ライフサイエンスコーパス: interactor

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

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

3 oprocessor component DROSHA as a novel DNMT1-interactor.

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

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

6 ly receptor transmembrane activator and CAML interactor.

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

8 atty acid (VLCFA) synthesis pathway and core interactor.

9 mass spectrometry to identify BIRC3 protein interactors.

10 ction of RPGR isoforms with their endogenous interactors.

11 subsequently validated many putative zDHHC17 interactors.

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

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

14 y to the nucleus when coexpressed with these interactors.

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

16 affimer" reagents as high-affinity ubiquitin interactors.

17 independent experiments, to filter bona fide interactors.

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

19 echanism for bringing together their diverse interactors.

20 A target, with relevance to other TPR domain interactors.

21 cribed PPIs as well as to identify novel NS1 interactors.

22 G-protein signaling components and G-protein interactors.

23 complex with cullin 3 (CUL3), are novel IRS1 interactors.

24 vel function of Shank3 in recruiting Abelson interactor 1 (ABI1) and the WAVE complex to the post-syn

25 ing G protein-coupled receptor (GPCR) kinase interactor 1 (GIT1), which we found to play an unexpecte

26 or HAI1-interacting proteins identified HAI1-Interactor 1 (HIN1), a nuclear protein of unknown functi

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

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

29 Abi1 (Abelson interactor 1) is an adapter protein that has been implic

30 protein 4)/TRIP10 (thyroid hormone receptor interactor 10) was identified as a new polyproline domai

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

32 Here, we provide evidence that Abelson interactor (Abi), a substrate for Abl kinase and compone

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

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

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

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

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

38 Here, we report on a new direct protein interactor and regulator of Feo we named Feo interacting

39 nctionally specific role of PFN2 as a stable interactor and regulator of the actin N-terminal acetylt

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

41 ts, we identified C19ORF57/BRME1 as a strong interactor and stabilizer of HSF2BP and showed that the

42 ate Kinase (MaGUK) PSD93 as a direct ZDHHC14 interactor and substrate.

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

44 actin module, each harboring specific actin interactors and actin isoforms.

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

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

47 ARHGEF12 and PPP1R12A as GluD1 intracellular interactors and downstream effectors.

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

49 We identified 22 UBE3B interactors and found that branched-chain alpha-ketoacid

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

51 rtin-like kinase 1 and 2 as bona fide KLHL15 interactors and mapped KLHL15 interaction regions to the

52 identified VCS and VARICOSE RELATED (VCR) as interactors and phosphorylation targets of SnRK2.5, SnRK

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

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

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

56 conserved repression motifs present on REL2 interactors and showed that two of these, RLFGV- and DLN

57 oID provides a tool for identifying new mRNA interactors and studying the dynamic view of the interac

58 major differences in their autophagy-related interactors and their post-translational and transcripti

59 e are no methods to accurately predict Hsp90 interactors and there has been considerable network rewi

60 ACTOR) transcription factor family are DELLA interactors and, at the same time, that several GRF gene

61 E, to populate the network of its functional interactors and, in doing so, to uncover new cancer-asso

62 s, identified as a zDHHC20 S-acyltransferase interactor, and annotated as a potential thioesterase.

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

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

65 GB1 is a huntingtin N17/PY-NLS ROS-dependent interactor, and this protein bridging is essential for r

66 ceptor-associated factor 6 (TRAF6) as a SOD1 interactor, and we determined that exposure of the SOD1

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 ion vector to allow paired-end sequencing of interactors, and the use of protein fragments rather tha

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

71 Sec1/Munc18 proteins and their interactors are important regulators of SNARE complex fo

72 ns) cells, the overwhelming majority of EBP1 interactors are part of ribonucleoprotein complexes regu

73 Interestingly, 70% of AGER negative interactors are switch genes including PRDX4, whose acti

74 identified a specific role for ATL3, and its interactor ARF4, in vesicle trafficking and virion matur

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

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

79 We identified a number of known interactors, but also ones including the GluA2 subunit o

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

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

82 recision with which transmembrane ectodomain interactors can be identified.

83 1 conformers as well as a high proportion of interactors common to both conformers.

84 nding dynamics of low and high affinity KRAS interactors contribute to rewiring.

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

86 the interaction between carboxyltransferase interactors (CTIs) and alpha-CT, which in turn attenuate

87 Inhibiting two or three interactors destabilizes silencing.

88 helical bundle, a docking site for many DAXX interactors (e.g. p53 and ATRX).

89 We will describe the properties of "interactor elements" (IEs) involved in direct physical i

90 Our results demonstrate that NFS1 and its interactor FH are involved not only in nonhost resistanc

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

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

93 ctrometry to map the glycan and glycoprotein interactors for galectin-3 in live human hepatic stellat

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

95 roposed as a therapeutic strategy, druggable interactors for rescue of ATP7B mutants remain elusive.

96 ost of the low mobility of strong nucleosome interactor FOXA1.

97 the NITROGEN FIXATION S-LIKE1 (NFS1) and its interactor FRATAXIN (FH), when silenced in Nicotiana ben

98 To distinguish genuine Cdc14-interactors from proteins that bound non-specifically to

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

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

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

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

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

104 es, we further focused on bona fide ribosome interactors (i.e. SEC61) and ER proteins (ribophorin I,

105 tinct classes of behavior for the 603 unique interactors identified.

106 predicted components and identify additional interactors implicated in histone acetylation and chroma

107 try demonstrated that cohesin is its primary interactor in the nucleus.

108 rotein interaction screen searching for KAT1 interactors in Arabidopsis (Arabidopsis thaliana).

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

110 have not previously been identified as Cdc14 interactors in C. albicans or S. cerevisiae.

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

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

113 ntified a large collection of UIM-based ATG8 interactors in plants, yeast, and humans.

114 tools for the discovery of Ub chain-specific interactors in proteomic studies, but their structural d

115 We see highly diverse networks with common interactors in similar lesions.

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

117 and thioredoxins, are substoichiometric RNA interactors in vivo.

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

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

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

121 Ki-67 interactors included proteins involved in nucleolar proc

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

123 others have previously identified novel eNOS interactors, including G protein-coupled receptor (GPCR)

124 tively charged motif in a subset of PP2A:B56 interactors, including KIF4A, to facilitate B56 binding

125 otif determinants uncovered unanticipated CN interactors, including NOTCH1, which we establish as a C

126 nt (MT) H-, K-, and N-Ras, identifying known interactors, including Raf and PI3K, as well as a common

127 pectrometry (MS), we identified several eNOS interactors, including the protein plasminogen activator

128 on screen identified numerous potential host interactors, including the Rho GTPases Rac1 and Cdc42.

129 n between RPGR isoforms and their endogenous interactors INPP5E, PDE6D, and RPGRIP1L.

130 In addition to 3'-UTR-independent interactors involved in known BIRC3 functions, we detect

131 of DOPr and revealed several endogenous DOPr interactors involved in protein folding, trafficking, an

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

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

134 One of the newly validated CTCF interactors is BRG1, the major ATPase subunit of the chr

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

136 As these small, globular proteins have many interactors, it has been difficult to ensure that method

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

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

139 ases, we also examined ATP1A3 and all of its interactors known to be expressed in the brain to establ

140 Depletion of the BAF interactors LEMD2 or emerin, and to a lesser extent lami

141 By mass spectrometry, we detected a RIT1 interactor, leucine zipper-like transcription regulator

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

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

144 ndently of TORC1 regulation through the Gtr1 interactor Ltv1.

145 Thus, IRGM and its interactors mAtg8s close a loop between the autophagosom

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 Whereas NCBP1 and 2 identify known CBC interactors, NCBP3 primarily interacts with components o

150 Es) directing their wiring within the "ncRNA interactor networks" through the emergence of secondary

151 tput) through complex "sentences" (the ncRNA interactor networks).

152 We also identified OsPT8 as an interactor of a rice mitogen-activated protein kinase BW

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

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

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

156 at ROP INTERACTIVE PARTNER b (RIPb; synonym: INTERACTOR OF CONSTITUTIVE ACTIVE ROP b) directly intera

157 teractor of the Rho of plants (ROP) effector interactor of constitutively active ROP (ICR1).

158 logy domain-containing protein 1) as a novel interactor of Cx43 in the heart.

159 Additionally, we identify EDG-1 as an interactor of DEPS-1 and PRG-1.

160 Our results demonstrate that NAA50, an interactor of EDR1, plays an important role in regulatin

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

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

163 In this study, we identify NLK as an interactor of huntingtin protein (HTT).

164 ion of the gene for alpha-parvin (Parva), an interactor of ILK.

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

166 vealed that FRS7 and FRS12 recruit the NOVEL INTERACTOR OF JAZ (NINJA) to assemble a transcriptional

167 ein deacetylase sirtuin 2 (SIRT2) as a novel interactor of LMAN2.

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

169 ults altogether demonstrate that LCBK1 is an interactor of MEA that positively regulates PTI-induced

170 We also discover NlpA as a novel interactor of MetNI complex.

171 dentifies mitochondrial protein ATAD3A as an interactor of mitochondrial fission GTPase, Drp1, in HD.

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

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

174 posed natural ligand, CXXC repeat-containing interactor of PDZ3 domain (CRIPT), and results from prev

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

176 ent, PROLINE-TRYPTOPHANE-TRYPTOPHANE-PROLINE INTERACTOR OF POLYCOMBS1, in Arabidopsis (Arabidopsis th

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

178 entified as a potential proximity factor and interactor of RHBDL4.

179 litates chromatin transcription (FACT) as an interactor of substrate-bound Cas9.

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

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 ly, we identify the small GTPase RAB11 as an interactor of the guanine nucleotide exchange factor DEF

185 h-mobility group box 1 (HMGB1) protein as an interactor of the intervening sequence within the PY-NLS

186 a2+-dependent modulator of ICR1 (CMI1) as an interactor of the Rho of plants (ROP) effector interacto

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

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

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

190 vered the leucine-zipper protein LUZP1 as an interactor of truncated SALL1, a dominantly-acting prote

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

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

193 Green Fluorescent Protein (GFP) to identify interactors of a GFP-tagged protein of interest by high-

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

195 mass spectrometry analysis to detect in vivo interactors of AtGET1 and identified a membrane protein

196 We identify RcsF and OmpA as bone fide interactors of BamA, and we show that MetQ association w

197 mplementary screens for genetic and physical interactors of BRD4, which converge on the folate pathwa

198 Two known interactors of FIH-1, apoptosis-stimulating of P53 prote

199 ggest that IQGAP proteins are not functional interactors of H-, K-, or N-Ras and challenge the ration

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

201 wo-hybrid assay, we discovered several novel interactors of MAFR-1 that are expressed in a sperm- and

202 therapeutic targets, we searched for unique interactors of mTOR complexes through proteomics analyse

203 Functional analyses of meiosis-specific interactors of MutLgamma-Exo1 identified Rtk1, Caf120, a

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

205 Eighteen novel interactors of Oxa-23 are identified.

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

207 th Bgh, we searched for potential downstream interactors of RACB.

208 Among these were four membrane-embedded interactors of RNF26, a polytopic E3 whose abundance is

209 g with mass spectrometry to identify protein interactors of SS-31 in mitochondria.

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

211 We identified both known and novel interactors of the endocytic TPLATE complex.

212 Finally, we identify interactors of the endogenous JJ-complex and propose tha

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

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

215 e KHD1 and SPEN3 proteins were identified as interactors of the HUB1 and HUB2 proteins with in vitro

216 e tool to reconstruct networks and query for interactors of the kinetochore complex as well as conser

217 Here, we identified protein interactors of the WASH complex by immunoprecipitation a

218 ure-proteolytic-release approach to identify interactors of the yeast importin Pdr6/Kap122.

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

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

221 s identified with FAMA-TurboID include known interactors of this stomatal transcription factor and no

222 We found that interactors of ULK1 and ULK2 all have different tissue-s

223 eal that the tagged protein pulls down known interactors of wild type RanBP9.

224 ing, was identified as a specific and direct interactor only of activated CD28.

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

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

227 ckers and/or SE-lockers that will change the interactor partners' spectrum of proteins, RNAs, DNAs, o

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

229 -3 (RGA) inhibits RGA binding to four of its interactors-PHYTOCHROME-INTERACTING FACTOR3 (PIF3), PIF4

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

231 oteins are epigenetic repressors and lamin A interactors, primarily involved in the maintenance of ce

232 terminal beta-strand shapes the broader ATG8 interactor profiles, defining interaction specificity wi

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

234 ly the second structure of a 14-3-3 mode III interactor, provides further insight into this less-well

235 TOR and its primary interactors, RAPTOR and LST8, have been remarkably evolu

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

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

238 lates with the activation of known COPD GWAS interactors SERPINE2, CD79A, and POUF2AF1.

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

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

241 s spectrometric identification of the OTULIN interactor SNX27 (sorting nexin 27), an adaptor of the e

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

243 These hits included expected PI3K interactors, such as the platelet-derived growth factor

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

245 (SCRIB) with >8x higher affinity than known interactors syntrophin, CASK and DLG1.

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

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

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

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

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

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

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

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

254 calpain 1 (CAPN1) as an exclusive rPhe508del interactor that prevents active EZR recruitment, impairs

255 igenome shRNA dropout screen, to define ZEB1 interactors that are critical to metastatic NSCLC.

256 volved in known BIRC3 functions, we detected interactors that bind only to BIRC3 protein encoded from

257 We identify PSD-95 interactors that differentially bind to the SH3-GK domai

258 Here we describe a new class of ATG8 interactors that exploit ubiquitin-interacting motif (UI

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

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

261 es, we identified novel high-confidence CTCF interactors that provide a still unexplored biochemical

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

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

264 velopment to this technique, allowing CENP-A interactors to be characterized within only a few minute

265 oinformatic analysis linked ER-E3s and their interactors to multiple homeostatic, regulatory, and met

266 n challenges through the introduction of new interactor types and data formats.

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

268 We identified KDR interactors using a combination of yeast two-hybrid scre

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 In addition, a novel conserved F&H interactor was identified, GxcU (in Dictyostelium) and t

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

273 Among these interactors, we further establish the heterotrimeric G p

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

275 Apart from the previously known interactors, we identified more than 60 additional beta-

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

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

278 modules consisting of driver genes and their interactors, we show that these interactions are associa

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

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

281 BjNRAMP4.1 interactors were particularly enriched in proteins takin

282 The interactors were predicted to function as components of

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

284 structure of a complex containing a mode III interactor, which is defined as a 14-3-3 interaction wit

285 pathway and cell adhesion molecule, as a CK5 interactor, which we confirmed by co-immunoprecipitation

286 howed that H2A.Z.1 and H2A.Z.2 have specific interactors, which can mediate their functional antagoni

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

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

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

290 g protein DJ-1 and non-muscle myosins as Tau interactors whose binding to Tau was profoundly influenc

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

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

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

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

295 lated protein (Hip1R) are mutually exclusive interactors with CLCa, and suggest a model for the seque

296 and cyclophilin, were found to be consistent interactors with G(N) These newly discovered thrips prot

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

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

299 UTX and its protein interactors within the COMPASS family, including the MLL

300 DGFRA), as well as novel RNA-binding protein interactors ZC3H14 (zinc finger CCCH-type containing 14)