ライフサイエンスコーパス: two-hybrid assay

1 , and the interaction was confirmed by yeast two-hybrid assay.

2 h FASN and (ii) NS3 interacts with FASN in a two-hybrid assay.

3 e combinations for binary interaction in the two-hybrid assay.

4 that interact with this region using a yeast two-hybrid assay.

5 th V(1) and V(0) subunits were identified by two-hybrid assay.

6 AG1 and other proteins by means of the yeast two-hybrid assay.

7 d is shown to bind Prp43p and Spp382p in the two-hybrid assay.

8 th multiple division proteins in a bacterial two-hybrid assay.

9 o p33 in vitro or in a split-ubiquitin-based two-hybrid assay.

10 lence HMRa and to interact with Orc1BAH in a two-hybrid assay.

11 teracts with both MEI-9 and ERCC1 in a yeast two-hybrid assay.

12 teracting protein(s) in apple, using a yeast two-hybrid assay.

13 d VirB2 and VirB5 were detected in the yeast two-hybrid assay.

14 confirmed that CgtA interacts with SpoT in a two-hybrid assay.

15 of the beta-catenin C terminus in the yeast two-hybrid assay.

16 barley aleurone and physically in the yeast-two-hybrid assay.

17 oprecipitation from HEK293 lysates and yeast two-hybrid assay.

18 lity to interact with Rab4A by using a yeast two-hybrid assay.

19 of yeast vacuolar proteins and in the yeast two-hybrid assay.

20 tigated by coimmunoprecipitation and a yeast two-hybrid assay.

21 teroid receptor coactivator-1 in a mammalian two-hybrid assay.

22 sing pure proteins in solution and the yeast two-hybrid assay.

23 py studies and subsequently confirmed by the two-hybrid assay.

24 modulate its function, we performed a yeast two-hybrid assay.

25 ith myocyte enhancer factor 2 in a mammalian two-hybrid assay.

26 sitive interaction with nucleolin in a yeast two-hybrid assay.

27 two polypeptides can be detected in a yeast two-hybrid assay.

28 cursors was affected, as judged by the yeast two-hybrid assay.

29 ed for interaction with pre-22a in the yeast two-hybrid assay.

30 subunits including Sgf29 and Spt7 in a yeast two-hybrid assay.

31 racting proteins were screened using a yeast two-hybrid assay.

32 at prevent DEPTOR binding to mTOR in a yeast-two-hybrid assay.

33 proteins were identified by a modified yeast two-hybrid assay.

34 high-throughput, array-based, directed yeast two-hybrid assay.

35 ing proteins with GLP-1R by a membrane yeast two-hybrid assay.

36 was further confirmed by Co-IP and mammalian two-hybrid assay.

37 ck proteins, Hsp16.9 and Hsp17.5, in a yeast two-hybrid assay.

38 amK and the two proteins interact in a yeast two-hybrid assay.

39 -interacting proteins using a modified yeast two-hybrid assay.

40 with FeoB or FeoC was detected in the BACTH two-hybrid assay.

41 s DEAD-box helicase/ATPase LOS4 in the yeast two-hybrid assay.

42 e ESCRT-III-related proteins CHMP1A in yeast two hybrid assays.

43 ters, subcellular localization and bacterial two hybrid assays.

44 length protein in vivo, as measured by yeast-two hybrid assays.

45 h other mitochondrial MORF proteins in yeast two hybrid assays.

46 teracted with both Mst12 and Mata-1 in yeast two-hybrid assays.

47 sactivator yeast two-hybrid or reverse yeast two-hybrid assays.

48 s Alix in both immunoprecipitation and yeast-two-hybrid assays.

49 immunoprecipitation, pulldown, and mammalian two-hybrid assays.

50 ) with activity levels measured in bacterial two-hybrid assays.

51 teract with other flavonoid enzymes in yeast two-hybrid assays.

52 with this, AGL61 and AGL80 interact in yeast two-hybrid assays.

53 tween Mst7 and Pmk1 is not observed in yeast two-hybrid assays.

54 an interact with both TTI1 and TTI2 in yeast two-hybrid assays.

55 inity for LEDGF in either pull-down or yeast two-hybrid assays.

56 pitate from the testis and interact in yeast two-hybrid assays.

57 and Hst 5 were tested by pull-down and yeast two-hybrid assays.

58 ts with Ras1, Ras2, Cdc42, and Mgb1 in yeast two-hybrid assays.

59 rotein (GCP)6, as a keratin partner in yeast two-hybrid assays.

60 EBNA2 and EBNA-LP were found with mammalian two-hybrid assays.

61 e pull-down, yeast two-hybrid, and mammalian two-hybrid assays.

62 was shown to ablate the Rad54 interaction in two-hybrid assays.

63 bind the other's cognate effectors in yeast two-hybrid assays.

64 ssary for inter-domain interactions in yeast two-hybrid assays.

65 and Bbp1p and the U2 snRNP protein Prp11p by two-hybrid assays.

66 the Rev nuclear export signal (NES) in yeast two-hybrid assays.

67 olishes this interaction, as determined with two-hybrid assays.

68 sing co-immunoprecipitation and in mammalian two-hybrid assays.

69 ned their impact on pRBR binding using yeast two-hybrid assays.

70 lutathione S-transferase pull-down and yeast two-hybrid assays.

71 cts with MBD2 and MBD3 in vitro and in yeast two-hybrid assays.

72 eciprocal coprecipitation experiments and by two-hybrid assays.

73 ptide aptamers for further analysis in yeast two-hybrid assays.

74 with UNC-116 kinesin-1 heavy chain in yeast two-hybrid assays.

75 g relatively little affected by ABA in yeast two-hybrid assays.

76 ies with coimmunoprecipitation and mammalian two-hybrid assays.

77 Using a yeast two-hybrid assay, a protein inhibitor of activated STAT1

78 cted between PMK1 and MST7 or MST11 in yeast two-hybrid assays, a homolog of yeast STE50 in M. grisea

79 that abolished the interaction in the yeast two-hybrid assay also abolished capsid assembly in insec

80 PYL6 and MYC2 interact in yeast two hybrid assays and the interaction is enhanced in the

81 Using the yeast two-hybrid assay and a co-immunoprecipitation assay, we

82 Bacterial two-hybrid assay and accumulation of Gp0.6 only in MreB-

83 Using the yeast two-hybrid assay and affinity chromatography, we demonst

84 high-throughput techniques such as the yeast two-hybrid assay and affinity purification, as well as f

85 Srs2 interacts with Rad51 in the yeast two-hybrid assay and also in vitro.

86 A1 physically interacts with HFR1 in a yeast two-hybrid assay and an in vitro co-immunoprecipitation

87 he globular tail which was verified by yeast two-hybrid assay and by in vivo bimolecular fluorescence

88 Employing yeast two-hybrid assay and coimmunoprecipitation followed by m

89 ally interacts with NLBD using the mammalian two-hybrid assay and coimmunoprecipitation studies in MN

90 anion exchanger 1 (kAE1), detected by yeast two-hybrid assay and confirmed by immunoprecipitation an

91 A mammalian two-hybrid assay and confocal microscopy were used to de

92 By yeast two-hybrid assay and ELISAs using purified proteins, UNC

93 ptic clustering domain, we performed a yeast two-hybrid assay and found that this stargazin domain bi

94 We performed a yeast two-hybrid assay and identified hematopoietically expres

95 GE cytoplasmic domain as "bait" in the yeast two-hybrid assay and identified the formin homology (FH1

96 interact with Hsp90Ecin vivo in a bacterial two-hybrid assay and in vitro in a bio-layer interferome

97 e in ClpB interaction in vivo in a bacterial two-hybrid assay and in vitro in a fluorescence anisotro

98 ns also directly interact in vivo in a yeast two-hybrid assay and in vitro through ammonium sulfate c

99 s transcription factor prey library by yeast two-hybrid assay and isolated six class I members of the

100 Ialpha was therefore used as bait in a yeast two-hybrid assay and microtubule affinity regulating kin

101 Here we show, by using the yeast two-hybrid assay and the glutathione S-transferase pull-

102 Despite the routine use of the two-hybrid assay and the potential of three-hybrid syste

103 Both proteins interacted with DDB1 in yeast two-hybrid assays and associated with DDB1 and CUL4 in v

104 ABD1 directly interacts with ABI5 in yeast two-hybrid assays and associates with ABI5 in vivo by co

105 Erm and TTF-1 were demonstrated by mammalian two-hybrid assays and by co-immunoprecipitation assays.

106 of the p12 subunit were determined by yeast two-hybrid assays and by pulldown assays.

107 By yeast-two-hybrid assays and chromatin immunoprecipitation we d

108 Yeast two-hybrid assays and co-fractionation studies using rec

109 Two-hybrid assays and coimmunoprecipitation analyses dem

110 Yeast two-hybrid assays and coimmunoprecipitation experiments

111 and TMC1 or TMC2 was observed in both yeast two-hybrid assays and coimmunoprecipitation experiments.

112 o the blue-light photoreceptor FKF1 in yeast two-hybrid assays and delays flowering in Arabidopsis wh

113 Yeast two-hybrid assays and fluorescence resonance energy tran

114 r the interaction of CRY2 with COP1 in yeast two-hybrid assays and in planta Mutations in the VP moti

115 with beta-catenin was confirmed using yeast two-hybrid assays and in vitro synthesized proteins.

116 fects in vivo, ARC3 interacted with FtsZ2 in two-hybrid assays and inhibited FtsZ2 assembly in a hete

117 Mammalian two-hybrid assays and pull-down experiments demonstrated

118 Yeast two-hybrid assays and studies in HEK293 cells and primar

119 AcrB, in the absence of both AcrA and TolC, two-hybrid assays and suppressor mutations indicate that

120 reement with these observations, using yeast two-hybrid assays and TAP-tagged protein pull-down analy

121 (I)48 was initially examined using the yeast two-hybrid assay, and a TBP-binding domain was identifie

122 eric interactions were observed in the yeast two-hybrid assay, and Gpr4 was shown to physically inter

123 p, a subunit of mRNA decapping enzyme in the two-hybrid assay, and is enriched in cytoplasmic P bodie

124 h deletion analysis, co-immunoprecipitation, two-hybrid assay, and pulldown assays with expressed pro

125 cessary for the interaction with FeoB in the two-hybrid assay, and when either of these amino acids w

126 Light-scattering studies, yeast two-hybrid assays, and analytical ultracentrifugation me

127 ified as Oas1b interaction partners in yeast two-hybrid assays, and both in vitro-transcribed/transla

128 tion of pull-downs, mass spectrometry, yeast two-hybrid assays, and chemical genomics, we demonstrate

129 le LIM protein) did not interact with WT1 in two-hybrid assays, and WTIP did not interact with an unr

130 based on yeast two-hybrid screens, mammalian two-hybrid assays, and/or coimmunoprecipitation assays.

131 h the CAR ligand-binding domain in mammalian two-hybrid assays; and 5) disrupts CAR binding to the pr

132 reliminary experiments involving a bacterial two-hybrid assay are presented that corroborate the exis

133 ing yeast Smc5/6 complex employing the yeast two-hybrid assay as well as in vitro biochemical approac

134 ted using the GST pull-down assay, the yeast two-hybrid assay, as well as by coimmunoprecipitation.

135 Surprisingly, yeast two-hybrid assays, bimolecular fluorescence complementat

136 ructure was corroborated using the bacterial two-hybrid assay, biochemical characterization of the pu

137 unoprecipitation in vitro and in vivo, yeast two-hybrid assay, bioluminescence resonance energy trans

138 Based on bacterial two-hybrid assays, CelR homodimerizes but does not inter

139 TIP clone, which interacted with WTIP in the two-hybrid assay, co-localized with WT1 in nuclei, co-pr

140 Furthermore, mammalian two-hybrid assays, coimmunoprecipitation analyses, and b

141 The two-hybrid assay confirmed these findings and revealed t

142 ions with core exocyst subunits in the yeast two-hybrid assay, cytoplasmic localization, and genetic

143 We report two-hybrid assay data that support this model, and resul

144 irect association between Nab2 and Gfd1, and two-hybrid assays delineated Gfd1 binding to the N-termi

145 A split-ubiquitin membrane yeast two-hybrid assay demonstrated specific interactions of t

146 Finally, a yeast two-hybrid assay demonstrated that SCP-2 directly intera

147 A yeast two-hybrid assay demonstrated that the last 22 amino aci

148 Functional analyses by the yeast two-hybrid assay demonstrated that the p.140 delN mutati

149 Mammalian two-hybrid assays demonstrated that PB selectively incre

150 Yeast two-hybrid assays detect interactions between the basola

151 In a bacterial two-hybrid assay, DnaK interacts with ClpB and with chim

152 that would occur with the traditional yeast two-hybrid assay due to the transactivating properties o

153 Yeast two-hybrid assays established a direct interaction of Ce

154 Yeast GAL4 two-hybrid assays established that both proteins contain

155 In yeast two-hybrid assays, FgMcm1 interacted with Mat1-1-1 and F

156 Here, using yeast two-hybrid assays followed by biochemical binding experi

157 were screened for function both in the yeast two-hybrid assay for interaction with VP19C and in a gen

158 Results from immunoprecipitation and a two-hybrid assay further indicated that Fliih directly i

159 Mammalian two-hybrid assay further indicates that the amino acids

160 ating enzyme, interacts with NOPO in a yeast two-hybrid assay; furthermore, ben-derived embryos arres

161 In two-hybrid assays, Ggamma13 interacted specifically with

162 esin light chain is demonstrated via a yeast two-hybrid assay, glutathione S-transferase pull down, a

163 The yeast two-hybrid assay has proven to be a powerful method to d

164 tion of protein-protein interactions through two-hybrid assays has revolutionized our understanding o

165 By using the yeast two-hybrid assay, here we identified HtrA2/Omi, a stress

166 genetic approaches exemplified by the yeast two-hybrid assay; however, neither assay works well for

167 Site-directed mutagenesis and yeast-two hybrid assays identified DnaA and DnaN binding sites

168 A yeast two-hybrid assay identified a novel, WT1-interacting pro

169 The yeast two-hybrid assay identified that proteasome subunit alph

170 pull-down, co-immunoprecipitation, and yeast two-hybrid assays identified a specific interaction betw

171 Yeast two-hybrid assays identified ETTIN (ETT, or AUXIN RESPON

172 Yeast two-hybrid assays identified the S10 region of the K(+)

173 xococcus xanthus was identified from a yeast two-hybrid assay in which MglA was used as bait.

174 By a combination of yeast-two hybrid assay, in vitro binding, and coimmunoprecipit

175 Using a combination of quantitative yeast two-hybrid assays, in planta co-localization studies, fl

176 Two-hybrid assays indicate that Ers1 also directly inter

177 Yeast two-hybrid assays indicate that these newly characterize

178 In vitro pull-down and yeast two-hybrid assays indicate that these splice variants ha

179 Yeast two-hybrid assay indicated that the PDH45 protein intera

180 Bacterial two-hybrid assays indicated strong interactions of M. tu

181 Analysis of mutated proteins in yeast two-hybrid assays indicated that mutations that inactiva

182 Co-immunoprecipitation and two-hybrid assays indicated that RARgamma interacts with

183 cular fluorescence complementation and yeast-two-hybrid assays indicated that the IDR3 domain does no

184 Consistent with these findings, two-hybrid assays indicated that the Sir1 N terminus cou

185 with P. blakesleeanus Ras homologs in yeast two-hybrid assays, indicating that MadC is a regulator o

186 amily member periplakin, identified in yeast two-hybrid assays, interacted with a membrane-proximal d

187 Yeast two-hybrid assays involving seven ABA receptor proteins

188 on between Cdc13 and Est1, as monitored by a two-hybrid assay, is dependent on S255 but Tel1-independ

189 s) in human cells, termed mammalian-membrane two-hybrid assay (MaMTH).

190 In yeast two-hybrid assays, MAS2 interacted with splicing and rib

191 r each Chlamydomonas FDX; (b) pairwise yeast two-hybrid assays measuring FDX interactions with protei

192 Here, a yeast two-hybrid assay of LOX-PP-interacting proteins identifi

193 tinal insulin receptor (IRbeta) and used the two-hybrid assay of protein-protein interaction in the y

194 According to a yeast two-hybrid assay, ORRM1 interacts selectively with penta

195 In yeast-two hybrid assays, ORRM3 interacts with RIP1, ORRM2 and

196 The remarkable impact of two-hybrid assay platforms derives from their speed, sim

197 , a cDNA library was screened with the yeast two-hybrid assay, resulting in the identification of hea

198 Yeast two-hybrid assay results indicated that MKT1 directly in

199 from reporter transactivation and mammalian two-hybrid assays reveal that DEHP activates CAR2 at low

200 Yeast two-hybrid assays reveal that RgsD can interact with the

201 A yeast two-hybrid assay revealed a p204-cytoplasmic Ras protein

202 A yeast two-hybrid assay revealed an interaction between amino a

203 ted from a high-throughput screen of a yeast two-hybrid assay revealed interactions between sigma(54)

204 rminus of the alpha1-subunit using the yeast two-hybrid assay revealed that a distal C-terminal pepti

205 Yeast two-hybrid assay revealed that the N-terminal region of

206 Yeast two-hybrid assays revealed four-and-a-half LIM domain (F

207 Yeast two-hybrid assays revealed that GPC3 interacts with CD81

208 co-immunoprecipitation, pull-down, and yeast two-hybrid assays revealed that mXinalpha directly inter

209 Yeast two-hybrid assays revealed the formation of a ternary co

210 In yeast (Saccharomyces cerevisiae) two-hybrid assays, rice CBLs interact with the kinase pa

211 30 as an ARNT-interacting protein in a yeast two-hybrid assay screen.

212 Yeast two-hybrid assays show that FCL1 interacts with a subset

213 Furthermore, our yeast two-hybrid assays show that MoVps17 and MoVps5 can inter

214 Furthermore, results of the mammalian two-hybrid assay showed that cyclin-dependent kinase 3 (

215 Yeast two-hybrid assays showed that an N-terminal region of GR

216 Co-immunoprecipitation and mammalian two-hybrid assays showed that retinoschisin and the N-te

217 Additional yeast two-hybrid assays showed that the Gbeta(1) subunit also

218 immunoprecipitation, Far-Western assays, and two-hybrid assays showed that TIN2, but not POT1 or PIP1

219 tion between these two proteins in the yeast two-hybrid assay similarly failed to complement the grow

220 In mammalian two hybrid assays, Smad factors recruited the hybrid gen

221 In yeast two-hybrid assays, stronger interactions between DRaf's

222 DLF1 in the yeast (Saccharomyces cerevisiae) two-hybrid assay strongly supports that ZCN8 plays an or

223 -seq and proteomics data together with yeast two-hybrid assays suggest that MS23 along with MS32, bHL

224 n experiments in transfected cells and yeast two-hybrid assays suggest that the C terminus of DFz2 in

225 Yeast two-hybrid assays suggested an interaction of Psb27 with

226 Yeast two-hybrid assays suggested that GID1a has the highest a

227 ocardin and SRF as determined by a mammalian two-hybrid assay, suggesting that Ang II-induced increas

228 fatty acid synthase II (FAS-II) in bacterial two-hybrid assays, suggesting essentiality may be linked

229 teracts with the other nucleoporins in yeast two-hybrid assays, suggesting that the proteins affect s

230 using a high-throughput version of the yeast two-hybrid assay that circumvents the difficulties in ex

231 We also show by yeast two-hybrid assay that MEIS proteins can interact with an

232 Bacterial two-hybrid assays that detected interaction between the

233 lyacrylamide gel electrophoresis and a yeast two-hybrid assay, the binding of copper was found to be

234 In a yeast two-hybrid assay, the thioredoxin-like domain of LTO1 in

235 In two-hybrid assays, the interaction of sigma(70) with eit

236 Here we show that in yeast two-hybrid assays, the non-EAR protein, Related to ABI3/

237 In direct two-hybrid assays, this portion of MAN1 bound to Smad2 a

238 n cross-linking protein filamin in the yeast two-hybrid assay through their highly conserved amino-te

239 otein fragment complement assay, and a yeast two-hybrid assay to analyze the protein-protein interact

240 ssisted RNA-RNA-binding protein [RBP] yeast) two-hybrid assay to assess binding of our CEH mutant RNA

241 of NUP98-HOXA9, we used a cytoplasmic yeast two-hybrid assay to avoid the nonspecific trans-activati

242 addressed this question using the bacterial two-hybrid assay to determine how the initiation protein

243 We used the yeast two-hybrid assay to determine that XPF interacts with th

244 In this study, we used a bacterial two-hybrid assay to identify cellular proteins that inte

245 In the current studies, we used a yeast two-hybrid assay to identify ten amino acids in Axin tha

246 tially screened for interaction in the yeast two-hybrid assay to identify the domains important for t

247 Here, we have used the yeast two-hybrid assay to isolate molecular partners of harmon

248 In a mammalian two-hybrid assay to measure PR agonist-induced interacti

249 We used a yeast two-hybrid assay to screen for interactors of the golgin

250 on with other proteins, we performed a yeast two-hybrid assay to search for novel interactors of AnxA

251 Initial difficulties in getting the two-hybrid assay to work with full-length Oas1b led to t

252 rt that CEA binds TRAIL-R2 (DR5) directly in two-hybrid assays to decrease anoikis through the extrin

253 ass spectrometry, split-luciferase and yeast-two-hybrid assays to generate a single reliability score

254 we used membrane-based split ubiquitin yeast two-hybrid assays to identify novel GLP1R interactors in

255 Here, we carry out directional yeast two-hybrid assays to identify the interactions between t

256 Furthermore, we used yeast two-hybrid assays to show that DYT1 forms homodimers and

257 Here, we utilized insect two-hybrid assays to show that FTZ-F1 interacts with two

258 and thermal shift assays, and membrane yeast two-hybrid assays, to define the mechanism mediating thi

259 d a human prostate cDNA library by the yeast two-hybrid assay using full-length MDM2 protein as the b

260 A yeast two-hybrid assay using IIp45 as bait identified HDAC6 pr

261 reened a kidney cDNA library through a yeast two-hybrid assay using NKCC2 C terminus as bait.

262 n the N-terminus of XPF by the reverse yeast two-hybrid assay using randomly mutagenized XPF.

263 Binary two-hybrid assays using DNA encoding this isoform as bai

264 We searched for such proteins by yeast two-hybrid assay, using GARP as a bait to screen a human

265 Here, a yeast two-hybrid assay was performed to identify FGFR1-binding

266 A yeast two-hybrid assay was used to identify putative OAT3-asso

267 The yeast two-hybrid assay was used to test for interactions betwe

268 interactions with corepressors in mammalian two-hybrid assays was unexpected.

269 By using the yeast two-hybrid assay we found that the ESCP tyrosine-based m

270 eptor-associated factor 2 (TRAF2) in a yeast two-hybrid assay, we demonstrate that Na interacts with

271 Using a modified version of the mammalian two-hybrid assay, we demonstrate that the interaction st

272 Utilizing a yeast two-hybrid assay, we discovered several novel interactor

273 Using an E. coli two-hybrid assay, we do not detect an interaction betwee

274 Using the yeast two-hybrid assay, we found an interaction between CaM an

275 Using a yeast two-hybrid assay, we found that Prox1 strongly and speci

276 Using the above-mentioned two-hybrid assay, we found that zebrafish Tmc1 and Tmc2a

277 Using the yeast two-hybrid assay, we have identified ribosomal S6 kinase

278 Using the yeast two-hybrid assay, we have now identified the histone ace

279 Using a two-hybrid assay, we have shown that RocS1 interacts wit

280 Using a two-hybrid assay, we present evidence that FliX regulate

281 ntaining plastidial proteins in binary yeast two-hybrid assays, we also gained insights into the spec

282 ion of cross-linking/affinity pull-downs and two-hybrid assays, we determined that TraK self-associat

283 Using yeast two-hybrid assays, we determined the interactions among

284 Using yeast two-hybrid assays, we have identified a Rev7-binding sur

285 By yeast two-hybrid assays, we have now demonstrated that Myosin

286 combination of immunoprecipitation and yeast two-hybrid assays, we identified a series of protein-pro

287 Using yeast two-hybrid assays, we identified Spermidine Synthase2 (S

288 By using yeast two-hybrid assays, we identified the carboxyl-terminal r

289 ons coupled with mass spectrometry and yeast two-hybrid assays, we show the Saccharomyces cerevisiae

290 Yeast-two hybrid assays were used to identify two new and inde

291 All interactions identified by yeast two-hybrid assays were confirmed by in vitro binding ass

292 Yeast two-hybrid assays were employed to identify important in

293 Drosophila S2 cell two-hybrid assays were used to describe a novel homotypi

294 Yeast two-hybrid assays were used to identify ABA signaling co

295 Yeast two-hybrid assays were used to identify rice proteins in

296 und state failed to bind to AvrL567 in yeast two-hybrid assays, while binding was detected to the sig

297 moylation sites, and it interacts in a yeast two-hybrid assay with the UBC-9 and GEI-17 components of

298 All four proteins interacted in yeast two-hybrid assays with phragmoplastin, and showed differ

299 hb-21 and ESE1 are able to interact in yeast two-hybrid assays with the ABA responsive element bindin

300 In yeast two-hybrid assays ZYX-1 interacts with several known den