ライフサイエンスコーパス: heterodimerize

1 In vitro, HuR and CUGBP2 heterodimerize.

2 We further show that APS and SH2-B isoforms heterodimerize.

3 s show that all of them have the capacity to heterodimerize.

4 lly expressed homologs TAF4 and TAF12, which heterodimerize.

5 ream caspases to p12 and p20 subunits, which heterodimerize.

6 tis elegans LIN-2 and LIN-7 can specifically heterodimerize.

7 eucine zippers that homodimerize rather than heterodimerize.

8 s and that this depended on their ability to heterodimerize.

9 dicate that AT1 and B2 receptors efficiently heterodimerize.

10 teins that are capable of homodimerizing and heterodimerizing.

11 wild-type receptor, are shown by BRET(2) to heterodimerize, accounting for their dominant-negative e

12 The ability of Her3 and Her4 to heterodimerize and activate other family members is stud

13 n factors APETALA3 (AP3) and PISTILLATA (PI) heterodimerize and are required to specify petal identit

14 Pbx proteins also stably heterodimerize and bind DNA with Meis and Pknox1-Prep1,

15 ribonucleoprotein (hnRNP)-like proteins that heterodimerize and bind RNA.

16 t, low amounts of CREB-1 and C/EBP appear to heterodimerize and bind to a site consisting of a half s

17 Since Dectin-2 and MCL heterodimerize and both CLRs use FcRgamma as the signali

18 pUL50 and pUL53 heterodimerize and form a core nuclear egress complex (N

19 ays showed the ability of PGHS1 and PGHS2 to heterodimerize and form prostaglandins.

20 2 genes, hamartin and tuberin, respectively, heterodimerize and inhibit the mammalian target of rapam

21 have 86% amino acid identity; they homo- and heterodimerize and partially co-localize to TRE.

22 B2 and erbB3, receptor tyrosine kinases that heterodimerize and signal in Schwann cells in response t

23 rtain developmental disorders constitutively heterodimerize and that their signaling activity can als

24 Furthermore, CD97 heterodimerized and functionally synergized with LPAR1,

25 ctivate the expression of SHP, which in turn heterodimerizes and suppresses FTF transactivation activ

26 se proteins can only homodimerize but do not heterodimerize, and lacking significant homology to Jun

27 lication to yield two homodimers that cannot heterodimerize, and the mutants we identified represent

28 Both methods showed that NHERF2 and NHERF3 heterodimerize as the strongest interaction among all NH

29 eins, the ZTA and C/EBPalpha subunits do not heterodimerize, as indicated by an in vitro cross-linkin

30 static interactions that are used to specify heterodimerizing B-ZIP proteins in H.sapiens are not pre

31 The two L27 domains heterodimerize by building a compact structure consistin

32 idated the DNA-assisted binding method using heterodimerizing coiled-coil proteins.

33 he ErbB-4 receptor tyrosine kinase homo- and heterodimerizes following heregulin binding, which provo

34 es may result in preferential binding to the heterodimerized forms.

35 me by the addition of rapamycin, a drug that heterodimerizes Fpr1 and Tor1.

36 oform, and the finding that the two proteins heterodimerize, further suggests that the amphiphysins a

37 -6Ralpha hexameric complex, CNTF/CNTF-Ralpha heterodimerizes gp130 and LIF-R via noncooperative energ

38 1A-with alpha1D-adrenoceptors, which did not heterodimerize, had no effect on receptor density or pro

39 These agents could be useful for imaging heterodimerized HER2 and HER3 receptors because their bi

40 ddition to forming homodimers, Mst1 and Mst2 heterodimerize in cells, this interaction is mediated by

41 ITLUPE (ZTL) and clock element GIGANTEA (GI) heterodimerize in the cytosol, thereby stabilizing ZTL.

42 e, we demonstrate that the two NblA proteins heterodimerize in vitro and in vivo using pull-down assa

43 We also demonstrate that BMP7 and GDF7 heterodimerize in vitro and that, under these conditions

44 o be stable homodimers with no propensity to heterodimerize in vitro.

45 DTX family members homodimerize and heterodimerize in vivo, suggesting that physical interac

46 ARNT heterodimerizes in vivo with other bHLH PAS proteins to

47 ost cells express multiple ErbB members that heterodimerize, leading to receptor cross-activation.

48 , used to monitor thermal denaturations of a heterodimerizing leucine zipper system containing either

49 We use a heterodimerizing leucine zipper system to examine the co

50 le (MT) motor protein consisting of distinct heterodimerized motor subunits associated with an access

51 a are homeodomain transcription factors that heterodimerize on DNA and are down-regulated during norm

52 y, pairs of complementary ZFNs are used that heterodimerize on the target DNA sequence; however, conv

53 These data suggest that MOR and DOR heterodimerize only at the cell surface and that the oli

54 ion of a ligand that activates LXRs or their heterodimerizing partner, the retinoid X receptor.

55 per 53 (bZIP53) transcription factor and its heterodimerizing partners, bZIP10 and bZIP25.

56 ion, indicating that HIV-1 and HIV-2 RNA can heterodimerize prior to packaging using the DIS sequence

57 F (prolamin box-binding factor) and OHP1 (O2-heterodimerizing protein 1), were also analyzed.

58 retinoid X receptor alpha (RXRalpha), which heterodimerizes readily with other receptors.

59 The heterodimerizing self-assembly between a phosphoric acid

60 omponents assemble only in the presence of a heterodimerizing small molecule.

61 nal region and the BH3 domain were unable to heterodimerize, suggesting that BNIP1 may bind to BCL-XL

62 modynamic preference for erbB ectodomains to heterodimerize, thereby creating erbB receptor assemblie

63 NKD1 and NKD2 can homo- and heterodimerize through their ID domains.

64 iochemical studies reveal that SAV1 and MST2 heterodimerize through their SARAH domains.

65 its a much weaker ability to homodimerize or heterodimerize; thus the binding of RASSF1C to Nore is v

66 The domains heterodimerize to become transcriptionally competent and

67 er (bHLH/LZ) proteins, ChREBP and Mlx, which heterodimerize to bind DNA.

68 ion-leucine zipper (B-ZIP) proteins homo- or heterodimerize to bind sequence-specific double-stranded

69 Moreover, two non-functional receptors heterodimerize to form a functional receptor, suggesting

70 ing SLC7A5 and SLC3A2, the products of which heterodimerize to form an amino acid transporter in HT-2

71 related G-protein-coupled receptors have to heterodimerize to form the functional GABA(B) receptor a

72 ammalian homologues of Escherichia coli MutL heterodimerize to form three distinct complexes: MLH1/PM

73 composed of two distinct proteins that must heterodimerize to generate transport activity, but the r

74 g cassette (ABC) half-transporters that must heterodimerize to move to the apical surface of cells.

75 es generating N320 and C180 fragments, which heterodimerize to stabilize the complex and confer its s

76 sess lower free Bax but higher levels of Bax heterodimerized to Bcl-2 and Bcl-xL.

77 solated tissue-specific bHLH protein, BETA2, heterodimerized to the ubiquitously expressed bHLH prote

78 In this system, rapamycin is used to heterodimerize two chimeric proteins.

79 induced using two custom-designed ZFNs that heterodimerize upon binding DNA to form a catalytically

80 age is induced when two custom-designed ZFNs heterodimerize upon binding DNA to form a catalytically

81 s of IKK alpha and IKK beta, which homo- and heterodimerize, varied among cell types.

82 Ring1b are critical components of PRC1 that heterodimerize via their N-terminal RING domains to form

83 Given that NAC53 and NAC78 homo- and heterodimerize, we propose that they work as a pair in a

84 ndings show that PHOX2B forms homodimers and heterodimerizes weakly with mutated proteins, exclude th

85 alpha(2A)-adrenergic receptor (alpha(2A)AR) heterodimerize when coexpressed in cells.

86 Upon binding to E2, ERs homo- and heterodimerize when coexpressed.

87 ns reveal that these proteins both homo- and heterodimerize, which may contribute to greater selectiv

88 igned a pair of proteins, Prb and Pdar, that heterodimerize with a Kd of 130 nM, 1000-fold tighter th

89 dicate that at 37 degrees C myogenin and E12 heterodimerize with a Kd of 36 microM (k(on) of 573 M(-1

90 fter Fas (CD95) ligation as well as directly heterodimerize with and activate caspase-8.

91 e the function of PML through its ability to heterodimerize with and delocalize PML from the nuclear

92 basic helix-loop-helix (bHLH) proteins that heterodimerize with and negatively regulate bHLH transcr

93 x family of homeobox genes has been found to heterodimerize with and thereby augment the DNA binding

94 As expected, however, max(USF) was unable to heterodimerize with any of the tested max partner protei

95 elix-loop-helix PAS (bHLH-PAS) proteins that heterodimerize with ARNT.

96 VBP does not heterodimerize with B-ZIP domains from C/EBP alpha, JUND

97 hough this construct retained the ability to heterodimerize with Bax and to inhibit apoptosis, when a

98 oth wild-type and Bax knock-out mice, it can heterodimerize with Bax in normal lymphocytes, and it is

99 nd phosphorylated Bcl-2 lost its capacity to heterodimerize with Bax.

100 motes cell death as a homodimer but that can heterodimerize with Bcl-2 to promote cell viability.

101 thout significantly affecting its ability to heterodimerize with BCL-2.

102 ility to homodimerize with themselves and to heterodimerize with Bcl-2.

103 odimerized via its POZ domain but it did not heterodimerize with BCL-6, which heterodimerizes with PL

104 ibit survival correlated with the ability to heterodimerize with Bcl-x(L).

105 taining the BH3 deletions were still able to heterodimerize with BCL-XL while mutants lacking both th

106 he bHLH transcription factors, and when they heterodimerize with bHLH proteins, the complexes are ina

107 roup reduces the ability of BCCP Delta 67 to heterodimerize with BPL, and emphasizes that a network o

108 er domain and correlated with its ability to heterodimerize with C/EBPbeta and inhibit C/EBPbeta DNA

109 tivity of C/EBPgamma required its ability to heterodimerize with C/EBPbeta.

110 However, full-length c-FLIPL can also heterodimerize with caspase-8 independent of death recep

111 encodes one of three class I E proteins that heterodimerize with class II bHLH proteins such as TWIST

112 Recent studies have shown that GPCRs heterodimerize with closely related members, resulting i

113 They are also able to heterodimerize with coexpressed wild-type Stat1.

114 otes the formation of survivin monomers that heterodimerize with CRM1 and facilitate its nuclear expo

115 rast, Atonal and Scute, which are thought to heterodimerize with Daughterless to promote furrow progr

116 dE2F1 and dE2F2 both heterodimerize with dDP and bind to the promoters of E2F

117 In contrast, MGAT2 did not heterodimerize with DGAT2 when co-expressed in COS-7 cel

118 Gli1 reduced the ability of MyoD to heterodimerize with E12 and bind DNA, providing one mech

119 like motif in BNIP3 abrogates its ability to heterodimerize with E1B-19K and BCL-xL.

120 The members of the Mix family heterodimerize with each other and overexpression of eac

121 lating Bcl-2 family of proteins can homo- or heterodimerize with each other at neutral pH and can als

122 SOHLH1 and SOHLH2 heterodimerize with each other in vivo, as well as homod

123 ASSF1A can each efficiently homodimerize and heterodimerize with each other through their nonhomologo

124 and its related family members TFE3 and TFEB heterodimerize with each other, recognize the same DNA s

125 he FKBP ligand AP1510, or instead induced to heterodimerize with EGFR or HER3 by adding the heterodim

126 However, the isoforms can heterodimerize with ER-beta1 and enhance its transactiva

127 The predilection of p95ErbB2 to heterodimerize with ErbB3 provides an explanation for it

128 Ralpha co-receptors, and have the ability to heterodimerize with full-length RET.

129 (B(2)), not only does the truncated receptor heterodimerize with GABA(B(2)), the association is of su

130 s ability to be secreted, and its ability to heterodimerize with hCG-beta.

131 In vitro, LIN-32 can heterodimerize with HLH-2 and bind to an E-box-containin

132 partner (Shp-1), an orphan receptor that can heterodimerize with Hnf-4alpha and inhibit its transcrip

133 ivative of Pbx1, both retains its ability to heterodimerize with Hox proteins and arrest myeloid diff

134 o dispensable for the ability of E2a-Pbx1 to heterodimerize with Hox proteins and immortalize myelobl

135 d both its binding to DNA and its ability to heterodimerize with Hox proteins.

136 s differentiation and retains its ability to heterodimerize with Hox proteins.

137 as a higher order structure and that it may heterodimerize with its closely related receptor, the lu

138 urpose, we exploited the ability of c-Jun to heterodimerize with its native protein partner, c-Fos, a

139 Since the loss of function S70A mutant can heterodimerize with its partner protein and death effect

140 proteins, including DeltaFosB, are known to heterodimerize with Jun family proteins to create active

141 analysis assessed the effects on genes that heterodimerize with known nuclear receptors.

142 d factor and from putative factors likely to heterodimerize with kreisler.

143 hown to both influence beta(1) integrins and heterodimerize with LAT-2, which confers amino acid tran

144 cular understanding of the ability of RXR to heterodimerize with many nuclear receptors and of the pe

145 HLH-ZIP proteins, Mad1, Mxi1, Mad3 and Mad4, heterodimerize with Max and also repress transcription o

146 proteins, Mad1, Mxi1, Mad3, and Mad4, which heterodimerize with Max and function as transcriptional

147 embers of the Mad family of bHLHZip proteins heterodimerize with Max and function to repress the tran

148 helix leucine zipper (bHLH-LZ) proteins that heterodimerize with Max to bind DNA and thereby influenc

149 Fos proteins heterodimerize with members of the Jun family to form ac

150 alian PAF49 resulted in a protein that could heterodimerize with mouse PAF53.

151 t of mouse liver environment and that it can heterodimerize with mouse retinoid X receptor, and this

152 hich lacks the homeodomain completely, could heterodimerize with NKX2-5 wild type and its cofactors,

153 The preferential ability of RASSF1A to heterodimerize with Nore and thereby associate with Ras-

154 ene promoter as a homodimer, it is unable to heterodimerize with O2.

155 in of MEK5 but do not significantly homo- or heterodimerize with one another in vitro.

156 PDZK1, are expressed in the apical membrane, heterodimerize with one another, and, at least in vitro,

157 nd MEK5 encode Phox/Bem1p (PB1) domains that heterodimerize with one another.

158 mediate a repressor effect because ATF2 can heterodimerize with other bZIP molecules.

159 trated that CXCR4 can form homodimers or can heterodimerize with other G-protein-coupled receptors to

160 HT) receptors were shown to homodimerize and heterodimerize with other GPCRs, although the details an

161 ately influences the availability of Hes6 to heterodimerize with other Her proteins.

162 Csx/Nkx2.5 can heterodimerize with other NK2 homeodomain proteins, Nkx2

163 in the retinoid and, through its ability to heterodimerize with other nuclear hormone receptors, non

164 can be explained by the ability of PIPKH to heterodimerize with other type I PI(4)P 5-kinases.

165 (-) fibronectin isoform does not efficiently heterodimerize with other V-region splice variants of fi

166 can bind DNA as heterodimers, both can also heterodimerize with Pbx proteins.

167 HEC1 and HEC2 heterodimerize with PIF family members.

168 nic fibroblasts, both proteins competitively heterodimerize with pre-B-cell leukemia homeobox-1 (Pbx1

169 it of G protein (Gbeta), previously shown to heterodimerize with RACK1 in vitro.

170 Nuclear hormone receptors that heterodimerize with retinoid X receptor (RXR), such as t

171 he nuclear hormone receptor superfamily that heterodimerize with retinoid X receptor and are activate

172 Retinoic acid receptors (RARs) heterodimerize with retinoid X receptors (RXRs) and bind

173 Furthermore, the double mutant did not heterodimerize with RXR or RAR but was still able to dim

174 However, RARbeta' retains the ability to heterodimerize with RXRalpha and interact with transcrip

175 member of the Bcl-2 family whose ability to heterodimerize with survival proteins such as Bcl-X(L) a

176 protein Bax can homodimerize with itself and heterodimerize with the anti-apoptotic protein Bcl-2, bu

177 NPAS1 and NPAS3 must each heterodimerize with the aryl hydrocarbon receptor nuclea

178 The D-Ns specifically heterodimerize with the B-HLHZip dimerization domain of

179 Like other class II bHLH proteins, Tal1 can heterodimerize with the class I bHLH proteins, such as E

180 nemia, and of APL, in view of its ability to heterodimerize with the FANC-C and PLZF proteins, respec

181 erum response factor (SRF) has been shown to heterodimerize with the myogenic basic helix-loop-helix

182 of neuronal nitric oxide synthase (nNOS) can heterodimerize with the PDZ domains of postsynaptic dens

183 CASTOR1 homodimerizes and can also heterodimerize with the related protein, CASTOR2.

184 on by RXR for the ability of the receptor to heterodimerize with the retinoic acid and the vitamin D

185 uperfamily of nuclear hormone receptors that heterodimerize with the retinoid X receptor and regulate

186 receptors (PPARs) are nuclear receptors that heterodimerize with the retinoid X receptor and then mod

187 ite results in loss of the ability of BAD to heterodimerize with the survival proteins BCL-XL or BCL-

188 espectively) the resulting construct did not heterodimerize with the wild-type HNF4alpha, although it

189 GALLEX experiments, show that these peptides heterodimerize with their complementary TMDs on their re

190 TREK1 and TREK2 can each heterodimerize with TRAAK, but do so less efficiently th

191 ular domain and TM1 could self-associate and heterodimerize with wild type receptors.

192 e NodD1 mutant proteins can homodimerize and heterodimerize with wild-type NodD1.

193 ally inactive cancer-associated PTEN mutants heterodimerize with wild-type PTEN and constrain its pho

194 by maintaining the protein in the cytoplasm, heterodimerized with antiapoptotic Bcl-2 family members.

195 Bif-1 did not directly interact with Bak, it heterodimerized with Bax on mitochondria in intact cells

196 CHOP heterodimerized with C/EBPepsilon and negatively regulat

197 When co-expressed in COS-7 cells, MGAT2 heterodimerized with DGAT1 without treatment with a cros

198 dly acts in a dominant-negative fashion when heterodimerized with ERbeta1 or ERalpha.

199 nuclear transporter-2 (ARNT2/HIF-2beta) also heterodimerized with HIF-1alpha and -2alpha.

200 d sNix, was not targeted to mitochondria but heterodimerized with Nix and protected against Nix-media

201 aining the Ostbeta transmembrane (TM) domain heterodimerized with Ostalpha, although the resulting co

202 g mitochondria, suggesting that BAD is often heterodimerized with other Bcl-2 family proteins in vivo

203 PACT heterodimerized with PKR and activated it in vitro in th

204 ins were tyrosine phosphorylated by JAK2 and heterodimerized with STAT5B except for the WKR mutant, s

205 zed with the bivalent FKBP ligand AP1510 and heterodimerized with the bifunctional FKBP-FRB ligand ra

206 In vivo, Sse1sbd successfully heterodimerized with the yeast cytosolic Hsp70s Ssa and

207 Y297A NRP1, however, heterodimerized with wild-type NRP1 and NRP2 indicating

208 Moreover, Mitf-mc heterodimerizes with a closely related transcription fac

209 This is the first documented case where Max heterodimerizes with a transcription factor that has aff

210 f high mannose form of ABCG8, a protein that heterodimerizes with ABCG5 to control sterol balance.

211 ErbB2 heterodimerizes with and activates the ErbB3 receptor, a

212 1(201-549), has RNA triphosphatase activity, heterodimerizes with and stimulates Ceg1 in vitro, and s

213 unstable and functionally inactive unless it heterodimerizes with another phytochrome.

214 It heterodimerizes with BARD1 to acquire an E3 ubiquitin (U

215 g 4 (ID4) is a helix-loop-helix protein that heterodimerizes with basic helix-loop-helix transcriptio

216 on of the E protein Daughterless (Da), which heterodimerizes with bHLH proteins to activate them, wit

217 xpressed in the suprachiasmatic nucleus that heterodimerizes with BMAL1 and regulates circadian rhyth

218 rs with ErbB3, but not EGFR, while p185ErbB2 heterodimerizes with both EGFR and ErbB3.

219 htly linked to that of BARD1, a protein that heterodimerizes with BRCA1.

220 its procaspase-8, which in turn recruits and heterodimerizes with c-FLIPL/S via a hierarchical bindin

221 We show that c-Fos heterodimerizes with c-Jun to repress transcription of c

222 odes a homeodomain transcription factor that heterodimerizes with Deformed and other homeotic Hox pro

223 Like other bHLH family members, N-Twist heterodimerizes with E protein and binds DNA at a consen

224 A-SREBP-1 heterodimerizes with either B-SREBP-1 or B-SREBP-2, and

225 fied by in a recent issue of Molecular Cell, heterodimerizes with FANCM, binds unwound DNA, and revea

226 GABPalpha binds to DNA, and GABPbeta heterodimerizes with GABPalpha and possesses the ability

227 Instead, IL-4Rbeta heterodimerizes with gammac or IL-13Ralpha' and mediates

228 MOR1D heterodimerizes with gastrin-releasing peptide receptor

229 Because ARNT heterodimerizes with HIFalpha, we assessed whether CUL2

230 E2a-Pbx1 heterodimerizes with Hox but not with Meis/Prep1 protein

231 We show that KSHV vBcl-2 heterodimerizes with human Bcl-2 in a yeast two-hybrid s

232 gene which encodes an Ikaros homologue that heterodimerizes with Ikaros proteins.

233 n 13 receptor alpha1 (IL-13R alpha 1), which heterodimerizes with IL-4R alpha.

234 s, such as the S107 protein of lambda, which heterodimerizes with its cognate holin, S105.

235 and translocates into the nucleus, where it heterodimerizes with its DNA binding partner, the AhR nu

236 The BRCA1 tumor suppressor protein heterodimerizes with its partner protein, BARD1, via the

237 and ovarian susceptibility protein 1 (BRCA1) heterodimerizes with its structural relative, the BRCA1-

238 We reported that the kinin B1 receptor (B1R) heterodimerizes with membrane carboxypeptidase M (CPM),

239 ent death agonist, BAX, forms homodimers and heterodimerizes with multiple antiapoptotic members.

240 dantly interacts with protein substrates and heterodimerizes with MuRF1.

241 xclusion chromatography indicate that DRBP76 heterodimerizes with nuclear factor of activated T cells

242 receptor and glycoprotein 130-like receptor) heterodimerizes with oncostatin M receptor beta to bind

243 equence of their 3' half-sites, and E2a-Pbx1 heterodimerizes with only a subset of Pbx partners, rest

244 The transcription factor CHOP (GADD153) heterodimerizes with other C/EBP family members, especia

245 There is evidence APJ heterodimerizes with other GPCRs; however, the existence

246 Under physiologic levels of expression, HER2 heterodimerizes with other members of the EGF receptor/H

247 The p62 PB1 domain homodimerizes as well as heterodimerizes with other PB1 domains.

248 erizes with p35 to form bioactive IL-12, and heterodimerizes with p19 to comprise the cytokine IL-23.

249 ifically in macrophages and dendritic cells, heterodimerizes with p35 to form bioactive IL-12, and he

250 Human MafG heterodimerizes with p45 NF-E2 and binds DNA with specif

251 PACT heterodimerizes with PKR and activates it by direct prot

252 it did not heterodimerize with BCL-6, which heterodimerizes with PLZF.

253 t1 interacts with Skp1, a small protein that heterodimerizes with proteins containing the F-box motif

254 sociating with the vitamin D receptor, which heterodimerizes with retinoic acid X receptors to bind v

255 T3 binds to thyroid hormone receptor, which heterodimerizes with retinoid X receptor (RXR) and regul

256 through the vitamin D receptor (VDR), which heterodimerizes with retinoid X receptor, gamma (RXRG).

257 eptor-alpha, a nuclear hormone receptor that heterodimerizes with retinoid X receptor, stimulate epid

258 iated by the vitamin D receptor (VDR), which heterodimerizes with retinoid X receptors (RXR).

259 ing and priming is only possible when Munc13 heterodimerizes with RIM via its C2A domain.

260 bunit of core binding factor (CBFbeta), that heterodimerizes with RUNX3, could co-immunoprecipitate r

261 f the vertebrate orphan receptor, BXR, which heterodimerizes with RXR and binds high-affinity DNA sit

262 Nrf2 heterodimerizes with small Maf proteins, but the role of

263 Boo inhibits apoptosis, homodimerizes or heterodimerizes with some death-promoting and -suppressi

264 STR heterodimerizes with STR2, and the resulting transporter

265 T2 either forms homodimers or heterodimerizes with T1 subunits that provide essential

266 a ligand-activated transcription factor that heterodimerizes with the AhR nuclear translocator (ARNT/

267 ins, and the AHR nuclear translocator, which heterodimerizes with the AHR to form a competent transcr

268 The C-alpha(1) sGC variant heterodimerizes with the beta(1) subunit and produces a

269 e most tissue-restricted bHLH factors, HAND2 heterodimerizes with the broadly expressed bHLH factors,

270 CeBNIP3 also efficiently heterodimerizes with the cell death protease proCED-3 by

271 he retinoid X receptor, ultraspiracle (USP), heterodimerizes with the ecdysone receptor (EcR) to form

272 CRLF2 heterodimerizes with the IL7 receptor (IL7R) and signals

273 Although missing a DNA-binding domain, SHP heterodimerizes with the ligand-binding domains of other

274 ress a PB1 domain, and we have shown that it heterodimerizes with the PB1 domain of MEKK2.

275 With regard to the latter, POT1 heterodimerizes with the protein TPP1 to foster binding

276 by binding to a nuclear receptor, EcR, which heterodimerizes with the retinoid X receptor homologue U

277 A common non-DNA binding CBFbeta subunit heterodimerizes with the Runt domain of the Runx protein

278 ent on TCR expression, suggesting that CXCR4 heterodimerizes with the TCR to couple to ZAP-70 and mob

279 A-VBP heterodimerizes with this mutant C/EBP, preventing it fr

280 is a ubiquitin-conjugating enzyme (E2) that heterodimerizes with UEV1A (also known as UBE2V1) and sy

281 ubiquitin-conjugating enzymes, Ubc13, which heterodimerizes with Uev1a, specifically mediates lysine

282 DHR38 also heterodimerizes with USP, and this complex responds to a

283 article shows that MAPKBP1 homodimerizes and heterodimerizes with WDR62.

284 Our results demonstrate that c-RelER heterodimerizes with wild-type c-Rel and forms specific

285 jRXR also heterodimerizes with Xenopus TR beta on a thyroid respon

286 d DNA affinity chromatography prove that Sp1 heterodimerizes with ZBP-89 when bound to the silencer e

287 able of either homodimerizing with itself or heterodimerizing with Bcl-2 and was inactive at promotin

288 ating that Mtd does not promote apoptosis by heterodimerizing with Bcl-2 or Bcl-XL.

289 nique role in the ubiquitination reaction by heterodimerizing with cullin 1 to catalyze ubiquitin pol

290 xtracellular region and signals primarily by heterodimerizing with ErbB2/HER2/Neu.

291 r (SHP) suppresses bile acid biosynthesis by heterodimerizing with FTF.

292 the wild-type (WT) G-CSFR by constitutively heterodimerizing with it.

293 yeast from the lethal effects of Bax without heterodimerizing with it.

294 t stabilization of beta-catenin, which after heterodimerizing with lymphocyte enhancer factor-1/T-cel

295 llular processes by either homodimerizing or heterodimerizing with other basic HLH-PAS proteins.

296 -mediated homodimers but are also capable of heterodimerizing with other C/EBPs in vitro.

297 bits PIF1 target gene expression by directly heterodimerizing with PIF1 and preventing DNA binding an

298 ediates its actions on gene transcription by heterodimerizing with retinoid X receptors (RXRs) on dir

299 cate that each isoform of ARNT is capable of heterodimerizing with the AhRin vitro.

300 pe TBP suppresses these mutants, possibly by heterodimerizing with them.