ライフサイエンスコーパス: ternary complex

1 m the MYOCD/SRF/CArG box triad (known as the ternary complex).

2 nal entropy of the kinase:nucleotide:peptide ternary complex.

3 eukaryotic initiation factor 4F (eIF4F) and ternary complex.

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

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

6 stal structure of the MbtI-Mg(2+)-salicylate ternary complex.

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

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

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

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

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

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

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

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

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

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

17 hat showed benefit to patients targeted this ternary complex.

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

19 ters FXII and HK into a higher-order 500-kDa ternary complex.

20 g in the formation of the BRCA2-MEILB2-BRME1 ternary complex.

21 meric CD40L and generate integrin-CD40L-CD40 ternary complex.

22 inding energy landscape of the Fis1:Fis2:DNA ternary complex.

23 eases the level of eIF2-GTP-Met-tRNA(i)(Met) ternary complexes.

24 interacted with the salivary protein to form ternary complexes.

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

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

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

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

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

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

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

32 f MAIT T cell antigen receptor (TCR)-MR1-AML ternary complexes, along with biochemical and functional

33 hermodynamics of the formation of binary and ternary complexes among TTR, Abeta(1-42) peptide, and TT

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

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

36 increase the efficiency of the formation of ternary complex and enhance the protein degradation effi

37 ing shows that NAA80, actin, and PFN2 form a ternary complex and that NAA80 has partly disordered reg

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

39 ontinued formation of the eIF2-GTP-Met-tRNAi ternary complex and unabated global translation at high

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

41 rmation of conventional agonist-5-HT(7)-G(s) ternary complexes and subsequent G(s) activation.

42 ational rearrangement, which strengthens the ternary complex, and contributes to enlarging a "hydroph

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

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

45 The ternary complex architecture explains how Rab11 vesicles

46 that only LCR segments heavily bound by this ternary complex are essential for its function.

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

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

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

50 ther areas of biology and chemistry in which ternary complexes are observed.

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

52 1, 36 formed a stable NDM-1:Zn(II):inhibitor ternary complex, as demonstrated by (1)H NMR, electron p

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

54 subunit Thermococcus onnurineus Csm effector ternary complexes, as well as X-ray studies on Csm1-Csm4

55 support t-SNARE interactions and accelerate ternary complex assembly.

56 driven by elongation and the formation of a ternary complex at filament barbed ends, or by nucleatio

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

58 hiG) and presents the crystal structure of a ternary complex between c-di-GMP, sigma(WhiG), and its a

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

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

61 We have used the ternary complex between p27(Kip1) (p27), Cdk2, and cycli

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

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

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

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

66 dependently to spike protein in vitro, and a ternary complex can be generated using heparin as a scaf

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

68 A ternary complex comprised of SHOC2, MRAS, and PP1 (SHOC2

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

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

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

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

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

74 ty through its ability to form high-affinity ternary complexes containing CEP250 and FKBP12.

75 apoCaM complex with the Na(V)1.5 CT and for ternary complexes containing fibroblast growth factor ho

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

77 We show that the ternary complexes containing proliferating cell nuclear

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

79 uated insertion kinetics and high-resolution ternary complex crystal structures of a configurationall

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

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

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

83 tion results in low availability of the eIF2 ternary complex (eIF2-GTP-tRNAi) by affecting the intera

84 nzyme to a nearly closed conformation of the ternary complex entails a disordered-to-ordered transiti

85 crystal structures of BmLDH in apo state and ternary complex (enzyme-NADH-oxamate) solved at 2.79 and

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

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

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

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

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

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

92 n be explained by the formation of transient ternary complexes favored at high protein concentrations

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

94 ormation of RdRp-RNA binary and RdRp-RNA-NTP ternary complexes for the poliovirus RdRp, including an

95 thways that coordinate eIF4F regulation with ternary complex formation after treatment with genotoxic

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

97 trometry were used to investigate binary and ternary complex formation between ProRS, YbaK, and tRNAP

98 servations suggest that additional rounds of ternary complex formation can occur on the ribosome duri

99 We characterize the role of ternary complex formation in driving selectivity, showin

100 assembly and secretion, suggesting that the ternary complex formation is required for PRAP1 to facil

101 ated unbinding component likely occurs via a ternary complex formation mechanism.

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

103 tic profiles, and ubiquitination, as well as ternary complex formation thermodynamics.

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

105 Mechanisms for ternary complex formation were characterized by Fourier

106 i) diffusion-limited binding, (ii) transient ternary complex formation, and (iii) fast exchange of mo

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

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

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

110 dation by O(2) and by stabilizing Mn(II) via ternary complex formation.

111 The ternary complex formed by Chz1 and H2A.Z-H2B dimer is th

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

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

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

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

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

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

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

119 apamycin, and the FKBP12-photo-rapamycin-FRB ternary complex formed readily in vitro.

120 ter being distinct from those seen in FKBP12 ternary complexes formed by FK506 and rapamycin.

121 and inter-relationships between the critical ternary complexes formed by the auto- and crosscatalytic

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

123 ned the crystal structures of bGalE in three ternary complex forms: NAD(+)/UDP, NAD(+)/UDP-GlcNAc, an

124 alpha binary, and RNAP-TFEalpha-promoter DNA ternary complexes from archaea, Thermococcus kodakarensi

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

126 For TGFbetas and BMPs, structures of ternary complexes have revealed differences in receptor

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

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

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

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

134 minus of CENP-H, leading to formation of the ternary complex in which CENP-H is sandwiched between CE

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

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

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

138 rget RNA and Csm(crRNA)-target RNA(anti-tag) ternary complexes in the 3.1 angstrom range.

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

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

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

142 A hypothesis about the nature of the ternary complex involving a MAPK, its substrate, and ATP

143 However, we did not detect a ternary complex involving E2A-AD1, KIX, and TAZ2 and fou

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

145 g that the conformational equilibrium of the ternary complex is biased toward the open conformation o

146 d D2 binds, and (iii) the fully-formed fuzzy ternary complex is formed concomitantly with an extensio

147 Bi sequential kinetic mechanism, in which a ternary complex is formed, indicating that both substrat

148 The resulting active-state ternary complex is the basis for conventional stimulus-r

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

150 Despite attempts to isolate the ternary complex, it is not known if Galphaolf and Galpha

151 both the Mg(2+) form (KARI:2Mg(2+)) and its ternary complex (KARI:2Mg(2+):NADH:inhibitor) are temper

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

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

154 This ternary complex likely reflects the state of repair bubb

155 Thus, a NgR1/PlexinA2/CRMP2 ternary complex limits neural repair after adult mammali

156 e, we report the structures of MavC/UBE2N/Ub ternary complex, MavC/UBE2N-Ub (product) binary complex,

157 ator of ERalpha and that Ajuba/DBC1/CBP/p300 ternary complex may be a new target for developing thera

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

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

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

161 l advances, including the formulation of the ternary complex model of G protein-coupled receptor sign

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

163 o heretofore underappreciated aspects of the ternary complex model.

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

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

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

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

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

169 The neutral ternary complex of [Zn(XDPAdeCage)](+) with the anionic

170 the cryo-electron microscopy structure of a ternary complex of catalytically competent DNMT3A2, the

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

172 s actively engaged in protein synthesis is a ternary complex of elongation factor Tu (EF-Tu), aminoac

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

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

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

176 Thus, in characterizing the ternary complex of photo-rapamycin by MS, we applied bin

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

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

179 port here the high-resolution structure of a ternary complex of SARS-CoV-2 nsp16 and nsp10 in the pre

180 )) tails by poly(A) polymerase, binding of a ternary complex of T(30)-biotin/horseradish peroxidase (

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

182 yo-EM structures of the extracellular region ternary complexes of GDF15/GFRAL/RET, GDNF/GFRalpha1/RET

183 Here we determined the crystal structures of ternary complexes of MEF2 and NKX2-5 bound to myocardin

184 The stability derives from the formation of ternary complexes of the initiator with the single- and

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

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

187 97-cyclin H and CDK7-cyclin H as well as the ternary complex pUL97-cyclin-H-CDK7 are detectable in an

188 and comparing it with that obtained with the ternary complex (receptor-agonist-G protein) we show tha

189 The LIN28:pre-let-7:TUTase ternary complex regulates pluripotency and oncogenesis b

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

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

192 the helix 6 environment in the active-state ternary complexes resides in a well-defined conformation

193 radiation, digestion, and MS analysis of the ternary complex revealed a McLafferty rearrangement prod

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

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

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

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

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

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

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

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

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

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

204 the first example of human MADS-box/homeobox ternary complex structures involved in cardiogenesis.

205 Compared with the apo, binary, and ternary complex structures of the original KOD polymeras

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

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

208 s to translating ribosomes associated with a ternary complex (TC) consisting of elongation factor Tu

209 rated dissociation of the eIF2.GTP.Met-tRNAi ternary complex (TC) from reconstituted PICs with a UUG

210 itiation complex (PIC) containing eIF1 and a ternary complex (TC) of GTP-bound eIF2 and Met-RNAi scan

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

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

213 arget engagement requires the formation of a ternary complex (TC) when the ligand brings its target p

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

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

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

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

218 that the act of codon testing of noncognate ternary complexes (TCs) at the ribosomal A-site enhances

219 decrease in k(trl) arises from a shortage of ternary complexes (TCs) under nutrient limitation and fr

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

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

222 library against a stabilized ligand-receptor ternary complex that acted as a "molecular cast" of the

223 receptor-G protein complexes, a conventional ternary complex that activates G proteins and an inverse

224 investigation, a catalytic cycle involving a ternary complex that binds to both the coupling partners

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

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

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

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

229 By strengthening the interactions of the ternary complex, the WW2 domain stabilized the WW1 domai

230 In such PNA:DNA ternary complexes, the two duplexes share a common PNA b

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

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

233 Ajuba recruits DBC1 and CBP/p300 and forms a ternary complex to co-activate ERalpha transcriptional a

234 ent recruitment of the eIF2*GTP*Met-tRNAiMet ternary complex to the ribosome and for its proper respo

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

236 (d) = 0.32 muM, indicating the presence of a ternary complex TTR/IDIF/Abeta(1-42).

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

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

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

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

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

242 ind simultaneously to the receptor to form a ternary complex, where the allosteric modulator affects

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

244 Fig4 is active as a lipid phosphatase in the ternary complex, whereas PIKfyve within the complex cann

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

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

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

248 tures of the POL domain, as apoenzyme and as ternary complex with 3'-dideoxy-terminated DNA primer-te

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

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

251 1 binding, and MLL1-bound KIX did not form a ternary complex with BMAL1, indicating that the MLL-bind

252 nally disordered protein CP12, which forms a ternary complex with both enzymes.

253 n by causing cell cycle arrest when bound in ternary complex with cyclin-dependent kinase (Cdk2) and

254 essive motility is activated when it forms a ternary complex with dynactin and a cargo adaptor.

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

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

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

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

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

262 an appended side chain of GdL(1) and forms a ternary complex with HSA (GdL(1)-Cu(2+)-HSA).

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

264 roduced later in the program, and it forms a ternary complex with Isc10 and Smk1 during MII that is p

265 Ccr4-Not binds Rsp5 and forms a ternary complex with it and the RNAPII elongation comple

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

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

268 inity motif for binding TCRs, and may form a ternary complex with MHCII.

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

270 in, redistributes to the cell periphery in a ternary complex with podocalyxin and ezrin, where it pro

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

272 EM structures of DOCK2-ELMO1 alone, and as a ternary complex with RAC1, together with the crystal str

273 show that SGEF, a RhoG-specific GEF, forms a ternary complex with Scribble and Dlg1, two members of t

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 available crystal structures of HCV NS5B in ternary complex with template-primer duplexes and nucleo

277 85 (E85V) impairs PRAP1's ability to form a ternary complex with TG and MTTP, as well as impairs its

278 hange in the RNA structure that stabilizes a ternary complex with the AUF1 protein, thus repressing t

279 for germinal center (GC) formation, forms a ternary complex with the lymphoid-enriched OCT2 and GC-s

280 avidly bound human (h) IgG1 IC and formed a ternary complex with the neonatal Fc receptor (FcRn) und

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

282 lex macrocyclic natural product that forms a ternary complex with the proteins FKBP12 and FRB.

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

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

285 tas, BMPs, and activins, signal by forming a ternary complex with type I and type II receptors.

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

287 eticulum (ER)-resident protease that forms a ternary complex with ubiquitinated substrates and p97/VC

288 rystal structure of macroPROTAC-1 bound in a ternary complex with VHL and the second bromodomain of B

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

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

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

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

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

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

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 a shared FKBP-binding domain before forming ternary complexes with their respective targets, mechani

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

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