ライフサイエンスコーパス: heterotrimer

1 no acid sequence and glycosylation patterns (heterotrimers).

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

3 ical modulators of the Galpha protein of the heterotrimer.

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

5 freely rotates with angles much larger than heterotrimer.

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

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

8 roduction and folding of the type I collagen heterotrimer.

9 o the Galpha subunit and dissociation of the heterotrimer.

10 formation of a zwitterionically neutral AAB heterotrimer.

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

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

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

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

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

16 we report the first structure of a collagen heterotrimer.

17 s for more efficient folding of the collagen heterotrimer.

18 three polymerase subunit proteins to form a heterotrimer.

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

20 lently closing defined interfaces within the heterotrimer.

21 thout formation of a classic Galphabetagamma heterotrimer.

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

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

24 ubunits are very different from those of the heterotrimer.

25 of freedom of the membrane-bound transducin heterotrimer.

26 ndent of its function in the Galphabetagamma heterotrimer.

27 ed to the quaternary structure of the intact heterotrimer.

28 five different AAB heterotrimers and one ABC heterotrimer.

29 s rather than disassembly of Galphabetagamma 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 ides to promote the formation of an abc-type heterotrimer.

34 nsfectants five times more strongly than B27 heterotrimers.

35 cated, under various conditions, with hybrid heterotrimers.

36 mammalian systems contain hundreds of unique heterotrimers.

37 ficantly elevated in cells expressing mutant heterotrimers.

38 agen peptides that specifically associate as heterotrimers.

39 le helices that can be either homotrimers or heterotrimers.

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

41 sequesters the PHI through the formation of heterotrimers.

42 s are regulated exclusively by one family of heterotrimers.

43 lity and less efficient fibrillogenesis than heterotrimers.

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

45 and fibrillogenesis in mixtures with normal heterotrimers.

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

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

48 for efficient assembly of type I procollagen heterotrimers.

49 y disrupting the formation of PP2A(BalphaAC) heterotrimers.

50 side chain charge pairs on the stability of heterotrimers.

51 complex is a hexamer consisting of dimers or heterotrimers.

52 two VDAC molecules forming heterodimers and heterotrimers.

53 through the formation of fusion incompetent heterotrimers.

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

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

56 ollowing endosomal recycling of cell surface heterotrimers.

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

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

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

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

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

67 xes: the cargo recognition VPS26-VPS29-VPS35 heterotrimer and a membrane-targeting heterodimer or hom

68 plexes, namely, a Vps26-Vps29-Vps35 obligate heterotrimer and a SNX1/2 alternative heterodimer or hom

69 Complex formation between the heterotrimer and activated rhodopsin leads to a dramatic

70 ach of the Galpha(GDP), Galpha(GDP)betagamma heterotrimer and Galpha(GTPgammaS) conformations are con

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

72 hat nonetheless shares similarities with the heterotrimer and GTPgammaS/Mg(2+)-bound ChiT.

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

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

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

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

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

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

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

80 ully show the assembly of five different AAB heterotrimers and one ABC heterotrimer.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

98 ype I collagen, the most abundant form, is a heterotrimer assembled from two identical alpha1 chains

99 ubunits have distinct functions in different heterotrimer assemblies.

100 synthetic protein folding prior to G protein heterotrimer assembly.

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

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

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

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

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

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

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

108 ta-subunit (Sip2) interacts with Snf4 in the heterotrimer but should still be able to bind carbohydra

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

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

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

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

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

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

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

116 Therefore, a heterotrimer can divulge specific information about any

117 Because collagen heterotrimers can be designed to have substitution in on

118 These results show that the stability of heterotrimers cannot be directly determined from the ana

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

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

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

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

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

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

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

126 calization and functional specificity to the heterotrimer complex.

127 B27 heterotrimers complexed with the L6M variant of the GAG

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

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

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

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

132 Human replication protein A (RPA), a heterotrimer composed of RPA70, RPA32, and RPA14 subunit

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

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

135 Heterotrimers composed of collagen type IV alpha 1 (COL4

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

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

138 e cupin superfamily), and a nuclear factor Y heterotrimer comprised of A5, B9, and possibly C9.

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

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

141 e predominant form of PP2Ac assembles into a heterotrimer comprising the scaffolding PR65/A subunit t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

173 tatic interactions can be utilized to direct heterotrimer formation.

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

175 at an isotope-labeled G(alpha) reconstituted heterotrimer forms functional complexes under NMR experi

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

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

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

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

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

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

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

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

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

185 This heterotrimer has a stability comparable to that of a (PO

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

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

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

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

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

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

192 re, causes prominent changes relative to the heterotrimer in the structure of switch I and contiguous

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

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

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

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

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

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

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

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

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

202 The heterotrimer is electrostatically stabilized via multipl

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

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

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

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

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

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

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

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

211 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

212 These heterotrimers maintain the native oligomeric structure o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

227 Heterotrimers of the LIGHT variants decreased binding av

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

243 Independent homo- and heterotrimer solubility measurements in mixtures confirm

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

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

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

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

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

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

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

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

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

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

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

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

256 Binding of the heterotrimer to activated rhodopsin to form the nucleoti

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

258 Ski-(16-192) interacted with an R-Smad.Smad4 heterotrimer to form a pentamer.

259 r to form a hexamer and with an R-Smad.Smad4 heterotrimer to form a pentamer.

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

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

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

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

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

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

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

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

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

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

270 ptides were mixed, and their ability to form heterotrimers was assessed.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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