report the structures of MavC/UBE2N/Ub ternary complex, MavC/UB

114 ve framework based on demography to show how the structure of migration flows between cities, togethe

115 We solved the structure of MKP5 in complex with this inhibitor, wh

116 on a core theme in their arguments; namely, the structure of models that generate predictions.

117 Previously, the structures of MRP1 were determined in an inward-faci

118 h day are forgotten, those integrated within the structure of multiple prior memories tend to endure.

119 The structure of MX(3) transition metal trichalcogenides

120 Moreover, we present the structure of N6-methyl-dAMP-bound human MTH1, reveal

121 e this essential leak channel and determined the structure of NALCN in complex with a distinct auxili

122 The structure of nano-sized PST-5 crystals is determined

123 Here, we studied the structure of native bovine IRBP in complex with a mo

124 hich is critical for motility, we determined the structure of native flagellar filaments from the spi

125 The structure of NdCCD in complex with its apocarotenoid

126 The structure of NdCCD revealed a tapered active site ca

127 eory can provide an unprecedented picture of the structure of neutral biomolecules in the gas phase.

128 and function of chromatin, we must determine the structures of nucleosomes containing native DNA sequ

129 The structure of one rhesus antibody, capable of neutral

130 To further support this model, we altered the structure of osteoblast HS genetically to make it in

131 In particular, we report the structure of PAICS with CAIR bound in the active sit

132 We investigated the structure of PbS NC SLs with grazing-incidence small

133 further elucidating the relationship between the structures of polymorphic fibrils, including their P

134 hnique was used to collect information about the structure of polypeptides that interact with a suppo

135 This study showed that small differences in the structure of polyphenols such as RES and RESAn1 infl

136 y and personal breeding experience influence the structure of populations at the landscape scale.

137 collective behavior is strongly dependent on the structure of preference sharing within the group, as

138 perform a much broader role in generalizing the structure of problems.

139 n view of the challenges involved in probing the structure of proteins within monomolecular films ass

140 ntitatively programs both the expression and the structures of proteins in diverse fungi.

141 Determining the structures of proteins is a critical step to underst

142 ve (with P5C) inhibition constant of 100 mum The structure of PYCR1 complexed with NFLP shows that in

143 her heterocyclic aromatic amines (HAAs) with the structure of quinoxaline is proposed.

144 The structure of rabbit Ca(v) 1.1 bound to an achiral dr

145 logical traits may contribute to forecasting the structure of reef fish communities on novel reef eco

146 In conclusion, the structure of RNF213 uncovers a distinct type of an E

147 The structure of SAVED reveals links to the CRISPR syste

148 The structure of self-other representation in the mPFC a

149 Due to the structure of silk fibroin (possessing lots of functi

150 tanding the contribution of soil protists to the structure of soil microbiomes.

151 timescale sediment tracer in soils to reveal the structure of soil mixing.

152 ly determined under solvent-free conditions, the structures of solvated 2D COFs are largely unexplore

153 we develop here may be useful to reconstruct the structure of some of the Precambrian orogenic belts

154 We elaborate on the structures of some notable SLPs required for binding

155 The structure of spider web and its material properties

156 The structure of Ste2 bears similarities in overall topo

157 rom charge density projections, and uncovers the structures of sublayer surfaces and their evolution

158 t the actual interdependencies that comprise the structure of such systems, particularly when the cau

159 E1A spacer region and oncogenicity of HAdVs, the structures of synthetic peptides identical or very s

160 e we use cryo-electron microscopy to analyse the structures of tau filaments extracted from the brain

161 Here we report the structure of TbIMPDH at room temperature utilizing f

162 se proteins in viral maturation and presents the structure of TerS(P76-26), revealing key differences

163 g feature of each technology is organized by the structure of that material.

164 ot bind modified bases due to differences in the structure of the active site compared with other zin

165 synthesis, the molecular-level insights into the structure of the active sites, catalytic mechanisms,

166 o understand better the relationship between the structure of the AdE1A spacer region and oncogenicit

167 Finally, the structure of the anticipated ring-opening product, d

168 In this work, we investigate how the structure of the bacterial arrangements influences t

169 Here we report the structure of the BAM complex of Escherichia coli fol

170 m which they originated, which differed from the structure of the body and head of the same thrombi.

171 The structure of the bovine dimer also demonstrates that

172 Modeling of the structure of the C-terminal part of Opi3 was consist

173 To achieve higher resolution detail, the structure of the C5_MG4-CirpT complex was solved by

174 Here we determine the structure of the C9orf72-SMCR8-WDR41 complex by cryo

175 We solved the structure of the CAK complex from the model organism

176 We have also determined the structure of the CAK in complex with the covalently

177 Here we report the structure of the catalytic domain of human MANEA and

178 Here we report the structure of the catalytic half of LRRK2, and an ato

179 Inspired by the structure of the catalytically active center of natu

180 dies provided partial structures(10-14), but the structure of the central core module is unknown.

181 The method uses only the structure of the chemical and polymer, the weight fr

182 any additional descriptors depending only on the structure of the chemical compound will be of big he

183 iral amine (the inductor) forces a change in the structure of the chromophore system through the poin

184 ptide fusion IN have enabled us to determine the structure of the cleaved synaptic complex intasome,

185 , an observation that is mostly explained by the structure of the complex [2].

186 We solve the structure of the complex formed by an improved teixo

187 otein-binding protein 1 (GPIHBP1) and solved the structure of the complex.

188 Detailed solution NMR studies on the structure of the CTD showed that a serine/threonine-

189 time to reveal hidden factors accounting for the structure of the data.

190 Although the structure of the desmosomal cadherins is known, the

191 sphatase enzyme activity of SrrB and present the structure of the DHp-CA catalytic core.

192 re pronounced and/or distinct alterations in the structure of the DMPC bilayer than the deprotonated/

193 Many DNA-binding proteins induce changes in the structure of the DNA outside the intrinsic B-DNA env

194 The structure of the emergent trophic network and the ra

195 ic molecular dynamics simulation, we present the structure of the entire dimeric insulin receptor ect

196 quence similarity to other transporters, and the structure of the entire inner-membrane MlaFEDB compl

197 her is model-based learning, which considers the structure of the environment.

198 ne residues and the aziridinyl moiety within the structure of the epothilone molecule and providing n

199 In this study, inspired by the structure of the ferroconcrete, a high-strength bifu

200 heterodimer structure has been resolved(16), the structure of the full-length receptor and its transm

201 We compare the structure of the genome and genes involved in penici

202 astfed, rural African infants did not affect the structure of the gut microbial communities until the

203 ts showed that open-to-closed transitions in the structure of the headpiece underlie PLB inhibition o

204 Here, we provide insight into the structure of the high-energy transition state of Glt

205 chitectural staining techniques, we analyzed the structure of the hippocampal formation in the banded

206 We have previously determined the structure of the HIV-1 strand transfer complex intas

207 SC constituents have been reported; however, the structure of the holo-MSC has not been resolved.

208 e impact of naturally occurring variation on the structure of the HPV capsid proteins of vaccine-rele

209 We found that the structure of the human brain remains self-similar wh

210 We determined the structure of the human EMC in a lipid nanodisc to an

211 ith the neurotransmitter noradrenaline model the structure of the human heart after myocardial infarc

212 ence of multiple pathways is rationalized by the structure of the imidate intermediate, mainly influe

213 ption, and emission are governed not only by the structure of the individual molecules but also by th

214 In conclusion, the structure of the infant fecal microbiota is affected

215 However, the structure of the intact cap complex, and the molecul

216 As compared to the structure of the isolated core complex, Set1 undergo

217 The structure of the lever in each head is competent to

218 d helicate formation was highly sensitive to the structure of the ligand, with minor modifications in

219 The work unveils the structure of the liver blood flow architecture as a

220 s involved in EPS recognition, we determined the structure of the Lotus japonicus (Lotus) exopolysacc

221 Although recent work has shed light on the structure of the LPL monomer, the inactive oligomer

222 ption and emission properties that vary with the structure of the macrocycle.

223 cture of human DEC-205, thereby illuminating the structure of the mannose receptor protein family.

224 We further solved the structure of the MastR-T74D mutant, which contains a

225 The structure of the multi-parametric data was shaped pr

226 We report the structure of the nanobody-stabilized complex of nucl

227 Finite element modeling is used to show that the structure of the nanoboxes is not responsible for th

228 ach populations, including information about the structure of the networks connecting the individuals

229 We show that the structure of the networks describing who infects who

230 -cell EPR using nitroxide-based spin labels, the structure of the nitroxides must confer reduction re

231 Here, we revealed that the structure of the nociceptive terminal tree determine

232 By comparison with the structure of the non-ubiquitinated ID complex bound

233 Finally, the structure of the NPC1-NPC2 complex at 4.0 angstrom r

234 study provides high-resolution insights into the structure of the PD-associated protein alpha-synucle

235 The structure of the PG, however, encompasses a variety

236 tagged, apex-binding Fab PG16 and determined the structure of the PG16-Env complex by cryo-EM to an o

237 The structure of the pretriggered Env conformation, pref

238 rtmentalization, as well as an alteration of the structure of the protein bodies and of the cell wall

239 hat this crisis will have lasting effects on the structure of the radiology field.

240 tic pathways were postulated many years ago, the structure of the reaction intermediates remained elu

241 eutical isoniazid and show that CSP provides the structure of the recently obtained, but unsolved, Fo

242 We present the structure of the RsiG-(c-di-GMP)(2)-sigma(WhiG) comp

243 The structure of the second zinc finger of SALL4 in comp

244 mmunostimulatory activities, suggesting that the structure of the side chain, triterpenoid core, and

245 ent instabilities in fluid turbulence, while the structure of the simulated patterns is indicative of

246 urce conservation optimization is encoded in the structure of the standard genetic code, providing ro

247 The structure of the synthetic material was further corr

248 losely related oroidin alkaloids, supporting the structure of the synthetic material.

249 The structure of the TB19 Fab with CD73 reveals that it

250 The structure of the tightest binding peptide was solved

251 Here, we solve the structure of the TR LysG of Corynebacterium glutamic

252 Although the structure of the TSWV G(N) is different from other b

253 ty for branching, we demonstrate that either the structure of the ubiquitin-ubiquitin junction or its

254 he rates of this surrogate model encode both the structure of the underlying network and disease dyna

255 tes that frameshift stability is embedded in the structure of the universal genetic code and may have

256 By solving the structure of the virus, and through sequence compari

257 This work illuminates the structure of the VSD intermediate state and demonstr

258 n latent variables probabilistically mapping the structure of the world.

259 evealed only small differences compared with the structure of the WT receptor.

260 We determine the structure of the yeast histone H3-H4 complex based o

261 incubation at 4 degrees C, for up to 6 days, the structures of the arteries were significantly disrup

262 We present the structures of the bacterial HeR-48C12 in two states

263 The structures of the bovine and human BBSome reveal tha

264 Here we present the structures of the ferroportin from the primate Phili

265 ne, and phenolics compounds by HPLC-DAD, and the structures of the latter were confirmed by LC-MS.

266 Here, we focus on the structures of the peptide-lipid aggregates occurring

267 The structures of the precursor, two intermediates, and

268 The structures of the radical in WT, V172I, and V172C va

269 The structures of the sponge-derived dibrominated bis-in

270 The structures of the substrate-bound CntA help to defin

271 ic contacts, which was notably distinct from the structures of the TCR:HLA-DQ2.5:gliadin epitope comp

272 We used NMR spectroscopy to characterize the structures of the three native S. epidermidis AIP si

273 Here we report the structures of the TrkH-TrkA complex in the presence

274 isms underlying these unusual properties and the structures of their corresponding epitopes is crucia

275 ts' mouse movements reveal that they learned the structures of their environments, despite the fact t

276 However, the structure of these intermediates is difficult to stu

277 We find that the structure of these networks is extremely variable, w

278 The structures of these WTA transferases provide new ins

279 role of niche dimensional complementarity on the structuring of these anuran assemblages over fine-te

280 ngle X-ray scattering (SAXS) to characterize the structure of this carotenoprotein in two distinct ol

281 The first total synthesis now proves that the structure of this compound had originally been misas

282 The structure of this double layer predicts the eventual

283 However, the structure of this highly reactive, unisolable interm

284 The structure of this network impacts not only the socio

285 Using cryo-electron microscopy, we determine the structures of this constitutively active form (Mec1(

286 The structures of tolyporphins L and M have been revised

287 Therefore, characterizing the structure of toxic intermediate oligomers plays an e

288 ch is present in excess during catalysis, on the structure of transient Rh(2) nitrenoids.

289 -catalysts and intermediates, elucidation of the structures of transient reactive intermediates, whic

290 We examined the structure of two of the novel orbitides by NMR, find

291 We define the structures of two unique species-specific components

292 lations that provide insight into changes in the structure of ultrathin a-C films during deposition a

293 rm to estimate UHI intensities based only on the structure of urban sites, as well as their relative

294 Prior to the SNARE assembly, the structure of VAMP2 is unclear.

295 The results revealed that the structure of variability in naturalistic human behav

296 The structure of VCBC-Cullin5 has recently been solved b

297 We modeled the structure of VcChiP, revealing a trimeric cylinder t

298 is based entirely on what was inferred from the structure of VcINDY, a related transporter in bacter

299 There has been no direct information on the structure of VP40 matrix layers within viruses or vi

300 son with large-sized channels, we determined the structure of YbiO, which showed larger portals and a