ライフサイエンスコーパス: protein subunit

1 ulates the excitation energy from the entire protein subunit.

2 ion modulating the allosteric network in the protein subunit.

3 bled from two mutant forms of the same basic protein subunit.

4 e complexes that contain no other detectable protein subunits.

5 his inner membrane complex is composed of 11 protein subunits.

6 ed by the highly interlocked organization of protein subunits.

7 d of the long backbone helix of major capsid protein subunits.

8 onal interaction between biologically active protein subunits.

9 the activity of endogenous heterotrimeric G protein subunits.

10 ifferences in (15)N incorporation into their protein subunits.

11 -based assay that monitors dissociation of G protein subunits.

12 ned by a conformational change in one of the protein subunits.

13 e diacylglycerol addition to GerD and GRs' C protein subunits.

14 wer of drift and the structural integrity of protein subunits.

15 ic8 strains have greatly reduced levels of G-protein subunits.

16 ts effects in the structural features of the protein subunits.

17 ional roles through their interaction with G-protein subunits.

18 as the ribosome, composed of many different protein subunits.

19 ae, OT is composed of nine integral membrane protein subunits.

20 aic virus (TMV) from its constituent RNA and protein subunits.

21 between distinct structural features on the protein subunits.

22 energy of association between the assembling protein subunits.

23 the composition of complexes formed by PBAF protein subunits.

24 virus capsids are assembled from virus-coded protein subunits.

25 meter and is assembled from several thousand protein subunits.

26 posed of a catalytic RNA that is assisted by protein subunits.

27 have a novel Fe-S center formed between four protein subunits.

28 d by acylation similar to the shuttling of G protein subunits.

29 ticulum from Sar1-GTP, Sec23/24 and Sec13/31 protein subunits.

30 liday junction (HJ) bound specifically by 11 protein subunits.

31 receptor-binding GP1, and transmembrane GP2 protein subunits.

32 , the other half is actively exchanging core protein subunits.

33 subunits connected to the two different MoFe-protein subunits.

34 vage site (N(-4)) and the RNase P protein (P protein) subunit.

35 and mitochondria of a tiny minority of their protein subunits?

36 the quasi-equivalent conformers of the coat protein subunit (A, B, and C) in the T=3 capsid.

37 In the presence of the E.T proteins, the M protein subunits accumulated into detergent-insoluble co

38 itant loss of the mitochondrial acyl carrier protein subunit ACPM1 from the enzyme complex and paraly

39 act to temporally modulate the activity of G protein subunits after G protein-coupled receptor activa

40 A (PRKACA) or the guanine nucleotide-binding protein subunit alpha (GNAS) gene, the CYP11B1 promoter

41 evious work showed that the heterotrimeric G protein subunit alpha(q) contains a polybasic region in

42 ways after allergen challenge and, through G-protein subunit alpha, ERK, and Pin1 signaling, likely p

43 -coupled receptor that signals through the G-protein subunit alpha11 (Galpha11).

44 ray and RNAi that guanine nucleotide-binding protein subunit alpha13 (Galpha13) is a negative regulat

45 G protein subunit alphai2 mediates the effects of dopamine

46 pathways that are dysregulated in PDAC was G protein subunit alphai2, which has not been previously a

47 s dependent on activation of the G(alpha)s G-protein subunit and cAMP-cAMP-dependent protein kinase a

48 that sequence-specific contacts between the protein subunit and the leader sequences of pre-tRNAs ma

49 ed endoribonuclease composed of 10 different protein subunits and a single RNA.

50 ract with YbbN, including multiple ribosomal protein subunits and a strong interaction with GroEL.

51 NP pseudouridine synthase comprises multiple protein subunits and an RNA subunit.

52 ions with deletion mutations of both capping protein subunits and cofilin mutations with severing def

53 reased expression of mitochondrial complex I protein subunits and concomitant changes in glucose meta

54 ed but differing interactions between capsid protein subunits and each type of nucleotide in each of

55 involving a complex interplay between these protein subunits and IP6 that in turn controls nucleosom

56 ccurs with a substoichiometric ratio of coat protein subunits and is followed by a gradual increase i

57 isoforms are stimulated by heterotrimeric G protein subunits and members of the Rho GTPase family of

58 in the overall structure of the helices, the protein subunits and the location of the various cofacto

59 We also show that the same G-protein subunits and their modulators exhibit distinct p

60 nique, unequal association of GIRK1/2 with G protein subunits, and the cooperative nature of GIRK gat

61 ssembly state or through the gain or loss of protein subunits, and these processes can be driven by b

62 x, yet do this by interacting with different protein subunits, and using steric or non-steric modes o

63 Moreover, some G protein subunits are able to traffic reversibly from the

64 valent and divalent ion concentrations, four protein subunits are associated with archaeal RNase P ac

65 The coat protein subunits are mostly alpha-helical and curved, an

66 le into large, organized structures in which protein subunits are positioned by interactions with RNA

67 the 'pointed-end complex' that includes the protein subunits Arp11, p62 and the p27/p25 heterodimer.

68 form a 20-nm-diameter particle comprising 60 protein subunits, arranged with 532 symmetry when crysta

69 al. demonstrate that the NPC loses essential protein subunits as cells age, resulting in increased nu

70 y of nucleus-encoded and chloroplast-encoded protein subunits as well as the insertion of hundreds of

71 atic interactions stabilize four betagamma G-protein subunits at the interfaces between four K(+) cha

72 The protein subunits, at least those surrounding the Q(P) po

73 gene encoding the guanine nucleotide-binding protein subunit beta-1, Gbeta.

74 mutations in the guanine nucleotide-binding protein subunit beta-3 gene (GNB3).

75 ic reticulum (ER) in a complex with the COPI protein subunit beta-COP1.

76 ctional role(s) of PilB, the major GBS pilus protein subunit, by coupling analysis of an isogenic GBS

77 leoprotein complex minimally consisting of a protein subunit called telomerase reverse transcriptase

78 Their protein subunits can be modified by genetic engineering

79 erior surface, or the interface between coat protein subunits, can be independently functionalized to

80 ix-loop-helix PER-ARNT-SIM (bHLH-PAS) domain protein subunits, CLOCK and BMAL1.

81 TtCmr complex, is composed of six different protein subunits (Cmr1-6) and one crRNA with a stoichiom

82 ricus, this complex is composed of seven CAS protein subunits (Cmr1-7) and carries a diverse "payload

83 tial to IL12Rbeta1's binding of IL12p40, the protein subunit common to both IL-12 and IL-23.

84 An RNA and reverse transcriptase protein subunit comprise its enzymatic core.

85 cleotides are bound asymmetrically by the Fe-protein subunits connected to the two different MoFe-pro

86 A concentric array of six protein subunits constitutes a hemichannel; electrical s

87 ound 61-nucleotide crRNA spans the entire 11-protein subunit-containing complex, where it interacts w

88 imate recombination of fragments that encode protein subunits could have quickly led to diversificati

89 s)) are composed of large complexes of multi-protein subunits creating ion channels in the cell plasm

90 TtCsm is composed of five different protein subunits (Csm1-Csm5) with an uneven stoichiometr

91 nserved protein complex composed of 8 unique protein subunits (CSN1 through CSN8).

92 clinical evaluation include live attenuated, protein subunit, DNA, and viral-vectored approaches.

93 llowed us to directly evaluate the role of G-protein subunits during nodulation.

94 n IL-12 p35 subunit and an IL-12 p40-related protein subunit, EBV-induced gene 3 (EBI3).

95 kinase (Fak) is composed of two dissociable protein subunits encoded by separate genes.

96 i (MTP) are composed of low-molecular-weight protein subunits encoded by the predicted M. tuberculosi

97 haromyces cerevisiae Est3p and the catalytic protein subunit (Est2p) by demonstrating that recombinan

98 to precisely direct tRNA 3' end to the other protein subunit for aminoacylation in a conformation-dep

99 dulate the electrostatic interactions of the protein subunits for various association strengths.

100 us, triggering TLR2 with an antigen-specific protein subunit formulation is a possible strategy for t

101 2 double-stranded DNA genome is bound to one protein subunit from a connector complex that also forms

102 Disassembly of RecA protein subunits from a RecA filament has long been know

103 ry growth; reduced expression of respiratory protein subunits from complexes I, II, III, and IV; mark

104 larities between the MUN domain and a set of protein subunits from several related vesicle tethering

105 mic swelling, translocation of dissociated G-protein subunits from the disc membranes into the cytopl

106 ), bound NKB but impaired dissociation of Gq-protein subunits from the receptor compared with WT NK3R

107 cell bodies in the basal layer express the G-protein subunit G alpha(o) and members of the V2R superf

108 nhibitors and a strong interactor with the G-protein subunit G alpha(o), localizes to retinal ON bipo

109 ntracellular domain and the heterotrimeric G-protein subunit Galpha(S), and demonstrate that Galpha(S

110 rotein, and by showing that heterotrimeric G-protein subunits Galpha (GPA1) and Gbeta (AGB1) interact

111 to NF-kappaB activation through recruiting G protein subunits Galphai and Galpha12 to activate PKCbet

112 covery of a signalling platform comprising G protein subunit, Galphai and GIV, its guanine exchange f

113 Putative functions of the heterotrimeric G-protein subunit Galphai2-dependent signaling include ion

114 The G-protein subunit Galphai3, a well-documented partner of G

115 tors signal through the olfactory-specific G-protein subunit, Galphaolf.

116 C-73E RhoGEF-2 isoform is activated by the G-protein subunit Galphaq and is required for normal rates

117 on molecule-1 (PECAM-1) and heterotrimeric G protein subunits Galphaq and 11 (Galphaq/11) are junctio

118 on system to inactivate the heterotrimeric G protein subunit Gbeta and find that this acute perturbat

119 ular application of antibodies against the G protein subunit Gbeta and was mimicked by the myristoyla

120 signal transduction by the heterotrimeric G protein subunit Gbeta1 is essential for proper pLLP migr

121 ising pTyr-PAK1, Etk/Bmx, the heterotrimer G-protein subunits Gbeta1, Ggamma2, and/or Ggamma5, PAK-as

122 bfamily RGS proteins are stabilized by the G-protein subunit Gbeta5, such that the knockout of the Gn

123 on of phospholipase C-beta3 (PLC-beta3) by G protein subunits Gbetagamma and Galpha(q), the relevant

124 ation, we found that signaling mediated by G protein subunits Gbetagamma is required to regulate cell

125 s of AC5 N terminus (5NT) bind to purified G protein subunits (GDP-Galpha(s) and Gbetagamma) with app

126 ene, encoding the pan-neuronally expressed G-protein subunit GOA-1, with a degradation-tagged transge

127 n their interaction with and regulation of G protein subunits: group I, guanine nucleotide exchange f

128 The heterotrimeric G protein subunit Gsalpha stimulates cAMP-dependent signal

129 diffraction data to 2.0-A revealed that each protein subunit harbors a hot dog-fold and that the TE6

130 previously solved C-protein structures, each protein subunit has two extra helices at the C-terminus,

131 Reduced gene dosage of ribosomal protein subunits has been implicated in 5q- myelodysplas

132 ue (R160) of the active site containing EutB protein subunit have been characterized.

133 he VAX003 and VAX004 trials of a recombinant protein subunit HIV-1 vaccine and in the Step study, we

134 triction-modification enzymes comprise three protein subunits; HsdS and HsdM that form a methyltransf

135 tream of the regulatory IkappaB kinase-gamma protein subunit in the NF-kappaB signaling pathway, and

136 ervation of the spatiotemporal response of G protein subunits in a living cell to receptor activation

137 bacterial form, employing multiple essential protein subunits in addition to the catalytic RNA subuni

138 nted tool for assessing the involvement of G protein subunits in chemoattractant receptor function.

139 modelling the backbone conformations of the protein subunits in other macromolecular assemblies at n

140 Furthermore, the specific G-protein subunits in P. patens are essential for its life

141 spholipase Cbeta (PLCbeta) is activated by G protein subunits in response to environmental stimuli to

142 ase in the level of mRNA encoding proteasome protein subunits in response to MG132 treatment and an i

143 ity to maintain interactions between soluble protein subunits in the gas phase of a mass spectrometer

144 urther show preferential usage of distinct G-protein subunits in the presence of an additional signal

145 DNA, acts in the flagellar motor to organize protein subunits in the rotor.

146 into sectors corresponding to the number of proteins (subunits) in a complex/process.

147 aS incorporation at D(2S) coexpressed with G-protein subunits indicated significant bias for promotio

148 Loss of G protein subunits, inhibition of multiple signal transduc

149 pected interactions such as heterotrimeric G protein subunit interactions and aquaporin oligomerizati

150 Previous studies of G protein subunit interactions have used stoichiometric am

151 nding site serves to promote and stabilize G protein subunit interactions in the presence of competin

152 guanine nucleotide binding and hydrolysis, G protein subunit interactions, and/or serve as alternativ

153 ighly efficient self-assembly of hundreds of protein subunits into highly stable capsids.

154 The assembly of individual protein subunits into large-scale symmetrical structures

155 hrine, differences depended on the Galphai/o protein subunit involved.

156 these results and to further identify the G protein subunits involved, the blocking effects of pepti

157 uble-strand break intermediate in which each protein subunit is covalently linked to the target DNA s

158 two-state transition with a dimer where one protein subunit is denatured, N-D.

159 glycoprotein of M(r) 41,000 (gp41) envelope protein subunit is the target of 3 such human broadly ne

160 Internal water between protein subunits is identified as an essential mediator

161 mechanisms of regulation by heterotrimeric G protein subunits is isoform-specific.

162 ement in the interfaces between proteins and protein subunits is not always recognized.

163 of stoichiometric amounts of the respective protein subunits is of utmost importance.

164 n-6 and RhoGAP (Rho-family GTPase-activating protein) subunits, is essential for the formation of the

165 nges involving cooperativity between the two protein subunits, it has been hypothesized that conforma

166 the azithromycin-binding region of ribosomal protein subunit L4 (rpl4).

167 e 20 equivalent capsomers (trimers of capsid protein subunits) leading to a stable, nearly complete p

168 e are cross-molecular interactions among the protein subunits linearly along the nucleocapsid to stab

169 Chemical shift analysis indicates that the protein subunits making up the fibril adopt a compact co

170 gh movement of a flexible loop in one of the protein subunits may represent a general mechanism for t

171 act of genomic RNA on the association of the protein subunits may therefore provide further insights

172 The MfR protein subunits Met and SRC, cloned from Daphnia pulex,

173 lex denoted as "Mnx" that includes accessory protein subunits MnxE and MnxF, with an estimated stoich

174 cted with Kir2.4 mRNA and a combination of G-protein subunit mRNAs.

175 mma-secretase complex, as suppression of the protein subunit nicastrin with small interfering RNA (si

176 However, G protein subunit numbers in diploid plant genomes are gre

177 tion of the alpha4 nAChR and regulation of G protein subunit o, G protein regulated-inducer of neurit

178 o binding either the biotin carboxyl carrier protein subunit of acetyl-CoA carboxylase or a second Bi

179 Here we show that CasA, the largest protein subunit of Cascade, is required for nonself targ

180 bunit of Pol epsilon, known to bind the Psf1 protein subunit of CMG, allows stable synthesis with CMG

181 ns isp-1 gene encodes the Rieske iron-sulfur protein subunit of cytochrome c oxidoreductase (complex

182 the fimA and rgpA genes, encoding the major protein subunit of fimbriae and an arginine-specific pro

183 xpression of fimA, a gene encoding the major protein subunit of long fimbriae in P. gingivalis; as a

184 use binding site predictions on tubulin, the protein subunit of microtubules, with molecular docking

185 gene of Saccharomyces cerevisiae codes for a protein subunit of mitochondrial RNase P and has another

186 surface exposure of the minor fimbrial (Mfa) protein subunit of P. gingivalis, which stimulates biofi

187 endent replication, but addition of the Dpb2 protein subunit of Pol epsilon, known to bind the Psf1 p

188 Rpp29 is a protein subunit of RNase P.

189 inciple, we show that fish deficient for the protein subunit of telomerase exhibit the fastest onset

190 reverse transcriptase (hTERT; the catalytic protein subunit of telomerase) is subjected to numerous

191 binds the oligomycin sensitivity-conferring protein subunit of the enzyme at the same site as the AT

192 the expression and alternate splicing of the protein subunit of the telomerase enzyme.

193 TolR is a 15-kDa inner membrane protein subunit of the Tol-Pal complex in Gram-negative

194 C5 is the protein subunit of the transfer RNA processing ribonucle

195 eletion of Thoc1, which encodes an essential protein subunit of THO.

196 cancer cells contain high levels of eIF3h, a protein subunit of translation initiation factor eIF3, a

197 letion of (13)C and/or (15)N for one or more protein subunits of a complex can greatly simplify the m

198 320 kDa complex was composed of glycosylated protein subunits of about 50 and 37 kDa.

199 press three yeast (Saccharomyces cerevisiae) protein subunits of DNA REPLICATION FACTOR A (RFA) were

200 e hypothesis is that expression of genes for protein subunits of energy-transducing enzymes must resp

201 tations in connexins (Cxs), the constitutive protein subunits of gap junction (GJ) intercellular chan

202 e Pdu shell is assembled from a few thousand protein subunits of several different types.

203 formation about (i) sequences of the RNA and protein subunits of telomerase, (ii) sequence alignments

204 of all 13 mitochondrial DNA (mtDNA)-encoded protein subunits of the human oxidative phosphorylation

205 nant b and oligomycin sensitivity-conferring protein subunits of the mitochondrial F1FO ATP synthase.

206 The protein subunits of the telomerase holoenzyme counteract

207 While catalytic and many structural protein subunits of these complexes have been identified

208 RNA (crRNA) of the complex and includes six protein subunits of unknown functions.

209 oplast-localized proteins, such as ribosomal proteins, subunits of the RNA polymerase, and thylakoid

210 Within these proteins, subunits of the vacuolar ATPase, small GTPases

211 n to predict the relative arrangement of the protein subunits on the cell surface.

212 We then tested the effect of G-protein subunits on the surface expression of the channe

213 iently associating with multiple diffusing G protein subunits or by activating a G protein that is st

214 unted for by the incorporation of additional protein subunits or RNA rather than PRC2 dimerization.

215 ination with higher protein content, certain protein subunits or their polypeptides can also be targe

216 h AMPARs (via transmembrane AMPAR regulatory protein subunits) or NMDARs [via glutamate ionotropic re

217 ically active RNA subunit (PRNA) and a small protein subunit (P protein), catalyzes the 5'-end matura

218 ndent RNA polymerase consists of three viral protein subunits: PA, PB1, and PB2.

219 otoinactivation outran the clearance of PSII protein subunits, particularly in cells grown at sub- or

220 ciency is a function of the number of capsid protein subunits per gold nanoparticle.

221 of attachment proteins and a trio of fusion protein subunits play the cell entry concert of parainfl

222 of the single RNA with four previously known protein subunits (POP5, RPP21, RPP29, and RPP30), we sho

223 etase is made of four integral transmembrane protein subunits: presenilin (PS), nicastrin, APH1, and

224 Although ion channels are composed of protein subunits, previous mathematical models of modal

225 roscopy analyses of the Salmonella inner rod protein subunit PrgJ we present evidence that the assemb

226 tory (Galphai2) and stimulatory (GalphasL) G-protein subunits produced minor atrophic and hypertrophi

227 ically impact relative amino acid or storage protein subunit profiles; and (3) glutamine supply contr

228 of activators that includes heterotrimeric G protein subunits, protein tyrosine kinases, small G prot

229 ~500-kDa complex that contains 12 different protein subunits, providing many possible surfaces for i

230 The Mu wedges are comprised of only three protein subunits rather than the seven found in the equi

231 o using their respective constituent RNA and protein subunits, recognize and cleave such substrate-EG

232 mechanistic target of rapamycin complex 1/2 protein subunit regulatory associated protein of the MTO

233 characterization and stoichiometry of their protein subunits remains largely unknown.

234 local environment of the iron-sulfur (Fe/S) protein subunit residing in the Q(o) site on the other (

235 lexes A and B, that contain up to six and 15 protein subunits, respectively.

236 exes, A and B, composed of at least 6 and 15 protein subunits, respectively.

237 diester backbone and the EF-loop in one coat protein subunit result in the FG-loop of that subunit be

238 ary fibrosis disrupt the binding between the protein subunit reverse transcriptase of the telomerase

239 ation, comprises one essential RNA (RPR) and protein subunits (RPPs) numbering one in bacteria, and a

240 However, the number of RNase P protein subunits (RPPs) varies from 1 in bacteria to 9 o

241 Unexpectedly, G protein subunits shuttle rapidly (t1/2 < 1 min) between

242 has been to design interactions between the protein subunits so that they specifically assemble into

243 wo protein domains is important to allow the protein subunits sufficient freedom to assemble into the

244 nts of this unique activity in the catalytic protein subunit telomerase reverse transcriptase (TERT)

245 e appendages primarily comprised of a single protein subunit termed pilin, play a crucial role in the

246 ce appendages primarily composed of a single protein subunit termed pilin, which is encoded by pilA i

247 -finger DNA- and double-stranded RNA-binding protein subunit that binds specifically to the antigen r

248 ome editing approaches to target BRCC36, the protein subunit that confers the BRCA1-A complex its DUB

249 SCF complexes have a variable F-box protein subunit that determines substrate specificity fo

250 in the RNA-binding domain of Srp54, the SRP protein subunit that directly interacts with helix 8.

251 ne, only in the presence of BSSbeta, a small protein subunit that forms a tight complex with BSSalpha

252 americ complex composed of the 84 kDa portal protein subunit that forms the central channel of the ph

253 named gerWB) is shown to encode a receptor B-protein subunit that interacts with the GerUA and GerUC

254 We have identified FBXO17 as an F-box protein subunit that recognizes and mediates GSK3beta po

255 evidence that SEO genes in tobacco encode P-protein subunits that affect translocation.

256 ESCRT-III is composed of four protein subunits that are monomeric in the cytosol and o

257 lls are complex organizations of hundreds of protein subunits that assemble into intricate quaternary

258 During assembly of the bacterial flagellum, protein subunits that form the exterior structures are e

259 tion apparatus that functions to deliver the protein subunits that form the filament and other struct

260 the tertiary structures of both gp7 and gp10 protein subunits that form the T = 7 icosahedral lattice

261 mer epitope (EDE), that bridges two envelope protein subunits that make up the 90 repeating dimers on

262 olymer network was fully cross-linked across protein subunits that make up the cage and extended the

263 is displayed along a helical arrangement of protein subunits that protect the crRNA from degradation

264 Spherical capsids are shells of protein subunits that protect the genomes of many viral

265 apped by thousands of copies of a major coat protein subunit (the capsid).

266 subunit, the telomerase RNA and a catalytic protein subunit, the telomerase reverse transcriptase (T

267 e, but the molecular function of their major protein subunits, the BAR domain-containing proteins Pil

268 an GIRK2 channel in complex with betagamma G-protein subunits, the central signalling complex that li

269 stent with a parallel arrangement of DNA and protein subunits, the N termini of RAG1 and RAG2 are pos

270 overy after photobleaching of GFP-tagged MCM protein subunits through the cell cycle.

271 ion apparatus in its base that pumps certain protein subunits through the growing structure to their

272 o occur by the sequential addition of capsid protein subunits to a nucleus, with the final step compl

273 recruiting and organizing multiple copies of protein subunits to form a closed shell for genome packa

274 a surprisingly unrestricted ability of the G-protein subunits to form heterotrimeric complexes, inclu

275 ands of the DNA template and three dedicated protein subunits to trigger the highly controlled releas

276 ons of the entire structure consisting of 31 protein subunits together with solvent molecules contain

277 These are assembled from thousands of protein subunits translocated across the cell membrane b

278 governing the differential proteolysis of RC protein subunits under divergent cellular conditions.

279 nificant change in the orientation between G protein subunits upon activation that allows the G prote

280 e distinct and distal epitopes on Env during protein subunit vaccination.

281 Given their admirable safety records, protein subunit vaccines are attractive for widespread i

282 Many therapeutic proteins and protein subunit vaccines contain heterologous trimerizat

283 bcutaneous immunization of C57BL/6 mice with protein subunit vaccines containing one or two of these

284 ated vaccines present safety challenges, and protein subunit vaccines induce primarily antibody respo

285 mental implications for the design of future protein subunit vaccines.

286 ing mice deficient in individual Galphai/o G-protein subunits, we demonstrate that Galphai1 and Galph

287 Protein subunits were not observed in globulin and prola

288 Domains on the surface of both protein subunits were resistant to modification, indicat

289 a sets, whereas the models of the individual protein subunits were validated adopting the best practi

290 For GNAQ, a stimulatory alpha(q) G-protein subunit which was recently found to be mutated i

291 activation of an EGFP-tagged L10a ribosomal protein subunit, which allows translating ribosome affin

292 veal the C-terminal region of the small coat protein subunit, which is essential for virus assembly a

293 ignificant changes to the profile of storage protein subunits, which may have contributed to the impr

294 of a large number of symmetrically organized protein subunits whose local movements can be essential

295 in diameter, and is composed of thousands of protein subunits with a combined mass of approximately 2

296 cetylcholine (M3-ACh) receptor as well as Gq-protein subunits with high spatiotemporal resolution in

297 n mitochondria is an L-shaped assembly of 44 protein subunits with one arm buried in the inner membra

298 n the telomerase complex which shares common protein subunits with the H/ACA box snoRNPs.

299 composed of helically arranged single pilin-protein subunits, with a unique biomechanical ability to

300 Protein subunits within complexes of variable compositio