ライフサイエンスコーパス: heterotrimer

1 no acid sequence and glycosylation patterns (heterotrimers).

2 ides to promote the formation of an abc-type heterotrimer.

3 ated with the Gbeta subunit of the G-protein heterotrimer.

4 freely rotates with angles much larger than heterotrimer.

5 d monomeric beta(2)AR and nucleotide-free Gs heterotrimer.

6 s, allowing it to form three versions of the heterotrimer.

7 roduction and folding of the type I collagen heterotrimer.

8 o the Galpha subunit and dissociation of the heterotrimer.

9 formation of a zwitterionically neutral AAB heterotrimer.

10 superfamily that signal through a RI:RII:RII heterotrimer.

11 characterized alpha1(V) alpha2(V) alpha3(V) heterotrimer.

12 to displacement of Gbeta(1)gamma(1) from the heterotrimer.

13 modimeric interfaces to form an ExbD(2)-TonB heterotrimer.

14 orroborated the specific assembly of the ABC heterotrimer.

15 we report the first structure of a collagen heterotrimer.

16 s for more efficient folding of the collagen heterotrimer.

17 three polymerase subunit proteins to form a heterotrimer.

18 to the pol3/pol31 subunits of the pol delta heterotrimer.

19 lently closing defined interfaces within the heterotrimer.

20 thout formation of a classic Galphabetagamma heterotrimer.

21 ity of free rhodopsin and the free G protein heterotrimer.

22 NA, the PCNA of Sulfolobus solfataricus is a heterotrimer.

23 along with the structure of the GDP-bound Gs heterotrimer.

24 ubunits are very different from those of the heterotrimer.

25 of freedom of the membrane-bound transducin heterotrimer.

26 acies, in the absence and presence of the Gs heterotrimer.

27 ndent of its function in the Galphabetagamma heterotrimer.

28 ical modulators of the Galpha protein of the heterotrimer.

29 depends on energy but not on the intact AMPK heterotrimer.

30 to receptor coupling to the Galphabetagamma heterotrimer.

31 7TM receptor coupling to the Galphabetagamma heterotrimer.

32 stent with the formation of a UL15-UL28-UL33 heterotrimer.

33 sociation of active receptors with G protein heterotrimers.

34 nsfectants five times more strongly than B27 heterotrimers.

35 AP1 functions as a ferric reductase in STEAP heterotrimers.

36 cated, under various conditions, with hybrid heterotrimers.

37 mammalian systems contain hundreds of unique heterotrimers.

38 ficantly elevated in cells expressing mutant heterotrimers.

39 ster-specific assembly of synthetic collagen heterotrimers.

40 agen peptides that specifically associate as heterotrimers.

41 ssembly and activation of heterogeneous PP2A heterotrimers.

42 le helices that can be either homotrimers or heterotrimers.

43 ore, we show that adiponectin and CTRP9 form heterotrimers.

44 sequesters the PHI through the formation of heterotrimers.

45 s are regulated exclusively by one family of heterotrimers.

46 lity and less efficient fibrillogenesis than heterotrimers.

47 spond primarily to dimers released by G(i/o) heterotrimers.

48 and fibrillogenesis in mixtures with normal heterotrimers.

49 amma dimers derived specifically from G(i/o) heterotrimers.

50 ers dissociate more readily than active G(s) heterotrimers.

51 for efficient assembly of type I procollagen heterotrimers.

52 subunits from activated Galpha(i)-Gbetagamma heterotrimers.

53 of Au-Fe3O4 heterodimers to form Au-Ge-Fe3O4 heterotrimers.

54 -Fe3O4 heterodimer seeds to form Ag-Pt-Fe3O4 heterotrimers.

55 ollowing endosomal recycling of cell surface heterotrimers.

56 homotrimers and MEC-4 and MEC-10 form 4:4:10 heterotrimers.

57 er persistence length is half of that of the heterotrimer (96 A vs. 215 A), indicating it is more fle

58 A second heterotrimer, ABC-2, also stabilized by axial salt-bridg

59 These two heterotrimers act as a scaffold to assemble the remainin

60 iants (GNG11, RGS6) that influence G-protein heterotrimer action in GIRK-channel induced pacemaker me

61 resonance energy transfer (BRET) readout of heterotrimer activation with high temporal resolution re

62 a, Galphaibetagamma, or Galpha12/13betagamma heterotrimer activity.

63 ruption of the alpha3-alpha4-alpha5 collagen heterotrimer allowing autoantibody binding.

64 y of the most common collagens in humans are heterotrimers, almost all studies of collagen helices ha

65 agen type IV alpha 1 and alpha 2 chains form heterotrimers ([alpha1(IV)](2)alpha2(IV)) that represent

66 ivated (thiophosphorylated) recombinant AMPK heterotrimers (alpha2beta2gamma1 or alpha1beta1gamma1).

67 The number of active GPCRs governs G protein heterotrimer (alphabetagamma) dissociation, thereby cont

68 etagamma/AC5 interactions involving inactive heterotrimer and Gbetagamma stimulation of AC5 were sepa

69 tic simulations of a section of mouse type I heterotrimer and homotrimer collagen molecules are devel

70 he expression level of the entire transducin heterotrimer and that heterotrimer formation is essentia

71 ot with the PB1/PA heterodimer or PB2/PB1/PA heterotrimer and translocated into the nucleus with PB2

72 , alpha 1 (COL4A1) and alpha 2 (COL4A2) form heterotrimers and are abundant components of basement me

73 inhibited by intracellular dialysis of AMPK heterotrimers and by A769662, the effects of which were

74 stronger ligands for LILRB2 than HLA class I heterotrimers and H chains.

75 t purified by this method formed more stable heterotrimers and interacted more efficiently with membr

76 n other than regulating the assembly of PP2A heterotrimers and suggest that selective PP2A trimer inh

77 to assemble with proalpha1(I) chains to form heterotrimers and that were retained intracellularly.

78 NP and/or tER ligands couple two Myo4p*She3p heterotrimers and thereby generate a transport-competent

79 tion and cell killing both through PP2A(BAC) heterotrimers and through a B regulatory subunit-depende

80 disrupted the stable formation of PP2A(BAC) heterotrimers and thus E4orf4/C subunit association by P

81 I) polypeptides (required for folding of the heterotrimer), and their increased intracellular degrada

82 at were predicted to preferentially form the heterotrimer, and a rational annealing process led to th

83 motic stress requires energy sensing by AMPK heterotrimer, and osmotic stress leads to decreased intr

84 units to form the Galpha(i1)(GDP)-Gbetagamma heterotrimer, and that activation to Galpha(i1)(GTP) res

85 ocollagen, small populations of overmodified heterotrimers, and proalpha1(I) homotrimers that are com

86 determined that CD4, CXCR4, and CCR5 formed heterotrimers, and that CCR5 coexpression altered the co

87 subunit (AGB1) of the Arabidopsis G-protein heterotrimer are specifically involved in the regulation

88 We find that G(oA) heterotrimers are more effective activators of GIRK chan

89 Since all active heterotrimers are thought to dissociate and release free

90 ture also populates a single composition ABC heterotrimer as confirmed by circular dichroism (CD) and

91 tion of Gbetagamma dimer and Galphabetagamma heterotrimer, as well as their signaling upon GPCR activ

92 Collagen type I is an AAB heterotrimer assembled from two alpha1 chains and one al

93 It is an AAB heterotrimer assembled from two identical alpha1 and one

94 ubunits have distinct functions in different heterotrimer assemblies.

95 angstrom cryo-electron microscopy map of the heterotrimer assembly provides insight into the druggabl

96 synthetic protein folding prior to G protein heterotrimer assembly.

97 al images indicated segregation of homo- and heterotrimers at a subfibrillar level throughout the pro

98 ed receptors (GPCRs) must reorient G protein heterotrimers at lipid bilayers to catalyze nucleotide e

99 An electrostatic map of the EEEV E1/E2 heterotrimer based upon the recent Chikungunya virus cry

100 ATI-2341, a Galphaibetagamma heterotrimer-biased CXCR4 agonist, induced more robust p

101 previously showed that the Galphas-betagamma heterotrimer binds to the N terminus (NT) of type 5 AC (

102 sterically regulated by coupled G(i) protein heterotrimer both in insect cell membranes and as purifi

103 B) chromophore in a heterodimer (SB) and two heterotrimers (BSB and SBS) by alkyne bridges leads to t

104 eassociation of the pepsin-treated homo- and heterotrimers, but this remixing did not significantly r

105 inogen-in complex with an engineered Galphaq heterotrimer by cryoelectron microscopy (cryo-EM).

106 Gbetagamma in vitro from Galphai1beta1gamma2 heterotrimers by causing its dissociation from GalphaGDP

107 cleavage of full-length human procollagen I heterotrimers by either meprin alpha or meprin beta led

108 und that secretion of alpha3alpha4alpha5(IV) heterotrimers by podocytes into a preformed, abnormal, f

109 Activation of G-protein heterotrimers by receptors at the plasma membrane stimul

110 The PLD2-Grb2-WASp heterotrimer can be visualized in early phagocytic cups

111 diffusion along ssDNA and find that an hRPA heterotrimer can diffuse rapidly along ssDNA.

112 Therefore, a heterotrimer can divulge specific information about any

113 structural model of the CB1 receptor and Gi heterotrimer (CB1-Gi), guided by the x-ray structure of

114 Comparative analysis of the homo- and heterotrimer cleavage kinetics revealed that MMP-1 bindi

115 The Nsp1*Nup49*Nup57 channel nucleoporin heterotrimer (CNT) attaches to the IRC solely through th

116 ses and increase the repertoire of G protein heterotrimer combinations from three to 12.

117 may indicate differences in conformation and heterotrimer complex formation between the two preparati

118 Our findings reveal a heterotrimer complex with a key role in trastuzumab resi

119 tt-Aldrich syndrome protein (WASp) to form a heterotrimer complex, PLD2-Grb2-WASp, and present the me

120 calization and functional specificity to the heterotrimer complex.

121 B27 heterotrimers complexed with the L6M variant of the GAG

122 Teb2 and Teb3 assembled into other heterotrimer complexes, which when recombinantly express

123 otrimers including a surprisingly stable ABC heterotrimer composed of (DOG)10, (PKG)10, and (POG)10 c

124 It is a heterotrimer composed of a catalytic alpha and two regul

125 PP2A is a heterotrimer composed of a scaffold, catalytic and one o

126 Protein Phosphatase 2A (PP2A) is a heterotrimer composed of scaffolding (A), catalytic (C),

127 in expression of predominantly a single PP2A heterotrimer composed of the A/B charge-swap pair and th

128 Type I procollagen is a heterotrimer composed of two proalpha1(I) chains and one

129 Heterotrimers composed of B cell CLL/lymphoma 10 (BCL10)

130 Heterotrimers composed of collagen type IV alpha 1 (COL4

131 The results suggest that PP6 functions as a heterotrimer, composed of the PP6 catalytic subunit boun

132 G-protein heterotrimers, composed of a guanine nucleotide-binding

133 Yeast pol delta is a heterotrimer comprised of three subunits: the catalytic

134 Protein phosphatase 2A (PP2A) is a heterotrimer comprising catalytic, scaffold, and regulat

135 ENaC is probably a heterotrimer consisting of three well characterized subu

136 ctive F variant enriched the F oligomers for heterotrimers containing a single disulfide bond, withou

137 collagen triple helices can be "rescued" in heterotrimers containing amino acids with known high tri

138 tive or inactive state interacts with R7-RGS heterotrimers containing any R7-RGS isoform.

139 anine nucleotide exchange on Galphabetagamma heterotrimers containing Gq family G proteins.

140 a novel approach for the generation of PCNA heterotrimers containing one or two mutant monomers that

141 Unexpectedly, we found that PCNA heterotrimers containing only one functional binding sit

142 MT-1 knockdown reduced the formation of PP2A heterotrimers containing the Balpha regulatory subunit a

143 Because the Myo4p*She3p heterotrimer contains only one myosin molecule, it is no

144 t the interface of the kinase domain and the heterotrimer core exhibits normal regulation of phosphor

145 in which kinase domain association with the heterotrimer core is needed for kinase activation.

146 icating that our structure may represent the heterotrimer core of SNF1 in its activated state.

147 crystal structure at 2.6 A resolution of the heterotrimer core of SNF1.

148 which the kinase domain association with the heterotrimer core results in activation of the kinase ca

149 ny vasoconstrictive hormones signal via G(q) heterotrimer-coupled receptors, it is perhaps not surpri

150 IV alpha1 (COL4A1) and alpha2 (COL4A2) form heterotrimers critical for vascular basement membrane st

151 ement resembling that observed in a receptor-heterotrimer crystal complex.

152 According to the PP2A heterotrimer crystal structure, Glu153 (B'beta numbering

153 We also find that active G(oA) heterotrimers dissociate more readily than active G(s) h

154 On the basis of experimental evidence, both heterotrimer dissociation and rearrangement have been po

155 lasma membrane, GIRK channel activation, and heterotrimer dissociation.

156 the homologous short arm tips of the laminin heterotrimer, each consisting of a globular laminin N-te

157 he laminin alpha2 subunit of the laminin-211 heterotrimer expressed by astrocytes and pericytes, have

158 activation in cells where we could quantify heterotrimer expression at the plasma membrane, GIRK cha

159 r fibrils that served as seeds for mixed and heterotrimer fibrils.

160 To assess the requirement of the heterotrimer for regulated Thr-210 phosphorylation, we e

161 t that the CdtA and CdtC subunits of the Cdt heterotrimer form two putative lectin domains with a cen

162 ix electrostatic interactions, which promote heterotrimer formation and simultaneously discourage hom

163 on pathway that shifts the driving force for heterotrimer formation away from surface-driven nucleati

164 the entire transducin heterotrimer and that heterotrimer formation is essential for normal transduci

165 act of such abnormalities on efficient SNARE heterotrimer formation is poorly understood.

166 imilar affinities, suggesting that G protein heterotrimer formation occurred independently of nucleot

167 ped a discrete computational model to design heterotrimer-forming collagen-like peptides.

168 structure of the PE5(mt)-PPE4(mt)-EspG(3mm) heterotrimer from the ESX-3 system.

169 We designed a heterotrimer from three pairs of heterodimeric coiled co

170 oid-shaped ring structures of Pnkp1-Rnl-Hen1 heterotrimer fused at the Pnkp1 dimer interface.

171 g complex comprising pTyr-PAK1, Etk/Bmx, the heterotrimer G-protein subunits Gbeta1, Ggamma2, and/or

172 ergy transfer (FRET) and the binding site of heterotrimer Galpha(s) x betagamma mapped to amino acids

173 existence of a preformed complex of inactive heterotrimer (Galpha(s) x betagamma) and the effector ty

174 on of the assembly and function of G-protein heterotrimers (Galpha.GDP/Gbetagamma) is a complex proce

175 GNB3 encodes the beta subunit of G protein heterotrimer (Galphabetagamma) and is known to modulate

176 Galphaqbetagamma heterotrimer (Gq), an important mediator in the patholog

177 rgent-solubilized complex between Rho* and a heterotrimer (GT*) comprising a GalphaT/Galphai1 chimera

178 All previous reports on synthetic collagen heterotrimers have shown mixed populations with respect

179 ded some insight into the function of the C8 heterotrimer; however, there is no structural informatio

180 results indicated that the predominant AMPK heterotrimer in human liver is alpha1beta2gamma1 but tha

181 eceptor (B(2)R) and the Galpha(q)/Gbetagamma heterotrimer in living human embryonic kidney 293 cells

182 e report that Myo4p*She3p forms a stable 1:2 heterotrimer in solution.

183 specific G-protein alpha(olf)beta(2)gamma(7) heterotrimer in the striatum.

184 for novel proteins that interact with R7-RGS heterotrimers in the mouse brain.

185 al for the formation of laminin-211 and -221 heterotrimers in the muscle basal lamina.

186 alyze the stability of four AAB and four ABC heterotrimers including a surprisingly stable ABC hetero

187 ely for GPCRs coupled to alphai/o and alphas heterotrimers, including light-sensitive GPCRs.

188 suggest that these two phosphatases mediate heterotrimer-independent regulation of Thr-210 phosphory

189 action between activated Galpha13 and R7-RGS heterotrimers, indicating that these effector RhoGEFs ca

190 e find that the formation of the Ag-Pt-Fe3O4 heterotrimers initiates with indiscriminate Ag nucleatio

191 dings provide the first evidence that R7-RGS heterotrimers interact with Galpha13 to augment signalin

192 ranscription 1 (STAT1) and STAT2, which form heterotrimers (interferon-stimulated gene factor 3 [ISGF

193 Fitting of the elongated Z-shaped heterotrimer into electron microscopy (EM) envelopes of

194 The heterotrimer is electrostatically stabilized via multipl

195 trimers, the PE-PPE heterodimer of our ESX-3 heterotrimer is interacting with its chaperone at a dras

196 l that a single defined interface within the heterotrimer is opened during the loading process.

197 n with EMSA titrations suggest that one hRPA heterotrimer is sufficient to form a stable complex with

198 peptides (EOGPOG)(5) and (PRG)(10), the AAB heterotrimer is the dominant structure in solution and m

199 e provide evidence that the polymerase gamma heterotrimer is well-adapted to efficiently synthesize D

200 t structural characterization of PE-PPE-EspG heterotrimers is from the ESX-5 system.

201 ion of 5-HT(7) serotonin receptors with G(s) heterotrimers is necessary for agonist-induced signaling

202 STAT1 is an indispensable component of a heterotrimer (ISGF3) and a STAT1 homodimer (GAF) that fu

203 -Fe3O4, allowing tuning between two distinct heterotrimer isomers with different configurations.

204 ugh KLHL15 can interact with the PP2A/B'beta heterotrimer, it only degrades B'beta, thus promoting ex

205 nstrate that loss of this specific G-protein heterotrimer leads to reduced A(2A)R activation of adeny

206 As a biologically active heterotrimer, Lymphotoxin(LT)alpha1beta2 is unique in th

207 include M-Pt-Fe(3)O(4) (M = Au, Ag, Ni, Pd) heterotrimers, M(x)S-Au-Pt-Fe(3)O(4) (M = Pb, Cu) hetero

208 These heterotrimers maintain the native oligomeric structure o

209 firm the participation of B chains in an AAB heterotrimer molecule.

210 s of Gbeta1gamma2 and the Galphaibeta1gamma2 heterotrimer more precisely than could be achieved using

211 sights into the pathway by which Ag-Pt-Fe3O4 heterotrimer nanoparticles form and uncover new design g

212 The predominant form of PP2A is a heterotrimer of catalytic (C), scaffolding (A), and dive

213 on with epithelial cells by forming a stable heterotrimer of gH/gL/gp42.

214 mere-specific DNA binding of Teb1 or the TEB heterotrimer of Teb1, Teb2, and Teb3.

215 Normal type I collagen is a heterotrimer of two alpha1(I) and one alpha2(I) chains,

216 collagen, synthesized in all tissues as the heterotrimer of two alpha1(I) polypeptides and one alpha

217 The retromer complex is a heterotrimer of VPS29, VPS35, and VPS26.

218 peptide chains in the triple helix, distinct heterotrimers of different registers can be formed.

219 postulate that the mature NMDARs consist of heterotrimers of NR1-1b-NR2A-NR2C.

220 hospho-ser70 is dephosphorylated by specific heterotrimers of protein phosphatase 2A (PP2A).

221 plex is composed of stochastically assembled heterotrimers of RhAG, RhD, and RhCE.

222 ASICs are formed as homotrimers or heterotrimers of several isoforms (ASIC1a, ASIC1b, ASIC2

223 Heterotrimers of the LIGHT variants decreased binding av

224 s exposed in the 6-HB and is also present in heterotrimers of the N-HR and N36(Mut(e,g)) peptide.

225 he biological functions of precisely defined heterotrimers of various family members that had not bee

226 tor complex assembly requires two Myo4pShe3p heterotrimers, one She2p tetramer, and at least a single

227 zing agent consisting of a double-tagged VHH heterotrimer--one Stx1-specific VHH, one Stx2-specific V

228 The homotrimers completely replace the heterotrimers only in rare recessive disorders.

229 Thus, select PP2A heterotrimers oppose desensitization of the TrkA recepto

230 le-stranded DNA-binding protein Teb1 and its heterotrimer partners Teb2 and Teb3.

231 The Mre11-Rad50-Nbs1 (MRN) heterotrimer plays various and complex roles in DNA dama

232 The heterotrimer PLD2-Grb2-WASp then enables actin nucleatio

233 e discovered that the protein phosphatase 2A heterotrimer, PP2A(Ppp2r2d), regulates the phosphorylati

234 PriX, PriL and PriS form a stable heterotrimer (PriSLX).

235 Thus, XLG-Gbetagamma heterotrimers provide additional signaling modalities fo

236 In contrast, heterotrimers reconstituted with Teb2 and Teb3 and two o

237 e STAT1/STAT2/IRF9 (IFN regulatory factor 9) heterotrimers remained in the cytoplasm of PRRSV-infecte

238 t of the general single-stranded DNA binding heterotrimer replication protein A (RPA).

239 Our heterotrimer reveals that EspG(3mm) interacts exclusivel

240 at a remote location without perturbing the heterotrimer selectivity, suggesting a unique strategy t

241 Independent homo- and heterotrimer solubility measurements in mixtures confirm

242 the sterically less demanding layer removes heterotrimer specificity.

243 that Gbeta(3) participates in the G-protein heterotrimer that couples mGluR6 to TRPM1.

244 rotein phosphatase 2A (PP2A), representing a heterotrimer that is comprised of catalytic, scaffolding

245 yeast Gcn5, Ada2, and Ada3 components form a heterotrimer that is important for the enzymatic functio

246 r origins for the different type IV collagen heterotrimers that appear during development are unknown

247 SNF1/AMPKs are alphabetagamma heterotrimers that are activated by phosphorylation of t

248 novel model system based upon collagen-like heterotrimers that can mimic the glycine mutations prese

249 V, broadly expressed as alpha1(V)2 alpha2(V) heterotrimers that regulate collagen fibril geometry and

250 activated protein kinases are alphabetagamma-heterotrimers that sense and regulate energy status in e

251 The checkpoint protein Rad9/Rad1/Hus1 heterotrimer (the 9-1-1 complex) is structurally similar

252 We identified a naturally occurring heterotrimer, the Escherichia coli aldehyde oxidoreducta

253 ural analyses reveal that in contrast to the heterotrimer, the homotrimer easily forms kinks and free

254 In contrast, in a heterotrimer, the individual chains may be tailored in o

255 In contrast to the previously solved ESX-5 heterotrimers, the PE-PPE heterodimer of our ESX-3 heter

256 In solution, FluPol(A) forms dimers of heterotrimers through the C-terminal domain of the PA su

257 of the individual subunits of the G-protein heterotrimer to assemble into a functional complex.

258 o initiates cross-linking of two Myo4p*She3p heterotrimers to an ensemble that contains two myosin mo

259 of the Gbetagamma subunits of G(i) and G(o) heterotrimers to interact with G-protein regulated inwar

260 reen on coupling preference of all G-protein heterotrimers to NTR1 wild type and a stabilized mutant

261 and corresponding structures of a G-protein heterotrimer, to measure changes in structural stability

262 Normal type I collagen is a heterotrimer triple-helical molecule consisting of two a

263 multaneous specific assembly of two collagen heterotrimers using a genetically inspired operation, ci

264 tive design for the assembly of specific AAB heterotrimers using charged amino acids to form intrahel

265 americ (2:1:1:1) complex of Rho dimer and Gt heterotrimer, validating the oligomeric structure of the

266 The resulting non-covalent heterotrimer was exported in a Tat-dependent manner, del

267 In BN-PAGE, the SNARE heterotrimer was identified as a 150-kDa complex, increa

268 icates that the nuclear translocation of the heterotrimers was blocked.

269 d Thr-210 phosphorylation of the mutant SNF1 heterotrimers was substantially elevated during growth o

270 To this heterotrimer, we could then add CSN5 in vitro to reconst

271 rystal structure of the influenza polymerase heterotrimer, we generated a comprehensive functional ma

272 s of Gbeta1gamma2 and the Galphaibeta1gamma2 heterotrimer were both determined to fall within a simil

273 focal imaging of fibrils, in which homo- and heterotrimers were labeled with different fluorescent co

274 ective activators of GIRK channels than G(s) heterotrimers when comparable amounts of each are availa

275 hains of the collagen alpha3alpha4alpha5(IV) heterotrimer, which forms the major collagen IV network

276 ivated by thrombin to form an A1/A2/A3-C1-C2 heterotrimer, which functions as a cofactor for factor I

277 F2 preferentially form the TRAF1: (TRAF2)(2) heterotrimer, which interacts with cIAP2 more strongly t

278 It is a heterotrimer, which is probably located at the periplasm

279 he 1.2-MDa complex contains 12 copies of the heterotrimer, which unexpectedly form a spherical protei

280 Three-component hybrid nanoparticle heterotrimers, which are important multifunctional const

281 reaction for transforming heterodimers into heterotrimers, which is based on a supersaturation-preci

282 to favor charge-pair interactions in an ABC heterotrimer, while disfavoring the 26 competing oligome

283 substitution in an a site yields Pb(II)A(2)B heterotrimers, while d sites provide pure Pb(II)C(2)D or

284 This is the first report of a collagen heterotrimer whose thermal stability is greater than tha

285 cture of human VIP1R bound to PACAP27 and Gs heterotrimer, whose complex assembly is stabilized by a

286 , alpha2, and alpha3 chains of NC2, a stable heterotrimer with a disulfide bridge between alpha1 and

287 t is possible to selectively form a collagen heterotrimer with a well defined composition and registe

288 yeast Ada2, each have the ability to form a heterotrimer with ADA3 and GCN5L but that only the ADA2b

289 is communication we describe an AAB collagen heterotrimer with controlled composition and register.

290 Bacterially expressed Chz1 forms a heterotrimer with H2AZ-H2B, stabilizing the association

291 This receptor usually forms a heterotrimer with the IL2 receptors IL2RB and IL2RG, whi

292 LILRB1 bound to B27 heterotrimers with a K(D) of 5.3 +/- 1.5 muM but did not

293 CARD9, CARD10, and CARD11) are known to form heterotrimers with B-cell lymphoma 10 (BCL10) and mucosa

294 nalyze this process, recombinant laminin-111 heterotrimers with deletions and point mutations were ge

295 PP2A is an enzyme family of dozens of heterotrimers with different subcellular locations and c

296 nd forms a huge complex consisting of FrhABG heterotrimers with each a [NiFe] center, four Fe-S clust

297 homotrimers and normal alpha1(I)(2)alpha2(I) heterotrimers with fibroblast collagenase (MMP-1).

298 LILRB2 bound to B27(2) and B27 FHC and B27 heterotrimers with K(D)s of 2.5, 2.6, and 22 +/- 6 muM,

299 of strands that fold into A(2)B and ABC-type heterotrimers with only three salt bridges per triple he

300 S. solfataricus PCNA is a heterotrimer, with each subunit having a distinct specif