ライフサイエンスコーパス: subunit

1 bunits) and methyltransferase (HsdM and HsdS subunits).

2 ribosomal RNA (rRNA) of the large ribosomal subunit.

3 ifferent genes and CAPZA2 encodes the alpha2 subunit.

4 ia a SUMO-interacting motif in the HDAC Cpr1 subunit.

5 noglobulin G (IgG) class and targeted the S2 subunit.

6 y a single phosphorylation site on the GluA2 subunit.

7 oribosomes and the maturation of their small subunit.

8 gineered into receptors containing the delta subunit.

9 a large (TerL) and a small (TerS) terminase subunit.

10 suggesting an interaction with this protein subunit.

11 om the N-terminal segment of the neighboring subunit.

12 and prevents its association with the small subunit.

13 ncert with components of the large ribosomal subunit.

14 genes of either the small or large ribosomal subunit.

15 he conserved N terminus of the Rubisco large subunit.

16 ur data showing mislocalization of the gamma subunit.

17 washer" conformation and dock onto the STAG1 subunit.

18 ma as a tetramer of two A-subunits and two B-subunits.

19 ich selectively removes and degrades damaged subunits.

20 tion that generated distinct alpha- and beta-subunits.

21 al gating cooperativity between Nav1.5 alpha-subunits.

22 e smallest and the least conserved among ORC subunits.

23 that accepts the two mitochondrially encoded subunits.

24 s for 30 proteins, including 23 radial-spoke subunits.

25 lpha-subunit and one or more associated beta-subunits.

26 ion proteins, including three RNA polymerase subunits.

27 omplex formation, and the degradation of its subunits.

28 en assembled from multiple simpler identical subunits.

29 AMPARs that contain fast desensitizing flop subunits.

30 rest-neighbor distances between Nav1.5 alpha-subunits.

31 erotetramer comprising two GyrA and two GyrB subunits.

32 ributed to cytochrome c (1) being one of its subunits.

33 , depending on the presence of distinct beta-subunits.

34 n synthesis by immature Escherichia coli 30S subunits.

35 ng of the properties of its light-responsive subunits.

36 stem that allows ectopic targeting of Ctf19c-subunits.

37 f eukaryotic translation initiation factor 2 subunit 1 (eIF2alpha), the SG assembly G3BP paralogs, or

38 cluding core-binding factor alpha1, mediator subunit 12, transcriptional coactivator CBP and TATA-box

39 ariants in protein phosphatase 1, regulatory subunit 12a (PPP1R12A), an important developmental gene

40 Small subunit 18S rRNA gene sequencing and accessory pigment a

41 ransferase general transcription factor IIIC subunit 4 and decreased histone deacetylase 5 expression

42 minal residues within the NADH dehydrogenase subunit 4.

43 its phenylpropanoid production in a Mediator Subunit 5 (MED5)-dependent manner.

44 broblasts showed reduced levels of the AP4E1 subunit, a surrogate for levels of the AP-4 complex.

45 isomeric, yet, different, 8pai antiaromatic subunits, a benzocyclobutadiene (BCB) and a pentalene, a

46 e with four Zn(2+) binding sites within each subunit: a highly conserved primary site in transmembran

47 d pathway regulating interleukin-27 receptor subunit alpha (IL-27Ra) expression on hematopoietic stem

48 In the hippocampus, subunits alpha1, alpha2, alpha5, beta2, beta3, gamma2, a

49 These EMC subunits also bind to the ER-resident fusion machinery c

50 mination microscopy that knockdown of the a3-subunit altered the diameter and density of individual C

51 reased expression of the IL-2 receptor alpha-subunit and activation of the transcriptional regulator

52 eal the specific coupling between ENaC gamma-subunit and claudin-8 expression.

53 In Bacillus subtilis, the RNAP delta subunit and NTPase HelD have been implicated in RNAP rec

54 ium channels comprise an ion-selective alpha-subunit and one or more associated beta-subunits.

55 nds to uL14 protein onto the large ribosomal subunit and prevents its association with the small subu

56 ysical properties of the pore-forming alpha1 subunit and trigger excitatory synaptogenesis.

57 on, scaffolds the L-type pore-forming alpha1 subunit and, through its C-terminal region, scaffolds th

58 livery was dependent on presence of both C2C subunits and blocked by receptor competition.

59 quired for the stability of the EARP complex subunits and for the localization of EARP and its associ

60 m, we engineered an HA tag onto Cx26 or Cx30 subunits and imaged hemichannels that were liganded by F

61 Interactions with auxiliary subunits and other factors modify the intrinsic kinetic

62 ing either alpha1, alpha2, alpha3, or alpha5 subunits and the molecular dissection of the pharmacolog

63 ms to follow the interactions between SMC5/6 subunits and the relative stability of the complex.

64 understood about presynaptic auxiliary GluR subunits and their functions.

65 circulates in plasma as a tetramer of two A-subunits and two B-subunits.

66 RNAs coding for nAChR monomeric subunits and/or concatamers were injected into Xenopus o

67 t of a DNA endonuclease (HsdR, HsdM and HsdS subunits) and methyltransferase (HsdM and HsdS subunits)

68 ion involving the regulatory domain of sigma subunit, and potentially pinpoint a novel target for dev

69 s by varying calcium permeability, auxiliary subunits, and activation levels and show that Zn(2+) inh

70 the carboxy-terminal domains of both of its subunits, and this inhibition is released by interaction

71 that BRI1 binds directly to the medium AP-2 subunit (AP2M).

72 f-assembling nanoparticles, including the 60-subunit Aquifex aeolicus lumazine synthase (LuS) and the

73 classes, revealing how contacts to the small subunit are maintained throughout intersubunit rotation.

74 rrelates with nucleotide occupancy: five MCM subunits are bound to either ATPgammaS or ADP, whereas t

75 While most of its subunits are conserved, recent data have shown that the

76 ontacts between the penultimate and terminal subunits are consistent with existing cryogenic electron

77 e describe that alpha9, but not the alpha10, subunits are enriched in zebrafish HCs.

78 he quinone-binding site to the transmembrane subunits are found to be responsible for proton pumping.

79 The data imply that free subunits are more rapidly degraded than those incorporat

80 Here, we report that beta1 subunits are phosphorylated by FYN kinase.

81 e cytosolic portions of beta- and gamma-ENaC subunits as being important for PIP(2)-ENaC interactions

82 eric receptors that contain binding-impaired subunits, as we show for both kainate and GluA2 AMPA rec

83 Although much is known about the auxiliary subunits associated with postsynaptic GluRs, far less is

84 Because of the transient subunit association, an atomic resolution structure of a

85 intersubunit bridges to the small ribosomal subunit, assumes different conformations in the five cla

86 almodulin, the distance across the two GluN1 subunits at the entrance of the first transmembrane segm

87 tly tagged retrograde tracers (cholera toxin subunit B) into retinotopically-matched locations in var

88 of these molecules to pop out of this second subunit before finally re-entering to form a stable comp

89 ts, we investigated the effects of G protein subunit beta 5 (Gnb5) knockout on insulin secretion.

90 itor of interleukin-23 (IL-23) via IL-23 p19 subunit binding, significantly improved psoriatic arthri

91 This enzyme consists of four catalytic subunits: biotin carboxylase (BC), carboxyltransferase (

92 EM) structures of DNA-PKcs (DNA-PK catalytic subunit) bound to a DNA end or complexed with Ku70/80 an

93 The bacterial ribosome is recycled into subunits by two conserved proteins, elongation factor G

94 d, oxidized, and depleted of its stabilizing subunit calstabin-1 6 hours after the onset of the mecha

95 subtilis gyrase is a minimal enzyme, and its subunits can functionally interact with subunits from ot

96 es can self-assemble from smaller individual subunits, can be produced from prokaryotic and human exp

97 n mutants; the heterodimeric capping protein subunit CAPZB and its partner TWF2 never concentrated at

98 d silencing, we identified that the GABA(A)R subunit combination alpha3beta2gamma1 conforms the bulk

99 in-containing TCP-1 (CCT or TRiC) is a multi-subunit complex that folds many of the proteins essentia

100 stinct cellular functions, but how the multi-subunit complexes influence deacetylase activities and s

101 kinase module (CKM) is a detachable Mediator subunit composed of cyclin C and one each of paralogs Cd

102 e further investigated mTOR complex-specific subunit composition and phosphorylation state, and found

103 nopus oocytes to obtain receptors of defined subunit composition and stoichiometry.

104 All MCM subunits contact DNA, from MCM2 at the 5'-end to MCM5 at

105 ster is only moderately selective for alpha5-subunit-containing GABA(A) receptors, the derivative SH5

106 s of brain injury, drugs that inhibit alpha5 subunit-containing gamma-aminobutyric acid type A recept

107 Thus, we postulated that inhibiting alpha5 subunit-containing gamma-aminobutyric acid type A recept

108 The catalytic R1 subunit contains an overall activity site that can allos

109 The CPSF30 subunit contains five CCCH zinc fingers (ZFs), with ZF2-

110 f Kir6.1 (Kir6.1(-/-) ) or SUR2 (SUR2[STOP]) subunits, contractile parameters were not significantly

111 over, in the absence of Pob3, the FACT Spt16 subunit controls the 3' end of genes.

112 To understand how an accessory subunit (CoREST) enables a chromatin enzyme (LSD1) to fu

113 l lines depleted of the catalytic complex IV subunit COX1 or COX2.

114 te EC* that contains RTF1, a dissociable PAF subunit critical for chromatin transcription.

115 id precipitate, secretion of the major curli subunit, CsgA, is tightly regulated.

116 OSCP and F(6) The final component of the PS, subunit d, is added subsequently to form a key intermedi

117 IFT54 directly interacted with IFT dynein subunit D1bLIC, and deletion of residues 261-275 reduced

118 controlled Pol II kinetics by coupling rapid subunit degradation with orthogonal experimental readout

119 n all cases, intermediates between 35 and 90 subunits did not accumulate.

120 ough distinct mechanisms in which individual subunits differentially participate.

121 complexes form a core to which the catalytic subunit dimers are attached, adopting the shape of a Mal

122 formational changes are local and limited to subunits directly contacting bound cofilin.

123 of dystonia, although variants in different subunits display different phenotypic and inheritance ch

124 structural changes ranging from unfolding to subunit dissociation.

125 In contrast, the Galpha subunit distinctly affected both the efficacy and potenc

126 s a powerful tool for obtaining insight into subunit diversity, post-translational modifications, sto

127 identify inhibitors of the DNA-PK catalytic subunit (DNA-PKcs) with good selectivity versus the stru

128 h the DNA-dependent protein kinase catalytic subunit (DNA-PKcs).

129 nd higher-order changes induced by the beta3-subunit do not alter the degree of electrophysiological

130 th Kv4.3 (or Kv4.2), KChIP2 and another beta-subunit, DPP6-L (long isoform).

131 rising from the inactivation of the N-module subunits due to attrition caused by its constant activit

132 atekeepers MICU1 and MICU2, and an auxiliary subunit, EMRE, essential for Ca(2+) transport(3-8).

133 cetylcholine receptors containing the alpha5 subunit encoded by Chrna5 Disruption of this gene impair

134 Vertebrate genomes contain three alpha subunits encoded by three different genes and CAPZA2 enc

135 tes, and deletion of the only G-protein beta-subunit-encoding gene of A. oligospora nearly abolished

136 e complex 2 (PRC2) is composed of three core subunits, enhancer of zeste 2 (EZH2), embryonic ectoderm

137 es the ratio of ATP synthase enzyme to its c-subunit, enhancing ATP production efficiency and synapti

138 gamma-Secretase is a multi-subunit enzyme whose aberrant activity is associated wit

139 ncreased (+63%) the activation energy of 3HM subunit exchange.

140 out of both AMPK catalytic alpha1 and alpha2 subunits exhibited significantly higher fasting blood gl

141 erotrimeric complex, and its catalytic alpha subunit exists in 2 isoforms: AMPKalpha1 and AMPKalpha2.

142 Using GABA(A)R subunit expression and silencing, we identified that the

143 cer of zeste 2 polycomb repressive complex 2 subunit (EZH2).

144 of a large subunit (LiGPPS.LSU) and a small subunit for which two different cDNAs (LiGPPS.SSU1 and L

145 ere also fast, but absolutely required Kv3.3 subunits for fast repolarization (half-widths: 0.25 +/-

146 its subunits can functionally interact with subunits from other bacteria.

147 of major capsid proteins and terminase large subunits further suggests they form a distinct clade wit

148 The inhibitory G protein alpha-subunit (Galpha(z)) is an important modulator of beta-ce

149 t non-coding gap in a phage T4 topoisomerase subunit gene (gp60) requires several recoding signals.

150 whole brain and regional signatures of AMPAR subunit gene expression in healthy human brains as well

151 ha3 nicotinic acetylcholine receptor (nAChR) subunit gene, increases risk of tobacco dependence but u

152 on under redox control include NMDA receptor subunits GluN1 and GluN2A as well as KEAP1 (regulator of

153 tes phosphorylation of NMDA receptor (NMDAR) subunit GluN2B and that GluN2B-containing NMDARs also re

154 pecific knockdown or deletion of a key NMDAR subunit, GluN2B, implicated in the actions of ketamine.

155 ne brain with all the subunits including the subunit H, which is essential for ATPase activity.

156 ndothelium-specific expression of Kir6.1 GoF subunits had negligible effects on lymphatic contraction

157 new azacryptand containing three azobenzene subunits has been developed, and its photoisomerization

158 Terminase subunits have been studied in-depth, especially in class

159 aeolicus lumazine synthase (LuS) and the 24-subunit Helicobacter pylori ferritin.

160 ng measurements performed on cholera toxin B subunit homopentamer (CTB(5)) and nanodiscs containing a

161 also indicates a central role for the ArpC3 subunit in stabilizing the active conformation.

162 a receptor bearing multiple light-switchable subunits in a confined space is critical for the design

163 ) mapping of the static positions of SBF/MBF subunits in fixed cells revealed each transcription fact

164 ntegrator, but the roles of other Integrator subunits in gene regulation have yet to be elucidated.

165 regulatory subunits with conserved catalytic subunits in holoenzyme complexes.

166 rotein abundance of specific nuclear-encoded subunits in oxidative phosphorylation complexes I and V

167 Subunits in the ClpX hexamer assume a spiral conformatio

168 tions elucidating the role of dedicated AMPK subunits in the modulation of gene expression.

169 tact V-ATPase from bovine brain with all the subunits including the subunit H, which is essential for

170 atin regulatory regions of the NADPH oxidase subunits increases in the mdx muscle and JQ1 administrat

171 Depletion of PP4-complex subunits increases phosphorylation of both Ser666 and th

172 s regulated through interactions with the RC subunits inside.

173 Asymmetry also induces distinct inter-subunit interactions around the ring, suggesting a coord

174 Structural analyses reveal subunit interfaces responsible for the functionality of

175 al vector-induced re-expression of the beta4 subunit into either the MHb or IPN restored a "stop" sig

176 idic pocket of nucleosomes and the accessory subunit Ioc3 with nucleosomal DNA.

177 These results show that the alpha2 subunit is important for the potentiation of GlyRs in th

178 antitative analysis indicates that the beta3-subunit is not required for this clustering but beta3 do

179 The Orc6 subunit is the smallest and the least conserved among OR

180 erences in the interactions of the catalytic subunit Isw1 with the acidic pocket of nucleosomes and t

181 esidues, and ultimately serves to coordinate subunit joining through the release of late-stage mtLSU

182 pecific manner through co-assembly with beta subunits KCNE1-5.

183 n of CG with the microtubule network upon a3-subunit knockdown.

184 onditional kidney tubule-specific ENaC gamma-subunit knockout mice displayed decreased claudin-8 expr

185 e quantified and corrected for at the single-subunit level.

186 s heteromeric protein, consisting of a large subunit (LiGPPS.LSU) and a small subunit for which two d

187 d that expression of select GABA(A) receptor subunits may be one of the underlying mechanisms.

188 calcium uniporter complex (MCUC) inhibitory subunit MCUb overexpression.

189 ort that ablation of m(6)A methyltransferase subunit METTL14 in myeloid cells exacerbates macrophage

190 mitochondrial localization of the core MICOS subunit Mic60 in relation to two other MICOS proteins, M

191 ith the alpha-carboxyltransferase (alpha-CT) subunit of ACCase and participate in an original mechani

192 CAPZA2 encodes a subunit of an F-actin-capping protein complex (CapZ).

193 lase accumulated very low levels of the beta-subunit of beta-conglycinin.

194 opsis thaliana mutant of the POL2A catalytic subunit of DNA polymerase epsilon and show that POL2A is

195 Presenilin 1 (PS1) is the catalytic subunit of gamma-secretase, an enzyme complex responsibl

196 on requires RNA cleavage by the endonuclease subunit of Integrator, but the roles of other Integrator

197 Depletion of Raptor, the defining subunit of mTORC1, by small interfering RNA (siRNA) nega

198 ion of Cybb, the gene encoding the catalytic subunit of NADPH oxidase gp91phox.

199 r of zeste homolog 2 (EZH2) is the catalytic subunit of polycomb repressive complex 2 (PRC2), which s

200 aration-of-function mutations into the SUZ12 subunit of PRC2 to drive it into a PRC2.1 or 2.2 subcomp

201 loss of phosphorylation in RPB1, the largest subunit of RNA polymerase (pol) II.

202 mice with a genetic deletion of the specific subunit of system x(c)(-), xCT (xCT(-/-) mice), we uncov

203 nactivation of the gene SMARCB1, a conserved subunit of the chromatin remodeling BAF complex, which h

204 ELP1 is the largest subunit of the evolutionarily conserved Elongator comple

205 ection of inhibitory antibodies to the alpha subunit of the Gs heterodimeric protein (GalphaS) into w

206 on genetic ablation of METTL3 (the catalytic subunit of the major m(6)A methyltransferase complex), m

207 alently modify cysteine-54 (C54) of the MPC2 subunit of the mitochondrial pyruvate carrier (MPC) is p

208 his study, we examine the role of the NCKAP1 subunit of the pentameric cytoskeletal SCAR/WAVE complex

209 ntracellular C-terminal segment of the GluN1 subunit of the receptor.

210 tracellular HA-DAT colocalized with VPS35, a subunit of the retromer complex mediating recycling from

211 eshape and remodel, and thus mature, the 60S subunit of the ribosome.

212 osomal proteins, especially of the large 60S subunit of the ribosome.

213 riants in EXOSC5, which encodes a structural subunit of the RNA exosome.

214 Here we show that BAF60a, a subunit of the SWI/SNF chromatin-remodeling complexes, s

215 lytic region of tyrosine kinase) to the CD3e subunit of the TCR.

216 gh its C-terminal region, scaffolds the beta subunit of VGCC and the p11/Anxa2 complex.

217 BARP, an auxiliary subunit of voltage-dependent calcium channels, promoted

218 The CMV UL56 and UL89 genes, encoding subunits of CMV DNA terminase, were sequenced from plasm

219 ulating effect, i.e. they can bind to Galpha subunits of different classes and either stimulate or in

220 ilencing of endogenous genes that encode two subunits of magnesium chelatase, an enzyme necessary for

221 ight the importance of both Calpha and Cbeta subunits of PKA during human development.

222 from inactivating variants in genes encoding subunits of succinate dehydrogenase.

223 ss-of-function variants in genes that encode subunits of the adaptor protein complex 4 (AP-4) lead to

224 Mutations in genes encoding subunits of the cohesin complex are common in several ca

225 al density attributed to the pUL17 and pUL25 subunits of the CVSC.

226 cating privileged contacts between these two subunits of the MED middle module.

227 We found that the regulatory subunits of these AHAS complexes form a core to which th

228 Auxiliary alpha2delta subunits of VGCCs modulate trafficking and biophysical p

229 impact of loss-of-function variants in AP-4 subunits on intracellular protein trafficking using pati

230 interaction modes are modulated by accessory subunits, oncogenic histone mutations, and the methylati

231 n about turn in order to enter a neighboring subunit, only for some of these molecules to pop out of

232 hase leak channel by mild depletion of its c-subunit or pharmacological inhibition normalizes stimulu

233 The six-subunit origin recognition complex (ORC), a DNA replicat

234 s bound to the preformed F(1)-c(8) module by subunits OSCP and F(6) The final component of the PS, su

235 and tissue localization of Gly decarboxylase subunit P (GLDP) in nine Neurachninae species.

236 d an 11% decrease of AMY levels of the GluA1 subunit (p = 0.05) and a 21.5% decrease of aHIP levels o

237 the helicases XPB, XPD and five 'structural' subunits, p62, p44, p34, p52 and p8.

238 ) retains binding to an NADPH oxidase (NOX2) subunit, p67(phox), and to the RAC-binding domain of p21

239 xis toward host serum, and these ion channel subunits partially rescue sensory defects in Caenorhabdi

240 ptimal temperature accumulate immature large subunit particles missing several proteins.

241 A receptor (AMPAR) and NMDA receptor (NMDAR) subunit phosphorylation that likely contribute to increa

242 PC, requiring cooperation with a methylosome subunit pICln.

243 2A-dependent dephosphorylation of the alpha2 subunit play a role in the dynamic regulation of GABA(A)

244 monstrate that alpha2delta1 and alpha2delta3 subunits play distinct but complementary roles in drivin

245 Mutations of the regulatory subunit (PRKAR1A) of the cyclic adenosine monophosphate

246 contrast, later in development, alpha2delta1 subunits promote the glutamatergic neurotransmission and

247 Large ribosomal subunit protein bL31, which forms intersubunit bridges t

248 ule-specific expression of an L10a ribosomal subunit protein fused with enhanced green fluorescent pr

249 that conditional loss of a Mediator complex subunit protein, Med23 in mouse neural crest cells (Med2

250 loroplast and nuclear genes encoding the PSI subunits (psaA, psaB, and PSAN), the PSII subunits (psbA

251 SI subunits (psaA, psaB, and PSAN), the PSII subunits (psbA, psbB, and PSBW), the antenna proteins (L

252 ), the ribulose 1.5-bisphosphate carboxylase subunits (rbcL and RbcS), and enzymes of chlorophyll bio

253 r antagonist with high selectivity for GluK1 subunits, reduces the desensitization of GluK1/GluK2 het

254 s the turnover of immature glycoforms of BCR subunits, reducing total cellular BCR levels.

255 In this work, we examined Spo7, a regulatory subunit required for Nem1 catalytic function, to identif

256 Global deletion of Kir6.1 or SUR2 subunits results in severely impaired lymphatic contract

257 eeping genes such as that encoding the small subunit ribosomal RNA has revealed the extensive diversi

258 The catalytically active subunit Rrp44/Dis3 of the exosome in budding yeast (Sacc

259 plant toxin, ricin, is due to its enzymatic subunit, RTA, which inactivates mammalian ribosomes with

260 This effect is mirrored by subunit-selective agonists and heteromeric receptors tha

261 idal output neurons showed age-related nAChR subunit-selective reductions in postsynaptic responses t

262 reviously established that the Med1 Mediator subunit serves as a cofactor of GATA TFs in Drosophila,

263 deling complex, including its core catalytic subunit, SMARCA4.

264 Spt3 and the adjacent subunit Spt8 interact with the TATA box-binding protein

265 roduced that lacked cognate Se Rubisco small subunits (SSU) and expressed the Se LSU in place of toba

266 c stabilization of the Plasmodium TRiC delta subunit, suggesting an interaction with this protein sub

267 etry showed that F302L does not impair KCNA2 subunit surface trafficking.

268 re, we analyze the requirements for core CPC subunits, survivin and INCENP, and the mitotic kinesin-l

269 nd the cyclic nucleotide-gated (CNG) channel subunit tax-4 in larval chemotaxis toward host serum, an

270 termed CDTa, and a pore-forming or delivery subunit termed CDTb.

271 p52Shc binding and activating the p47(phox) subunit that results in redox stress and accelerated fib

272 heterotetramer of paralogous alpha- and beta-subunits that mediates respiratory oxygen transport and

273 SERCA is regulated by small membrane protein subunits, the most well-known being phospholamban (PLN)

274 hromatin association of individual replisome subunits, thereby challenging the notion that lagging-st

275 that each TF interacts with a dedicated MED subunit to induce specific transcriptional responses.

276 n in macromolecular complexes with accessory subunits to regulate brain function.

277 The pairing of KCNQ1 and KCNE1 subunits together mediates the cardiac slow delayed rect

278 ses, by stimulus-dependent ATP synthase beta subunit translation; this increases the ratio of ATP syn

279 f this variant in a member of the core TRAPP subunit, TRAPPC4 that associates with vesicular traffick

280 The K(2P) channel subunits TRESK and TREK-2 provide the predominant backgr

281 duced in mice lacking all 3 immunoproteasome subunits (triple-ip(-/-)) or lacking either the gene enc

282 Eukaryotic TSEN is comprised of four core subunits (TSEN54, TSEN2, TSEN34 and TSEN15).

283 on and structure of assembling 60S ribosomal subunits undergo numerous changes as pre-ribosomes trans

284 MF59-adjuvanted glycoprotein B (gB) protein subunit vaccine (gB/MF59) is the most efficacious vaccin

285 ion would be the development of an effective subunit vaccine; however, no approved vaccine currently

286 Using this strategy, the fused pyrrolidine subunit was constructed with exceptionally high regio- a

287 al knock-out mouse in which the Cav1.2 alpha subunit was deleted in GFAP-positive astrocytes.

288 We investigated how a 40S subunit was recruited by the cricket paralysis virus int

289 e (PI3K) comprised of the p110beta catalytic subunit was recruited to the gB/EGFR complex despite p11

290 motif linked to the 1,2,5-oxadiazole 2-oxide subunit was synthesized, indicating the stability of pre

291 ns of the LHCII trimers and of the monomeric subunits were affected in the phosphatase mutants.

292 Unassembled subunits were generally degraded within 3 h.

293 tions in the expression level of alpha2delta subunits were implicated in several syndromes and diseas

294 d rheological properties of gluten and their subunits were studied.

295 t also allows the minimal number of distinct subunits when designing artificial nucleic acid structur

296 uncovered differential binding of these NPC subunits, where Nup107 preferentially targets active gen

297 incoming monomers, and flatten the terminal subunit, which likely promotes ATP hydrolysis and rapid

298 ibosome via specific interaction of the Not5 subunit with the ribosomal E-site in Saccharomyces cerev

299 nsors using porphyrinoid dimers of nonplanar subunits with biased reactivity.

300 rough the interaction of distinct regulatory subunits with conserved catalytic subunits in holoenzyme