ライフサイエンスコーパス: interactor

1 ly receptor transmembrane activator and CAML interactor.

2 found that U1 snRNP is the most abundant FUS interactor.

3 dulation of CRISPR-Cas activity by a protein interactor.

4 or and calcium-modulating cyclophilin ligand interactor.

5 dentified tumor suppressor p27 as a PCTAIRE1 interactor.

6 nine kinase [8], as a putative novel anillin interactor.

7 t chain-related protein-1 (KLCR1) as an IQD1 interactor.

8 mbrane scaffolding protein, CASK, as a FRMD7 interactor.

9 L3MBTL3 (also known as MBT1) as a novel RBPJ interactor.

10 oprocessor component DROSHA as a novel DNMT1-interactor.

11 d DNA (ssDNA)-binding protein, as a novel G4 interactor.

12 th SR34 as bait and discovered SR45 as a new interactor.

13 ctions of PLEKHA7, we looked for new PLEKHA7 interactors.

14 echanism for bringing together their diverse interactors.

15 nexplored, as well as the discovery of novel interactors.

16 creened a siRNA library targeting known CFTR interactors.

17 ral sclerosis perturb a defined community of interactors.

18 unctions, likely via recruitment of specific interactors.

19 to be important for binding to many of these interactors.

20 nt for either PKA or PKG and their secondary interactors.

21 nvironments containing a myriad of potential interactors.

22 des to isolate each kinase and its secondary interactors.

23 damaged DNA (translesion synthesis) as TRIP interactors.

24 oup-level traits are neither replicators nor interactors.

25 stinct diseases, identified disease-specific interactors.

26 e mutations identified 50 disease-associated interactors.

27 raction with FD or 14-3-3 proteins, known FT interactors.

28 uency of both mutation genes and their close interactors.

29 t together with some of the newly identified interactors.

30 brid screen to identify potential substrates/interactors.

31 me, identifying 37 high-confidence candidate interactors.

32 eled cell lysates to quantitatively identify interactors.

33 ously identified to be in vivo genetic CLASP interactors.

34 sically linked to each other in vivo are LBC interactors.

35 subsequently validated many putative zDHHC17 interactors.

36 ating RNAPII, while P-TEFb was not among the interactors.

37 roteins, here we sought to identify new PP1c interactors.

38 affimer" reagents as high-affinity ubiquitin interactors.

39 independent experiments, to filter bona fide interactors.

40 pUL135 interacted directly with abl interactor 1 (ABI1) and ABI2 to recruit the WAVE2 regula

41 Abl interactor 1 (Abi1) is a scaffold protein that plays a c

42 the association of the adapter protein c-Abl interactor 1 (Abi1) with neuronal Wiskott-Aldrich syndro

43 identified mitofusin2 (MFN2) and Rab and Ras Interactor 1 (RIN1) as new Smad2 binding partners requir

44 Ras and Rab interactor 1 (RIN1) is predominantly expressed in the ne

45 anonical synaptic vesicle SNAREs Vps10p-tail-interactor-1a (vti1a) and vesicle-associated membrane pr

46 PPIs included both previously characterized interactors, along with a large subset of interactors th

47 Further, many interactors also had a suggested role in cellular redox

48 tantly, we determined that a subset of these interactors also modified hLRRK2(I2020T) induced dopamin

49 ctivated C-kinase 1, GNB2L1) as a novel ATG5 interactor and an autophagy protein.

50 a tomato UspA, is, to our knowledge, a novel interactor and phosphorylation target of a member of the

51 re mimicked by downregulation of OSBP, a VAP interactor and PI4P transporter that participates in VAP

52 -S100A10 protein complex as a novel Munc13-4 interactor and show that AnxA2-S100A10 participates in r

53 Here we show that EZH2 is a novel interactor and substrate of the SCF E3 ubiquitin ligase

54 fied the tumor suppressor Pdcd4 as IBtkalpha interactor and ubiquitylation substrate of CRL3(IBTK) fo

55 tified several proteins including known BAK1 interactors and a previously uncharacterized LRR-RLP tha

56 f G-protein signaling (RGS) proteins are key interactors and critical modulators of the Galpha protei

57 sought to identify additional WW domain host interactors and demonstrate that the PPxY L domain motif

58 identify 638 individual high-confidence CFTR interactors and discover a F508 deletion-specific intera

59 ckdowns of sixteen previously identified Tat interactors and found that a novel E3 ligase, PJA2, ubiq

60 In this study, we investigated Pih1 interactors and identified a specific interaction betwee

61 ge analysis revealed that although some HP1a interactors and regulators are broadly distributed withi

62 ority of the over four hundred putative HP1a interactors and regulators identified were previously un

63 performed a proteomic screen for novel HEG1 interactors and report that HEG1 binds directly to Rasip

64 a systematic map of disease-relevant lamin A interactors and suggest loss of tissue-specific lamin A

65 rane activator and calcium modulating ligand interactor, and B cell maturation antigen, at a stoichio

66 Ag (BCMA), transmembrane activator and CAML interactor, and BAFF receptor, in sorted human immune ce

67 cription, longer canonical transcripts, more interactors, and a higher number and more types of post-

68 on, we purified Drosophila melanogaster HP1a interactors, and performed a genome-wide RNAi screen to

69 Indeed, most GR/PR interactors are components of membrane-less organelles s

70 These interactors are selected and optimized using the Random

71 Trx-like proteins, whose functions and redox interactors are unknown.

72 itially identified in DNA damage repair, ATM-interactor (ATMIN) further functions as a transcriptiona

73 Recently, the ATM interactor (ATMIN) was identified as critical for replic

74 Importantly, as a GLP1R interactor, ATP6ap2 was required for GLP1-induced Ca(2+)

75 We further show that one interactor, ATP6ap2, plays a novel dual role in beta cel

76 ork are discussed, with the most significant interactors being responses to hypoxia, regulation of ce

77 ence) of hnf4 and its predicted gene pathway interactors beta-catenin and hh Interestingly, the model

78 Lastly, we establish that regulation of interactor binding by ubiquitylation occurs more general

79 bonucleoprotein (hnRNP)-A2/B1 and hnRNP-R as interactors binding directly to the ASCL1 mRNA 5'- and 3

80 the affinity of RAB11B to a series of binary interactors, both effectors and guanine nucleotide excha

81 We refined our list of interactors by comparing the interactomes using quantita

82 ort, we identified additional host WW-domain interactors by screening for potential interactions betw

83 , providing high-certainty identification of interactors by their direct access during cycling infect

84 We identify and validate two strong interactors, C10orf12 and C17orf96, which display enrich

85 NonO and its interactors can activate rhodopsin promoter in HEK293 ce

86 g properties of each SH3 domain to the known interactor Casitas B-lineage lymphoma protein (c-CBL), c

87 ding to Ccm2l and its previously established interactors Ccm2 and Heg.

88 kinase1 (BAK1) and several other known BRI1 interactors coimmunoprecipitated with BRL3, no evidence

89 The analysis reveals several novel interactors confirmed by their localization to microvill

90 , we show that Dyrk2 kinase, a reported UBR5 interactor, cooperates with UBR5 in mediating MOAP-1 ubi

91 A strong novel interactor, dADD1 (Drosophila ADD1) (CG8290), is highly

92 Inhibiting two or three interactors destabilizes silencing.

93 sues and reproducibly retrieved at least one interactor for 81.4 % of the baits screened for in callu

94 focus on well-conserved yet uncharacterized interactors for further study.

95 y, our TAP protocol enables the discovery of interactors for low abundance proteins in rice and opens

96 ndidate synaptic cell-adhesion molecules, as interactors for the lectin-like domain of latrophilins.

97 deficient in several of the newly identified interactors for their capacity to secrete CCL22 in respo

98 two ALB proteins may engage similar sets of interactors for their specific functions.

99 Here we identify novel TDP-43 protein interactors found in a yeast two-hybrid screen using an

100 homologues of human fused toes (FTS) and its interactor FTS- and Hook-interacting protein.

101 metry generated a roster of disease-specific interactors functionally linked to lipid metabolism.

102 c protein partners were identified, with the interactors functioning mainly in DNA maintenance and mi

103 oplasmic domain (NCD), but not the known NCD interactor GIPC1.

104 Although many LC8-interactors have roles in signaling cascades, LC8's role

105 Identification of this novel eVP40 interactor highlights the functional interplay between c

106 aps with the binding site of known LEDGF/p75 interactors-HIV-1 integrase, PogZ, and JPO2.

107 x protein CHD4, and the repressive chromatin interactor HP1BP3, by co-immunoprecipitation combined wi

108 regulated together with other specific HSPB8 interactors (HSPB2 and HSPB3).

109 e the downstream analysis of >2000 potential interactors identified in high-throughput experiments.

110 2-dependent, and proteomic analysis for Rac2 interactors identified the 226 kD protein Myh9.

111 A targeted screen for PI interactors identified the PHD finger of TAF3, a TATA bo

112 -specific Lyn substrate-1) is a cytoskeletal interactor in the B-cell receptor (BCR) signaling pathwa

113 article argues that whole groups can act as interactors in an evolutionary process.

114 st two-hybrid assays to identify novel GLP1R interactors in both mouse and human islets.

115 ass spectrometry to identify HIV RNA-protein interactors in HIV-1 infected cells.

116 ity to detect proximal proteins and putative interactors in intact tissues, and to quantify changes c

117 ealed several TCR adaptor proteins acting as interactors in stimulated cells, of which LAT and Trat1

118 Specific interactors include HnrnpK, which participates in Xist-m

119 The interactors include protein complexes involved in chromo

120 The 215 amk2-specific negative interactors included genes functioning in chromatin sile

121 The 120 gsk3-specific negative interactors included genes functioning in translation an

122 Ki-67 interactors included proteins involved in nucleolar proc

123 The inventory of identified BetaM interactors includes lamina-associated protein LAP-1, my

124 analysis of four ncRNAs captures key protein interactors, including a U1-specific link to the 3' RNA

125 lar RNAs (snoRNAs) were identified as coilin interactors, including numerous unannotated mouse and hu

126 suppression, since the expression of several interactors, including some of the above-noted transcrip

127 coimmunoprecipitates with several key Atg11 interactors, including the Atg1/Unc-51-like autophagy ac

128 We discover multiple classes of interactors-including cohesins, condensins, topoisomeras

129 thus able to discover a number of novel Rif1 interactors, involved in chromatin metabolism and phosph

130 e assembly of complexes comprising the Cdc42-interactor IQGAP1, the Rho GTPase-activating protein ARH

131 The most abundant KCC2 interactor is a neuronal endocytic regulatory protein te

132 One interactor is MAK-1, C. elegans orthologue of MAPKAP kin

133 A list of non-specific and false positive interactors is presented, based on re-occurrence over mo

134 orted that expression of NMI (N-myc and STAT interactor) is compromised in invasive breast cancers.

135 Although OCRL, a direct clathrin interactor, is recruited to late-stage clathrin-coated p

136 Although Xist attracts some interactors, it repels architectural factors.

137 identified a novel and functional EBOV VP40 interactor, ITCH, that regulates VP40-mediated egress.

138 y described functions of several known CLASP interactors, its multiparametric resolution reveals more

139 IM-actin-MKL1 sequence, we identify the MKL1 interactor Jumonji domain demethylase 1A (JMJD1A) as a n

140 aging, we identified the Kif1B motor and its interactor Kif1 binding protein (KBP) as critical for SC

141 conformation, which prevents its binding to interactors known to be involved in membrane fission and

142 A proteomic analysis of DOUBLETIME interactors led to the identification of an unstudied pr

143 and identity of component species, as strong interactors like foundation species have the potential t

144 We suggest that PrP(C) and its interactor, LR/37/67 kDa, could be potential therapeutic

145 ndently of TORC1 regulation through the Gtr1 interactor Ltv1.

146 We show that one of these interactors, matrin-3 (matr3), localizes to mRNA process

147 e possibility that targeting NRP1 or its NCD interactors may be a useful therapeutic strategy in neov

148 ural response appeared not influenced in the interactor mutants katA and acnB in steady-state behavio

149 Phenotyping of 124 Arabidopsis effector-interactor mutants revealed a correlation between intras

150 bind to either the LIM cofactor nuclear LIM interactor (NLI) or another LIM homeodomain factor, Isl1

151 Based on this approach, we identified N-Myc interactor (NMI) as an IRE1alpha-interacting/modulator p

152 e have observed that the expression of N-myc interactor (NMI) decreases significantly during progress

153 Thus, specific interactors, not merely oligomeric structure, drive path

154 giectasia mutated) phosphorylation-dependent interactor of 53BP1 and show that absence of Rif1 result

155 ALG-2 interacting protein X (Alix/AIP1), an interactor of apoptosis-linked gene protein 2 (ALG-2).

156 the tumour suppressor protein Niam (Nuclear Interactor of ARF and Mdm2).

157 identify a protein named TSSC1 as a specific interactor of both GARP and EARP and as a novel componen

158 d heat shock protein 70 (HSP70) as a protein interactor of both wild type and Crohn mutant NOD2.

159 ntified the RING finger protein RNF181 as an interactor of CARD11, a key signaling scaffold in the an

160 olvement of the RHO of Plants (ROP) effector INTERACTOR of CONSTITUTIVELY active ROP 1 (ICR1) in regu

161 5' RNA degradation machinery, as a physical interactor of CP190-dependent chromatin insulator comple

162 een, we show here that N-cadherin is a novel interactor of Fbxo45.

163 ting protein 2 (Cyfip2) was identified as an interactor of FMRP, and its mRNA is a highly ranked FMRP

164 Subsequently, we identified Sp110 as a novel interactor of HBx and found this association to be essen

165 Here, we identified TRAP1 as an interactor of HTRA2 using an unbiased mass spectrometry

166 One particular novel interactor of interest is the glycerol transporter Fps1p

167 By analogy to the related Novel Interactor of JAZ (NINJA) protein, it was suggested that

168 All three lines harbored mutations in Novel Interactor of JAZ (NINJA), which encodes part of a repre

169 or interactome, we identify PAXX as a direct interactor of Ku.

170 at NS5A protein represents the most probable interactor of M3R or that this viral protein could elici

171 d kinetochore-associated protein, as a novel interactor of NuMA.

172 a screening assay, we identified CRKII as an interactor of oncogenic EGFR(L858R) and showed that CRKI

173 entified Matrin 3 (MATR3) as a novel protein interactor of PABPN1.

174 main-containing protein 11 (PDZD11) as a new interactor of PLEKHA7 by yeast two-hybrid screening and

175 dentified cortactin as a novel substrate and interactor of proline-rich tyrosine kinase 2 (Pyk2).

176 ET) we identified alpha-synuclein as a novel interactor of PSEN1 in wild-type mouse brain tissue.

177 P11), a known DDR-component, as a functional interactor of RNF4.

178 he signaling protein TIF1gamma as a specific interactor of SnoN1 but not the closely related isoform

179 it tethering complex and GEF for RAB1, as an interactor of TBC1D14.

180 ow tract development, and is a known genetic interactor of Tbx1.

181 on experiments established DGCR8 as a direct interactor of Tcf7l1 mRNA, a core component of the pluri

182 We identify a novel substoichiometric interactor of the complex, transcription factor ZNF131,

183 Cactin was originally identified as an interactor of the Drosophila IkappaB factor Cactus and s

184 P and Naa15 as well as Naa50 (NatE), another interactor of the NatA complex.

185 RGO-1 pathway, including eri-12, encoding an interactor of the RNAi-defective protein RDE-10, and ntl

186 alling and identify Axin1 as a novel protein interactor of the widely-expressed gamma-Pcdh-C3 isoform

187 like (Mid1ip1l), previously identified as an interactor of the X-linked Opitz G/BBB syndrome gene pro

188 Here, we identify TOPBP1 as a novel interactor of TOP2A, and reveal that it is required for

189 biquitinating enzyme YOD1 (OTUD2) as a novel interactor of TRAF6 in human cells.

190 s of 135 candidate CCM proteins and physical interactors of 38 of these proteins.

191 Fifty protein interactors of a Brassica juncea NRAMP protein was ident

192 vidence for existence of Gly-Trp (GW) repeat interactors of AGO proteins acting in the plant microRNA

193 mass spectrometry analysis for brain-derived interactors of ArPIKfyve-Sac3 and unraveled the alpha-sy

194 Quantitative proteomics for protein interactors of ATG16L1 identified previously unknown non

195 inhibitors have been identified, designated interactors of CDKs or Kip-related proteins (KRPs).

196 eleton regulators as previously unrecognized interactors of complexes associated with the Hermansky-P

197 rtin (IMP) family of nuclear transporters as interactors of Ei24 and characterize an IMPbeta-binding-

198 etabolism, UL39 and UL50, as novel candidate interactors of ICP0.

199 mary tissue as well as the identification of interactors of insoluble proteins that form higher-order

200 precipitation of Dock7, Sec16a, and Vac14 as interactors of Nbeal2.

201 l-based system to screen for protein-protein interactors of NOD2.

202 Eighteen novel interactors of Oxa-23 are identified.

203 hermore, transposon mutagenesis of oxa-23 or interactors of Oxa-23 demonstrates changes in meropenem

204 finity-purification and mass spectrometry of interactors of the centrosomal and ciliopathy protein, C

205 proaches to identify genetic and biochemical interactors of the Drosophila SMN homolog.

206 study, we identified NFIB and YBX1 as novel interactors of the estrogen receptor (ESR1).

207 pressed genes showed enrichment for putative interactors of the first three identified COPD GWAS gene

208 This opens a novel view on the use of interactors of the ICOS:B7h system as immunomodulatory d

209 interactions, including seven novel putative interactors of the tumor suppressor p53.

210 we found differential expression of putative interactors of these genes, and we replicated previous h

211 domain-containing proteins and ALKBH5, known interactors of this modification, we find that FMR1 and

212 were also detected between BRCA1 and certain interactors of TONSL, including both members of the FACT

213 While the influence of some CLASP interactors on MT behavior is known, a comprehensive sur

214 and calcium modulator and cyclophilin ligand interactor) on GC B cells, thus limiting their capacity

215 xpressing AMLs, that Hoxa genes and selected interactors or downstream targets are required for survi

216 These data sets include known interactors PABPC1 and MOV10 and, with in-cell imaging s

217 Microtubules and their interactors, particularly end-binding proteins (EBs), ha

218 re complex because they are affected by both interactors' phenotypes and external variables.

219 -3 (RGA) inhibits RGA binding to four of its interactors-PHYTOCHROME-INTERACTING FACTOR3 (PIF3), PIF4

220 h diverse proteins, and its most predominant interactors play important roles in postsynaptic recepto

221 ion, disease association, protein structure, interactors, posttranslational modifications, and inhibi

222 URI (unconventional prefoldin RPB5 interactor protein) is an unconventional prefoldin, RNA

223 ion, the tail-anchored pUL34 and its soluble interactor, pUL31.

224 ppGpp, but not the previously described YfgM interactors RcsB and PpiD, influence YfgM degradation.

225 ed that caveolin 1 (CAV1), a well-known eNOS interactor, regulates eNOS activity in sinusoidal endoth

226 We have identified a conserved protein and interactors required for maintaining cell adhesion durin

227 dependent deacetylase, Sirt2, as a novel AKT interactor, required for optimal AKT activation.

228 We identified the LINKIN interactors RUVBL1, RUVBL2, and alpha-tubulin by using S

229 mutants did not depend on the SHR functional interactor SCARECROW and the sugar signaling component A

230 alysis of Arabidopsis homologs of BjNRAMP4.1 interactors showed enrichment of many protein components

231 Quantitative proteomic analysis of polyQ interactors showed that expression of Gts1p reduced the

232 F-dependent transmembrane activator and CAML interactor signals in atherosclerosis pathogenesis, of p

233 re under-represented within the 305 positive interactors specific for the amk2 gsk3 query.

234 oes not affect the action of other secondary interactors, such as GreA or GreB.

235 ding the transcriptional repressor and MeCP2 interactor switch-insensitive 3 family member A (SIN3A;

236 or and calcium-modulating cyclophilin ligand interactor (TACI) are found in 8% to 10% of subjects wit

237 gen (BCMA), transmembrane activator and CAML interactor (TACI) but not to the BAFF receptor (BAFFR).

238 or and calcium-modulating cyclophilin ligand interactor (TACI) controls differentiation of long-lived

239 How mutant transmembrane activator and CAML interactor (TACI) influences wild-type TACI function is

240 brane activator and calcium modulator ligand interactor (TACI) is important for T-independent antibod

241 Transmembrane activator and CAML interactor (TACI) signals are critical for BAFF-mediated

242 and calcium-modulator and cyclophilin ligand interactor (TACI) was severely reduced in XID B cells.

243 ro of CD86, transmembrane activator and CAML interactor (TACI), and CD23 activation markers after TLR

244 and calcium-modulator and cyclophilin ligand interactor (TACI), is a key molecule for plasma cell mai

245 tor calcium modulator and cyclophilin ligand interactor (TACI).

246 y involving transmembrane activator and CAML interactor (TACI).

247 ctivating protein ARHGAP10, and the integrin interactors Talin-1/2 or Filamin A.

248 ng sites, with Vps39 being the stronger Ypt7 interactor than Vps41.

249 n 102 (SAP102) was identified as a candidate interactor that bound to the A2A receptor C terminus.

250 unconventional prefoldin, RNA polymerase II interactor that functions as a transcriptional repressor

251 roduced to enlarge the range of proteins and interactors that can be assayed by hybrid-based approach

252 ed interactors, along with a large subset of interactors that have not been previously identified as

253 e of which are potential stage-specific mRNA interactors that likely reflect the dynamics of RNA-prot

254 We have identified 36 candidate interactors that modify LRRK2 induced toxicity in the Dr

255 Identifying interactors that stabilize toxic oligomeric complexes co

256 viability, we uncovered a novel role for its interactor, the ESCRT-I protein TSG101: it directly part

257 A third interactor, the histone methyltransferase MES-4, is also

258 teraction with Slx5, SUMO, Slx8, and a novel interactor, the SUMO E3 ligase Siz1.

259 ty-regulated cytoskeleton-associated protein interactors, the fragile X mental retardation protein co

260 Among the variety of PrP(C) protein interactors, the neuronal cell adhesion molecule (NCAM)

261 tellite proteins localize their cognate MCPH interactors to centrosomes and also promote centriole du

262 Harnessing the ability of these protein interactors to transform the oncogenic mutant p53 to the

263 were detected between BRCA1 and four of the interactors: TONSL, SETX, TCEANC, and TCEA2.

264 Among these interactors, TPCs were resolved to scaffold Rab GTPases

265 monstrate that unconventional prefoldin RPB5 interactor (URI) expression in hepatocytes leads to hepa

266 expression of unconventional prefoldin RPB5 interactor (URI) leads to a multistep process of HCC dev

267 in 6 (DPP6) was first identified as a PrP(C) interactor using in vivo formaldehyde cross-linking of w

268 P, we sought to identify direct IRF6 protein interactors using a combination of yeast 2-hybrid screen

269 tome of PAX3-FOXO1 and screened 60 candidate interactors using siRNA-mediated depletion to identify c

270 AF patients, with CSDA and PDE5A being novel interactors validated by bioinformatics, immunocytochemi

271 identified polypeptides represent bona fide interactors versus those that are background contaminant

272 ins, including several highly specific ACTN4 interactors, was globally decreased in the patient-deriv

273 In an unbiased BioID screen for Plk4 interactors, we identified members of the Arp2/3 complex

274 Searching for IYO interactors, we identified RPAP2 IYO Mate (RIMA), a homo

275 From a screen for functionally relevant ERG interactors, we identify the arginine methyltransferase

276 A total of 135 and 78 putative PP1c interactors were captured from mouse and human cardiac l

277 Nonetheless, the first described OFD1 interactors were components of the TIP60 histone acetylt

278 Both amk2- and gsk3-specific interactors were enriched in phenotype categories relate

279 Three such interactors were identified-hnRNPA1, hnRNPA3 and hnRNPU-

280 BjNRAMP4.1 interactors were particularly enriched in proteins takin

281 The interactors were predicted to function as components of

282 ore proteins ABC1K3, PES1, and CCD4 as PGM48 interactors, whereas several other PG-localized proteins

283 rification allowed copurifying PSBS with its interactors, which were identified by mass spectrometry

284 Proteomics identified 16 new IRF5 interactors while RNAi-mediated knockdown found 43 regul

285 dentified the pseudokinase PTK7 as an AMIGO2 interactor whose function is regulated by AMIGO2.

286 interactome remodelling identifies key novel interactors, whose loss promote F508 CFTR channel functi

287 g approaches, we demonstrate that the N-WASP-interactors WIP and WICH/WIRE play non-redundant roles i

288 transferase, which we identified as a strong interactor with all three TET proteins, catalyzes the ad

289 se inhibitor Matrimony (Mtrm) as a potential interactor with Cort.

290 TLR4 interactor with leucine-rich repeats (TRIL) is a brain-e

291 ment binding protein superfamily, as a DELLA interactor with physiological relevance in the context o

292 analysis identified annexinA2 as a potential interactor with the extracellular domains of PLA2R.

293 d the ubiquitin-modifying enzyme TRAF6 as an interactor with the integrin beta1 subunit and regulator

294 ting Protein 1 (Cnrip1) was discovered as an interactor with the intracellular region of Cannabinoid

295 ow that Scribble PDZ1 and PDZ3 are the major interactors with beta-PIX and reveal a distinct binding

296 tively, including many previously unreported interactors with conserved PP1c docking motifs.

297 Among 126 interactors with miRNAs, we surprisingly found the CED-3

298 WP1 and all four of its WW domains as strong interactors with the PPXY motif of eVP40.

299 Here we used mAb technology to identify interactors with Z alpha1-antitrypsin that comply with b

300 d 69 negative and 82 positive common genetic interactors, with functions related to cellular growth a