ライフサイエンスコーパス: complex of

1 tains the overall architecture of the native complex of 14-3-3 and phosphorylated HSPB6 that has rece

2 The mIg is a symmetric complex of 2 identical membrane-bound heavy chains (mHC)

3 ethod is shown by synthesizing several metal complexes of 2-(benzo[d]thiazol-2-yl)phenol that can be

4 ydroxyphenyl)benzoxazole and hydrogen-bonded complexes of 2-aminopyridine with protic substrates] var

5 To detect labile complexes of 40S subunits with RNA by DEER/PELDOR spectr

6 l cations among which the hexanuclear Cd(II) complex of 6 + 3 + 3 imine was isolated and characterize

7 of pyridine moieties, and hexanuclear Cd(II) complex of 6 + 3 + 3 imine, which gives a deeper insight

8 f an imine (kinetic product) to the zinc(II) complex of a hydrazone (thermodynamic product).

9 synthetic route gives access to the gold(I) complex of a phosphine displaying a chiral phosphoric ac

10 irst structurally characterized hexafluorido complex of a tetravalent actinide ion, the [UF(6) ](2-)

11 3d metallocenates, which consist of anionic complexes of a metal centre (manganese, iron or cobalt)

12 Several cyclopalladated complexes of a new series of 6,6'-binicotinates and 2,2'

13 Formation of IL (n-1) (zi) and IL (n) (zi) complexes of a primary ion is less of a concern because

14 e determined that it is composed of multiple complexes of a supramolecular volume of up to 0.5 um(3)

15 further improves proteostasis by eliminating complexes of aberrant composition(2), but how it detects

16 n from a set of N-heterocyclic carbene (NHC) complexes of alkenylboranes bearing two tert-butyl ester

17 here the target of investigation is the most complex of all biological systems.

18 tionary relative in the Semliki Forest virus complex of alphaviruses.

19 Anionic molecular imide complexes of aluminium are accessible via a rational syn

20 id amide hydrolase (FAAH) in the basolateral complex of amygdala (BLA) is thought to buffer against t

21 rogenated, catalyzed for the first time by a complex of an earth-abundant metal.

22 ions, the latter changing from the silver(I) complex of an imine (kinetic product) to the zinc(II) co

23 odorant receptors (ORs) are believed to be a complex of an odorant binding subunit, OrX, and an ion c

24 ncurrent formation of JL (zj) and JL(2) (zj) complexes of an interfering ion is shown here to shift t

25 Complexes of anionic CNCs and cationic LAE (CNCs/LAE) we

26 SCEptRe extracts weekly updated 3D complexes of antibody-antigen, TCR-pMHC and MHC-ligand f

27 accharomyces cerevisiae and dodecameric AHAS complexes of Arabidopsis thaliana.

28 ted wing drosophila Drosophila suzukii, is a complex of at least two cryptic species.

29 arbenes (NHCs) to create organometallic -ate complexes of Au(I) that serve both as WCAs and functiona

30 esent crystal structures of the fully active complex of AURKC bound to INCENP, consisting of phosphor

31 y molecular redox) in memristors based on Ru-complexes of azo-aromatic ligands.

32 Complexes of bacteria were delineated that related to sp

33 sensor of activated GPCRs, and the BBSome, a complex of Bardet-Biedl syndrome (BBS) proteins, are req

34 data reveal that by replacing an activating complex of Batf and Irf-4 at the Bcl-6 promoter, Bach2 r

35 The structural differences between these complexes of beta(1)AR provide a foundation for the desi

36 Racemic rhodium complexes of bidentate phospholane phosphites derived fr

37 tivation method for the study of noncovalent complexes of biological significance.

38 Complexes of bis(trimethylsilyl)acetylene Me3SiC2SiMe3 (

39 In addition, LYAR binds a complex of BRD4 and KAT7, which is then recruited to rDN

40 e the first structurally characterized boryl complexes of calcium and strontium, {(Me(3) Si)(2) N}M{B

41 ve at a structural model for the dodecameric complex of CaMKII with F-actin.

42 motif in the subunit G1 of the glycoprotein complex of Can, which is otherwise present in the wild-t

43 ip leads to the formation of a sandwich-like complex of capture probe-analyte-detection probe on the

44 to this paradigm) operate as heterotrimeric complexes of catalytic-alpha and regulatory beta- and ga

45 o-electron microscopy structure of a ternary complex of catalytically competent DNMT3A2, the catalyti

46 ylates the replicative DNA helicase CMG (the complex of CDC45, MCM2-7 and GINS).

47 ium exchange-MS (HDX-MS) study of functional complexes of CF, CheA, and CheW bound to vesicles in nat

48 inhibitor avibactam to trap the acyl-enzyme complex of class A beta-lactamase CTX-M-14 at varying pH

49 trong binding resulted in the removal of the complex of cognate peptide and major histocompatibility

50 hydrazine hydrate and Et(3)N affords a Cn(-) complex of copper(I), [(Cn(-))Cu(I)(PPh(3))(2)] (1).

51 herefore, in this study, the copper and iron complexes of COTI-2 were synthesized and evaluated for t

52 Here, we present observations on the crystal complexes of COX-2 with two indomethacin-dansyl conjugat

53 ary tissue persistence of a lipophilic metal complex of CPX and Zinc (CPXZn) after intraductal admini

54 In complexes of CsgG bound to a 35-residue CsgF constrictio

55 ivity enhancement, compared to the molecular complex of Cu with an identical coordination site.

56 bing protein present in the light-harvesting complex of cyanobacteria and red algae.

57 n improved method for the deprotection of Co-complexes of cyclic enediynes using tetrabutylammonium f

58 on, we present a strategy based on targeting complexes of D(1)R and histamine H(3) receptors (H(3)R).

59 n be effectively activated by the cobalt(II) complexes of D(2)-symmetric chiral amidoporphyrins for e

60 Specifically, we have prepared dipyrrin complexes of dichlorogallate (GADIPY) or phenylphospheni

61 have been made to synthesize molybdenum-oxo complexes of different ligand environments.

62 e show here that the presence of two or more complexes of different stoichiometries for a given ion m

63 , the concurrent presence of two primary ion complexes of different stoichiometries, such as IL (zi)

64 study the binding interfaces of RNA/protein complexes of different stoichiometry, and provides a det

65 The bis-boron(III) complex of diphenanthrioctaphyrin has been obtained, pro

66 Complexes of diploid and polyploid species have formed f

67 LCOs are perceived by a heteromeric receptor complex of distinct Lys motif (LysM)-type transmembrane

68 pecific contact formation with generation of complexes of distinct signal-triggering topology on biom

69 adder with a nephropore (exit opening) and a complex of diverticula, spread throughout the cephalotho

70 Here we generated covalent enzyme-substrate complexes of DNMT3A and DNMT3B, and performed bisulfite

71 lease degradation and trapping transient RNA complexes of E. coli DsrA-rpoS derived bulge-loop intera

72 The reaction is catalyzed by a pincer complex of earth-abundant manganese in the presence of a

73 In this context, a complex of EDS1 with PHYTOALEXIN DEFICIENT4 (PAD4) is re

74 experiments demonstrated transient encounter complexes of EI(Ntr) not only with the expected partner,

75 The BBSome, a complex of eight Bardet-Biedl syndrome (BBS) proteins in

76 This complex of eight closely related species was exhaustivel

77 ly engaged in protein synthesis is a ternary complex of elongation factor Tu (EF-Tu), aminoacyl-tRNA

78 mally stable GH8 from the cellulose synthase complex of Enterobacter sp. R1, for deconstruction of be

79 ools, a webserver called SCEptRe (Structural Complexes of Epitope-Receptor) was created.

80 wn adipocytes lacking the Sel1L-Hrd1 protein complex of ER-associated protein degradation (ERAD).

81 Here we report the structure of the BAM complex of Escherichia coli folding BamA itself.

82 y heterologously expressing the HpaBC enzyme complex of Escherichia coli, which hydroxylates tyrosol

83 tensive research toward their replacement by complexes of essential metal ions, like Mn(II).

84 , which complement the classical established complexes of expensive precious metals and rare-earth el

85 rials replaces the natural electron transfer complex of Fe protein and ATP and provides low-potential

86 The complex of Fe-SRFA showed a strong synergistic effect in

87 The capability of the complexes of Fe(II) and Cu(II) with Suwanee river fulvic

88 Although alkyl complexes of [Fe(4)S(4)] clusters have been invoked as i

89 lar tension in a nesprin protein of the LINC complex of fibroblastic and epithelial cells in culture.

90 Six complexes of formula [Ir(eta(5):kappa(1)-C(5)Me(4)CH(2)p

91 a crassa, negative feedback is executed by a complex of Frequency (FRQ), FRQ-interacting RNA helicase

92 Recent studies have implicated a complex of FtsW and FtsI (FtsWI) as the essential PG syn

93 imal system consisting of Rab5, RabGDI and a complex of full length Rabex5/Rabaptin5 was necessary to

94 by monitoring the sizes and conformations of complexes of Gag with very short oligonucleotides.

95 and then applied to a >300 kDa precipitated complex of GB1 with full length human immunoglobulin G (

96 ructures of the extracellular region ternary complexes of GDF15/GFRAL/RET, GDNF/GFRalpha1/RET, NRTN/G

97 Herein, we report isostructural halide complexes of Ge(II), Sn(II), and Pb(II) with a 1-butyl-1

98 In contrast to strand transfer complexes of genuine transposases, where severe kinks oc

99 verely than 600 MPa; however, tightly-packed complexes of globular starch granules-protein-cell wall

100 alculation of ice sheet retreat rates from a complex of grounding-zone wedges on the Larsen continent

101 ific to two distinct HLA-A*02:01/HBV epitope complexes of HBV nucleocapsid and envelope proteins, we

102 Luminescent complexes of heavy metals such as iridium, platinum, and

103 The [M(CN)8]n- ions comprise a series of complexes of heavy transition metals in high oxidation s

104 Synthetic strategies to yield molecular complexes of high-valent lanthanides, other than the ubi

105 more common than the exclusive formation of complexes of higher stoichiometry unless the ionophore i

106 d by deposition of methyl groups by multiple complexes of histone lysine methyltransferase 2 (KMT2) f

107 s (mAbs) specific for the peptide-MHC (pMHC) complex of HLA-DQ2.5 and the immunodominant gluten epito

108 The lifetime of a 1:1 complex of htt(ex1) with profilin, determined using a sh

109 HAMLET is a complex of human alpha-lactalbumin (ALA) and oleic acid

110 We also generated complexes of human alphaA-crystallin or alphaB-crystalli

111 The Co(II) complexes of HuPhyrin, [Co(HuPhyrin)], represent new-gen

112 d for structure determination of IgE and the complex of IgE with the anti-IgE antibody ligelizumab.

113 glomerular deposition of circulating immune complexes of IgG bound to galactose-deficient IgA1 (Gd-I

114 t impacts can be directed in vivo by forming complexes of IL-2 and anti-IL-2 mAbs (IL-2C) to target I

115 solubility of the protein and nucleoprotein complexes of IN with viral DNA ends (intasomes).

116 ohols is achieved using an in situ generated complex of inexpensive NiBr(2) and readily available 8-a

117 7 outbreaks by characterizing the polymerase complex of influenza A(H5N8) viruses from both outbreaks

118 etry, an integrative structural model of the complex of interest can be generated.

119 ented here can be applied to any peptide-MHC complex of interest with a structural model as input, re

120 ation of cellular regions containing protein complexes of interest.

121 States for classical biological control of a complex of invasive saltcedar species and their hybrids

122 tion spectra (XAS) for distinct inner-sphere complexes of iron.

123 rlying multimotor transport, we analyzed the complexes of kinesin-1 and kinesin-3 motors attached thr

124 cellular receptor for the gH/gL glycoprotein complex of KSHV.

125 adhesion receptors and was found to activate complex of latent transforming growth factor beta (TGFbe

126 ciation constants for different cation-bound complexes of LCo, as determined by (1)H NMR spectroscopy

127 ohydrate determinants and Der p 2 as well as complexes of ligelizumab-Fab with IgE and IgE Fc were as

128 results demonstrate how an intimately linked complex of lineage- and stage-specific factors converges

129 ut of the 14 lanthanide (Ln) ions, molecular complexes of Ln(IV) were known only for cerium and more

130 btained a 2.10 angstrom structure containing complex of lsBSH bound to GCA and cholic acid (CA), a pr

131 ulosis, the T. curvata aldolase is a protein complex of Ltp2 with a DUF35 domain derived from the C-t

132 miya sp, consists of a high molecular weight complex of luciferin and proteins, apparently associated

133 m mouse brain tissue, and identified it as a complex of lysine-acetylated actin (KAc-actin) and cycla

134 The salivary complex of mammals consists of 3 major pairs of glands:

135 determined the crystal structures of ternary complexes of MEF2 and NKX2-5 bound to myocardin enhancer

136 n proteins are required for the formation of complexes of membrane proteins including cell-wall synth

137 The formation of ternary aqua complexes of metal-based diagnostics and therapeutics is

138 nd "side-to-side" phi back-bonding, found in complexes of metallacyclopropenes and metallacyclocumule

139 DAT co-exist and that higher-order molecular complexes of mGFP-hDAT are absent at the plasma membrane

140 present in the matrix and respiratory chain complexes of mitochondria.

141 While high-valent oxygenated complexes of Mn, Fe, Co, and Cu are increasingly well-kn

142 vel of single molecules or small interacting complexes of molecules.

143 mined the structure of a DNA-strand transfer complex of mouse RAG at 3.1- angstrom resolution.

144 role of MNK1-eIF4E-mediated translation of a complex of mRNAs that control mechanistic target of rapa

145 Complexes of Mto2 and Mto1 with gamma-tubulin regulate m

146 Here we identified a minimal stable complex of murine Rab33B(30-202) Q92L and Atg16L1(153-21

147 We also show that the AHAS complex of Mycobacterium tuberculosis adopts a similar s

148 Here, within a young species complex of neotropical cichlid fishes (Amphilophus spp.)

149 determined high-resolution structures of the complex of neurexophilin-1 and the second laminin/neurex

150 f livers in control mice revealed sinusoidal complexes of neutrophils and platelets and formation of

151 This finding is demonstrated by comparing complexes of nido-C(2) B(9) H(11) (2-) and nido-[o-xylyl

152 The synthesis of two well-defined rhodium(I) complexes of nitrous oxide (N(2) O) is reported.

153 Tightly packed complexes of nucleocapsid protein and genomic RNA form t

154 ort the structure of the nanobody-stabilized complex of nucleotide-free Galpha bound to phosphorylate

155 fused carbatriphyrins(2.1.1) and organo P(V) complex of one of the meso-fused carbatriphyrins were ob

156 ch the target and interfering ions each form complexes of only one stoichiometry.

157 e absence of ORC1 revealed a compact, stable complex of ORC2-5.

158 droanthracene (DHA) compared to diamond core complexes of other first-row transition metals including

159 Among those, only the complexes of oxidative phosphorylation (OXPHOS) affected

160 Although multimeric complexes of p100 (IkappaBdelta) are known to inhibit pr

161 Heteromeric receptor complexes of P2X7A and P2X7L are predicted to have reduc

162 ation interactions, and their importance for complexes of Pa and U in particular.

163 Th and U complexes, our calculations include complexes of Pa, Np, and Pu.

164 y, we examined the binding of free PAI-1 and complexes of PAI-1 with low-molecular-weight urokinase-t

165 es of this individual within two other major complexes of passage tombs 150 km to the west of Newgran

166 gstrom resolution reveals a compact globular complex of PCBP2 interacting with the cruciform RNA via

167 at gap-filling synthesis is carried out by a complex of PCNA, Pol delta, FEN1 and LigI.

168 Several new structures of non-covalent complexes of PGA with different substrates, as well as s

169 As a result, metal complexes of phosphangulene are predisposed to cocrystal

170 Thus, in characterizing the ternary complex of photo-rapamycin by MS, we applied binding sit

171 of chloroplasts in plants to accommodate the complexes of photosynthesis.

172 els with the function of the oxygen evolving complex of photosystem II, and provides new insights int

173 , but the extent to which the two endogenous complexes of PI3Kgamma, p101/p110gamma and p84/p110gamma

174 It is well-established that complexes of plasminogen-activator inhibitor 1 (PAI-1) w

175 s between PTMs and associated reader protein complexes of Plasmodium falciparum, a unicellular parasi

176 nvolves the assembly of defective initiation complexes of Pol III.

177 ed using coacervates (Coa) (i.e., a tertiary complex of poly(ethylene argininylaspartate diglyceride)

178 In this aspect, luminescent complexes of precious metals such as iridium, platinum,

179 at least five distinct nuclei, the pulvinar complex of primates includes two large visually driven n

180 ce of cation and pH homeostasis in the Golgi complex of professional secretory cells and the critical

181 A complex of protein interactions with enhancer RNAs empha

182 are manufactured by ribosomes-macromolecular complexes of protein and RNA molecules that are assemble

183 x sensitive units of the H3K4-trimethylating complex of proteins (COMPASS).

184 The COMPASS (complex of proteins associated with Set1) complex repres

185 Here we report that yeast Set1C/COMPASS (complex of proteins associated with Set1) is dimeric and

186 numerous sugars, is made in the cytoplasm; a complex of proteins forms a membrane-to-membrane bridge

187 nnelling metabolon which is part of a larger complex of proteins including pyruvate kinase.

188 y actin dynamics at the leading edge where a complex of proteins known as the WAVE regulatory complex

189 The kinetochore is a complex of proteins, broadly conserved from yeast to man

190 a developmental model, that specific hetero-complexes of Ptch2/Gas1 and Ptch1/Boc mediate the proces

191 hion and mediate the formation of tripartite complexes of Ras, immunophilin, and the ligand.

192 ct, explaining the 726 nm band based on a CT complex of reduced ET-FAD and oxidized Bf-FAD.

193 onnect the membrane stacks, as suggested for complexes of reticulon proteins.

194 parameters consistent with a triplet nitrene complex of Rh(2).

195 report the synthesis of PAlP and PBP pincer complexes of Rh with a central bis(N-pyrrolyl)aluminyl o

196 Here, we examined the structure of the complex of Ric8A with minimized Galpha(i) (miniGalpha(i)

197 hereas other ANAs bind protein components of complexes of RNA and RNA-binding proteins (RBPs).

198 Replication complexes of (+)RNA viruses of eukaryotes are associated

199 orbing organic molecules or transition-metal complexes of ruthenium, iridium, chromium or copper(5,6)

200 lculation demonstrated that a supramolecular complex of saccharide-fullerene was formed through CH-pa

201 The in vitro re-constituted transcriptional complexes of Saccharomyces cerevisiae (yeast) and humans

202 escribe structures of the hexadecameric AHAS complexes of Saccharomyces cerevisiae and dodecameric AH

203 nicotinamide adenine dinucleotide phosphate) complexes of SARM1 and plant NLR RUN1 TIR domains, respe

204 e the high-resolution structure of a ternary complex of SARS-CoV-2 nsp16 and nsp10 in the presence of

205 ss A penicillin-binding proteins (aPBPs) and complexes of SEDS proteins and class B PBPs (bPBPs).

206 e active translation proximal to replication complexes of several coronaviruses.

207 I), cleanly gives a borole half-sandwich pai-complex of Si(II) and silicocene.

208 tural characterization of a stable hexameric complex of six Escherichia coli FabZ dehydratase subunit

209 duction is transcriptionally controlled by a complex of six virally encoded proteins that hijack the

210 U2-type or the U12-type spliceosomes, large complexes of small nuclear ribonucleoprotein particles a

211 To date, synthetic model complexes of sMMO-Q have shown limited abilities to oxid

212 ich then activate proPO in the presence of a complex of SPH1 and SPH2.

213 ses the rate, relative to that of the parent complex of strain-free ligand.

214 either considered a polymorphic species or a complex of subspecies, due to its numerous morphological

215 can be either the proteins themselves or the complexes of sugars that decorate these membrane protein

216 Dyspepsia is a complex of symptoms referable to the gastroduodenal regi

217 igraine is characterized by a well-described complex of symptoms.

218 by poly(A) polymerase, binding of a ternary complex of T(30)-biotin/horseradish peroxidase (HRP)-bio

219 In this work it is shown that copper hydride complexes of tertiary phosphorus ligands (L) can be tune

220 ia their projections to the medial posterior complex of thalamus (POm).

221 report on the catalytic activity of a pincer complex of the abundant earth metal manganese for an unp

222 thermostable enzyme comprising a multimeric complex of the alpha(2) beta(2) or (alpha(2) beta(2) )(2

223 tree pangolin, the superior olivary nuclear complex of the auditory system, while not exhibiting add

224 trom resolution structure of the periplasmic complex of the C-terminal CSS domain (CCSSD) of PupR, th

225 Complex I, the first and the largest protein complex of the chain, harvests electrons from NADH to re

226 and either PB1, NP, or the entire polymerase complex of the chicken isolate, caused higher and earlie

227 DS is among the most genetically complex of the conditions that are compatible with human

228 In the absence of Jdp2, a complex of the cyclin-dependent kinase inhibitor 1 (p21(

229 o-EM), we report reconstructions of the core complex of the Dot/Icm T4SS that includes a symmetry mis

230 Features of the QRS complex of the electrocardiogram, reflecting ventricular

231 by conformational changes that the Michaelis complex of the enzyme and natural substrate undergoes wh

232 oscopy structure of a membrane-embedded core complex of the ESX-3/type VII secretion system from Myco

233 g of CheY proteins to the cytoplasmic switch complex of the flagellar motor, resulting in changes in

234 trans product, which corresponds to the gold complex of the head-to-head E-enyne.

235 usion spike incubated with EY6A Fab reveal a complex of the intact spike trimer with three Fabs bound

236 Previously, we reported that a complex of the Islet-1 (Isl1) transcription factor and t

237 tionary origins with the DA-enriched central complex of the Mandibulata.

238 The P(V) complex of the meso-fused carbatriphyrin(2.1.1) was foun

239 e Mn(4)CaO(5) cluster of the water oxidation complex of the photosystem II (PSII) complex.

240 UDP-glucosyltransferase UGT76G1, including a complex of the protein with UDP and rebaudioside A bound

241 This results in an irreversible inhibitory complex of the serpin with the protease.

242 e U5 small nuclear ribonucleoprotein (snRNP) complex of the spliceosome.

243 ic studies suggest that the formation of the complex of the substrates (alpha-halo carbonyl compounds

244 Here, we show that the Ech complex of the thermophilic acetogenic bacterium Thermoa

245 viously detailed the unusual locus coeruleus complex of the tree pangolin, the superior olivary nucle

246 termediates, namely, of the Ubc9*Pdr6 import complex, of the RanGTP*Pdr6 heterodimer, and of the trim

247 terferon beta (IFN-beta) than the polymerase complexes of the 2016-17 outbreak viruses, mediated via

248 The first enantiopure chiral-at-rhenium complexes of the form fac-ReX(CO)(3) (:C^N) have been pr

249 acterization of a series of thermally stable complexes of the general formula [Tp'(CO)(2)MSiC(R(1))C(

250 and Au(I)-azide PPh(3)AuN(3) provide digold complexes of the general formula R-1,5-bis-triphenylphos

251 Phosphinidene complexes of the general formula RPM(CO)(n) (R = an alky

252 bility derives from the formation of ternary complexes of the initiator with the single- and double-s

253 Inflammasomes are multiprotein complexes of the innate immune system that orchestrate d

254 Inflammasomes are multiprotein complexes of the innate immune system.

255 ystal structures and modeled substrate-bound complexes of the LCP enzymes reported here provide insig

256 Complexes of the LGN and NuMA proteins, fundamental comp

257 Dihapto-coordinate 1,2-dihydropyridine complexes of the metal fragment {WTp(NO)(PMe(3))} (Tp =

258 rane called cristae that contain the protein complexes of the oxidative phosphorylation system.

259 his region possesses multiple YY1 sites, and complexes of the promoter/enhancer combination were isol

260 report structures of core and complete vRNAP complexes of the prototypic Vaccinia poxvirus (Grimm et

261 le synthetic precedent, we show here that Ni complexes of the redox-active ligand (tBu,Tol)DHP ((tBu,

262 Mammalian mitochondria assemble four complexes of the respiratory chain (RCI, RCIII, RCIV, an

263 Aguada Fenix and other ceremonial complexes of the same period suggest the importance of c

264 The binary complexes of the two most promising compounds binding ND

265 tion experiments suggest that silylpalladium complexes of the type (PCy(3))(2)Pd-SiR(3)(+) are three-

266 e that the formally Class IIIA mixed valence complexes of the type [((R)dmx)Cu(2)(mu(2)-NAr)](-) feat

267 we describe a series of iridium(III) pincer complexes of the type [(PEP)IrCl(CO)(H)] (q) enabling th

268 The lanthanide complexes of these ligands were investigated by NMR spec

269 transmitted extracellularly through protein complexes of these molecules, called adhesions.

270 Finally, we determined the structure of a complex of this antibody bound to PvDBP, indicating the

271 The cytosolic ATPase complex of this injectisome is proposed to play an impor

272 Complexes of this type are potentially involved in catal

273 However, there is little knowledge about complexes of this type.

274 ch have uncovered the mechanism by which the complex of tissue factor (TF) and the plasma serine prot

275 hilic, Lewis acidic character, which renders complexes of titanium less functional group tolerant tha

276 ation and activation of heteromeric receptor complexes of transmembrane, dual-specificity kinases and

277 y of mtHsp70 is regulated by a heterodimeric complex of two J-domain proteins (JDPs), Pam18 and Pam16

278 tructure of McrB, we propose that McrBC is a complex of two McrB hexamers bridged by two subunits of

279 This technique was tested on complexes of two model DNA fragments and four ligands, n

280 roach is illustrated by application to three complexes of two subunits and a large assembly of 10 sub

281 activin A are capable of signaling through a complex of type II and type I receptors.

282 Complexes of type 1 combine the virtues of previous gene

283 s into structure and electronic character of complexes of type 1.

284 structural results published previously for complexes of type I L-asparaginase (EcAI) from E. coli.

285 es of palladium N-heterocyclic carbene (NHC) complexes of type trans-{(NHC)PdCl(2)L} (L = C(5)H(5)N,

286 e(3))(2) ligand have generated a new nitride complex of U(III), which is highly reactive toward C-H b

287 These data demonstrate that nitride complexes of U(III) are accessible with amide ligands an

288 h and found that the TCRdelta locus houses a complex of V segments from multiple lineages.

289 rs to produce an ensemble of interconverting complexes of variable stoichiometries, binding energetic

290 d in reactions with three electrophilic iron complexes of varying electronic properties, affording th

291 ity is demonstrated for a variety of protein complexes of varying topologies.

292 imed to determine if the recently identified complex of VASH1/2 (vasohibin 1/2) and SVBP (small vasoh

293 r detyrosination were recently identified as complexes of vasohibins (VASHs) one or two with small VA

294 is order, VSV encodes a unique polymerase, a complex of viral L (large, the enzymatic component) prot

295 ruses assemble a multi-subunit RNA-synthesis complex of viral non-structural proteins (nsp) responsib

296 beta- and gammaherpesviruses, a specialized complex of viral transcriptional activators (vTAs) coord

297 eport the crystal structure of the GMP bound complex of Vrg4, revealing the molecular basis for GMP r

298 G1-phase, there are ~250,000 nuclear cohesin complexes, of which ~ 160,000 are chromatin-bound.

299 ngineered the formation of heteropolynuclear complexes of [(YbL)(2)Tb (x)] compositions ( x = 1 and 2

300 The neutral ternary complex of [Zn(XDPAdeCage)](+) with the anionic ligand p