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

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

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

5 U5 small nuclear ribonucleoprotein particle assembly factor.

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

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

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

9 tro, demonstrating that HJURP is a chromatin assembly factor.

10 n combination with voa1Delta, a nonessential assembly factor.

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

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

13 edicated transcription factor and a ribosome assembly factor.

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

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

16 mplicated multistep process that is aided by assembly factors.

17 pwise fashion through the actions of several assembly factors.

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

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

20 action by transportin binding and inhibiting assembly factors.

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

22 mplexes depends on the activity of dedicated assembly factors.

23 eotide cofactor require the participation of assembly factors.

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

25 nuclear-encoded accessory proteins known as assembly factors.

26 cellular distribution of several soluble COX assembly factors.

27 regulated process that requires a number of assembly factors.

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

29 2 of the nuclear-encoded subunits and in six assembly factors.

30 2 and Cox10 are previously characterized CcO assembly factors.

31 uding strains with deletions or mutations of assembly factors.

32 ecause it locally activates critical spindle assembly factors.

33 Formins are potent actin assembly factors.

34 ents for most genes encoding OXPHOS subunits/assembly factors.

35 participation of a large number of ribosome assembly factors.

36 l (dTACC), two MAPs that function as spindle assembly factors.

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

38 is a complex process facilitated by several assembly factors.

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

40 ermediate that exhibits low affinity for the assembly factors.

41 Chromatin assembly factor 1 (CAF-1) and Rtt106 participate in the

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 Chromatin assembly factor 1 (CAF-1) deposits histones H3 and H4 ra

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

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

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

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

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

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

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

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

53 ereas the histone chaperone CAF-1 (chromatin assembly factor 1) in humans and Caf1 in Drosophila are

54 -associated protein 1 (NuSAP1) and chromatin assembly factor 1, subunit B (p60; CHAF1b) as targets of

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

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

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

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

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

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

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

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

63 The ATP-dependent chromatin assembly factor (ACF) forms such structures in vitro and

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

65 aryotes requires approximately 200 essential assembly factors (AFs) and occurs through ordered events

66 Assembly factors (AFs) prevent premature translation ini

67 More than 170 assembly factors aid the construction and maturation of

68 Two additional assembly factors, AIFM1 and ACAD9, coimmunoprecipitated

69 ast Saccharomyces cerevisiae with two mutant assembly factor alleles, VMA21 with a dysfunctional ER r

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

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

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

73 e functions of most of the approximately 200 assembly factors and 79 ribosomal proteins required to c

74 , small nuclear ribonucleoprotein-associated assembly factors and beta-actin mRNA.

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

76 Complexes of specific assembly factors and generic endoplasmic reticulum (ER)

77 Specific assembly factors and generic ER chaperones, collectively

78 ns and mechanisms of function of the various assembly factors and pathways by which exogenous antigen

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

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

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

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

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

84 initiation factor, securin gene, nucleosome assembly factor, and a subunit of the cohesin complex) b

85 of the viral RNA polymerase complex, a viral assembly factor, and an inhibitor of host interferon (IF

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

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

88 Scm3 functions as a Cse4-specific nucleosome assembly factor, and that the resulting octameric nucleo

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

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

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

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

93 includes replication factor C, the chromatin assembly factor Asf1p, and the K56-specific acetyltransf

94 The chromatin assembly factor Asf1p, as well as the acetylation of his

95 ing defect of pol30 mutants to the chromatin assembly factors Asf1p and CAF-1, we found pol30 mutants

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

97 In Saccharomyces cerevisiae, more than 180 assembly factors associate with preribosomes to enable f

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

99 In the absence of these assembly factors, at least one exonuclease can switch fr

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

101 During convertase assembly, factor B associates with C3b and Mg(2+) formin

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

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

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

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

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

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

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

109 re, we show the involvement of two chromatin assembly factors (CAFs), Asf1 and CAF-1, in turning off

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

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

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

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

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

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

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

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

118 cells lacking the cytochrome c oxidase (CcO) assembly factor Coa2 are impaired in Cox1 maturation and

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

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

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

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

123 re shared with mutants lacking the chromatin assembly factor complex CAF1.

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

125 ich Scm3(Sp) acts as a CENP-A(Cnp1) receptor/assembly factor, cooperating with Mis16 and Mis18 to rec

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

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

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

129 in yeast mitochondria is dependent on a new assembly factor designated Coa2.

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

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

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

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

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

135 However, how assembly factors drive the construction of ribonucleopro

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

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

138 ratus, newly synthesized Cox1, and other COX assembly factors during Cox1 maturation/assembly.

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

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

141 The SdhE assembly factor enhances covalent flavinylation of Compl

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

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

144 Removal of the assembly factor eukaryotic initiation factor 6 (eIF6) is

145 Specialized assembly factors facilitate the formation of many macrom

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

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

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

149 CD147 is an obligatory assembly factor for monocarboxylate transporters.

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

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

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

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

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

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

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

157 Here, we show that four conserved assembly factors govern biogenesis of the yeast RP base.

158 To identify novel assembly factors, high sensitivity proteomic analysis of

159 ion mediator Rad22 (Sc Rad52), the chromatin assembly factor Hip1 (Sc Hir1), and the Msc1 protein rel

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

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

162 mbly into nucleosomes requires the chromatin assembly factor HJURP.

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

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

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

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

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

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

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

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

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

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

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

174 eveal functional redundancy between specific assembly factors in the chromatin pathway, suggesting in

175 atory control and is aided by a multitude of assembly factors in vivo, but can also be carried out in

176 Yvh1 is a novel ribosome assembly factor: in yvh1Delta cells, free 60S and 80S ri

177 les with peptides is orchestrated by several assembly factors including the transporter associated wi

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

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

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

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

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

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

184 ith mutations in genes that encode other OMP assembly factors leads to severe synthetic phenotypes, s

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

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

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

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

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

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

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

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

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

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

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

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

199 The essential and conserved ribosome assembly factor Nob1 has been suggested to be the endonu

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

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

202 The Nop7-subcomplex contains three assembly factors: Nop7, Erb1, and Ytm1, each of which is

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

204 Our data imply that the snoRNP assembly factor NUFIP can regulate the interactions betw

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

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

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

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

209 Hundreds of assembly factors, organized into sequential functional g

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

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

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

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

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

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

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

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

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

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

220 shown here to be distinct from the chromatin assembly factors previously shown to load other histone

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

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

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

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

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

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

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

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

229 er enzymes, transport proteins, and membrane assembly factors relative to their equivalent gel bands

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

231 Six of seven assembly factors required for this step (A(3) factors) a

232 ngly, additional copies of an extraribosomal assembly factor, RimJ, rescued all the phenotypes associ

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

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

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

236 lamin B, the spindle matrix contains spindle assembly factors (SAFs) such as Eg5 and dynein which are

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

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

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

240 r form the binding surface for the H/ACA RNP assembly factor SHQ1 and that DC mutations modulate the

241 iana by an interaction between ARC6, an FtsZ assembly factor spanning the inner envelope membrane, an

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

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

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

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

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

247 xes between calreticulin and the MHC class I assembly factor tapasin and are important for maintainin

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

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

250 the ERp57 binding site and the glycan of the assembly factor tapasin.

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

252 irected SAGA complex versus the housekeeping assembly factor TFIID.

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

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

255 TPX2 is a Ran-regulated spindle assembly factor that is required for kinetochore fiber f

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

257 ce showing that Cox25 is a new essential COX assembly factor that plays some roles similar to Cox14.

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 he spatial coordination of the ribosome with assembly factors that are critical for enzyme biogenesis

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

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

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

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

266 Formins are potent actin assembly factors that protect the growing ends of actin

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

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

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

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

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

272 Ran control the abundance of active spindle assembly factors to achieve the accurate formation of th

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

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

275 nesin-5 motor Eg5 interacts with the spindle assembly factor TPX2, but how this interaction contribut

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

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

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

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

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

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

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

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

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

285 We have discovered a fifth V(0) assembly factor, Voa1p (YGR106C); an endoplasmic reticul

286 7orf32) as a human homolog of yeast V-ATPase assembly factor Vph2p (also known as Vma12p).

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

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

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

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

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

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

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

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

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

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

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