ライフサイエンスコーパス: subcomplex

1 nd the cargo-binding alphabeta'epsilon-COP B-subcomplex.

2 on of CENP-HIKM and of CENP-TW, another CCAN subcomplex.

3 hich along with APC1 form the APC/C platform subcomplex.

4 ic F1 region via rotation of a central rotor subcomplex.

5 d the trimeric Atg17-Atg31-Atg29 scaffolding subcomplex.

6 s a bridge between VPS34 and the ATG14:BECN1 subcomplex.

7 e Xeroderma pigmentosum B (XPB) and a kinase subcomplex.

8 for connecting the stalk to the catalytic F1 subcomplex.

9 king site for the formation of eIF3(a:b:i:g) subcomplex.

10 ecessary for the formation of the CSN4-5-6-7 subcomplex.

11 vacuolar Q(a) SNARE, leaving behind a Q(bc)R subcomplex.

12 n is further regulated by the 19S proteasome subcomplex.

13 nchored to the cell envelope by the membrane subcomplex.

14 063w, which is also a component of the Cef1p subcomplex.

15 tory IC138 phosphoprotein and its associated subcomplex.

16 ex of the CSN, we reconstituted a CSN4-5-6-7 subcomplex.

17 sis of the EcoP15I holoenzyme and the Mod(2) subcomplex.

18 fy the interplay between BamA and the BamCDE subcomplex.

19 interactions with the Nup107-160 nucleoporin subcomplex.

20 cific subunits, Vps39 and Vps41, also form a subcomplex.

21 3 endonucleases associate with the insertion subcomplex.

22 ing modulators that target SF3B1 in the SF3b subcomplex.

23 complex with the human VPS29-VPS35 retromer subcomplex.

24 e-embedded VO region via rotation of a rotor subcomplex.

25 ith a 315-kDa subassembly, forms the 550-kDa subcomplex.

26 ents efficient formation of this midassembly subcomplex.

27 orting Pex10 and Pex12, but with the docking subcomplex.

28 he cytosolic V1 and the integral membrane V0 subcomplex.

29 ts than deletion of single MICOS subunits or subcomplexes.

30 fferent nucleoporins, typically organized in subcomplexes.

31 hilus with those of its membrane and soluble subcomplexes.

32 between IFT88/70/52/46 and IFT81/74/27/25/22 subcomplexes.

33 lex and the Nup93 complex, two conserved NPC subcomplexes.

34 einhardtii IFT70/52 and Tetrahymena IFT52/46 subcomplexes.

35 but finite exchange of even its most stable subcomplexes.

36 arity and structural independence of the IFT subcomplexes.

37 origins of the IFT-A, IFT-B, and the BBSome subcomplexes.

38 ic protein, C3orf1, were associated with the subcomplexes.

39 nto separate cavin1-cavin2 and cavin1-cavin3 subcomplexes.

40 Complex I is put together from preassembled subcomplexes.

41 mposed of 13 proteins, which assemble in two subcomplexes.

42 s and consequently the masses of the various subcomplexes.

43 icles (19S RPs) subdivided into base and lid subcomplexes.

44 the interaction between the BamAB and BamCDE subcomplexes.

45 Nuclear pore complexes consist of several subcomplexes.

46 The RP is divisible into base and lid subcomplexes.

47 res that the SNAREs assemble into functional subcomplexes.

48 rtners the APH-1/nicastrin and PS1-NTF/PEN-2 subcomplexes.

49 alyses of isolated FlaH and archaellum motor subcomplexes.

50 s are released as individual molecules or as subcomplexes.

51 ghts into the structure and function of FoF1 subcomplexes.

52 he Rpc82/34/31 and Rpc53/37 Pol III-specific subcomplexes.

53 g the mutually exclusive composition of PRC2 subcomplexes.

54 e carrier protein, NADH dehydrogenase 1alpha subcomplexes 2 and 3, translocase of inner mitochondrial

55 osphate carrier or NADH dehydrogenase 1alpha subcomplexes 2 or 3 in 3T3-L1 cells results in decreased

56 nds on two evolutionarily conserved modules, subcomplexes A (IFT-A) and B (IFT-B), to drive ciliary a

57 The RMI subcomplex also associates with FANCM, a component of th

58 etry, crystal structure of the CPSF160-WDR33 subcomplex and biochemical assays, we define the molecul

59 comet)-dependent disassembly of a Cdc20-Mad2 subcomplex and identify it as Thyroid Receptor Interacti

60 complex, comprising the Mis18alpha:Mis18beta subcomplex and M18BP1, is crucial for CENP-A homeostasis

61 VET-specific subunits, Vps3 and Vps8, form a subcomplex and physically and genetically interact with

62 elix domains that form the eIF2Bgammaepsilon subcomplex and propose a model for domain interactions b

63 ssociate with mtHsp70 as a hetero-oligomeric subcomplex and regulate mtHsp70 function.

64 nally, we discovered the presence of a CcoNQ subcomplex and showed that CcoN is the required anchor f

65 Importantly, the presence of the Nup84 pore subcomplex and Slx5/8 suppresses CAG repeat fragility an

66 s through a mechanism involving the shoulder subcomplex and the cytoskeletal-associated protein glyci

67 sponsible for the formation of eIF3(a:b:i:g) subcomplex and, because of mutually exclusive nature of

68 aled the presence of active CcoNQO and CcoNO subcomplexes and also showed that the CcoP subunit is no

69 ugh Dsc5, showing that the Dsc proteins form subcomplexes and display defined connectivity.

70 vealing both novel and previously identified subcomplexes and hub proteins, including Nop4.

71 m mitochondria lacking gRNA-bound RNP (gRNP) subcomplexes and identified REH2-associated cofactors 1

72 cose-dependent manner, positioning V1 and V0 subcomplexes and orienting the V1 C subunit to promote a

73 The MRB1 core associates with multiple subcomplexes and proteins through RNA-enhanced or RNA-de

74 CI subunits demonstrated rapid generation of subcomplexes and revealed that their specific abundance

75 n of complexes, including the delineation of subcomplexes and subunit stoichiometry.

76 unfolded GLFG repeats as Velcro to link NPC subcomplexes and thus add a new layer of connections to

77 between the RNP catalytic core, p75-p19-p45 subcomplex, and the DNA-binding Teb1.

78 mass spectrometry measurements of complexes, subcomplexes, and subunits are necessary to build comple

79 ow that inactive EGFR, LAPTM4B, and the Sec5 subcomplex are required for basal and starvation-induced

80 We further demonstrate that both subcomplexes are associated with intron RNA, which is a

81 The archaeal box C/D and C'/D' RNP subcomplexes are each assembled with three sRNP core pro

82 into CI and CI+CIII(2), indicating that the subcomplexes are productive intermediates of assembly.

83 phic data obtained from the E1p-E2p didomain subcomplex as well as with other biochemical and NMR dat

84 e 26 S proteasome comprises two multisubunit subcomplexes as follows: 20 S proteasome and PA700/19 S

85 HoxEFUYH, HoxFUYH, HoxEFU, HoxFU, and HoxYH subcomplexes as well as association of the immature, unp

86 or interaction with the membrane-embedded Fo subcomplex, as its transmembrane helix can be removed.

87 brane-spanning (subM) and the luminal (subL) subcomplexes, as well as subA, subB, and subE.

88 We find that individual spliceosomal subcomplexes associate with pre-mRNA sequentially via an

89 essential role for HoxF and HoxU in complex/subcomplex association.

90 atalysis requires interaction of the protein subcomplex (BchX)2 with the catalytic (BchY/BchZ)2 prote

91 e experiments revealed a [4Fe-4S] cluster of subcomplex (BchX)2.

92 in a gamma-CA mutant is consistent with this subcomplex being a key initiator of CI assembly in plant

93 We here report the crystal structure of a subcomplex between E1p and an E2p didomain containing a

94 Further, early subcomplex binding events do not fully commit a pre-mRNA

95 ng, whereas the opposite face of the NELF-AC subcomplex binds NELF-B.

96 The NELF-AC subcomplex binds single-stranded nucleic acids in vitro,

97 ility was discovered in the E1p-E2p didomain subcomplex, both of which probably have consequences in

98 S proteasome from 20 S proteasome and PA700 subcomplexes but has no effect on in vitro activity of t

99 ized roles and normally function in distinct subcomplexes but retain the ability to substitute for on

100 tinating histone H2B, which is mediated by a subcomplex called the deubiquitinating module (DUBm).

101 also found evidence suggesting that the WRAD subcomplex catalyzes weak H3K4 monomethylation within th

102 teracted directly with the four-subunit CCAN subcomplex CENP-HIKM.

103 Deletion of genes encoding alignment subcomplex components, PilM or PilP, but not other T4P c

104 rane subcomplexes, connected by an alignment subcomplex composed of PilMNOP.

105 Furthermore, we have identified a novel subcomplex composed of the B-factors Nop2 and Nip7.

106 We identify a RQC-trigger (RQT) subcomplex composed of the RNA helicase-family protein S

107 One of these subcomplexes, composed of subunits that share structural

108 SC activity and that UBAP2L is part of a PcG subcomplex comprising BMI1, we propose a model in which

109 are carried out by a lagging strand-specific subcomplex comprising DnaG, DnaEBs and DnaC, which stimu

110 netically and biochemically define a minimal subcomplex comprising just three proteins (FANCB, FANCL,

111 ochemical characterization of influenza RdRP subcomplex comprising PA, PB1, and N terminus of PB2, wh

112 re of NuRD by determining the structure of a subcomplex comprising RbAp48 and MTA1.

113 nce, is composed of inner and outer membrane subcomplexes, connected by an alignment subcomplex compo

114 A subcomplex consisting of eIF3a, eIF3b, eIF3g, and eIF3i

115 r's tail module is highly dynamic and that a subcomplex consisting of Med2, Med3, and Med15 can be in

116 Cells lacking NDUFA9 contained a complex I subcomplex consisting of membrane arm subunits but not m

117 found that components of the inner membrane subcomplex consisting of PilMNOP were not essential for

118 Here we describe a heterotrimeric TFIID subcomplex consisting of the TAF2, TAF8 and TAF10 protei

119 of proteins called the divisome, of which a subcomplex consisting of three bitopic inner membrane pr

120 Each of these subcomplexes contain 9 +/- 2 cavin molecules and appear

121 the daughter cell requires members of an NPC subcomplex containing Nsp1p and its interacting partners

122 h other at endosomes and recruit the exocyst subcomplex containing Sec5.

123 MLL1 associates with a subcomplex containing WDR5, RbBP5, Ash2L, and DPY-30 (WR

124 MLL1 associates with a subcomplex containing WDR5, RbBP5, ASH2L, and DPY-30 (WR

125 ETd1A/B, which all interact with a conserved subcomplex containing WDR5, RbBP5, Ash2L, and DPY-30 (WR

126 Although subcomplexes containing VP22 and ICP0 can be formed when

127 The 200-kDa subcomplex, containing the ancestral gamma-carbonic anhy

128 0-subunit yeast TFIIH and of a nested set of subcomplexes, containing 5, 6, and 7 subunits, have been

129 The individual RdRP subcomplex contains all the characterized motifs and app

130 size, thus enabling the removal of distorted subcomplex data in downstream models.

131 ected via Mic19, which functions to regulate subcomplex distribution, and thus, potentially also cris

132 The VPS34 catalytic domain and BECN1:ATG14 subcomplex do not touch, and it is unclear how allosteri

133 s, prefabrication of a native-like r-protein subcomplex drives efficient and accurate construction of

134 observations support that the 19S proteasome subcomplex enhances the targeting of co-activator at the

135 our data demonstrate that the 19S proteasome subcomplex enhances the targeting of NuA4 HAT to activat

136 ndividual components, we reconstituted a PLC subcomplex, excluding the Transporter Associated with An

137 ing sites, which are on different proteasome subcomplexes, explains the specificity of Ecm29 for prot

138 f and eIF3h, are stabilized by eIF3m through subcomplex formation.

139 We identify a NELF core subcomplex formed by conserved regions in subunits NELF-

140 t the reconstitution and characterization of subcomplexes formed by the cytoplasm-exposed synaptotagm

141 , we inferred that MET1 associates with PSII subcomplexes formed during the PSII repair cycle.

142 Moreover, subcomplexes formed in solution and gas phases reveal th

143 Among the subcomplexes formed were a-bI-alpha, bII-beta, alpha-bI-

144 ble nanoscale organization of these separate subcomplexes, forming individual striations on the surfa

145 The Mcm2-7 subcomplex forms a cracked-ring, right-handed spiral whe

146 Electrophysiology studies show that the Ton subcomplex forms pH-sensitive cation-selective channels

147 tic and biochemical evidence that a PTIP-PA1 subcomplex functions independently from the MLL3/MLL4 co

148 We show that the Mod(2) subcomplex has a relatively compact shape with a radius

149 in mammalian cells, the individual retromer subcomplexes have functionally diverged to organize mult

150 Mediator is organized in three distinct subcomplexes: head, middle, and tail modules.

151 structures of individual MAC components and subcomplexes; however, the molecular details of its asse

152 s a prerequisite for the correct assembly of subcomplex I.

153 This supercomplex contains two subcomplexes (I and II) that are responsible for trans-s

154 The IFT system consists of three subcomplexes [i.e., intraflagellar transport (IFT)-A, IF

155 comparing the structures and composition of subcomplex Ibeta and complex I, supported by comparisons

156 esolution X-ray crystallography structure of subcomplex Ibeta, a large portion of the membrane domain

157 mass spectrometry revealed that the largest subcomplex (IIa) represents the succinate dehydrogenase

158 Another subcomplex (IIb) is composed of the SDH3, SDH4, SDH6, an

159 corporation of new subunits into the 200-kDa subcomplex in a gamma-CA mutant is consistent with this

160 meric cohesin requires the Ctf19 kinetochore subcomplex in budding yeast [16-18].

161 e providing a new role of the 19S proteasome subcomplex in establishing a specific regulatory network

162 is dispensable for forming an active CcoNOP subcomplex in membranes.

163 F(1) subcomplex in mitochondrial samples is often considered

164 We investigated the role of the Eaf3/5/7 subcomplex in NuA4 binding to nucleosomes.

165 approach to explore the role of Sec71-Sec72 subcomplex in post-translational protein translocation.

166 CcoP associates to CcoNQO subcomplex in the late maturation step, and once the Cco

167 However, the role of the 19S proteasome subcomplex in transcriptional activation of the TFIID-de

168 atin-remodeler form an abundant and distinct subcomplex in vivo and stimulate INO80-mediated activity

169 I, A34.5 and A49, that form a TFIIF-related subcomplex in yeast RNA polymerase I.

170 d our understanding of this highly conserved subcomplex, in part by demonstrating a direct interactio

171 reduced by phosphomimetic mutations on both subcomplexes, in an additive manner, indicating that bot

172 interactions with components of the BRCA1-A subcomplex, including ABRA1 and RAP80.

173 Our data suggest that MICOS subcomplexes independently localize to cristae junctions

174 import showed the further assembly of these subcomplexes into CI and CI+CIII(2), indicating that the

175 s the first structure of an E1p-E2p didomain subcomplex involving a homodimeric E1p, and the results

176 The retromer trimer subcomplex is an effector of Rab7 (Ypt7 in yeast).

177 The core of the subcomplex is based on a stable heterotrimeric associati

178 The p75-p45-p19 subcomplex is identified as another RPA-related complex,

179 The assembly of 19S RP base subcomplex is mediated by multiple dedicated chaperones.

180 embles into the axoneme, but the IC138 IC/LC subcomplex is missing.

181 The results indicate that the IC138 IC/LC subcomplex is necessary to generate an efficient wavefor

182 We find that the 19S proteasome subcomplex is recruited to the promoters of these riboso

183 l spliceosomes and that association of every subcomplex is reversible.

184 The subcomplex is stabilized by three types of interactions:

185 report that PHF5A, another component of this subcomplex, is also targeted by these compounds.

186 c80 outer kinetochore complex, but not other subcomplexes, is shed upon meiotic entry.

187 The essential nature of this subcomplex, its low abundance, and its multiple interact

188 ) coactivator, which contains a four-protein subcomplex known as the deubiquitinating (DUB) module.

189 SAGA contains a separable subcomplex known as the histone acetyltransferase (HAT)

190 cs and reveal the existence of an EZH1-SUZ12 subcomplex lacking EED.

191 3/5/7 within NuA4 came from mutations in the subcomplex leading to approximately 40% reductions in H4

192 molecular architecture and roles of the NPC subcomplexes, little is known about the regulation of NP

193 in an additive manner, indicating that both subcomplexes make independent contributions to attachmen

194 ents captured for both intact assemblies and subcomplexes match expected values from available X-ray

195 of MICOS and identify two independent MICOS subcomplexes: Mic27/Mic10/Mic12, whose assembly is depen

196 To understand how the IC138 IC/LC subcomplex modulates I1 activity, we characterized the m

197 es the major microtubule-binding kinetochore subcomplexes, Ndc80 and (in yeast) Dam1, to promote rele

198 ionally relevant form of the proteasome is a subcomplex of 19S base proteins, which functions as an A

199 n particular, the S-shaped Atg17-Atg31-Atg29 subcomplex of Atg1 is critical for phagophore nucleation

200 structure of Arf1 bound to the gammazeta-COP subcomplex of coatomer.

201 rtant for the maintenance of the MRPP1-HSD10 subcomplex of RNase P and that loss of HSD10 causes impa

202 not affect Wapl-Pds5 binding to the cohesin subcomplex of sister chromatid cohesion protein 1 (Scc1)

203 onsists of a 10-subunit catalytic core and a subcomplex of subunits Rpb4 and Rpb7 (Rpb4/7).

204 nt of the cyclin-dependent activating kinase subcomplex of TFIIH).

205 h along with APC4 and APC5 form the platform subcomplex of the APC/C, is an additional target of the

206 structure and assembly of a CSN5-containing subcomplex of the CSN, we reconstituted a CSN4-5-6-7 sub

207 the Nup107-160 complex, the major structural subcomplex of the NPC.

208 ough a mechanism dependent on the Nup107-160 subcomplex of the nuclear pore complex and is modulated

209 a-helix in HsiB1 (TssB) thus forming a novel subcomplex of the T6SS.

210 ted, CMG unloading is inhibited, and a large subcomplex of the vertebrate replisome that includes DNA

211 cking, suggesting that vesicles derived from subcomplexes of COPII coat proteins have a role in the s

212 dings of eIF3a and eIF3j to eIF3b, different subcomplexes of eIF3 likely exist and may perform noncan

213 It is also not clear whether or not some subcomplexes of MCC inhibit the APC/C and whether Mad2 i

214 CT chaperonin further binds and disassembles subcomplexes of MCC that lack Mad2.

215 Water-soluble subcomplexes of membrane-bound [NiFe]-hydrogenases (MBH)

216 Subcomplexes of mitochondrial respiratory complex I (CI;

217 We used purified subcomplexes of mitotic checkpoint proteins to examine t

218 ed differences in the subunit composition of subcomplexes of ovine complex I as compared with bovine,

219 and XPD ATPases, and how the core and kinase subcomplexes of TFIIH are connected.

220 Multiple protein subcomplexes of the kinetochore cooperate as a cohesive

221 We have previously proposed a model where subcomplexes of vRNA are exported from the nucleus and a

222 , Fap7 ATPase activity unloads the uS11:eS26 subcomplex onto its rRNA binding site, and therefore ens

223 Teb1, and the p75 subunit of the holoenzyme subcomplex p75/p19/p45.

224 r pilin PilE depends on the putative priming subcomplex PilVWX and the non-pilin protein PilY1 for in

225 at mutant ESCs assemble atypical hybrid PRC2 subcomplexes, potentially accounting for enhancement of

226 a major component of an adaptor nucleoporin subcomplex proposed to link the NPC coat with the centra

227 Although the docking subcomplex proteins (Pex13, Pex14, and Pex17) also requi

228 ory particle, consisting of the lid and base subcomplexes, recognizes and processes polyubiquitinated

229 Phosphomimetics on either subcomplex reduced attachment lifetimes under constant f

230 lar waveforms reveals that loss of the IC138 subcomplex reduces shear amplitude, sliding velocities,

231 ntified an RNA editing helicase 2-associated subcomplex (REH2C) and showed that REH2 binds RNA.

232 lation and in formation of the eIF3(a:b:i:g) subcomplex remain to be solved.

233 e of these proteins and how they assemble in subcomplexes remain poorly defined.

234 The PP2A subcomplex required for stable G0 contains the B56gamma

235 For these exceptions, we find that distorted subcomplexes result from extreme disruption conditions,

236 ndant functions as the absence of both MICOS subcomplexes results in more severe morphological and re

237 n amc1, -2, -5-7, the detection of a 700 kDa subcomplex retaining NADH dehydrogenase activity indicat

238 The RMI subcomplex (RMI1/RMI2) functions with the BLM helicase a

239 liberated upon dissection of complex II into subcomplexes, SDH6 and SDH7 also add some hydrophilic ma

240 ated by association with different accessory subcomplexes: SecYEG (forming SecYEG dimers) or SecDF-Ya

241 This subcomplex serves as an acceptor for a Q(a) SNARE from t

242 ein 3, NADH dehydrogenase (ubiquinone) 1beta subcomplex subunit 8, and NADH dehydrogenase (ubiquinone

243 fied NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9 (NDUFA9) and inosine-5'-monophospha

244 , and NADH dehydrogenase (ubiquinone) 1alpha subcomplex subunit 9 of respiratory complex I, and decre

245 d find additional functions of the Top3-Rmi1 subcomplex that are critical for the completion of meios

246 complex I and probably stabilizes a 400-kDa subcomplex that forms the initial nucleus of the periphe

247 eins, IFT144/140/122, can form a stable 12 S subcomplex that we refer to as the IFT A core.

248 eatments, the holo complex is dissected into subcomplexes that are analyzed by a three-dimensional ge

249 romatin-modifying complexes are organized by subcomplexes that harbor unique and distinct activities.

250 ase-resistant EMRE mutants produce uniporter subcomplexes that induce constitutive Ca(2+) leakage int

251 y mutants and isolated histidine-tagged PSII subcomplexes that Psb27 associates with the "unassembled

252 active minimal complexes, we identify stable subcomplexes that, through newly defined protein-protein

253 sis culminates with the joining of two large subcomplexes, the lid and base.

254 s regulatory particle (RP) consisting of two subcomplexes, the lid and the base.

255 plex (NDH-C) is assembled from five distinct subcomplexes, the membrane-spanning (subM) and the lumin

256 The APC/C assembly contains two subcomplexes: the "Platform" centers around a cullin-RIN

257 The 26S proteasome can be divided into two subcomplexes: the 19S regulatory particle and the 20S co

258 Coatomer consists of two subcomplexes: the membrane-targeting, ADP ribosylation f

259 The APC/C assembly comprises two scaffolding subcomplexes: the platform and the TPR lobe that togethe

260 hat F(O)F1 is assembled in a modular way via subcomplexes, thereby preventing the formation of a func

261 aging, and budding of peroxisomal importomer subcomplexes, thereby preventing their premature assembl

262 is the core component of the inner membrane subcomplex thought to be involved in both recognition of

263 solating mitochondria, we have identified CI subcomplexes through differences in (15)N incorporation

264 rmational switch in both FtsA and the FtsBLQ subcomplex to de-repress septal peptidoglycan synthesis

265 that with FimU, PilE may couple the priming subcomplex to the major pilin PilA, allowing for efficie

266 PilXNm and PilVNm, likely connects a priming subcomplex to the major pilin, promoting efficient assem

267 Here we used heterologously expressed BBSome subcomplexes to analyze the complex architecture and to

268 quiring 66 subunits distributed over several subcomplexes to associate in a coordinated fashion.

269 ing of the MIS12 and NDC80 outer kinetochore subcomplexes to CENP-C and CENP-T.

270 ators include components of the spliceosomal subcomplex U1 small nuclear ribonucleoprotein (U1 snRNP)

271 The formation of this subcomplex was critical for conferring stability to the

272 ammadelta)(4) kinase core, because a beta(4) subcomplex was observed through both chemical cross-link

273 Proper fractionation of PSII super- and subcomplexes was achieved by critical selection of eluti

274 teracts with the Rags and is composed of two subcomplexes we call GATOR1 and -2.

275 d throughout the extremely stable Nup107-160 subcomplex, we refined our understanding of this highly

276 try of the FtsQpBpLp complex and the FtsQpBp subcomplex were determined in complementary surface plas

277 mutations in the conserved PilMNOP alignment subcomplex were previously shown to have distinct effect

278 ver, intact PA700 accumulated as an isolated subcomplex when cellular 20 S proteasome content was red

279 ften more compact and reflect native protein subcomplexes when compared with unmodified complexes act

280 EPB7, and KREPB8 associate with the deletion subcomplex, whereas the KREN1, KREN2, and KREN3 endonucl

281 Mediator contains the Cdk8 regulatory subcomplex, which directs periodic transcription and inf

282 ith the highly conserved YidC and SecDF-YajC subcomplex, which facilitates translocation into and acr

283 DNA repair, while the CDK-activating kinase subcomplex, which includes the kinase activity of CDK7 a

284 Far3, Far7, and Far8 form a subcomplex, which is recruited to the ER by Far9/10.

285 (Arf1):GTP-binding betagammadeltazeta-COP F-subcomplex, which is related to the adaptor protein (AP)

286 r membrane and forms a approximately 300 kDa subcomplex with complex IV subunits.

287 an mRNA-associated ribonucleoprotein (mRNP) subcomplex with editing substrates, intermediates, and p

288 somal central protuberance, assembles into a subcomplex with MrpL7 (uL5), Mrp7 (bL27), and MrpL36 (bL

289 on display reduced affinity to form a stable subcomplex with NFS1, and thereby fails to prevent NFS1

290 of RNA polymerase II (RNAP II) that forms a subcomplex with Rpb7, play important roles in transcript

291 paring the CD spectrum of an alphagammadelta subcomplex with that of the native (alphabetagammadelta)

292 the overall coat complex, and form distinct subcomplexes with cavin 1.

293 Both DnaJC15 and DnaJC19 formed two distinct subcomplexes with Magmas at the import channel.

294 I disrupted the assembly of the complex, and subcomplexes with masses of 550 and 815 kDa accumulated.

295 ions suggest that the complex is composed of subcomplexes with RNA-dependent and independent interact

296 Eaf3, Eaf5, and Eaf7 form a subcomplex within NuA4 that may also function independen

297 n distinct conformations of the Rpn1-p28-AAA subcomplex within the p28-bound RP at subnanometer resol

298 e determined the structure of a four-protein subcomplex within the SWI/SNF remodeler that comprises t

299 amidase autoinhibition governed by conserved subcomplexes within the cytokinetic ring.

300 tylation in regulating the formation of DUBm subcomplexes within the larger SAGA complex.