ライフサイエンスコーパス: ternary complex

1 idence that HS, OPG, and RANKL form a stable ternary complex.

2 nd UvsY and gp32 independently and also as a ternary complex.

3 ycling of RNAP by releasing the RNA from the ternary complex.

4 to one another in vivo forming a functional ternary complex.

5 hains of the T-cell receptor, thus forming a ternary complex.

6 ell as with PSD-95(PDZ3) domains, creating a ternary complex.

7 hat showed benefit to patients targeted this ternary complex.

8 h is required for forming the Scc4.Scc1.CopN ternary complex.

9 turns rigid to prevent the formation of the ternary complex.

10 rting specificity on the PPP1R15B-PP1G-actin ternary complex.

11 n, which joined PPP1R15-PP1 to form a stable ternary complex.

12 E when compared with the TRBV14(+) TCR-HLA-E ternary complex.

13 tremities induced stabilizing effects on the ternary complex.

14 an ionization of substrate within the enzyme ternary complex.

15 toplasmic domain regulates formation of this ternary complex.

16 nters the ClpA processing pore in the active ternary complex.

17 ceptors, the TCR and MHC class II, forming a ternary complex.

18 r of Notch signaling and binds to the Notch1 ternary complex.

19 a solution-based model for the Fen1/PCNA/DNA ternary complex.

20 protein 95 (PSD-95) and stargazin, forming a ternary complex.

21 nslocase and disfavor that of the elongation ternary complex.

22 previously disclosed 3-CRBN-GSPT1 cocrystal ternary complex.

23 t, H11, which enabled crystallization of the ternary complex.

24 membrane, organizing a K-Ras4B-CaM-PI3Kalpha ternary complex.

25 that joins dynein and dynactin into a stable ternary complex.

26 early symmetric for PR20, as dimer-inhibitor ternary complexes.

27 em with the previous nucleic acid-associated ternary complexes.

28 be effectively combined with Mg(2+) to form ternary complexes.

29 l-5 have exceptional delipidating effects on ternary complexes.

30 ic phases and at least two subpopulations of ternary complexes.

31 of HA-CR8020-FcgammaRIIa/HA-IgG-FcgammaRIIIa ternary complexes.

32 1 as shown by crystal structures of MAIT TCR ternary complexes.

33 ain generates a population of non-productive ternary complexes.

34 ext of translationally active GTP.EF-Tu.tRNA ternary complexes.

35 metic nanobody, between more and less active ternary complexes.

36 interacted with the salivary protein to form ternary complexes.

37 R-SCR binary and JACKDAW (JKD)/IDD10-SHR-SCR ternary complexes.

38 , and Klebsiella pneumonia SlmA-DNA-FtsZ CTD ternary complexes.

39 ese findings suggest that EF-Ts may regulate ternary complex abundance in the cell through mechanisms

40 ive site, whereas in the substrate-selective ternary complex, actin contributes to one face of a plat

41 NMR measurements reveal a partially plastic ternary complex active site.

42 Developing neutralizing mAb to disrupt the ternary complex and abrogate the resulting toxicity is a

43 binding ability could stabilize a mismatched ternary complex and destabilize a matched ternary comple

44 erved when challenged for the formation of a ternary complex and incorporation of the first nucleotid

45 ular interactions within the POT1-TPP1-ssDNA ternary complex and the conformational changes that cont

46 Molecular modeling of the TCR-peptide-HLA ternary complexes and alanine scanning revealed that the

47 ling suggest that varied competition between ternary complexes and release factors perturbs the UGA r

48 ystems such as the ternary complex, extended ternary complex, and cubic ternary complex models for 7T

49 ed ternary complex and destabilize a matched ternary complex, and provided evidence with structures i

50 ant forms: resting state, one binary and two ternary complexes, and a covalent, thioacyl intermediate

51 ions of phenylalanyl, methionyl, and arginyl ternary complexes, and the development of a strategy to

52 of RT-RNA/DNA-dATP complex resembles DNA/DNA ternary complexes apart from additional interactions of

53 The ternary complex architecture explains how Rab11 vesicles

54 e CSD1 and the Sxl protein components in the ternary complex are revealed by the combination of NMR a

55 WY 14,643) and reduced (hAR*NADPH*WY 14,643) ternary complexes are comparable to each other.

56 provide direct evidence that RTK-GIV-Galphai ternary complexes are formed in living cells and that Ga

57 pon formation of the transition state of the ternary complex, are reflected in the UVPD mass spectra.

58 in acidic conditions enabled trapping of the ternary complex as a dominant population.

59 1, 36 formed a stable NDM-1:Zn(II):inhibitor ternary complex, as demonstrated by (1)H NMR, electron p

60 ntial for formation of the A1R/neurabin/RGS4 ternary complex, as well as for stable localization of R

61 -healing requires a low energetic barrier to ternary complex association.

62 f apo-CalS8 and the CalS8.substrate.cofactor ternary complex (at 2.47 and 1.95 A resolution, respecti

63 e TOCA HR1 domain to Cdc42 and the potential ternary complex between Cdc42 and the G protein-binding

64 ired for the formation of a ligand-activated ternary complex between GIV, Galphai, and growth factor

65 appaB dissociation from DNA, and a transient ternary complex between NF-kappaB, its cognate DNA seque

66 ed, we determined the crystal structure of a ternary complex between the full-length NS5 protein from

67 ivery demonstrate that the two halves of the ternary complex between the MoFe protein and two reduced

68 ealing, we observe the formation of a stable ternary complex between U4 and U6 RNAs and Prp24, indica

69 apping conformational epitopes in binary and ternary complexes between SEB and Fab fragments.

70 Significantly, the open E295K ternary complex binds two metal ions indicating that met

71 ogenesis and integrity of the Rpn3-Sem1-Rpn7 ternary complex but becomes dispensable once the ternary

72 re we structurally characterize the >100-kDa ternary complex by NMR and negative stain EM and show a

73 are functionally separate, so that a stable ternary complex can be formed.

74 sured for each step in this strictly ordered ternary complex catalytic mechanism.

75 e MCR.methyl-SCoM complex to form the active ternary complex (CoB7SH.MCR(Ni(I)).CH3SCoM) is highly fa

76 r thapsigargin stimulated the formation of a ternary complex composed of Orai1, TRPC1, and STIM1, the

77 Here we solve the crystal structure of a ternary complex comprising full-length human papilloma v

78 In addition, a ternary complex consisting of Erv1, Mia40, and substrate

79 Purified membrane proteins are ternary complexes consisting of protein, lipid, and dete

80 nosylmethionine (AdoMet)-binary and abortive ternary complex containing 8-hydroxyquinoline, and contr

81 lecular dynamics simulation of an hPol kappa ternary complex containing a template-primer DNA with dC

82 xtended GPU-based computational studies of a ternary complex containing catecholate show a clear tren

83 The 1.85 A resolution structure of a ternary complex containing NADPH and a P5C/proline analo

84 Ternary complexes containing 7-azaindenoisoquinolines we

85 NACK is recruited to the ternary complexes containing Maml1 and Maml3, but not Ma

86 We show that the ternary complexes containing proliferating cell nuclear

87 dy of Thermus thermophilus Argonaute (TtAgo) ternary complexes containing single-base bulges position

88 ic barrier for the dissociation of the CB[8] ternary complex cross-links, whereas facile and rapid se

89 transfer mapping of key residues within this ternary complex demonstrates that the protein substrate

90 materials utilizing cucurbit[8]uril (CB[8]) ternary complexes displaying a range of binding, and the

91 A GTP-state locked Arl2 mutant inhibits ternary complex dissociation in vitro and causes severe

92 inase-phosphorylated Sld2 and Sld3 to form a ternary complex during S phase.

93 dentify the translation elongation factor-1A ternary complex (eEF1A.GTP.aminoacyl-tRNA) as a specific

94 he 40S ribosomal subunit, eIF1, eIF1A, eIF3, ternary complex (eIF2-GTP-Met-tRNAi), and eIF5.

95 The two structures of the ternary complex ESA/Dic/Nps, obtained by competitive coc

96 mic acid rather than due to the formation of ternary complexes, except at very low TC concentrations.

97 s ways to build receptor systems such as the ternary complex, extended ternary complex, and cubic ter

98 show that a dominant-negative mutant of the ternary complex factor (TCF) Elk-1 attenuated the upregu

99 ctor activity, focusing on the ERK-regulated ternary complex factor family of SRF partner proteins.

100 The ERK-regulated ternary complex factors (TCFs) act with the transcriptio

101 mplications for the application of the CB[8] ternary complex for the formation of hydrogels, as these

102 gest that signaling potency is determined by ternary complex formation ability, whereas efficacy depe

103 A transient kinetic analysis of the ternary complex formation aided by small molecule ligand

104 was a "Superspondin" that exhibited enhanced ternary complex formation and 10-fold stronger signaling

105 ROTACs exhibited positive cooperativities of ternary complex formation and were more potent degraders

106 contrasts with the three-step mechanism and ternary complex formation in ubiquitin-activating enzyme

107 Pu sorption to goethite at pH 3, suggesting ternary complex formation or, in the case of humic acid,

108 with doxorubicin (DOX) prodrug 2 via hetero-ternary complex formation to yield 7.

109 Mechanisms for ternary complex formation were characterized by Fourier

110 virus serotypes from subgroups A to D induce ternary complex formation, Dlg1-dependent PI3K activatio

111 f 20-bp guide RNA:target DNA heteroduplex on ternary complex formation.

112 ting cleft adopts a "locked" conformation on ternary complex formation.

113 tributing to the RecA homology search before ternary complex formation.

114 reconstruction at approximately 26 A of the ternary complex formed by 2G12 Fab2, soluble CD4, and En

115 ereospecificity during aldol addition, a key ternary complex formed by DHAP and d-G3P, comprising 2%

116 In Arabidopsis, a ternary complex formed by MYB, bHLH transcription factor

117 A notable exception is the ternary complex formed by proproteinase E, chymotrypsino

118 We identified a ternary complex formed by TBP and the histone fold (HF)

119 Crystal structures of the ternary complex formed by the extracellular domains reve

120 he TTR-Abeta interaction, as well as for the ternary complex formed in the presence of IDIF.

121 No gH/UL116/gL ternary complex formed in transfected cells, suggesting

122 6.5, and then extraction of the hydrophobic ternary complexes formed in presence of cetyltrimethylam

123 rization by the d-G3P aldehyde moiety in the ternary complex generates the active trans-isomer compet

124 The versatile CB[8] ternary complex has, therefore, proven to be a powerful

125 ures of {L + Mg(2+)} and its phosphate bound ternary complexes have been established by computational

126 addition of dNTPs induces the formation of a ternary complex having what appears to be a conformation

127 ing the suite of published KIR and CD94-NKG2 ternary complexes, highlight the features that allow NK

128 ither CRY1 or CLOCK disrupt formation of the ternary complex, highlighting the importance of this int

129 determination of the Apo2L/TRAIL-DR5-AMG 655 ternary complex illustrates how higher order clustering

130 action in PI3Kalpha activation involving the ternary complex in cell proliferation signaling by oncog

131 of Cu(I) with bathocuproine (BCP) to form a ternary complex in presence of sodium dodecyl sulfate (S

132 ecreased expression of any component of this ternary complex in RPE1 cells causes a defective recruit

133 lex, we observe the formation of a transient ternary complex in the first few milliseconds of the flu

134 ata supports the existence of Kv4/KChIP/DPPL ternary complex in vivo.

135 cofactor TBCC onto this chaperone, forming a ternary complex in which Arl2 GTP hydrolysis is activate

136 , in turn, recruits HCF-1, thereby forming a ternary complex in which BAP1 bridges FoxK2 and HCF-1.

137 e three SMP-containing ERMES subunits form a ternary complex in which Mdm12 bridges Mmm1 to Mdm34.

138 ty (Ka = 1.3 x 10(4)) via the formation of a ternary complex in which one phosphate replaces both inn

139 ults suggest the existence of Kv4/KChIP/DPPL ternary complexes in ISA -expressing nociceptors and pai

140 on X-ray crystallographic unary, binary, and ternary complexes in order to decipher the molecular bas

141 ence suggests that neuronal Kv4 channels are ternary complexes including pore-forming Kv4 subunits an

142 been proposed that neuronal Kv4 channels are ternary complexes including pore-forming Kv4 subunits, K

143 ntigen (PfCyRPA) is a crucial component of a ternary complex, including Reticulocyte binding-like Hom

144 ary complex but becomes dispensable once the ternary complex incorporates into larger lid precursors.

145 -1alpha and VEGF, and a pStat3-pc-Jun-pATF-2 ternary complex induces CCL5 expression in LECs.

146 dicate that the galectin-3-U1 snRNP-pre-mRNA ternary complex is a functional E complex and that U1 sn

147 in pathway to the IL-36R.IL-36alpha.IL-1RAcP ternary complex is through the IL-36R.IL-36alpha binary

148 On formation of the ternary complex, ligand efficacy determines the quality

149 in neural lineages and the lens by forming a ternary complex likely facilitated allosterically throug

150 how an enzyme can enforce a strictly ordered ternary complex mechanism and serves as a template for i

151 ate that PvSHMT catalyzes the reaction via a ternary complex mechanism.

152 s product requires the binding of the other (ternary-complex mechanism).

153 sm of PglC, differing fundamentally from the ternary complex mechanisms of representative polytopic P

154 This ternary complex model may lead to development of novel M

155 preference for the symmetric FGF2-HS2-FGFR2 ternary complex model.

156 n for mu-ORs, determined using an allosteric ternary complex model.

157 ther layer of regulation in the classic GPCR ternary-complex model, with broad implications for the m

158 complex, extended ternary complex, and cubic ternary complex models for 7TMR function.

159 a bridge between the two enzymes to create a ternary complex named the transsulfursome.

160 The insights on ternary complexes obtained from the experimental results

161 lA-tRNA(Sec) complex, resulting in a 1.3-MDa ternary complex of 27.0 +/- 0.5 nm in diameter and 4.02

162 Here, we report the crystal structure of the ternary complex of 2OST, 3'-phosphoadenosine 5'-phosphat

163 In addition, the decreased stability of the ternary complex of 8-oxoG:dA extension results in furthe

164 The method is based on selective ternary complex of As(V) with acridine orange (AOH(+)) b

165 or the repressive cochaperone ATRX to form a ternary complex of BNRF1-Daxx-H3.3-H4, using coimmunopre

166 tion leads to a cooperative formation of the ternary complex of Cdc37 and kinase with Hsp90.

167 CT(EC536) binary complex and the neutralized ternary complex of CysK/CdiA-CT/CdiI(EC536) CdiA-CT(EC53

168 Excitingly, the ternary complex of HygX with cosubstrate alpha-ketogluta

169 nsfer to IsdB and growth of S. aureus, and a ternary complex of IsdB.Hb.Hp was observed.

170 the intact rhodanine led to observation of a ternary complex of MBL, a thioenolate fragment and rhoda

171 ucing koff, indicating formation of a stable ternary complex of myosin:Xa:Va.

172 se a model of the conformationally protected ternary complex of nitrogenase.

173 Here we report a stable ternary complex of Pol II, the replicative polymerase Po

174 major groove of the adducted DNA within the ternary complex of polymerase and dCTP.

175 We present the ternary complex of Vpx from SIV that infects mandrills (

176 Here we present the crystal structure of a ternary complex of Vpx with the human E3 ligase substrat

177 Here we report the crystal structures of two ternary complexes of a human NaV cytosolic C-terminal do

178 Binary and ternary complexes of DHFR containing cofactor NADPH, inh

179 otinamide cofactor (NADPH) for both reactive ternary complexes of the WT enzyme.

180 Although Fg and a subdomain of Fn can form a ternary complex on an FnBPA protein construct containing

181 cated in facilitating formation of an active ternary complex poised for chemistry.

182 ne to generate an AgmNAT*acetyl-CoA*agmatine ternary complex prior to catalysis.

183 eres with the recruitment of IFNAR1 into the ternary complex, probably by impeding complex stabilizat

184 lecule in a neurabin homo-oligomer to form a ternary complex, representing a novel mode of regulation

185 and ASXH domains formed a cooperative stable ternary complex required for deubiquitination.

186 A binary complex and the Phi29 DNAP-DNA-dNTP ternary complex, residues Tyr-226 and Tyr-390 in the pol

187 Crystal structures of hpol eta mutant ternary complexes reveal that polarized water molecules

188 The structures of these 12 ternary complexes reveal that relative to D-deoxycytidin

189 totypical Vbeta8.1(+) TCR-H-2D(b)-GAP5040-48 ternary complex revealed that germline-encoded complemen

190 rystal structure of the CtFabI.NADH.AFN-1252 ternary complex revealed the specific interactions betwe

191 The ternary complexes revealed a 180 degrees polarity revers

192 tion crystal structure of human GALT (hGALT) ternary complex, revealing a homodimer arrangement that

193 KDM4B.pyridine 2,4-dicarboxylic acid.H3K9me3 ternary complex, revealing the core active-site region a

194 Crystal structure of the ternary complex reveals a noncanonical binding site for

195 ling that includes formation constants for U ternary complexes reveals that the aqueous concentration

196 mponents showed a clear relationship between ternary complex reversibility and inhibitory activities

197 The crystallographic structure of the ternary complex scFv LR-Cn2-scFv RU1 allowed us to ident

198 SP15SART3 makes a complex with USP4 and this ternary complex serves as a platform to deubiquitinate P

199 The crystal structure of the [CYP121(cYY)CN] ternary complex showed a rearrangement of the substrate

200 To assemble the ternary complex, SPS undergoes a conformational change.

201 The ternary complex structure of hAR*NADP(+)*WY 14,643 revea

202 bCOMT crystal structures and established the ternary complex structure with 5-hydroxyconiferaldehyde

203 We determined two pre-catalytic ternary complex structures of polbeta with an incoming n

204 Ternary complex (TC) and eIF4F complex assembly are the

205 xit-channel, contacting the eIF2GTPMet-tRNAi ternary complex (TC) and mRNA context nucleotides; but i

206 IF1, eIF1A, eIF3, and the eIF2-GTP-Met-tRNAi ternary complex (TC) in stabilizing the 43 S PIC are poo

207 ex (PIC) bearing the eIF2.GTP.Met-tRNAi(Met) ternary complex (TC) scans the mRNA for an AUG codon in

208 orms part of an aminoacyl(aa)-tRNA.EF-Tu.GTP ternary complex (TC) that accelerates the binding of aa-

209 i to the small (40S) ribosomal subunit, in a ternary complex (TC) with eIF2-GTP, is stimulated by euk

210 on complex (PIC) bearing Met-tRNAi(Met) in a ternary complex (TC) with eukaryotic initiation factor (

211 ukaryotic initiation factor 2 (eIF2) forms a ternary complex (TC) with GTP and the initiator methiony

212 nds Met-tRNAi to form the eIF2-GTP*Met-tRNAi ternary complex (TC), which is recruited to the 40S ribo

213 ting the levels of active eIF2-GTP/Met-tRNAi ternary complexes (TC).

214 onylated tRNAi (Met-tRNA(i)) binding (in the ternary complex [TC] with eIF2-GTP) to reconstituted pre

215 D2 (BICD2) joins dynein with dynactin into a ternary complex (termed DDB) capable of processive movem

216 om DNA and formed a more stable intermediate ternary complex than that formed from IkappaBalpha(WT) b

217 ted a spectrum of occupancy by the BATF-IRF4 ternary complex that correlated with the sensitivity of

218 hoinositide 5-kinase PIKfyve in a ubiquitous ternary complex that couples PtdIns(3,5)P2 synthesis wit

219 nhydroMurNAc provide detailed insight into a ternary complex that forms preceding an operative Michae

220 a unique manner by forming a Rap60-ComA-DNA ternary complex that inhibits transcription of target ge

221 (Dlg1), a component of the Dlg1:E4-ORF1:PI3K ternary complex that mediates E4-ORF1-induced PI3K activ

222 on their own, the sgRNA recruits them into a ternary complex that recapitulates the activity of full-

223 ex3 and RING-domain proteins, resulting in a ternary complex that was critical for the intra-ER sorti

224 nsertion stage is confirmed by structures of ternary complexes that allow visualization of the extens

225 haracterized as a central component of these ternary complexes that control anthocyanin and PA biosyn

226 bly of these tubulin binding proteins into a ternary complex, the concentration-dependent formation o

227 While the Set A shows the formation of ternary complex, the Set B does not exhibit any intermed

228 In the resulting model for the ternary complex, the two copies of the HDACs are situate

229 In the remaining two similar ternary complexes, the L-nucleotide surprisingly interac

230 -Ts promotes the formation of GTP.EF-Tu.tRNA ternary complexes, thereby accelerating substrate turnov

231 NA as a binary complex and to target DNAs as ternary complexes, thereby capturing catalytically compe

232 the assembly of temporary Fcho1/2Eps15/RAP-2 ternary complexes to facilitate conformational activatio

233 sely, the dissociation rate constants of the ternary complexes varied dramatically with the guest str

234 of this process remained a puzzle because no ternary complex was observed, and structures show that t

235 The formed ternary complex was then revealed by the introduction of

236 Consistent with the formation of a ternary complex, we find that the inhibitory peptide is

237 nt polymers captured in the nanopore in such ternary complexes were clearly distinguishable and seque

238 Five x-ray crystal structures of hpol eta ternary complexes were determined, three at the insertio

239 s simulations to explore the protein-SAM-DNA ternary complex where the target adenine is flipped out

240 molecules are present, simulations uncover a ternary complex, where the originally bound Fis protein

241 II)-N,N'-o-phenylene bis (salicylideneimine) ternary complex wherein Zn (II) ion is the imprint ion a

242 K188 and K189 to recruit NACK to the Notch1 ternary complex, which results in the recruitment of RNA

243 presence of cAMP, RD and RegA form a stable ternary complex, while in the absence of cAMP they maint

244 Pu with TBP and DBP yielded the formation of ternary complexes whose stoichiometry was directly relat

245 d beta3 strands, inducing the formation of a ternary complex with a 2:1 hBD6:FX stoichiometry.

246 ts the first structure of mismatched polbeta ternary complex with a closed protein conformation and c

247 n (GAP) for the eIF2 . GTP . Met-tRNAi (Met) ternary complex with a critical role in initiation codon

248 two components of nitrogenase form a stable, ternary complex with a small [2Fe:2S] ferredoxin termed

249 orts, here we solve a structure of CCR2 in a ternary complex with an orthosteric (BMS-681) and allost

250 o far apart to react, but we have captured a ternary complex with both substrates bound in a closed f

251 rystal structure of the kinase captured as a ternary complex with bound lipid substrate and an ATP an

252 absence of domain I binding, BARP can form a ternary complex with Cavalpha1 and Cavbeta via domain II

253 The trapped ternary complex with coenzyme and product reveals five c

254 that, under basal conditions, IP6K1 forms a ternary complex with CSN and CRL4 in which IP6K1 and CRL

255 First, aa-tRNAs in ternary complex with EF-Tu.GDP are selected in a step wh

256 by the messenger RNA programmed ribosome in ternary complex with elongation factor Tu (EF-Tu) and GT

257 nitial codon selection of aminoacyl-tRNAs in ternary complex with elongation factor Tu and GTP on mes

258 pVHL forms a ternary complex with elongin C and elongin B, critical f

259 YbDTMA forms a ternary complex with fluoride in aqueous solution by dis

260 Pure RGS14 forms a ternary complex with Galphao-AlF4(-) and an AlF4(-)-inse

261 of Arabidopsis FUT1 in its apoform and in a ternary complex with GDP and a xylo-oligosaccharide acce

262 t-specific tRNA-binding protein that forms a ternary complex with glutamyl-tRNA synthetase (GluRSc) a

263 ailoring by CblC, and it also stabilized the ternary complex with GSH.

264 the eukaryotic elongation factor-1A and its ternary complex with GTP and aminoacyl-tRNA are common t

265 ggesting a means by which TACC3 could form a ternary complex with HIF-2alpha PAS-B and ARNT PAS-B via

266 GIGANTEA forms a ternary complex with HSP90 and ZEITLUPE and its co-chape

267 the CDI toxin from Escherichia coli NC101 in ternary complex with its cognate immunity protein and el

268 GlgE in a binary complex with maltose and a ternary complex with maltose and a maltosyl-acceptor mol

269 T. brucei brucei acidocalcisomal PPases in a ternary complex with Mg(2+) and imidodiphosphate.

270 uced in Arabidopsis protoplasts could form a ternary complex with NF-YC2 in vitro, providing a molecu

271 conformational changes upon formation of the ternary complex with primer/template DNA and substrate.

272 e VPS26 protomer and sequentially assemble a ternary complex with PTHR and SNX27.

273 INO80 forms a ternary complex with RNAPII and Cdc48 and targets Rpb1 p

274 displaces HIF-1alpha by forming a transient ternary complex with TAZ1 and HIF-1alpha and competing f

275 In vitro, Mot1 forms a ternary complex with TBP and DNA and can use ATP hydroly

276 Wss1 forms a SUMO-specific ternary complex with the AAA ATPase Cdc48 and an adaptor

277 lation of CREB stimulated the formation of a ternary complex with the KIX and BRD domains of CBP by N

278 MLL forms a ternary complex with the lens epithelium-derived growth

279 intersubunit cooperativity in formation of a ternary complex with the mechanism based inhibitor, 5F-d

280 omplementary-tagged nucleotide forms a tight ternary complex with the primer/template and polymerase,

281 e crystal structure of human TDO (hTDO) in a ternary complex with the substrates L-Trp and O2 and in

282 that the transmembrane protein TMIE forms a ternary complex with the tip-link component PCDH15 and i

283 tagonist that binds to syndecans and forms a ternary complex with the Wnt co-receptor Lipoprotein rec

284 ice sites of the major class of introns as a ternary complex with U2AF(65) and U2AF(35) splicing fact

285 Our results for ternary complexes with a non-complementary dNTP confirme

286 Among the four ternary complexes with a specific L-nucleotide, two are

287 ich is a precursor of various high-stability ternary complexes with actinides, is demonstrated.

288 ith MIC values <1 mug/mL) and to form stable ternary complexes with both wild-type and resistant muta

289 Meanwhile, the opening rate in ternary complexes with complementary nucleotide was 6 s(

290 ormula: see text] and its various binary and ternary complexes with DNA and the inhibitor IkappaB.

291 metal ions are required for the formation of ternary complexes with either of the two compounds.

292 ing crystal structures of stalled polymerase ternary complexes with enzymes, RNA templates, RNA prime

293 of this human enzyme as the holo form and as ternary complexes with estrone and with the first potent

294 as glucose, fructose or galactose by forming ternary complexes with high-epitope organic receptors fo

295 e end of SecA allowed us to efficiently form ternary complexes with SecYEG for spectroscopic studies.

296 ectron-rich aromatic moieties forming hetero-ternary complexes with the macrocycle cucurbit[8]uril (C

297 Structural comparison of C2c1 ternary complexes with their Cas9 and Cpf1 counterparts

298 her hand, the CDV IRES forms a 40S/eIF3/IRES ternary complex, with multiple points of contact.

299 gamycin specifically stabilizes near-cognate ternary complexes within the A site during the normally

300 nting the dominant population trapped in the ternary complex, would lead to re-face attack on the ald