ライフサイエンスコーパス: assembly factor

1 in-protein ligases), and E4 (ubiquitin chain assembly factors).

2 the flavoprotein of complex II and the SdhE assembly factor.

3 modulating the levels of TPX2, a key spindle assembly factor.

4 edicated transcription factor and a ribosome assembly factor.

5 s, we validated C17orf89 as a complex I (CI) assembly factor.

6 on in complex I assembly as a plant-specific assembly factor.

7 l for photoautotrophy, functioning as a PS I assembly factor.

8 Scm3 functions as a Cse4-specific nucleosome assembly factor.

9 RAVE is the first isoform-specific V-ATPase assembly factor.

10 U5 small nuclear ribonucleoprotein particle assembly factor.

11 am68l-1 mutant identifies PAM68L as an NDH-C assembly factor.

12 etion substrate, needle cap, and injectisome assembly factor.

13 g center preventing binding of YjeQ, another assembly factor.

14 ecificity control activities of a processive assembly factor.

15 ive hepatopathy due to mutated BCS1L, a CIII assembly factor.

16 y of Scm3(HJURP), the centromeric nucleosome assembly factor.

17 eta gradually tune the activities of spindle assembly factors.

18 se function of each of the approximately 200 assembly factors.

19 is a complex process facilitated by several assembly factors.

20 ompanied by the accumulation of PSI-specific assembly factors.

21 the 16S rRNA, and several mtLSU proteins and assembly factors.

22 ermediate that exhibits low affinity for the assembly factors.

23 ains filament networks generated by multiple assembly factors.

24 mplicated multistep process that is aided by assembly factors.

25 pwise fashion through the actions of several assembly factors.

26 ning through the release of late-stage mtLSU assembly factors.

27 also RNA-processing, translation and protein assembly factors.

28 r content of COX subunits and COX7A2L/HIGD2A assembly factors.

29 action by transportin binding and inhibiting assembly factors.

30 ith both the RNA surveillance system and SRP assembly factors.

31 eotide cofactor require the participation of assembly factors.

32 protein (HJURP) coupled with other chromatin assembly factors.

33 nuclear-encoded accessory proteins known as assembly factors.

34 cellular distribution of several soluble COX assembly factors.

35 regulated process that requires a number of assembly factors.

36 nd subunit assembly with the aid of numerous assembly factors.

37 2) is a member of the formin family of actin assembly factors.

38 in-like cochaperone complex and known dynein assembly factors.

39 stead of binding DNA, Teb2 and Teb3 are Teb1 assembly factors.

40 mplexes depends on the activity of dedicated assembly factors.

41 DNA (mtDNA)-encoded subunits or 14 known CI assembly factors.

42 ti-silencing function 1 (Asf1) and Chromatin Assembly Factor 1 (CAF-1) chaperone histones H3/H4 durin

43 Chromatin assembly factor 1 (CAF-1) deposits histones during DNA s

44 The histone chaperone Chromatin Assembly Factor 1 (CAF-1) deposits tetrameric (H3/H4)2 h

45 Chromatin assembly factor 1 (CAF-1) is a H3-H4 histone chaperone t

46 Chromatin assembly factor 1 (CAF-1) is a histone H3-H4 chaperone t

47 Chromatin assembly factor 1 (CAF-1) is the histone chaperone respo

48 anti-silencing factor 1 (Asf1) to chromatin assembly factor 1 (CAF-1), another histone chaperone tha

49 we show that the histone chaperone Chromatin Assembly Factor 1 (CAF-1), which is recruited to DNA rep

50 of nucleosome loading mediated by chromatin assembly factor 1 (CAF-1).

51 upled histone assembly mediated by CHROMATIN ASSEMBLY FACTOR 1 (CAF-1).

52 past history of a mutation for the chromatin assembly factor 1 (CAF1) complex causes rapid changes in

53 Here, we report that yeast chromatin assembly factor 1 (CAF1), a conserved histone chaperone

54 EMB1793, At1g76060), which we term COMPLEX I ASSEMBLY FACTOR 1 (CIAF1), contains a LYR domain and is

55 identify TMEM159, now re-named lipid droplet assembly factor 1 (LDAF1), as an interaction partner of

56 K-eIF2alpha-ATF4 axis increases supercomplex assembly factor 1 (SCAF1 or COX7A2L), promoting SCs and

57 subunit of the chromatin modifier chromatin assembly factor 1 and it regulates H3K9 trimethylation o

58 vestigate mutants dysfunctional in chromatin assembly factor-1 (CAF-1) (fas1 and fas2 mutants), which

59 Subunits of the chromatin assembly factor-1 (CAF-1) complex, including Chaf1a and

60 Chromatin assembly factor-1 (CAF-1) is a three-subunit protein com

61 cycle stages, whereas knockdown of chromatin assembly factor 1b (CAF-1b) revealed derepression predom

62 een, and a knockdown mutant (sdhaf2) for SDH assembly factor 2 that is required for FAD insertion int

63 codes NADH:ubiquinone oxidoreductase complex assembly factor 6, also known as C8ORF38.

64 lab suggests that a group of interdependent assembly factors (A(3) factors) is necessary to create e

65 facilitates UQ biosynthesis by acting as an assembly factor, a targeting factor, or both.

66 The ATP-dependent chromatin assembly factor (ACF) spaces nucleosomes to promote form

67 filopodia, by altering the balance of these assembly factors' activities.

68 In addition, several assembly factors (AFs) are absent from pre-ribosomes or

69 Assembly factors (AFs) prevent premature translation ini

70 Two additional assembly factors, AIFM1 and ACAD9, coimmunoprecipitated

71 se that multiple factors, including the SdhE assembly factor and bound dicarboxylates, stimulate cova

72 hese studies identify how the conserved SdhE assembly factor and its homologs participate in complex

73 his study defines a new membrane-embedded CI assembly factor and provides a resource for further anal

74 d by mutations in ribosomal proteins (RP) or assembly factors and are characterized by cellular hypop

75 proteins to interact with multiple, distant assembly factors and functional ribosomal RNA elements,

76 ucturing events coincide with the release of assembly factors and predict that completion of the head

77 ever, detailed insights into the function of assembly factors and ribosomal RNA folding events are la

78 ssemble gradually, chaperoned by a myriad of assembly factors and small nucleolar RNAs, before they r

79 s of the newly synthesized cytochrome b with assembly factors and structural complex III subunits.

80 tein-only pre-snoRNP complex containing five assembly factors and two core proteins, 15.5K and Nop58;

81 F1), II (SDHAF2), III (UQCC2), and IV (SCO1) assembly factors and was required for stability of respi

82 ting mitochondrial chaperone, OXPHOS complex assembly factor, and glycolysis genes, ATFS-1 bound dire

83 7 and cyclin H, explaining its role as a CAK assembly factor, and it forms interactions with the CDK7

84 -affected mutant68 (PAM68), a photosystem II assembly factor, and photosynthesis-affected mutant68-li

85 trates that axonemal dyneins, their specific assembly factors, and broadly-acting chaperones are conc

86 cytoplasm through stepwise release of bound assembly factors, and proofreading of their functional c

87 For instance, many mitotic spindle assembly factors are known to be sequestered in the nucl

88 Here, we report that active spindle assembly factors are protected from APC/C-dependent degr

89 In vivo, however, assembly factors are required (NUFIP, BCD1, and the HSP9

90 However, many envelope assembly factors are wholly extracytoplasmic.

91 ural subunits and specialized chaperone-like assembly factors, are formed.

92 Cox3, supporting the idea that supercomplex assembly factors associate with Cox3 and demonstrating t

93 as confirmed TMEM126B as the tenth complex I assembly factor associated with human disease and valida

94 they do in spindles, whereas two key midzone assembly factors, Aurora B and Kif4, act as they do in m

95 e deacetylase modifier SPOP and in chromatin assembly factor BAZ1A, in nearly two thirds of cases.

96 nce, and provide the first evidence of actin assembly factors being required to repair myofibrils.

97 functional inactivation of the 60S ribosome assembly factor Bop1 in a 3T3 cell model markedly increa

98 acer, which directs the early association of assembly factors but is absent from the mature ribosome.

99 e Cox1 degradation in cells lacking the Coa2 assembly factor, but not in a series of other mutants st

100 d at centromeres by the HJURP/Scm3 family of assembly factors, but homologues of these chaperones are

101 bosome biogenesis involves approximately 200 assembly factors, but how these contribute to ribosome m

102 for KAc-actin in the regulation of an actin assembly factor by a mechanism that we call facilitated

103 Here we show that chromatin assembly factor (CAF)-1 subunit A (CHAF1A), the p150 sub

104 er, the DNA replication-associated chromatin assembly factor, CAF-1, binds to and specifically mainta

105 of CENP-A, either alone or together with its assembly factor CAL1, drives stem cell self-renewal.

106 the release from the 30S subunit of a second assembly factor, called RbfA.

107 le, and loss or accumulation of such spindle assembly factors can result in aneuploidy and cancer.

108 Rubisco-interacting proteins, photosystem I assembly factor candidates, and inorganic carbon flux co

109 (3)-type cytochrome c oxidase (cbb (3)-Cox) assembly factor CcoG as a cupric reductase that binds Cu

110 zed in the absence of the cbb3 -Cox-specific assembly factors CcoGHIS.

111 ncluding the pathogenic bacteria lacking the assembly factor CcoH as in R. gelatinosus.

112 d that CENP-A nucleosomes recruit the CENP-A assembly factors CENP-C and M18BP1 independently.

113 tal of 21 known and potentially new ribosome assembly factors co-localized with various ribosomal par

114 The CcO assembly factor Coa2 appears important in coupling the p

115 hares sequence similarity with the yeast COX assembly factor Coa3 and was termed hCOA3.

116 een EGFL9 and the cytochrome c oxidase (COX) assembly factor COA3.

117 mutations were recently reported in one such assembly factor, COA6, and our previous work linked Coa6

118 A new study shows that assembly factors compete for actin monomers, leading to

119 ociated with multiple members of the MCIA CI assembly factor complex and core CI subunits and was loc

120 spliceosomal small nuclear ribonucleoprotein assembly factor conserved from yeast to humans, modulate

121 oroplast-located rubredoxin 1 (RBD1), a PSII assembly factor containing a redox-active rubredoxin dom

122 increased during development, whereas OxPhos assembly factors decreased.

123 abundance of several NPC components and NPC assembly factors decreases.

124 poorly understood how the timing of spindle assembly factor degradation is established during mitosi

125 The correct timing of spindle assembly factor degradation, as achieved by this regulat

126 strain, we show that the requirement for the assembly factor depends on the cellular redox environmen

127 phoinositide-rich membranes, whereas F-actin assembly factors Dia2 and N-WASP reside on phosphoinosit

128 anslocation, thereby releasing the essential assembly factor Dim1 from pre-40S subunits.

129 Thus, the two assembly factors directly interact to initiate filament

130 The dynein axonemal assembly factor (Dnaaf) protein family is involved in pr

131 t interacts with the cytoplasmic ODA and IDA assembly factor DNAAF2 (KTU).

132 DYX1C1 is a newly identified dynein axonemal assembly factor (DNAAF4).

133 However, how assembly factors drive the construction of ribonucleopro

134 well as the underlying actin structures and assembly factors driving the process are unknown.

135 east to human and functions as a spliceosome assembly factor during pre-mRNA splicing.

136 Soper et al. determine the specific role of assembly factors during the final stages of ribosomal su

137 Functional tests show that two key spindle assembly factors, dynein and kinesin-5, act during assem

138 The SdhE assembly factor enhances covalent flavinylation of Compl

139 Depletion of the assembly factor Erb1 prevents stable assembly of seven o

140 ar weight complexes combined with regulatory/assembly factors essential for expression of this subuni

141 Specialized assembly factors facilitate the formation of many macrom

142 pen reading frame YDR381C-A) as an important assembly factor for complex III, complex IV, and their s

143 in the survival motor neuron (SMN)1 gene, an assembly factor for loading the Sm complex on snRNAs and

144 Acyl-CoA dehydrogenase 9 (ACAD9) is an assembly factor for mitochondrial respiratory chain Comp

145 CD147 is an obligatory assembly factor for monocarboxylate transporters.

146 ssociates with the Ycf39 protein, a putative assembly factor for photosystem II, and with the YidC/Al

147 asizing the physiological importance of PSII assembly factors for light acclimation.

148 ular motor type-II myosin Myo2 and the actin assembly factor formin Cdc12.

149 questration, thus down-regulating release of assembly factors from importin beta, and 2) direct actio

150 er of ATP hydrolysis to drive the removal of assembly factors from pre-60S particles, but the mechani

151 bosome assembly intermediates and associated assembly factors from wild-type Escherichia coli cells u

152 wever, the precise mechanisms by which these assembly factors function are largely unknown.

153 er determine the order of association of all assembly factors functioning in one step of ribosome ass

154 ion (PARylation) in regulating the chromatin-assembly factor HIRA in ALT cancer cells.

155 The CENP-A chaperone and assembly factor HJURP induces decondensation of a noncen

156 er68 eliminates the binding of CENP-A to the assembly factor HJURP, thus preventing the premature loa

157 mbly into nucleosomes requires the chromatin assembly factor HJURP.

158 ng domain 1 (FOXRED1) protein is a complex I assembly factor; however, its specific role in the assem

159 have been described for eukaryotic ribosome assembly factors; however, this work describes an exampl

160 Instead, the CAF-1(chromatin assembly factor I) subunit Cac2 level decreased in the H

161 Specifically, mutations in four conserved assembly factors impinging the biogenesis of the mitocho

162 of the conformational changes induced by an assembly factor in a bacterial subunit intermediate.

163 ursor rRNA, ribosomal proteins, and ribosome assembly factors in a hierarchical manner.

164 ing of the 16S rRNA and is assisted by 10-20 assembly factors in bacteria.

165 the key membrane anchor for endocytic actin assembly factors in budding yeast.

166 is revealed an unexpected role for ribosomal assembly factors in controlling stem cell cytokinesis.

167 mework to dissect molecular roles of diverse assembly factors in eukaryotic ribosome assembly.

168 on, rRNA processing activities, and ribosome assembly factors in plants, focusing on data from Arabid

169 nges in the levels of ribosomal proteins and assembly factors in preribosomes when RPLs functioning i

170 Importin beta is known to act by repressing assembly factors in regions distant from chromatin, wher

171 bosome biogenesis requires approximately 200 assembly factors in Saccharomyces cerevisiae.

172 ough a transient interaction with Complex IV assembly factors, in particular the copper chaperone COX

173 multiple DNA replication-coupled nucleosome assembly factors, including Rtt106, CAF-1, and lysine re

174 interacts with 25S rRNA and with several 60S assembly factors, including the RNA exosome, specificall

175 e catalytic subunits of CIII and COX10 is an assembly factor indispensable for the maturation of Cox1

176 Thus, Cdc123 is a specific eIF2 assembly factor indispensable for the onset of protein s

177 Assembly factors interact with subunits of Complex I but

178 Mutations in genes encoding cytoplasmic assembly factors, intraflagellar transport factors, dock

179 ion or inhibition of human complex II or its assembly factors is often associated with neurodegenerat

180 With 44 structural subunits and over 10 assembly factors, it is unsurprising that complex I defi

181 be essential for biogenesis, since dedicated assembly factors keep immature ribosomal subunits apart

182 Defects in the ribosome assembly factor Las1L are associated with congenital let

183 d by the recruitment of evolutionarily novel assembly factors like PAM68L.

184 cal homology with Vma22p, the yeast V-ATPase assembly factor located in the endoplasmic reticulum (ER

185 stabilizing disulfides in crucial bacterial assembly factors (LptD, BamA, and FtsN) and stress senso

186 bosome assembly, where it phosphorylates the assembly factor Ltv1, which causes its release from nasc

187 we demonstrate an interaction between CENP-A assembly factor M18BP1 and acetyltransferase KAT7/HBO1/M

188 in biogenesis is orchestrated by hundreds of assembly factors, many of which are yet to be discovered

189 biogenesis, and defects in a single ribosome assembly factor may be lethal or produce tissue-specific

190 Because of concerns that vascular plant assembly factors may not be adequate for assembly of a c

191 itself, in the absence of any chaperones or assembly factors, may serve as a platform for the transf

192 that Mss116 interacts with the mitoribosome assembly factor Mrh4, is required for efficient mitoribo

193 SU lacks bL36m, accumulates an excess of the assembly factors MTG1, GTPBP10, MALSU1 and MTERF4, and c

194 ing mutations in FLASH, mutations in the HLB assembly factor Mxc, or depletion of the variant histone

195 A12), whereas a paralog of this subunit, the assembly factor N7BML (NDUFAF2), was found firmly bound

196 This latter process involves several assembly factors, NafH, NifW, and NifZ, and precedes FeM

197 Furthermore, the essential NPC assembly factor Ndc1 has altered interactions in the abs

198 t with the well-characterized complex I (CI) assembly factor NDUFAF5 in a large-scale protein-protein

199 identify Arp2/3, EVL, and CRMP-1 as 3 actin assembly factors necessary for microspike formation.

200 his network includes genes encoding core and assembly factors needed to build the complete 26S partic

201 pose that such mutual exclusivity of cluster assembly factor (Nfs1/Yfh1) and cluster transfer factor

202 sociated proteins, ribosomal protein uL4 and assembly factor Nog1, in NPET assembly.

203 s affinity-purified using the epitope-tagged assembly factor Nog2.

204 By comparing the nonessential assembly factors Nop12 and Pwp1, we show that misfolding

205 The yeast pre-60S assembly factor Nop53 has previously been shown to assoc

206 ins the NADH binding site, but contained two assembly factors not present in intact CI.

207 In Chlamydomonas, three assembly factors--ODA5, ODA8, and ODA10--show genetic in

208 risation, by deleting cox10 gene encoding an assembly factor of cytochrome c oxidase (COX) specifical

209 n together, our data suggest that GLDH is an assembly factor of the membrane arm of complex I.

210 Unlike the integral components and assembly factors of NADH:ubiquinone oxidoreductase, Mtln

211 tein, renamed here alpha-carboxysome RuBisCO assembly factor (or acRAF), is a novel RuBisCO chaperone

212 y defect is direct, i.e. New1 is a bona fide assembly factor, or indirect, for instance due to a defe

213 ain insertions in genes encoding components, assembly factors, or regulators of type IV pili or conta

214 Hundreds of assembly factors, organized into sequential functional g

215 ctor governing the usage of one Fe-S cluster assembly factor over another in the maturation of apo-pr

216 ions (e.g., antibiotics, deletion mutants of assembly factors, oxidative stress, nutrient deprivation

217 , we reveal a novel role for the microtubule assembly factor p25 in regulating stabilization and elon

218 tematic analysis of one such uncharacterized assembly factor, Pet117, and demonstrate in Saccharomyce

219 Eight of the known extrinsic assembly factors plus a hydrophobic protein, C3orf1, wer

220 ulation of the kinase into large spliceosome assembly factor-positive speckle domains within the nucl

221 by the presence of the photosystem II (PSII) assembly factor PratA (for processing-associated TPR pro

222 membrane subcompartment harboring the early assembly factor PratA and are referred to as PratA-defin

223 x10, a gene encoding a cytochrome IV oxidase assembly factor, prevented the metabolic shift induced b

224 lecular associations of 15 core subunits and assembly factors previously linked to human CI deficienc

225 terized partially, and at least 12 extrinsic assembly factor proteins are required for the assembly o

226 s coordinated by at least thirteen extrinsic assembly factor proteins that are not part of the fully

227 Assembly factors provide speed and directionality to the

228 ociated low molecular mass subunits, and the assembly factor Psb27.

229 and possible function of two homologous PSII assembly factors, Psb28-1 and Psb28-2, from the cyanobac

230 and possible function of two homologous PSII assembly factors, Psb28-1 and Psb28-2, from the cyanobac

231 of disassembled V-ATPase (V1 domain) to its assembly factor RAVE (subunit Rav1p) was 5-fold enhanced

232 ture and pre-30S complexes in the absence of assembly factors RbfA and RimM revealed global reorganiz

233 rol mechanism in which the abundant ribosome assembly factor, RbfA, suppresses protein synthesis by i

234 esolution, revealing in molecular detail how assembly factors regulate the timely folding of pre-18S

235 Collectively, our results suggest that 40S assembly factors regulate the timely incorporation of ri

236 To better define the roles of assembly factors required for eukaryotic ribosome biogen

237 PK) structure depends on the presence of the assembly factor RimP.

238 lude most of the major functional classes of assembly factors: RNA-binding proteins, scaffolding prot

239 tein Snu13p/15.5K bound to a fragment of the assembly factor Rsa1p/NUFIP.

240 hrough the release of importin-bound spindle assembly factors (SAFs), which stimulate microtubule (MT

241 els of ssDNA, reduced levels of Cse4 and its assembly factor Scm3, and mislocalization of histone H3

242 ay structure of human SDHA and its dedicated assembly factor SDHAF2.

243 racts with the endoplasmic reticulum droplet assembly factors seipin and Fit2 to maintain proper drop

244 Genetic defects in four of these V-ATPase assembly factors show overlapping clinical features, inc

245 Strikingly, multiple dynein arm assembly factors show structural similarities to either

246 These data indicate that WDR92 is a key assembly factor specifically required for the stability

247 (COX) deficiency caused by mutations in COX assembly factors such as Sco1 and Sco2.

248 zation is tightly regulated by activation of assembly factors such as the Arp2/3 complex and formins

249 Nucleosome assembly in vivo requires assembly factors, such as histone chaperones, to bind to

250 g MidA (C2orf56/PRO1853/Ndufaf7), another CI assembly factor, suggesting that autophagy activation mi

251 t msk-null mutants are depleted of the snRNP assembly factor, survival motor neuron, and the Cajal bo

252 In particular, dependence on the assembly factor tapasin is highly variable, with frequen

253 ty complex (MHC) class I molecules and their assembly factor tapasin, thereby influencing antigen pre

254 in linkage is facilitated by a small protein assembly factor, termed SdhE in E. coli.

255 COX18 is an additional COX2 assembly factor that belongs to the Oxa1 family of membr

256 ese results is that Mediator functions as an assembly factor that facilitates PIC maturation through

257 n Cep290/Mks4/Nphp6 orthologue) as a central assembly factor that is specific for established MKS mod

258 his work describes an example of a bacterial assembly factor that tests a specific translation mechan

259 Formin proteins are actin assembly factors that accelerate filament nucleation the

260 are nucleated at centrosomes and by spindle assembly factors that are activated in the vicinity of c

261 aryotes involves the activity of hundreds of assembly factors that direct the hierarchical assembly o

262 Bol1 and Bol3 as specific mitochondrial ISC assembly factors that facilitate [4Fe-4S] cluster insert

263 ess (Asl) are essential, conserved centriole assembly factors that induce centriole amplification whe

264 elusive, and the roles of any additional CcO assembly factors that may be involved remain unclear.

265 At least 14 assembly factors, the 'B-factor' proteins, are required

266 ogue 1 (PES1), an essential 60S-preribosomal assembly factor, thereby impairing exonuclease-mediated

267 One such event is found in the complex I assembly factor TIMMDC1 establishing a novel disease-ass

268 The characteristics of C3orf1, of another assembly factor, TMEM126B, and of NDUFA11 suggest that t

269 and two previously uncharacterised V-ATPase assembly factors, TMEM199 and CCDC115, stabilise HIF1alp

270 Outer dynein arms (ODAs) require assembly factors to assist their preassembly, transport,

271 es cellular mechanisms for recruiting CENP-A assembly factors to existing CENP-A nucleosomes for the

272 By mooring actin assembly factors to the plasma membrane, this myosin org

273 ation defects, inefficient recruitment of CP assembly factors to the TZ, and flagellum paralysis.

274 mportin alpha by GM130 liberates the spindle assembly factor TPX2, which activates Aurora-A kinase an

275 its key targets is the MT-associated spindle assembly factor TPX2.

276 beta5pro is functionally linked to the Ump1 assembly factor, trans-expressed beta5pro associates onl

277 S translational active sites, the associated assembly factors Tsr1, Enp1, Rio2 and Pno1 collectively

278 bonucleoprotein particles (UsnRNPs) requires assembly factors united in protein arginine methyltransf

279 nd VopF (VopL/F) are tandem WH2-domain actin assembly factors used by infectious Vibrio species to in

280 An exception is the assembly factor vacuolar ATPase assembly integral membra

281 e show the wBm is active since the essential assembly factor virB8-1, is transcribed in adult worms a

282 as the functional ortholog of yeast V-ATPase assembly factor Voa1 and reveals a novel link of tissue-

283 ong-sought human homologue of yeast V-ATPase assembly factor Voa1.

284 7orf32) as a human homolog of yeast V-ATPase assembly factor Vph2p (also known as Vma12p).

285 trate that eEF1A and Hsp70 coopted replicase assembly factors, Vps34 phosphatidylinositol 3-kinase (P

286 ystem from the Wnt5 guidance cue to an actin assembly factor, we propose that the Wnt5/PCP navigation

287 reconstitution of competition between actin assembly factors, we found that the small G-actin bindin

288 Strikingly, 70S ribosome and ribosome assembly factors were strongly overrepresented in nucleo

289 ions and determine the structures of over 20 assembly factors, which are enriched in two areas: an ar

290 ing nuclear-encoding structural subunits and assembly factors, whilst only 3 of the 10 patients with

291 s C20orf7) is a mitochondrial complex I (CI) assembly factor whose mutations lead to human mitochondr

292 acts as a scaffold to recruit multiple actin assembly factors whose functions are normally regulated

293 aracterize Arabidopsis thaliana MET1, a PSII assembly factor with PDZ and TPR domains.

294 rb1 mutants: association of twelve different assembly factors with domain V of 25S rRNA, including th

295 table assembly of seven other interdependent assembly factors with pre-60S subunits, resulting in tur

296 t co-transcriptional association of ribosome assembly factors with pre-ribosomal RNA results in the f

297 Unlike other known dynein assembly factors within the axoneme, CCDC103 is not solu

298 Interacting sets of actin assembly factors work together in cells, but the underly

299 SI but was reduced in the absence of the PSI assembly factor Ycf3.

300 ding indicates that, along with acting as an assembly factor, YjeQ has a role as a checkpoint protein