ライフサイエンスコーパス: -interacting

1 We identified three CLC-1-interacting proteins that are well-known heat shock prot

2 gulatory protein 2 ligase 1 (HOIL-1), HOIL-1-interacting protein, and SHANK-associated RH domain-inte

3 iron regulatory protein 2 ubiquitin ligase-1-interacting protein (HOIP).

4 ion of Pk3 may involve Wilms tumor protein 1-interacting protein (Wtip), which physically associates

5 entary proteomic approaches to identify ACR4-interacting protein candidates that are likely regulator

6 l may facilitate the identification of APOL1-interacting molecules that could serve as new drug targe

7 ugh another negative immune regulator ARLPK1-interacting receptor-like kinase 1 (AKIK1), an active ki

8 om replication stress, and impairment in ATR-interacting protein (ATRIP) focus accumulation of SIRT2

9 odulin-like protein 38 (CML38) as an AtRALF1-interacting partner.

10 east two-hybrid system to search for AtRALF1-interacting proteins in Arabidopsis, we identified calmo

11 At present, AtWRI1-interacting partners remain largely unknown.

12 reby prevents the BH3-only protein BIM (BCL2-interacting mediator of cell death)-dependent triggering

13 emerged as possibly the largest class of CaM-interacting proteins with undefined molecular functions

14 oliovirus 2C(ATPase), near a presumed capsid-interacting site, important for encapsidation.

15 development progressed, similar to the CAPZB-interacting protein TWF2.

16 containing a unique N-terminal beta-catenin-interacting domain.

17 neurin B-like calcium sensors (CBLs) and CBL-interacting protein kinases (CIPKs) are involved in Al r

18 Calcineurin B-like proteins (CBLs) and CBL-interacting protein kinases (CIPKs) signal network have

19 tive endosomes recruiting syntenin-1, a CD63-interacting adaptor protein.

20 421 residue is required for MCP1-induced CDK-interacting protein 1 (p21Cip1) nuclear export and degra

21 Here, we report that the CDKN1-interacting zinc finger protein CIZ1 is critical for loc

22 osomal RNA processing protein 6), as a CELF1-interacting protein.

23 binds epilepsy-associated potassium channel-interacting proteins including KCNAB2 and KCNIP1, and in

24 nd further investigated ENKUR, a TRP channel-interacting protein identified in the cilia of all three

25 Here we investigate a chromatin-interacting module, the bromodomain (BD) from the BET fa

26 Pf1 associates with a chromatin-interacting protein complex comprised of MRG15, Sin3B, a

27 nd mental retardation-type 3) as a chromatin-interacting protein that promotes DNA repair by homologo

28 cation of the entire repertoire of chromatin-interacting RNAs and their respective binding sites.

29 The nuclear matrix protein Cip1-interacting zinc finger protein 1 (CIZ1) promotes DNA re

30 -Pcdhs gammaA4 and gammaB2, which depict cis-interacting regions in monomeric form.

31 st 50 proteins, including clathrin, clathrin-interacting proteins, actin filaments, and actin binding

32 new data on the biological function of a CML-interacting partner, PRR2 (PSEUDO-RESPONSE REGULATOR 2),

33 lymerase II (Pol II) C-terminal domain (CTD)-interacting domain (CID).

34 the phosphorylated C-terminus of Pol II (CTD-interacting domain, CID).

35 he phosphorylated CTD via its N-terminal CTD-interacting domain.

36 ble-click stapled peptides encoding the Ctf4-interacting peptide (CIP) of the replicative helicase su

37 Loss of SET1B or its unique cytoplasmic-interacting protein, BOD1, leads to up-regulation of exp

38 inhibiting the tumor suppressor DAB2IP (DAB2-interacting protein) in the cytoplasm.

39 cterize planarian homologs of human DAZL/DAZ-interacting partners and DAZ family mRNA targets.

40 increased expression of a target gene, Disco-interacting protein 2 homolog B (Dip2b).

41 interaction with SHANK-associated RH domain-interacting protein was impaired in a male fetus with IP

42 ting protein, and SHANK-associated RH domain-interacting protein.

43 udes the MyoA light chain myosin tail domain-interacting protein (MTIP) and several glideosome-associ

44 ctor 1 (RIF1) and Pax transactivation domain-interacting protein (PTIP), in the past few years to elu

45 -containing PTIP (Pax transactivation domain-interacting protein) chromatin regulator is controlled b

46 -containing PTIP (Pax transactivation domain-interacting protein).

47 mmal damage involves dysferlin and dysferlin-interacting proteins such as annexins.

48 t differ substantially in their predicted E1-interacting residues is unknown.

49 hese data show how a deubiquitinating enzyme-interacting protein dictates the efficiency and specific

50 MED1 mutation in its ER-interacting LxxLL motifs was sufficient to delay tumor o

51 ively regulates TGF-beta signaling via ERBB2-interacting protein (ERBIN), a SMAD anchor for receptor

52 guish these functions for FIP200 (FAK family-interacting protein of 200 kDa), an Atg in autophagy ind

53 epair partners, we observed that many Fancd2-interacting proteins are mitochondrion-specific.

54 n of FUBP1 and antagonize the binding of FBP-interacting repressor to FUBP1, thereby coordinating the

55 cterized protein named cardiac-enriched FHL2-interacting protein (CEFIP), which exhibited a heart- an

56 defense responses and interacts with FIN219-interacting protein 1 (FIP1) under FR light conditions.

57 ) to a missense mutation in cytoplasmic FMR1-interacting protein 2 (Cyfip2).

58 led with mass spectrometry, identified FOXC1-interacting proteins including a group of heterogeneous

59 (FRQ), casein kinase 1a (CK1a), and the FRQ-interacting RNA Helicase (FRH) rhythmically represses ge

60 trength of FvTox1 with four different FvTox1-interacting peptides and experimentally confirmed the si

61 We identified SLIRP as a novel G4-interacting protein.

62 Mutating two G4-interacting residues (T1024G and T1086G) abrogated prefe

63 This mobility increase is dependent on Gag-interacting Env tail but not on changes in viral envelop

64 Galpha-interacting vesicle-associated protein (GIV, aka Girdin)

65 We recently described that Galpha-interacting, vesicle-associated protein (GIV), a protein

66 A TAT peptide containing the Gbetagamma-interacting domain of DAT blocked the ability of mSIRK t

67 pendent manner, and tumors bearing a non-GNA-interacting C668S-EZH2 mutation exhibited resistance to

68 GR-interacting protein-1 (GRIP1) is a GR corepressor in mac

69 st, Galphai1(Q204L) did not reverse Rap1-GTP-interacting adaptor molecule (RIAM)-dependent increases

70 sent a clear proof of principle that MT-Hec1-interacting compounds may represent novel powerful antic

71 onic hedgehog (Shh)-binding loop of hedgehog-interacting protein (HHIP) and subjected to multiple rou

72 Homeodomain-interacting protein kinase (HIPK) 2, a nuclear serine/th

73 Homeodomain-Interacting Protein Kinase 1 (HIPK1) phosphorylates PAGE

74 Homeodomain-interacting protein kinase 2 (HIPK2) is a nuclear serine

75 two closely related pathogens and their host-interacting partners.

76 e show that CHIP (carboxyl terminus of Hsc70-interacting protein), a U-box E3 ligase, suppresses tumo

77 2 degradation through COOH terminus of Hsp70-interacting protein (CHIP)-mediated ubiquitination.

78 mammalian ubiquitin ligase C-terminal Hsp70-interacting protein (CHIP), if freed from chaperones dur

79 and SNX1) that increase and four (huntingtin-interacting protein 1 [HIP1], HIP14, GASP-1, and Nedd4)

80 Other identified EEEV nsP3 HVD-interacting host proteins are also capable of supporting

81 ed the interactions between the isolated INT-interacting MVP domains (iMVP) and wild-type INT and com

82 and neurotransmitter release, as a novel IRP-interacting transcript, and studied its role in iron met

83 Furthermore, we identified potential JMJD8-interacting proteins that are known to regulate protein

84 tivated by these problems, we identified JNK-interacting protein 3 (JIP3) as an important regulator o

85 ulation of the axonal transport proteins JNK-interacting protein 1 and amyloid beta precursor protein

86 show that in mature tissues TMV 126/183-kDa-interacting Aux/IAAs predominantly express and accumulat

87 tophagy regulator BCL2/adenovirus E1B 19-kDa-interacting protein 3-like (BNIP3L, best known as NIX) a

88 eracting serine-threonine kinases MAP kinase-interacting kinase 1 (Mnk1/2), the eIF4E upstream kinase

89 Here we identify MAP kinase-interacting serine/threonine protein kinase 1a (MNK1a) a

90 nhibitor of mitogen-activated protein kinase-interacting serine-threonine kinases MAP kinase-interact

91 Using a proteome-wide kinase-interacting substrate screening (KISS) method, we identi

92 The family member in kinetoplastids, KKT-interacting protein 1 (KKIP1), associates with the kinet

93 inction is mirrored in the phylogeny of KNOX-interacting BELL proteins, in that a gene duplication oc

94 A screen for LATS2-interacting proteins in liver-derived cells identified t

95 nation of the arginine residue within an LC3-interacting region motif of immunodominant MOG peptides

96 tophagy inhibitor by competing with host LC3-interacting proteins for LC3 binding.

97 f RTN3 contains several newly identified LC3-interacting regions (LIR).

98 X1BP1 binding of LC3 and GABARAP via its LC3-interacting region (LIR), but not its ubiquitin-binding

99 ate peptides that possess bona fide LIR (LC3-interacting region) properties and are selective for ind

100 y of the serine 34/35-phosphorylated Nix LC3-interacting region (LIR) to LC3B and formation of a very

101 To this end, we showed that removing the LC3-interacting region of p62, which facilitates p62-mediate

102 f unknown function that we termed LDIP (LDAP-interacting protein).

103 One of the candidate LDAP3-interacting proteins was Arabidopsis At5g16550, which is

104 performed proteomic screens to map the lipid-interacting proteome for both lipids.

105 , and caspases have emerged as important LPS-interacting proteins.

106 Our approach identified 127 potential MALAT1-interacting proteins and established a highly connected

107 the signaling axis involving p38 MAPK, MAPK-interacting kinase (MNK), and eukaryotic translation ini

108 gen-activated protein kinase) and MNK1 (MAPK-interacting serine/threonine kinase 1) signaling.

109 ymerize into highly organized, cell membrane-interacting filaments.

110 by modifying residues away from the membrane-interacting domain.

111 ications introduced directly in the membrane-interacting loops and/or by modifying residues away from

112 ld form, likely in combination with membrane-interacting ACT segments, a proteolipidic toroidal pore

113 Kinetochores, the microtubule-interacting machines on chromosomes, restrain mitotic ex

114 Through proteomic analysis of the MSI2-interacting RBP network and functional shRNA screening,

115 nity purification was used to identify Mst50-interacting proteins (MIPs) in this study.

116 These MT-interacting elements overlap with the binding site of im

117 k-1 associated with FKBP12, an abundant mTOR-interacting protein, enabling accumulation of RapaLink-1

118 c-Myc-interacting zinc finger protein-1 (Miz-1) is a poly-Cys2

119 ANCE STATEMENT The deletion of the Miz1 (Myc-interacting zinc finger protein 1) POZ (POxvirus and Zin

120 domain of the transcription factor Miz1 (Myc-interacting zinc finger protein; encoded by Zbtb17) in m

121 hate transporter activity, as a novel NaStEP-interacting protein.

122 kinases consisting of MAP4K4, Traf2- and Nck-interacting kinase (TNIK or MAP4K7), and misshapen-like

123 1 (MINK1 or MAP4K6) and TNIK Traf2- and Nck-interacting kinase (TNIK or MAP4K7), as upstream regulat

124 amily member 21 (IgSF21) as a neurexin2alpha-interacting membrane protein that selectively induces in

125 f a peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (PIN1) to p53-RS, but not the p53 form wit

126 Ocean were dominated by low coercivity, non-interacting, single-domain (SD) magnetite particles, whe

127 We found distinct, non-interacting effects of both manipulations: Motor trainin

128 Arrays of non-interacting nanomagnets are widespread in data storage a

129 system, the coupling occurs via a second non-interacting qubit, initially quantum correlated with the

130 Our results show that non-interacting species can be as important as directly inte

131 othermal magnetisation behavior from the non-interacting case, indicating weak dipolar interactions.

132 that the effective dimensionality of the non-interacting lattice component can evolve from quasi-3D t

133 Compared with the non-interacting linear spin-wave theory, our results demonst

134 The non-interacting picture of electrons with field-dependent mo

135 ion temperature of 135 degrees C, as the non-interacting vesicles are converted into weakly interacti

136 Here we study the behaviour of two non-interacting particles performing a quantum walk on the l

137 es are typically designed to replace two non-interacting residues with a constraining, olefinic stapl

138 In contrast, we show that using non-interacting anions in apolar solvents can maximize favor

139 Inducible entry of the NuRD-interacting transcriptional regulator Ikaros into mouse

140 entified competitive and noncompetitive OCT1-interacting ligands in a library of 1780 prescription dr

141 This analysis revealed 90 OGA-interacting partners, many of which exhibited increased

142 cently, a new RBP-J (mammalian CSL ortholog)-interacting protein termed RITA has been identified and

143 nt binding protein (CBP), p300, and Cbp/p300-interacting transactivator 2 (Cited2) was increased in t

144 C-terminus of Hsc/p70-Interacting Protein (CHIP) is a homodimeric E3 ubiquitin

145 on is mediated by the newly identified PALB2-interacting domain (PID) in RNF168 and the WD40 domain i

146 that AcrIIA4 competitively occupies both PAM-interacting and non-target DNA strand cleavage catalytic

147 Introducing the identified PAM-interacting mutations at their corresponding positions i

148 mproved by introducing an additional non-PAM-interacting mutation.

149 Plakophilin 2 (PKP2), an influenza PB1-interacting protein, restricts IAV replication and compe

150 (Thr(6) and Tyr(8)) located within its PCNA-interacting motif (PIP-box).

151 ion lies near the binding site for most PCNA-interacting proteins.

152 Finally, proteomic analysis of the Pf1-interacting complexes highlighted proteins involved in r

153 lation of WD repeat domain, phosphoinositide-interacting protein 2 in B cells alone enhanced this non

154 ) mutant, which lacks one of the phototropin-interacting CPT proteins, shows reduced sensitivity to b

155 PHYTOCHROME-INTERACTING FACTORs (PIFs) are members of the basic heli

156 sion of the transcription factor PHYTOCHROME-INTERACTING FACTOR (PIF4) may contribute to hybrid vigor

157 by the bHLH transcription factor PHYTOCHROME-INTERACTING FACTOR 4 (PIF4) [6-8], and enhanced stabilit

158 negatively acting factors (e.g. phytochrome-interacting factors or PIFs) are degraded in response to

159 Among them is PHYTOCHROME-INTERACTING FACTOR 3 (PIF3), a key transcription factor

160 by mediating the degradation of phytochrome-interacting transcription factors (PIFs) through the N-t

161 We provide evidence that phytochrome-interacting factors (PIFs) are phosphorylated by phytoch

162 an be induced by CK and that the phytochrome-interacting factor 4 (PIF4) is required for this upregul

163 Piwi-interacting RNAs (piRNAs) are 26-30-nucleotide germ line

164 Piwi-interacting RNAs (piRNAs) are a class of short ( 26-31-n

165 Piwi-interacting RNAs (piRNAs) are a new class of small non-c

166 PIWI-interacting RNAs (piRNAs) are small non-coding RNAs esse

167 PIWI-interacting RNAs (piRNAs) protect the germ line by targe

168 Piwi-interacting RNAs are small regulatory RNAs with key role

169 the histone ubiquitin ligase RNF8 in a Piwi-interacting RNA (piRNA)-independent manner, and MIWI sta

170 -directed gene silencing, we employed a Piwi-interacting RNA (piRNA)-targeted reporter assay in Droso

171 The nict-1 locus contains a Piwi-interacting small RNA (piRNA) cluster; we observe that t

172 on: short interfering RNAs (siRNAs) and PIWI-interacting RNAs (piRNAs) [1, 2].

173 e conserved Piwi family of proteins and piwi-interacting RNAs (piRNAs) have a central role in genomic

174 Piwi proteins and their bound Piwi-interacting RNAs (piRNAs) are predominantly expressed in

175 analogous to Drosophila TE silencing by PIWI-interacting RNAs and siRNAs.

176 Small RNAs called PIWI-interacting RNAs (piRNAs) act as an immune system to sup

177 echanism of biogenesis for tRNA-derived Piwi-interacting RNAs (td-piRNAs) expressed in Bombyx BmN4 ce

178 ere we show that PNLDC1 is required for piwi-interacting RNA biogenesis, transposon silencing, and sp

179 ily deadenylase PNLDC1 is implicated in piwi-interacting RNA trimming in silkworms.

180 Pnldc1 mutation in mice inhibits piwi-interacting RNA trimming and causes accumulation of untr

181 se results define PNLDC1 as a mammalian piwi-interacting RNA biogenesis factor that protects the germ

182 our current understandings of mammalian PIWI-interacting RNAs (piRNAs) and their role in TE regulatio

183 , leading to severe reduction of mature piwi-interacting RNAs in the testis.

184 The production of mature piwi-interacting RNAs requires a critical step of trimming pi

185 f sncRNAs including microRNAs (miRNAs), Piwi-interacting (piRNAs), small nuclear, nucleolar, cytoplas

186 ntermediates to achieve optimally sized piwi-interacting RNAs.

187 nhibition is thought to occur via small Piwi-interacting RNAs (piRNAs).

188 The PIWI-interacting RNA (piRNA) pathway is a conserved defense s

189 The PIWI-interacting RNA (piRNA) pathway is essential for retrotr

190 The Piwi-interacting small RNA (piRNA) pathway is vital for the r

191 e, we showed that tsRNAs are similar to Piwi-interacting RNAs (piRNAs) and demonstrated that ts-101 a

192 As requires a critical step of trimming piwi-interacting RNA intermediates to achieve optimally sized

193 ng and causes accumulation of untrimmed piwi-interacting RNA intermediates with 3' end extension, lea

194 ein phosphatase 1 (PP1c) is dictated by PP1c-interacting proteins, here we sought to identify new PP1

195 and quantify several weakly bound proteasome-interacting proteins and examine their roles in stress-m

196 adapter protein Ecm29 is the main proteasome-interacting protein responsible for stress-triggered rem

197 ng BNIP3 (BCL2/adenovirus E1B 19-kDa protein-interacting protein 3) and GLUT1 (glucose transporter 1)

198 We identify a panel of Ptchd1-interacting proteins that include postsynaptic density p

199 Rab3-interacting molecules (RIMs) provide scaffolding at pres

200 t and activation of Munc13-1 depends on Rab3-interacting proteins (RIMs), we demonstrate here that bM

201 RAB3A-interacting molecule (RIM) proteins are important regula

202 icle exocytosis.SIGNIFICANCE STATEMENT RAB3A-interacting molecules 1 and 2 (RIM1/2) are essential reg

203 it tetratricopeptide repeat-containing Rab8b-interacting protein (TRIP8b) also produces antidepressan

204 5, tetratricopeptide repeat-containing Rab8b-interacting protein (TRIP8b), binds to and functions as

205 Rad50-interacting protein 1 (Rint1) associates with the DNA da

206 e show that the HPV E2 protein targets Rad50-interacting protein 1 (Rint1) to facilitate virus genome

207 inactivation of its ATP-binding site, RAD51-interacting domain, or phosphorylation site causes exces

208 Rap1-interacting adaptor molecule (RIAM) is a Rap1 effector t

209 (ATM) phosphorylates 53BP1 and recruits RAP1-interacting factor 1 (RIF1) to dissociate the 53BP1-TIRR

210 Rasip1 (Ras-interacting protein 1) is required for apical junction c

211 Receptor-interacting protein kinase 1 (RIPK1) induces apoptosis a

212 Receptor-interacting protein kinase-3 (RIPK3) is an activator of

213 Receptor-interacting serine/threonine-protein kinase (RIP)-3-medi

214 , TNF receptor-associated factor 2, receptor-interacting protein 1, Hemo-oxidized iron regulatory pro

215 h, we demonstrate the presence of a receptor-interacting protein kinase 3 (RIPK3)-mixed lineage kinas

216 lex interplay between caspase-8 and receptor-interacting protein (RIP) kinase RIP 3 (RIPK3) driving e

217 for left-handed helix (Z-form) and receptor-interacting protein homotypic interaction motif (RHIM) d

218 iated via death domain (TRADD), and receptor-interacting serine/threonine protein kinase 1 (RIPK1).

219 h as CD141, GATA3, OX40 ligand, and receptor-interacting serine/threonine-protein kinase 4 (RIPK4), w

220 Adaptor proteins such as receptor-interacting serine/threonine-protein kinase 1 (RIPK1), r

221 in the absence of NOD proteins, but receptor-interacting protein 2 is not involved in CD8 single-posi

222 crosis, or "necroptosis", driven by receptor-interacting protein kinase 3 (RIPK3).

223 tic form of cell death initiated by receptor-interacting protein kinase-3 (RIPK3) and mixed lineage k

224 cell suicide mechanism initiated by receptor-interacting protein kinase-3 (RIPK3) phosphorylation of

225 mixed lineage kinase-like (MLKL) by receptor-interacting protein kinase-3 (RIPK3) results in plasma m

226 ammed necrosis that is regulated by receptor-interacting protein kinases (RIPs).

227 gulatory factors (DAI) that contain receptor-interacting protein (RIP) homotypic interaction motifs (

228 receptor gamma (RARgamma) controls receptor-interacting protein kinase 1 (RIP1)-initiated cell death

229 These G protein-coupled receptor-interacting proteins also facilitate fine-tuning of rece

230 We found that knocking down receptor-interacting serine/threonine protein kinase 1 (Ripk1) in

231 blasts induced NOD2, the downstream receptor-interacting serine/threonine-protein kinase 2 (RIPK2), r

232 RNA interference for receptor-interacting protein kinase 3 (RIPK3) or mixed lineage ki

233 Aryl hydrocarbon receptor-interacting protein-like 1 (AIPL1) is a distinctive memb

234 e itself or AIPL1 (aryl hydrocarbon receptor-interacting protein-like 1), leads to retinal diseases c

235 terferon (IFN-I) response to induce receptor-interacting protein (RIP) kinase-mediated necroptosis in

236 ubiquitin-editing complex inhibits receptor-interacting Ser/Thr kinase (RIPK) activation by removing

237 Because this involves receptor-interacting protein (RIP) kinase 1/3, this study aimed t

238 ession of the necroptosis mediators receptor-interacting protein kinase 3 (RIPK3) and mixed lineage d

239 re, disruption of the LXXLL nuclear receptor-interacting motif present in ACTN4 results in reduced GR

240 sis requires the kinase activity of receptor-interacting protein kinase 1 (RIPK1), a key regulator of

241 tatin-1, an allosteric inhibitor of receptor-interacting serine/threonine kinase 1 (RIPK-1).

242 ll death that critically depends on receptor-interacting serine-threonine kinase 3 (RIPK3) and mixed

243 s-associated death domain (FADD) or receptor-interacting protein kinase 1 (RIP1) cell death regulator

244 tically, Traf2 critically regulates receptor-interacting proteins 1 and 3 and mixed lineage kinase do

245 threonine-protein kinase 1 (RIPK1), receptor-interacting serine/threonine-protein kinase 3 (RIPK3), T

246 ent, PKP1 (plakophilin-1) by RIPK4 (receptor-interacting serine-threonine kinase 4) during epidermal

247 We further demonstrate that receptor-interacting protein kinase 3 (RIP3), which is highly exp

248 phil extracellular traps (NETs) via receptor-interacting protein kinase (RIPK) 1/3- and mixed-lineage

249 QP2) and the lysosomal trafficking regulator-interacting protein LIP5 targets AQP2 to multivesicular

250 Geminivirus Rep-Interacting Kinase (GRIK)1 and GRIK2 phosphorylate SnRK1

251 tion site required the highly conserved Rev1-interacting region (RIR) motif in XRCC1 and included thr

252 ike Homologous protein 5 (PfRH5) and the RH5-interacting protein (PfRipr), essential for erythrocyte

253 ssense mutations in CIT, encoding citron rho-interacting kinase (CIT), which has established roles in

254 Notably, we identified citron Rho-interacting kinase (CRIK), which has known functions in

255 mutations in CIT, encoding CRIK (citron rho-interacting kinase)-a component of the central spindle m

256 e is required for the recruitment of the Rho-interacting kinase citron to the anaphase midzone.

257 viously unrecognized myosin phosphatase-RhoA-interacting protein-dependent pathway.

258 sis downregulated the abundance of RNA5SP141-interacting proteins, which allowed RNA5SP141 to bind RI

259 , our results implicate INPP5E, a novel RPGR-interacting protein, in the pathogenesis of RPGR-associa

260 Mutations in the RPGR-interacting protein 1 (RPGRIP1) gene cause recessive Leb

261 y of 89 pyrenoid proteins, including Rubisco-interacting proteins, photosystem I assembly factor cand

262 In fact, based on experiments using the self-interacting FM domain, it appears generally true that ag

263 CTD proteins hetero-oligomerize through self-interacting T1 and H1 homology domains.

264 CUL3 ubiquitin E3 ligase complex, as a SETD2-interacting protein.

265 receptor 2 (EphA2) was identified as a SOCS2-interacting protein.

266 r carboxylesterase 1 (CES1) as a novel SORT1-interacting protein.

267 ed MS-based approach to identify novel STAT5-interacting proteins.

268 acterization of a mouse mutation in striatin-interacting protein 1 (Strip1) that disrupts migration o

269 the biochemically defined mammalian striatin-interacting phosphatases and kinase (STRIPAK) complexes

270 r with other core components of the striatin-interacting phosphatase and kinase (STRIPAK) complex, we

271 of the STUbL SLX5 or disruption of its SUMO-interacting motifs, confirming that Tof2 is targeted for

272 ng and mutagenesis, we identified a new SUMO-interacting motif (SIM) in PIASy.

273 This activity requires the sumoylation-interacting motif within p150N, which is also required f

274 r 1 (IF1) is a nuclear-encoded, ATP synthase-interacting protein that selectively inhibits the hydrol

275 dentified DDX5, FUS, EWSR1 and LSM14A as TAD-interacting proteins sensitive to F32L and/or Y96L mutat

276 TEL2 (Telomere maintenance 2) and TTI1 (Tel2-interacting protein 1), to form the triple T complex tha

277 The maize dek38 gene encodes a TTI2 (Tel2-interacting protein 2) molecular cochaperone.

278 protein (CIRP or hnRNP A18) as a telomerase-interacting factor.

279 RT as well as other telomerase- and telomere-interacting proteins have provided insights into telomer

280 trate here that transcription factor COUP-TF-interacting protein 1 (CTIP1/BCL11A; hereafter CTIP1) is

281 Since we recently identified thioredoxin-interacting protein (TXNIP) as an upstream regulator of

282 mediated by the de-repression of thioredoxin-interacting protein, a major redox control molecule, and

283 els of the pro-apoptotic protein thioredoxin-interacting protein (TXNIP).

284 Silencing thioredoxin-interacting protein abrogated reactive oxygen species ac

285 Recently, the thioredoxin-interacting protein TXNIP, which is strongly induced by

286 phosphatase-1 (SHP-1) and TXNIP (thioredoxin-interacting protein).

287 Toll-interacting protein (TOLLIP) is a ubiquitin-binding prot

288 sential for Thr9 phosphorylation of the TRAF-interacting protein TIFA, triggering activation of the N

289 n genes encoding the shelterin proteins TRF1-interacting nuclear factor 2 (TIN2) and adrenocortical d

290 n, and reduced recruitment of a known TRP120-interacting host protein, PCGF5, to ehrlichial inclusion

291 In this study, we identified the Tudor-interacting repair regulator (TIRR) that specifically as

292 al extremity of Galphas contains a ubiquitin-interacting motif (UIM), a sorting element usually found

293 ia an amino acid sequence, known as the UFM1-interacting sequence (UIS), located outside the adenylat

294 eover, depletion of DHX38, encoding an USP39-interacting splicing factor, also reduces the viability

295 The vault-interacting domain of vault poly(ADP-ribose)-polymerase

296 ntified focal adhesion kinase (FAK) as a VHR-interacting molecule.

297 viperin and used CIA1 as the primary viperin-interacting protein.

298 elegans AMPylation enzymes-huntingtin yeast-interacting protein E (HYPE) and filamentation-induced b

299 Tubule formation depends on the Rab7/Ypt7-interacting retromer complex, consisting of the sorting

300 n disrupts colocalization with a known ZRSR2-interacting protein, U2AF2.