ライフサイエンスコーパス: complex of

1 ding constant of Zn(II) to the [enzyme-TPPS] complex of 1.3 10(4)mol/L and a first-order rate constan

2 y and a small-molecule radioactive hapten, a complex of (177)Lu and S-2-(4-aminobenzyl)-1,4,7,10-tetr

3 on a weak Kd value for the Rev-erbbeta.heme complex of 2 mum determined with isothermal titration ca

4 Main-group and transition-metal complexes of 2 have been accessed, and have revealed the

5 In the present study, the inclusion complexes of 2-nonanone (2-NN) with beta-cyclodextrin (b

6 tion, the decreased stability of the ternary complex of 8-oxoG:dA extension results in further loss o

7 lational optic flow detectors in the central complex of a bee has inspired a new model of path integr

8 hydrogenation catalyst based on a manganese complex of a chiral P,N,N ligand has been found to be es

9 Here we present the crystal structure of a complex of a cytidine deaminase with ssDNA bound in the

10 hinese as "DongChong XiaCao", is a parasitic complex of a fungus (Ophiocordyceps sinensis) and a cate

11 uI formed the unique, neutral Cu2 I2 (L(.) ) complex of a ligand-centered radical, whereas reaction w

12 nd theoretical study of the first borylimido complex of a rare earth metal, (NacNac(NMe2))Sc{NB(NAr'C

13 The first (N horizontal lineN)(2-) complex of a rare-earth metal with an end-on dinitrogen

14 re trimers in which the protomeric unit is a complex of a surface subunit (SU) and a fusion active tr

15 alpha-fluoroindanones catalyzed by palladium complexes of a BINOL-derived monophosphine and Segphos,

16 Supramolecular complexes of a family of positively charged conjugated p

17 (as measured by ESI-MS) of the carbohydrate complexes of a proxy protein (Pproxy), which binds to al

18 dies of the first double-H-bonded DD.AA-type complexes of a series of aromatic boronic acids that ado

19 Metal complexes of a tripodal hydroxylaminato ligand, TriNOx(3

20 of [Fe(II)]0 decay rates for the iron-peroxo complex of about 50 s(-1) were determined in absence and

21 t least two pathways, one involving the ASRT complex of actin, SNX27, and retromer and another possib

22 acid to form fluorescent trinitrophenylated complexes of Ado (TNP-Ado) and Ino (TNP-Ino).

23 e 6-coordinate heme Fe(III)-OH(-) and -CN(-) complexes of AfGcHK are also active, but the 5-coordinat

24 images can clearly differentiate R from its complex of Ag(+).

25 is based on the formation of anionic chelate complexes of Al(III) and Cr(VI) with o-hydroxy azo dye,

26 Molecular machines are among the most complex of all functional molecules and lie at the heart

27 y ionization has been used to generate ionic complexes of all-cis 1,2,3,4,5,6 hexafluorocyclohexane.

28 n, silver nanoparticles ensemble with Zn(II) complex of alpha-liopoic acid conjugated terpyridine (Zn

29 Complexes of alpha-lac/CMD-b-PEG formed at pH values nea

30 ed subtle electronic differences between the complexes of Am(III) and the lanthanides.

31 tandem reaction in group 3 metal (Y and Sc) complexes of amidine-amidopyridinate ligands.

32 The reaction is catalyzed by a pincer complex of an earth-abundant metal (manganese), in the a

33 e 3D X-ray structure of the pseudo-Michaelis complex of an inactive (D220N) variant of C. perfringens

34 Complexes of an ester-functionalized ligand were taken u

35 the location of Cy3 and Cy5 on dsRNA, using complexes of an RNA stem-loop bound to L5 protein determ

36 stinctive structural difference in the bound complexes of apoCaM-Ng13-49 and holoCaM-CaMKII delineate

37 the mitochondrial outer membrane and forms a complex of approximately 120 kDa.

38 pecifically but weakly in solution to form a complex of approximately 1:1 stoichiometry that depends

39 oth proteins co-migrated in native gels in a complex of approximately 200 kDa that also contained bet

40 ymer that assembles to form a spindle-shaped complex of approximately 6 MDa.

41 , and CK1delta were distributed into several complexes of approximately 0.9-1.1 MDa that appear to co

42 ed proteins that associate with the THO core complex of Arabidopsis TREX.

43 structures and properties of the adsorption complexes of arsenous acid (As(OH)3) on hydrated mackina

44 n microscopy (cryoEM) reconstructions of the complex of bacterial 30S subunit with initiator tRNA, mR

45 Composed of a trimeric complex of BAG6, TRC35 and UBL4A the BAG6 sortase is als

46 long fascinated biologists, but tracing this complex of behavioural repertoires is challenging, as th

47 sphorylated, binds with high affinity to the complex of betagamma-subunits of G protein transducin (G

48 over the last 4 million years, resulting in complexes of between two and six distinct Hodgkinia line

49 or allostery in several proteins and protein complexes of biological and pharmaceutical interest.

50 e subpallium, hypothalamus, and dorsal vagal complex of birds suggests that some of the functions of

51 al superfamilies and 1404 families; (ii) 446 complexes of bitopic proteins with known three-dimension

52 s the most taxonomically challenging species complex of black flies in the Oriental Region.

53 previously reported fluorescent copper(I) pi-complexes of boron-boron double bonds, the Cun-pi-dibory

54 We discovered that RSV infection induces a complex of bromodomain containing 4 (BRD4) with NF-kappa

55 alternate with those of a 1:2 supramolecular complex of BU6 and PF6(-).

56 Moreover, the data demonstrate that the complex of Ca(2+)/CaM and K-Ras4B is stable in the prese

57 A complex of Cas1 and Cas2 proteins is capable of insertin

58 The re-dispersed soluble complexes of casein-iron-orthophosphate generated using

59 Here we report the development of polyvalent complexes of CD1b proteins and carbohydrate backbones (d

60 ckpoint complex (MCC) is formed from two sub-complexes of CDC20-MAD2 and BUBR1-BUB3, and current mode

61 ranscription elongation factor b (P-TEFb), a complex of Cdk9 and cyclin T1, promotes release of pause

62 ial structures made by up to four chains and complexes of chains (e.g. in capsids).

63 Copigmented complexes of chondroitin sulfate and anthocyanin were pr

64 A published complex of Clostridium perfringens GH125 enzyme with a n

65 The complex of coagulation factor VIIa (FVIIa), a trypsin-li

66 arding the spatial structure of a population complex of coastal Atlantic cod (Gadus morhua).

67 2 gives a rare example of a side-on dioxygen complex of cobalt.

68 Herein are reported the first pi-complexes of compounds with boron-boron triple bonds wit

69 ous samples was converted into a hydrophobic complex of copper(II) diethyldithiocarbamate and subsequ

70 Hydride complexes of copper, silver, and gold encompass a broad

71 m, via differential localization of distinct complexes of core PCP factors.

72 We successfully identified stable complexes of crenezumab with Abeta pentamer (oligomer mo

73 Although the crystal structure of the complex of crossveinless-2 (CV-2) vWC1 and BMP-2 previou

74 g single-molecule spectroscopy, that the FCP complexes of Cyclotella meneghiniana switch frequently i

75 g interaction mimics the 'cysteine synthase' complex of CysK:CysE.

76 We propose a novel model by which stationary complexes of cytoplasmic dynein-1 are responsible for th

77 The Co(II) complex of D2-symmetric chiral amidoporphyrin 3,5-Di(t)B

78 The cobalt(II) complex of D2-symmetric chiral porphyrin [Co(3,5-Di(t)Bu

79 ent proteins are assembled into multiprotein complexes of defined stoichiometry.

80 The main light-harvesting complexes of diatoms, known as fucoxanthin-chlorophyll p

81 ) nature, DFT studies show that the Cu(I) pi-complexes of diborynes reported herein exhibit enhanced

82 tibility tensor differ significantly between complexes of different lanthanides with the same ligand:

83 sian (DoG) particle-picking method to detect complexes of different shapes and sizes under various cr

84 has properties that set it apart from serine complexes of different sizes or from complexes composed

85 to obtain reconstructions of macromolecular complexes of different sizes to better than 3-A resoluti

86 Complexes of different stoichiometries are observed rang

87 Our findings support that the AP-2 complex of dikarya has acquired, in the course of evolut

88 plicable to the biophysical investigation of complexes of disordered proteins and folded proteins.

89 dentified two macromolecular, cytosolic BRAF complexes of distinct molecular composition and phosphor

90 lease neutrophil extracellular traps (NETs), complexes of DNA, histones, and proteins capable of inhi

91 light intermediate chain and the pointed-end complex of dynactin.

92 that is catalyzed, for the first time, by a complex of earth-abundant iron.

93 and (ii) the first structural model for the complex of eIF2B with its substrate, eIF2-GDP, reaction

94 pair of the photosynthetic enzyme Rubisco, a complex of eight large (RbcL) and eight small (RbcS) sub

95 Complexes of Env trimers with broadly neutralizing antib

96 Chromatin is the complex of eukaryotic DNA and proteins required for the

97 malian neutrophils: Both cell types export a complex of extracellular DNA (exDNA) and antimicrobial p

98 ric determination of a mixture of overlapped complexes of Fe(3+), Mn(2+), Cu(2+), and Zn(2+) ions wit

99 Splicing is catalyzed by the spliceosome, a complex of five major small nuclear ribonucleoprotein pa

100 A complex of five Nus factors (NusB, NusE, NusA, NusG and

101 y machinery (BAM) is a approximately 203 kDa complex of five proteins (BamA-E), which is essential fo

102 e the cryo-electron microscopy structures of complexes of five neutralizing VHHs with the Mahoney str

103 The Fe(3+) ion complex of FONs based sensor was further tested with dif

104 ed rare-earth metal (N horizontal lineN)(2-) complexes of formula [A2Ln(THF)x]2[mu-eta(2):eta(2)-N2]

105 both the Sec61 translocation channel, and a complex of four additional proteins: Sec63, Sec62, Sec71

106 Neurospora crassa circadian clock, a protein complex of frequency (FRQ), casein kinase 1a (CK1a), and

107 ir crosstalk mechanism through a heteromeric complex of G protein-coupled receptors.

108 A chemical complex of gastrin and histamine is postulated as is als

109 water oxidation catalyst based on the copper complex of general formula [(Lpy)Cu(II)](2-), 2(2-), (Lp

110 of Ph-RF (RF = CF3 or CF2CF3) coupling at Pd complexes of general structure (P(t)Bu3)Pd(II)(Ph)(RF).

111 reactivity studies of organometallic Ni(III) complexes of general structure TpNi(III)(R)(R(1)) (Tp =

112 In both analyses, we detected a conserved complex of genes, including the helicase gene, showing c

113 Nuclear complex of glyceraldehyde-3-phosphate dehydrogenase and

114 nt virus-neutralizing antigen-the pentameric complex of glycoprotein H (gH), gL, and pUL128, pUL130,

115 Novel octanuclear NHC complexes of gold(I) and silver(I) form metallocavitand

116 ed structure of EBOV GP, and high-resolution complexes of GP with the anticancer drug toremifene and

117 The ability of complexes of hard and labile metal ions with one or more

118 sis of X-ray crystallographic studies of the complex of hCA II with 4-(3,4-dihydro-1H-isoquinoline-2-

119 The tongue is an elaborate complex of heterogeneous tissues with taste organs of di

120 This suggests that complexes of Hg(II) with DOM thiols have similar bioavai

121 Hyperactive BRAF(V)(600E) resides in large complexes of higher molecular mass and activity, while B

122 d to formation of a death-inducing signaling complex of Hip1, Hippi, and Caspase-8.

123 formation from the gas-phase hydrogen-bonded complexes of HMSA with (R1)(R2)NH on the water droplet i

124 The crystal structures of complexes of HpalphaCA with a family of acetazolamide-re

125 lectron microscopy structure of a quaternary complex of human CPSF-160, WDR33, CPSF-30, and an AAUAAA

126 potential exhaustion-associated system: the complex of human inhibitory receptor TIM3 (hTIM3) and it

127 the 2.4-A resolution crystal structure of a complex of human NPC1-MLD and NPC2 bearing bound cholest

128 ta class IVA (Tubb4a), result in the symptom complex of hypomyelination with atrophy of basal ganglia

129 t ZBP1 senses viral ribonucleoprotein (vRNP) complexes of IAV to trigger cell death.

130 Analysis of a complex of ICL1:2-VIC by electrospray ionization mass sp

131 The presence of circulating immune complexes of IgA bound to beta2-glycoprotein I (B2A-CIC)

132 ved mechanism, we purified a native effector complex of III-B Cmr-alpha from S. islandicus and charac

133 re we describe the crystal structures of the complexes of IL-6 with two Fabs derived from conventiona

134 MCPs manifest as a complex of insertions around a bacteriophage HK97 gp5-li

135 e noncovalent, tightly bound antagonist-GPCR complex of iodopindolol and beta-adrenergic receptor.

136 n (pin = pinacolate) using POCOP-type pincer complexes of Ir has been demonstrated, with turnover num

137 represent the first mononuclear coordination complexes of Ir(V) in an N,O-donor environment.

138 Polypyridyl complexes of iridium and ruthenium have served as popula

139 IsdB and growth of S. aureus, and a ternary complex of IsdB.Hb.Hp was observed.

140 O2 binding to the Fe(II) heme complex of its N-terminal globin domain strongly stimula

141 iation when we added cholesterol to isolated complexes of loops 1 and 7.

142 A complex of M2R and Gi1 was tetrameric in both, and activ

143 standing of the organization of the pulvinar complex of mammals.

144 lectrode, due to the use of a multinucleated complex of manganese with mu-oxo units, which was able t

145 ade of different polypeptide chains, the MCM complexes of many Archaea form homohexamers from a singl

146 We present crystal structures of the complex of Mettl3/Mettl14 methyltransferase domains in a

147 hydrogen cleavage reaction of ruthenium PNN complexes of Milstein and the PN(3) of Huang, with simil

148 ize grouped candidates into known regulatory complexes of mitosis or cytokinesis, respectively, and p

149 ys highlight that FeSII binds to a preformed complex of MoFe and Fe protein upon activation, primaril

150 In a simulation, each molecule (or complex of molecules) is taken to occupy a single lattic

151 Despite the prevalence of stable pi-complexes of most d(10) metals, such as Cu(I) and Ni(0),

152 Additionally, a stable complex of MRPP1 and MRPP2 has m(1)R9 methyltransferase

153 to negatively regulate Akt by downregulating complexes of mTORC2 and CDK2/cyclin A2 and upregulating

154 The complete condensin is a large tripartite complex of MukB, the kleisin, MukF, and an accessory pro

155 We found that the preintegration complex of murine leukemia virus (MLV) interacts with th

156 ff, indicating formation of a stable ternary complex of myosin:Xa:Va.

157 bound and are among the most strongly bound complexes of Na(+) and Cl(-) ever observed with molecula

158 For example, NatE is a complex of Naa10, Naa50, and Naa15 (auxiliary).

159 ral insights came from the unbound state and complexes of NagZ with the substrate, products and a mim

160 Repair is mediated by a core complex of NHEJ factors that includes a ligase (DNA Liga

161 el of the conformationally protected ternary complex of nitrogenase.

162 The surface properties and known complexes of nitrogenase component proteins allow us to

163 ities, characterize the stoichiometry of the complex of NS5 and SLA, and determine how solution condi

164 s of many proinflammatory mRNAs and recruits complexes of nucleases to promote rapid mRNA turnover.

165 ntensity of spectra for known donor-acceptor complexes of organic molecules.

166 rulopathy after rigorous exclusion of immune complexes of other cause, particularly recurrent glomeru

167 live cell microscopy showed that the Zn(II) complex of our lead compound, di-2-pyridylketone 4-cyclo

168 ents of mitochondria that harbor the protein complexes of oxidative phosphorylation, but how cristae

169 basic helix-loop-helix transcription factor complex of pancreatic acinar cells and critical to acina

170 affinity (1.0x10(6)M(-1)) between the copper complex of PDI-HIS receptor and PPi.

171 the ligand free protein and the acyl-enzyme complex of perdeuterated E166A Toho-1 beta-lactamase wit

172 e ions are shown to interact with lanthanide complexes of phenacylDO3A derivatives in aqueous solutio

173 y transfer in the Fenna-Matthews-Olson (FMO) complex of photosynthetic green sulphur bacteria, howeve

174 Diamagnetic metal complexes of phthalocyanines with n-butoxyl groups in al

175 (varphiphos = 0.45), strong 2PA makes Pt(II) complexes of pi-extended porphyrins a valuable class of

176 Here, we present an NMR structure of the complex of PI4KB and its interacting partner, Golgi adap

177 olved in degrading phycobilisomes, which are complexes of pigmented proteins that harvest light for p

178 hat by controlling the lifetime of the bound complex of pKID:KIX via altering the dissociation rate,

179 n of heparin therapy caused by antibodies to complexes of platelet factor 4 (PF4) and heparin.

180 ned the 4.5 A structure of the 2.2 MDa pore complex of pneumolysin, the main virulence factor of Str

181 Here we report a stable ternary complex of Pol II, the replicative polymerase Pol III co

182 be the structures of pre- and post-catalytic complexes of Pol mu with a ribonucleotide bound at the a

183 Notable aspects of the chemistry of complexes of polyether ligands including crown ethers, c

184 failure to assemble higher molecular weight complexes of PORB with its twin isoenzyme, PORA, as enco

185 The human primosome, a 340-kilodalton complex of primase and DNA polymerase alpha (Polalpha),

186 In the human and pig pancreas binary complexes of proCPA with proelastases were found.

187 rt sites to recruit the Wdr82-Set1A/COMPASS (complex of proteins associated with Set1) complex, which

188 Of the six members of the COMPASS (complex of proteins associated with Set1) family of hist

189 Although MLL/COMPASS (complex of proteins associated with Set1) family of hist

190 tions and translocations within the COMPASS (complex of proteins associated with Set1) family of hist

191 Proteins of the Rbfox family act with a complex of proteins called the Large Assembly of Splicin

192 t cells, the interaction between WASF3 and a complex of proteins, including CYFIP1, acts as a conform

193 ligand was also confirmed in vivo, where the complex of Pru p 3-ligand induced higher levels of IgE t

194 ent stabilities between the classical alkyne complexes of Pt(II) and their drastically more reactive

195 rt an association with dendritic trafficking complexes of Ptchd1.

196 spectroscopy of the Light-Harvesting 2 (LH2) complex of purple bacteria.

197 he article, we focus on the light-harvesting complexes of purple bacteria as a model to illustrate th

198 Structures of binary complexes of PYCR1 with NADPH or proline determined at 1

199 Transition-metal complexes of radical ligands can exhibit low-energy elec

200 loped a route to a new class of terminal oxo complexes of Re(III) supported by olefin moieties of sub

201 of bound cations on the reduction of cobalt complexes of redox active ligands and explored the react

202 A range of catalysts were used, including complexes of Rh(II) , Pd(II) , and Cu(II) , as well as S

203 itative comparison of cross-linking within a complex of RIIbeta and Cbeta, with or without the protot

204 and Med13, associate with the core mediator complex of RNA polymerase II.

205 rses for these efforts have been polypyridyl complexes of Ru(ii) and Ir(iii), compounds whose photoph

206 m cycle in higher plants, dead-end inhibited complexes of Rubisco must constantly be engaged and remo

207 charge-transfer-state lifetimes typical for complexes of ruthenium and other precious metals are oft

208 indicate that CozE is a member of the MreCD complex of S. pneumoniae that directs the activity of PB

209 e first crystallographically characterizable complex of Sc(2+) , [Sc(NR2 )3 ](-) (R=SiMe3 ), has been

210 Complexes of secretin (SecR) and angiotensin 1a (Atr1a)

211 Protein complexes of sequential metabolic enzymes, often termed

212 The tip complex of Shigella flexneri contains invasion plasmid a

213 the lanthanide ion to form an overhand knot complex of single handedness.

214 racting membrane protein (SCIMP), recruits a complex of SLP65/SLP76 and Grb2 adaptor proteins, known

215 d the gene silencing activity of Lipoplex, a complex of small interfering RNA (siRNA) and cationic li

216 stion whether retromer indeed functions as a complex of SNX-BAR proteins and the VPS26-VPS29-VPS35 tr

217 Along with the cross-linked polyion complex of SOD1 with polycation poly(ethylene glycol) (P

218 Most AMPA receptors (AMPARs) are heteromeric complexes of subunits GluA1/GluA2 or GluA2/GluA3, and th

219 s, including apo SuiB, SAM-bound SuiB, and a complex of SuiB with SAM and its peptide substrate, SuiA

220 xin binds to the 1:1 plasma membrane t-SNARE complex of syntaxin-1a and SNAP-25 while simultaneously

221 ly of Rieske oxygenase enzymes, nonheme iron complexes of tetradentate N4 ligands have been developed

222 We recently reported that Fe-N2 complexes of tetradentate P3(E) ligands (E = B, C) gener

223 ed out to be a good substrate for the Cu(II) complex of the 1,2-vicinal catalyst and a bad substrate

224 tion of A2ARs selectively in the basolateral complex of the amygdala, using a lentivirus with a silen

225 res of the apo enzyme and a binary Ago-guide complex of the archaeal Methanocaldococcus jannaschii (M

226 proceeds via dissociation of the metal-bound complex of the azirinium ylide to metal-free azirinium y

227 eed-encoding neurons converge in the central complex of the bee brain, and through block-face electro

228 Similar binding is observed for the Fe(III) complex of the bidentate hydrolysis product 2,3-dihydrox

229 ling pathway may regulate the tight junction complex of the BRB and may restore barrier properties af

230 lity of head-direction coding in the central complex of the cockroach, Blaberus discoidalis.

231 induces apoptosis via binding to a receptor complex of the common neurotrophin receptor (p75NTR) and

232 The reaction is catalyzed by a pincer complex of the earth abundant manganese and forms hydrog

233 new de-aromatized pyridine-based PNP pincer complex of the Earth-abundant, first-row transition meta

234 angement, whereas for the analogous Pd sigma-complex of the five-membered lactone the smallest Pd/end

235 re, we determined the crystal structure of a complex of the HAstV capsid protein and a virus-neutrali

236 h was previously thought to bind the Fe(III) complex of the hexadentate siderophore enterobactin (Kd

237 fects such as interference with the YAP-TEAD complex of the HIPPO pathway, resulting in growth inhibi

238 2 alone is sufficient to stabilize a similar complex of the interferon-alpha receptor and TYK2.

239 Here we report that the complex of the mannosidase Htm1p and the protein disulfi

240 ipheral division of the dorsal raphe nuclear complex of the minke whale, all indicate that the suite

241 oximately 1 MDa) and the least characterized complex of the mitochondrial electron transport chain.

242 idase (COX), the terminal electron-accepting complex of the mitochondrial respiratory chain.

243 observed reactivity, we prepared the Cu(II) complex of the mixed thia/aza 14-N2S2 ligand.

244 he primary substrate with the co-crystalized complex of the N169D mutant and NAD(+) led to the succes

245 surveys at two sites on the terminal moraine complex of the Ngozumpa Glacier, Nepal, to aid assessmen

246 The crystal structure of the complex of the oligonucleotide d[AAATTT]2 with compound

247 further functions into this smallest protein complex of the oxidative phosphorylation system (which i

248 After cargo delivery, a complex of the PEX1 and PEX6 ATPases and the PEX26 tail-

249 nce that five of the genes encoding the core complex of the T9SS are co-transcribed and that the gene

250 .1 microM), preferentially binds the Fe(III) complex of the tetradentate enterobactin hydrolysis prod

251 ave determined the structure of a quaternary complex of the translating Escherichia coli ribosome, th

252 The effector complex of the Type III-B Cmr system cleaves invader RNA

253 nspiration is generated by the pre-Botzinger complex of the ventrolateral medulla, where it is though

254 aleimide attachment protein receptor (SNARE) complex of the vesicle fusion apparatus.

255 The apical complex of the vitelliform lesion eventually degenerated

256 reduction process that affords Meisenheimer complexes of the clinical candidates BTZ043 and PBTZ169.

257 These reactions were catalyzed by palladium complexes of the commercially available bisphosphine Dif

258 slation, we use ribosome-nascent chain (RNC) complexes of the electron transfer protein flavodoxin.

259 for predicting the spin state of homoleptic complexes of the Fe(II) d(6) ion with chelating diimine

260 parameters and natures of dihydrogen-bonded complexes of the form M-H...H-X, as such species are now

261 Seven rhenium(I) complexes of the general formula fac-[Re(CO)3(NN)(OH2)](

262 ese findings identify the activation of AP-1 complexes of the Jun/ATF-type as an important element co

263 e the solution structures of the two central complexes of the pathways, C3 proconvertase and C3 conve

264 Single-crystal X-ray structures of complexes of the receptor with glutaric acid, alpha-keto

265 We determined the crystal structure of 13 complexes of the tetraphosphonate cavitand Tiiii[H, CH3,

266 kane complexes, we generated cationic alkane complexes of the type [(HEB)Re(CO)2(alkane)][Al(OR(f))4]

267 Molybdenum-based molecular alkylidyne complexes of the type [MesC identical withMo{OC(CH3)3-x(

268 Complexes of the ubiquitous beta-diketiminates (NacNac)

269 The secretin complex of Thermus thermophilus is an oligomer of the 75

270 Derived from complexes of these metals in their immutable +2 oxidatio

271 , affords the monoselenide and monotelluride complexes of thorium, [K(18-crown-6)][Th(E)(NR2)3] (E =

272 ve applied this strategy to the Clp protease complex of tobacco (Nicotiana tabacum) and identified a

273 The apical complex of Toxoplasma gondii and some other apicomplexan

274 The stoichiometry of the complex of TPEN and silver ion was established to be 2:1

275 ation of proanthocyanidins is regulated by a complex of transcription factors composed of R2R3 MYB, b

276 ted myocyte conversions, the core regulatory complex of transcription factors conveying myocyte ident

277 th small-angle X-ray scattering data for the complex of TRN-SR2 with truncated integrase, we propose

278 A complex of two related mammalian proteins, SFPQ and NONO

279 In contrast to the dimer complex of two single-domain lectins formed via protein-

280 y characterized heterobimetallic bis(mu-oxo) complex of two transition metals.

281 For Mb-RL, the analysis gives complexes of two connected micelles, each containing 10

282 ur types of subunits, evolved from ancestral complexes of two types of subunits through gene duplicat

283 the reactive species is a 1:1 urea-fluoride complex of type [UF](-) (U = urea) resulting from partia

284 Here, we use model complexes of type 1 Cu sites based on tris(pyrazolyl)bor

285 pores into membranes forming homo- or hetero-complexes of undetermined stoichiometry.

286 in human cells held together by a tethering complex of VAPA/B (vesicle-associated membrane protein-a

287 3 rProtein binds in slightly anticooperative complexes of various stoichiometries.

288 ibitor to show that the major brain TCP is a complex of vasohibin-1 (VASH1) with the small vasohibin

289 ehensive structural model for the tetrameric complex of vimentin has been obtained by X-ray crystallo

290 layer made of VP3 that encloses a replicase complex of VP1, VP4, and VP6 and a genome of 10 double-s

291 e a proteomic approach to identify a protein complex of Wdr5, Hdac1, Hdac2 that act together with RA

292 inc-chelating capacity and stability of zinc complexes of whey protein hydrolysates (WPH), produced w

293 for their elaborate visual system, the most complex of which possesses 12 types of color photorecept

294 date is the linear ubiquitin chain assembly complex, of which the catalytic core component is heme-o

295 We picked a dataset of 17 antibody-antigen complexes of which 11 have both bound and unbound struct

296 They form multiple complexes of which PRC1 and PRC2 are evolutionary conser

297 rones, adaptors, and folding enzymes-dynamic complexes of which regulate cellular homeostasis togethe

298 iation for transition metal cyclopentadienyl complexes, of which many have been used as catalysts for

299 ltiple emulsions stabilized by WPC alone and complex of WPC-pectin, respectively.

300 we explored the potential of a coordination complex of Zn(II) and anthracenyl-terpyridine as a modul