ライフサイエンスコーパス: multisubunit

1 One such E3 is the gigantic, multisubunit 1.2-MDa anaphase-promoting complex/cyclosom

2 her, this study demonstrates that SGF-2 is a multisubunit activator complex containing Awh.

3 e transport but are consistent with either a multisubunit, allosteric transporter, or a transporter i

4 Mediator is a multisubunit assemblage of proteins originally identifie

5 complex I in mitochondria are membrane-bound multisubunit assemblies of both hydrophilic and hydropho

6 regation of separate polypeptide chains into multisubunit assemblies.

7 monomers within the ER is a prerequisite for multisubunit assembly in the TGN.

8 gomeric integral membrane proteins, folding, multisubunit assembly, and recognition of conformational

9 omponent of both the proteasome and a second multisubunit assembly, the INO80 complex.

10 V-ATPases (H(+) ATPases) are multisubunit, ATP-dependent proton pumps that regulate p

11 The multisubunit bacterial RNA polymerase (RNAp) enzyme, whi

12 t these models in the structurally unrelated multisubunit bacterial RNA polymerase.

13 Intrinsic termination signals for multisubunit bacterial RNA polymerases (RNAPs) encode a

14 A multisubunit, bidirectional [NiFe]-hydrogenase has been

15 w protein interaction surface that creates a multisubunit-binding site for an S-phase protein kinase

16 esolution will allow the structure of large, multisubunit biological complexes in biologically releva

17 ovirus [HCMV] stimulates the assembly of the multisubunit, cap-binding translation factor eIF4F.

18 RNA polymerases are key multisubunit cellular enzymes.

19 equential rounds of linkage would generate a multisubunit chain that pulls successive subunits into a

20 Proteasomes are multisubunit chambered proteases and, until recently, we

21 r single copies of the mammalian double-ring multisubunit chaperonin TRiC/CCT in free solution using

22 Tagetitoxin (Tgt) inhibits multisubunit chloroplast, bacterial, and some eukaryotic

23 Whereas the multisubunit chromatin remodeler SWR1 is known to cataly

24 SWI/SNF is a multisubunit chromatin-remodeling complex that performs

25 Mediator is a multisubunit coactivator complex that facilitates transc

26 for controlling cell cycle transitions, is a multisubunit complex assembled from 13 different protein

27 In humans, the multisubunit complex cohesin is made up of SMC1, SMC3, R

28 HAT-B is a multisubunit complex composed of the histone acetyltrans

29 gether until mitosis by cohesin, a conserved multisubunit complex comprised of Smc1, Smc3, Scc1, and

30 nt-rich conditions, Atg1 is active only in a multisubunit complex comprising constitutive protein agg

31 A multisubunit complex containing chromatin remodeling pro

32 compartments, and FANCI-D2 interacted with a multisubunit complex containing the virus-encoded single

33 its (CesAs) are the catalytic sites within a multisubunit complex for cellulose biosynthesis in plant

34 Cytoplasmic dynein is a large multisubunit complex involved in retrograde transport an

35 The SWI/SNF multisubunit complex modulates chromatin structure throu

36 Here we report the identification of a multisubunit complex named BORC that regulates lysosome

37 ng of ScMcm10 on dsDNA and the assembly of a multisubunit complex on ssDNA suggests that, in addition

38 functional component of Integrator (INT), a multisubunit complex required for 3'-end processing of s

39 The proteasome is a multisubunit complex responsible for most nonlysosomal t

40 erts its effects on actin dynamics through a multisubunit complex termed Arp2/3.

41 The proteasome is a large, multisubunit complex that acts as the cell's 'protein-de

42 NADPH oxidase is a multisubunit complex that assembles during phagocytosis

43 I-E CRISPR-Cas system Cascade effector is a multisubunit complex that binds CRISPR RNA (crRNA).

44 The vacuolar ATPase (V-ATPase) is a multisubunit complex that carries out ATP-driven proton

45 The eukaryotic 26S proteasome is a large multisubunit complex that degrades the majority of prote

46 TIP60 resides within a multisubunit complex that has been shown to be targeted

47 s process also involves the DREAM complex, a multisubunit complex that has recently been identified a

48 Mediator is a large, multisubunit complex that is required for essentially al

49 omoting complex/cyclosome (APC/C) is a large multisubunit complex that regulates cell cycle progressi

50 the protein-protein interactions within the multisubunit complex were measured by isothermal titrati

51 It forms a multisubunit complex with TatB and binds the signal pept

52 Several proteins dedicated to this multisubunit complex, including BRG1 (also known as SMAR

53 Dynactin, a large multisubunit complex, is required for intracellular tran

54 4 (H3K4) methyltransferase that exists as a multisubunit complex.

55 ent viruses use different components of this multisubunit complex.

56 in the context of its biologically assembled multisubunit complexes (RDRCs).

57 proteins forms the core structures of three multisubunit complexes as follows: cohesin, condensin, a

58 regulation, and yet it is unclear how these multisubunit complexes coordinate their activities to fa

59 an innovative method to investigate PPIs of multisubunit complexes effectively and to identify new m

60 ATRX185 and ATRX125 form distinct multisubunit complexes in fly embryo.

61 istone acetyltransferases (HATs) function as multisubunit complexes in which accessory proteins regul

62 ic cells, oxidative phosphorylation involves multisubunit complexes of mixed genetic origin.

63 velopment incorporate peptides, subunits, or multisubunit complexes representing parts or all of the

64 Kinetochores are multisubunit complexes that assemble on centromeres to b

65 SWR-C/SWR1 and INO80 are multisubunit complexes that catalyze the deposition and

66 l insights into the assembly and function of multisubunit complexes that may not be revealed by using

67 Proteasomes are large, multisubunit complexes that support normal cellular acti

68 s, or remodelers, which are typically large, multisubunit complexes that use an ATPase subunit to tra

69 ATP-dependent motors that often function in multisubunit complexes to regulate chromatin structure.

70 conserved from yeast to humans, assemble in multisubunit complexes, and are needed to regulate gene

71 mTOR functions as part of either of the two multisubunit complexes, mTORC1 and mTORC2, but molecular

72 unction in leukemia occurs in the context of multisubunit complexes, which also protect the LMO2 onco

73 nover of proteasomes and several other large multisubunit complexes.

74 ding the molecular regulation of HATs within multisubunit complexes.

75 e stoichiometry of proteins participating in multisubunit complexes.

76 romatin-dependent processes are catalyzed by multisubunit complexes.

77 echanism to enforce hierarchical assembly in multisubunit complexes.

78 PHB complex participates in the assembly of multisubunit complexes; namely, respiratory complex I an

79 , and the sugar-specific membrane-associated multisubunit components enzymes IIC (EIIC) and IID (EIID

80 Whether vasoconstrictors regulate the multisubunit composition of surface BK channels to stimu

81 Whether the multisubunit composition of surface channels is fixed fo

82 The multisubunit composition of the transduction complex and

83 Understanding the diverse activities of the multisubunit core promoter recognition complex TFIID in

84 ox14 and Cox1 to facilitate the formation of multisubunit COX assembly intermediates.

85 n mammals, is specifically recognized by the multisubunit CPSF (cleavage and polyadenylation specific

86 The multisubunit cullin RING E3 ubiquitin ligases (CRLs) tar

87 s its overall architecture is reminiscent of multisubunit cullin-RING ubiquitin ligase complexes.

88 J-NAIP2-NLRC4 inflammasome is assembled into multisubunit disk-like structures through a unidirection

89 The multisubunit DNA repair and transcription factor TFIIH m

90 LMO2 is a component of multisubunit DNA-binding transcription factor complexes

91 ehensive multiple sequence alignments of the multisubunit DNA-dependent RNA polymerase (RNAP) large s

92 tch 3 is a polypeptide loop conserved in all multisubunit DNA-dependent RNA polymerases (RNAPs) that

93 , including eukaryotic, membrane, toxic, and multisubunit DNA/RNA-binding proteins.

94 on in all cellular organisms is performed by multisubunit, DNA-dependent RNA polymerases that synthes

95 Here we report the identification of a multisubunit Dot1 complex (DotCom), which includes sever

96 The TO cytoskeleton is organized as a multisubunit dynamic motor, including three main ultrast

97 Cilia motility requires the assembly of multisubunit dynein arms that drive ciliary bending.

98 he architecture of the Dsc E3 ligase and the multisubunit E3 ligase gp78 in mammals.

99 (linear ubiquitin chain assembly complex), a multisubunit E3 ligase.

100 advance our organizational understanding of multisubunit E3 ligases involved in endoplasmic reticulu

101 complex or cyclosome (APC/C) is a conserved, multisubunit E3 ubiquitin (Ub) ligase that is active bot

102 One such master regulator is the large, multisubunit E3 ubiquitin ligase anaphase-promoting comp

103 A central player in the pathway is a multisubunit E3 ubiquitin ligase complex or the FA core

104 phase Promoting Complex/Cyclosome (APC/C), a multisubunit E3 ubiquitin ligase targeting cell-cycle fa

105 se-promoting complex or cyclosome (APC/C), a multisubunit E3 ubiquitin ligase, is regulated by phosph

106 ing complex/cyclosome(Cdh1) (APC/C(Cdh1)), a multisubunit E3 ubiquitin ligase.

107 Cullin-RING ligases are multisubunit E3 ubiquitin ligases that recruit substrate

108 ely 300 human cullin-RING ligases (CRLs) are multisubunit E3s in which a RING protein, either RBX1 or

109 R-Cas systems are divided into Class 1, with multisubunit effector complexes, and Class 2, with singl

110 adaptable immune system that is mediated by multisubunit effector complexes.

111 uinone oxidoreductase (complex I/NDH-1) is a multisubunit enzymatic complex.

112 active site (C-cluster) of the bifunctional multisubunit enzyme complex carbon monoxide dehydrogenas

113 aryotic vacuolar H(+)-ATPase (V-ATPase) is a multisubunit enzyme complex that acidifies subcellular o

114 Gamma-secretase is a widely expressed multisubunit enzyme complex which is involved in the pat

115 ulation existing between two subunits of the multisubunit enzyme complex, GPI-N-acetylglucosaminyltra

116 t targeted, signal-dependent dissociation of multisubunit enzyme complexes is an important mechanism

117 It is a multisubunit enzyme embedded in the lipid environment of

118 (2+) into protoporphyrin IX catalyzed by the multisubunit enzyme magnesium chelatase.

119 proton-translocating ATPase (V-ATPase) is a multisubunit enzyme responsible for organelle acidificat

120 Oligosaccharyl transferase (OT) is a multisubunit enzyme that catalyzes N-linked glycosylatio

121 (NADH ubiquinone oxidoreductase) is a large multisubunit enzyme that catalyzes the first step in oxi

122 Telomerase is a multisubunit enzyme that maintains genome stability thro

123 Phosphodiesterase-6 (PDE6) is a multisubunit enzyme that plays a key role in the visual

124 ating that some basic regulation of the PDE6 multisubunit enzyme was maintained albeit by a unknown m

125 DPH oxidase (NOX), the superoxide-generating multisubunit enzyme.

126 gene expression trends was found for 65% of multisubunit enzymes and 75% of allosteric reactions.

127 Axonemal dyneins are multisubunit enzymes that must be preassembled in the cy

128 n order to operate in a coordinated fashion, multisubunit enzymes use cooperative interactions intrin

129 there is no structural information on these multisubunit enzymes.

130 h roles in assembly and nuclear transport of multisubunit eukaryotic RNA polymerases.

131 ce is dependent on Chs5p, a component of the multisubunit exomer complex.

132 as XRN4, or in the opposite direction by the multisubunit exosome complex.

133 In vivo, a multisubunit FA core complex catalyzes this step, but it

134 and its binding partner, FAAP24, anchor the multisubunit FA core complex to chromatin after DNA dama

135 duced by uropathogenic Escherichia coli, are multisubunit fibres crucial in recognition of and adhesi

136 esentative of a widespread class of adhesive multisubunit fibres in Gram-negative bacteria.

137 the presumptive catalytic components of the multisubunit gamma-secretase complex, which proteolyzes

138 The multisubunit gamma-tubulin complex (gamma-TuC) is critic

139 The multisubunit Golgi-associated retrograde protein (GARP)

140 ion of three tubulin cofactors and Arl2 as a multisubunit GTP-hydrolyzing catalytic chaperone that cy

141 tion of a DNA double-strand break (DSB) by a multisubunit helicase-nuclease machine (e.g. RecBCD, Add

142 l to the recombination pathway driven by the multisubunit helicase-nuclease machine RecBCD.

143 Together with CcmF and CcmH, CcmI forms a multisubunit heme ligation complex.

144 SAGA (Spt-Ada-Gcn5) complex, a well-studied multisubunit histone modifier, regulates gene expression

145 The multisubunit homotypic fusion and vacuole protein sortin

146 l stress response that antagonizes mTORC1, a multisubunit host kinase that controls protein synthesis

147 iated by single-subunit T7 RNA polymerase or multisubunit human RNA polymerase II in vitro and in hum

148 iated by single-subunit T7 RNA polymerase or multisubunit human RNA polymerase II in vitro and in hum

149 tations onto a model of the structure of the multisubunit IN-viral DNA complex, we found the lethal m

150 g to eIF4G, thereby reducing assembly of the multisubunit initiation factor eIF4F, viral protein prod

151 Why eukaryotes evolved a multisubunit initiator, and the roles of each component,

152 tic elements by an RNA-guided, RNA-targeting multisubunit interference complex.

153 nt-based drug design that were applicable to multisubunit ion channels.

154 rases METTL3 and METTL14 are components of a multisubunit m(6)A writer complex whose enzymatic activi

155 vacuolar H(+) ATPase (V-ATPase) is a complex multisubunit machine that regulates important cellular p

156 Structures of multisubunit macromolecular machines are primarily deter

157 any cyanobacteria use brilliantly pigmented, multisubunit macromolecular structures known as phycobil

158 hanism involving recruitment to ERSEs of the multisubunit Mediator and several histone acetyltransfer

159 Molecular Cell provide insights into how the multisubunit Mediator coactivator complex dynamically li

160 The multisubunit Mediator, comprising approximately 30 disti

161 Photosystem I (PS I) is a multisubunit membrane protein complex that functions as

162 that activate cells of the immune system are multisubunit membrane protein complexes in which ligand

163 rgy into chemical energy is catalyzed by two multisubunit membrane protein complexes, photosystem I (

164 PSII is a multisubunit membrane protein; the D1 and D2 polypeptide

165 Four multisubunit membrane proteins are involved: photosystem

166 iplasmic maltose-binding protein (MBP) and a multisubunit membrane transporter, MalFGK(2).

167 of yeast oligosaccharyl transferase (OT), a multisubunit membrane-associated enzyme complex catalyzi

168 In eukaryotes, it is catalyzed by a multisubunit membrane-associated enzyme, oligosaccharylt

169 plex I (NADH:ubiquinone oxidoreductase) is a multisubunit, membrane-bound enzyme of the respiratory c

170 of chlorophyllide a by the nitrogenase-like multisubunit metalloenzyme, chlorophyllide a oxidoreduct

171 The multisubunit mitochondrial contact site and cristae orga

172 They are synthesized by a multistep and multisubunit mitochondrial machinery that includes the s

173 t Swr1, brackets two independently assembled multisubunit modules.

174 reconstitution and characterization of this multisubunit monoubiquitin E3 ligase, providing key insi

175 ns that assemble into the FA core complex, a multisubunit monoubiquitin E3 ligase.

176 Cytoplasmic dynein is a large multisubunit motor protein complex and has a key role in

177 Cytoplasmic dynein is a 1.2-MDa multisubunit motor protein complex that, together with i

178 ecific protein-protein interactions within a multisubunit mRNA splicing complex.

179 The multisubunit mTORC1 complex integrates signals from grow

180 The transcriptional regulation of such a multisubunit, multichromosomal, and bigenomic enzyme is

181 However, as a multisubunit, multispan, integral membrane protein, even

182 e the combinatorial complexity inherent in a multisubunit, multistate system.

183 by coexpressing large transgenes encoding a multisubunit neuronal voltage-gated sodium channel (SCN1

184 damage responses through the formation of a multisubunit nuclear complex that facilitates the E3 ubi

185 Eukaryotes express three or more multisubunit nuclear RNA polymerases (Pols) referred to

186 The multisubunit nucleosome-remodeling enzyme complex SWR1,

187 Multisubunit outer dynein arm (ODA) motor complexes, pro

188 The IFT machinery is composed of motors and multisubunit particles, termed IFT-A and IFT-B, that car

189 sphatase 2A (PP2A), a ubiquitously expressed multisubunit phosphatase.

190 Photosystem II (PSII), a large multisubunit pigment-protein complex localized in the th

191 conservation of initiation mechanisms among multisubunit Pols and reveal a key function of yeast cor

192 DNA polymerase delta (Poldelta) is a multisubunit polymerase that plays an indispensable role

193 apsid, containing scaffolding proteins and a multisubunit portal but lacking DNA, which matures into

194 we identified a role for the proteasome, the multisubunit protease that degrades proteins in the nucl

195 the abundance of the proteasome, the complex multisubunit protease that destroys proteins.

196 Proteasomes are multisubunit proteases that initiate degradation of many

197 Multisubunit protein assemblies offer integrated functio

198 densin is a large, evolutionarily conserved, multisubunit protein assembly composed of dimers of the

199 The v-ATPase, a multisubunit protein complex composed of cytosolic V1-se

200 Escherichia coli RNA polymerase (RNAP) is a multisubunit protein complex containing the smallest sub

201 cle targeting and fusion require a conserved multisubunit protein complex termed the exocyst, which h

202 Cohesin is a conserved multisubunit protein complex that participates in chromo

203 terations in the function of the retromer, a multisubunit protein complex that plays a specialized ro

204 Mediator, an evolutionary conserved large multisubunit protein complex with a central role in regu

205 ullin4A-RING E3 ubiquitin ligase (CRL4) is a multisubunit protein complex, comprising cullin4A (CUL4)

206 The multisubunit protein complex, dynactin, is an essential

207 Condensin, an evolutionarily conserved multisubunit protein complex, is essential for chromosom

208 Mediator, a large multisubunit protein complex, plays a pivotal role in ge

209 Human Scml2 is a part of a multisubunit protein complex, PRC1 (Polycomb repressive

210 on of mRNA precursors is mediated by a large multisubunit protein complex.

211 The HVCCs are multisubunit protein complexes composed of a pore-formin

212 The constituents of large, multisubunit protein complexes dictate their functions i

213 Multisubunit protein complexes pose a challenge to the c

214 lated through the assembly onto chromatin of multisubunit protein complexes that license DNA for a fu

215 g to fold properly or to assemble into their multisubunit protein complexes.

216 cal reactions that are uniquely performed by multisubunit protein complexes.

217 dentify substrates and accessory subunits of multisubunit protein complexes.

218 define dominant trafficking domains in other multisubunit protein complexes.

219 used to target the subunit interfaces of any multisubunit protein having a similar mechanism of actio

220 alpha interacts with IkappaB kinase (IKK), a multisubunit protein kinase that consists of two catalyt

221 The GABA(A) receptor is a multisubunit protein that transduces the binding of a ne

222 d act within the cell to alter assembly of a multisubunit protein.

223 the importance of including all subunits of multisubunit proteins to map realistic kinetically acces

224 n, and Changeux (MWC) explained allostery in multisubunit proteins with a widely applied theoretical

225 e 26S proteasome is a 2.5-MDa, ATP-dependent multisubunit proteolytic complex that processively destr

226 The vacuolar H(+)-ATPase (V-ATPase), a multisubunit proton pump, has come into focus as an attr

227 hemoglobins of gnathostomes and cyclostomes, multisubunit quaternary structures provide the basis for

228 The T cell antigen receptor (TCR) is a multisubunit receptor on the surface of T cells that is

229 The RNA exosome is an essential multisubunit ribonuclease (RNase) that contributes to cy

230 ssRNA is channeled through its multisubunit ring-like core into the active site tunnel

231 protein complexes consisting of two stacked multisubunit rings, which open and close in an ATP-depen

232 ediate protein folding in a cavity formed by multisubunit rings.

233 Subunit D of multisubunit RNA polymerase from many species of archaea

234 a complete transcription system, including a multisubunit RNA polymerase, stage-specific transcriptio

235 xviruses are large DNA viruses that encode a multisubunit RNA polymerase, stage-specific transcriptio

236 Eukaryotic and archaeal multisubunit RNA polymerases (Pols) are structurally rel

237 The secondary channel (SC) of multisubunit RNA polymerases (RNAPs) allows access to th

238 Evolution-related multisubunit RNA polymerases (RNAPs) carry out RNA synth

239 Transcriptional pausing by multisubunit RNA polymerases (RNAPs) is a key mechanism

240 The active site of multisubunit RNA polymerases (RNAPs) is highly conserved

241 Evolutionary related multisubunit RNA polymerases (RNAPs) transcribe the geno

242 The flap domain of multisubunit RNA polymerases (RNAPs), also called the wa

243 Multisubunit RNA polymerases are complex protein machine

244 Parallels in the multisubunit RNA polymerases are discussed.

245 ntified the subunits of Arabidopsis thaliana multisubunit RNA polymerases I and III (abbreviated as P

246 Multisubunit RNA polymerases IV and V (Pols IV and V) me

247 In Arabidopsis, multisubunit RNA polymerases IV and V orchestrate RNA-di

248 with his presentation entitled "Five nuclear multisubunit RNA polymerases".

249 All eukaryotes have three essential nuclear multisubunit RNA polymerases, abbreviated as Pol I, Pol

250 ants are remarkable in having two additional multisubunit RNA polymerases, Pol IV and Pol V, which sy

251 tion may date back to the common ancestor of multisubunit RNA polymerases.

252 e importance of shared regions common to all multisubunit RNA polymerases.

253 ion factors that enhance the processivity of multisubunit RNA polymerases.

254 e thought to assemble into two non-canonical multisubunit RNAPs - a virion RNAP (vRNAP) that is injec

255 rity with the largest, catalytic subunits of multisubunit RNAPs and contains the conserved metal-bind

256 While other multisubunit RNAPs require multipartite cis-signals and/

257 action of two varphiKZ-encoded, noncanonical multisubunit RNAPs, one of which is packed within the vi

258 nalogous to the transcription factors of the multisubunit RNAPs, which provides an intriguing link be

259 vides an intriguing link between single- and multisubunit RNAPs.

260 ents of the two largest subunits of cellular multisubunit RNAPs.

261 The V-ATPase is a multisubunit, rotary proton pump whose precise role in h

262 oup of E3 ubiquitin ligases is formed by the multisubunit SCF complex, whose core complex (Rbx1/Cul1-

263 TCR is noncovalently coupled to a conserved multisubunit signaling apparatus, the CD3 complex, that

264 al component of the evolutionarily conserved multisubunit SIN3 complex that has roles in regulating g

265 The multisubunit Smc5-Smc6 holocomplex (Smc5/6) plays a crit

266 The role of the multisubunit sodium/proton antiporter (Mrp) of Methanosa

267 chemical complementation assay to discover a multisubunit stem cell coactivator complex (SCC) that is

268 cterized terms identified by NeXO, including multisubunit structures related to protein trafficking o

269 The 26 S proteasome comprises two multisubunit subcomplexes as follows: 20 S proteasome an

270 erichia coli, crRNAs are incorporated into a multisubunit surveillance complex called Cascade (CRISPR

271 RNAs (crRNAs) assemble into a 405-kilodalton multisubunit surveillance complex called Cascade (CRISPR

272 ipt by the Cas6 endonuclease and loaded into multisubunit surveillance/effector complexes, allowing h

273 The multisubunit SWI/SNF and RSC complexes utilize energy de

274 ype 2 behavior is not limited to cooperative multisubunit systems.

275 Inhibiting multisubunit targets with sequential actions resembles b

276 I (transport protein particle II) complex, a multisubunit tethering complex that is a GEF for the Rab

277 y which the exocyst, the exocytosis-specific multisubunit tethering complex, interacts with the exocy

278 ic fusion and vacuole protein-sorting (HOPS) multisubunit tethering complex, which is involved in the

279 COG, like other multisubunit tethering complexes (MTCs), is thought to f

280 7 shares structural similarity with cellular multisubunit tethering complexes (MTCs), which control v

281 s proposed to mediate tethering are a set of multisubunit tethering complexes (MTCs).

282 ition of Rab GTPase on transport vesicles by multisubunit tethering complexes and subsequent coupling

283 erly localized vesicle fusion, including the multisubunit tethering complexes and the SNARE complexes

284 s between MUN domain-containing proteins and multisubunit tethering complexes such as exocyst, conser

285 uctural similarity to components of cellular multisubunit tethering complexes, which control vesicula

286 bundle organization similar to that of other multisubunit tethering complexes.

287 mediated by SNARE proteins, Rab-GTPases, and multisubunit tethering complexes.

288 The multisubunit tethering homotypic fusion and vacuole prot

289 The multisubunit TFIID plays a direct role in transcription

290 Like the more complex multisubunit transcription systems, multiple steps may e

291 bosomes are loaded onto capped mRNAs via the multisubunit translation initiation factors eIF3 and eIF

292 Type IV secretion systems (T4SSs) are large multisubunit translocons, found in both gram-negative an

293 slationally imported into organelles through multisubunit translocons.

294 of cellulose synthase proteins in this large multisubunit transmembrane protein complex and the numbe

295 The large multisubunit transport protein particle (TRAPP) II compl

296 assembly is driven by crRNA and suggest that multisubunit type I CRISPR effectors may have evolved fr

297 phase-promoting complex/cyclosome (APC/C), a multisubunit ubiquitin E3 ligase that regulates the prog

298 itin ligase cascade involving parkin and the multisubunit ubiquitin ligase SCF(Fbw7beta).

299 ination is carried out by the Gid complex, a multisubunit ubiquitin ligase that consists of seven dif

300 s damage caused by interstrand crosslinks, a multisubunit ubiquitin ligase that monoubiquitinates two