ライフサイエンスコーパス: heterotrimeric

1 Despite the discovery of heterotrimeric alphabetagamma G proteins approximately 2

2 tes many cellular proteins, in the case of a heterotrimeric aminoacyl-tRNA synthetase complex, the ag

3 The enzyme family of heterotrimeric AMP-dependent protein kinases is activate

4 um, a basal chemotaxis pathway consisting of heterotrimeric and monomeric G proteins is sufficient fo

5 iverse array of processes and is part of the heterotrimeric Bag6 complex, which also includes ubiquit

6 NF-Y is a heterotrimeric CCAAT-binding complex consisting of A-C s

7 Prior studies suggested that the heterotrimeric ciliary kinesin may be dispensable for ce

8 e, which encodes the common motor subunit of heterotrimeric ciliary kinesins.

9 The RAD9A-HUS1-RAD1 (9-1-1) complex is a heterotrimeric clamp that promotes checkpoint signaling

10 t a thermally stable hydroxyproline-free ABC heterotrimeric collagen mimetic system composed of decap

11 ine-glutamate axial salt-bridges to design a heterotrimeric collagen triple helix, ABC-1, containing

12 , and coordinates their translation into the heterotrimeric collagen type I molecule.

13 Collectively, the data suggest that the heterotrimeric complex can work as a [2Fe-2S](2+) cluste

14 inase (AMPK) is an obligatory alphabetagamma heterotrimeric complex carrying a carbohydrate-binding m

15 protein phosphatase 2A (PP2A) functions as a heterotrimeric complex composed of a catalytic (C), scaf

16 Escherichia coli DNA polymerase V (pol V), a heterotrimeric complex composed of UmuD'2C, is marginall

17 ve channel show that the SecY subunit of the heterotrimeric complex consists of two halves that form

18 lB1 from Sulfolobus solfataricus exists as a heterotrimeric complex in cell extracts.

19 ochore-associated (Ska) protein complex is a heterotrimeric complex required for timely anaphase onse

20 Retromer is a heterotrimeric complex that associates with endosomal me

21 hat ectopically expressed cTalpha 1) forms a heterotrimeric complex with rod Gbeta(1)gamma(1), 2) sub

22 LKB1 is activated by forming a heterotrimeric complex with STRAD and MO25.

23 tions of which are poorly understood, form a heterotrimeric complex with Sufu and Gli.

24 t emerged that apo GRX3 and apo BOLA2 form a heterotrimeric complex, composed by two BOLA2 molecules

25 AMP-activated protein kinase (AMPK) is a heterotrimeric complex, composed of a catalytic subunit

26 -C subunits interact and form a stable NF-Y heterotrimeric complex.

27 and all possible betagamma-dimers to form a heterotrimeric complex.

28 VGSCs in mammalian brain are heterotrimeric complexes of alpha and beta subunits.

29 nd HSF2 interact directly, forming HSF1-HSF2 heterotrimeric complexes recruited to a specific heat sh

30 Although each R7-RGS subtype forms heterotrimeric complexes with Gbeta5 and R7-RGS-binding

31 ed ability of the G-protein subunits to form heterotrimeric complexes, including betagamma-dimers pre

32 elucidate the thermodynamic properties of a heterotrimeric DNA complex that portrays the structure o

33 The original purification of the heterotrimeric eIF4F was published over 30 years ago.

34 AMP-activated protein kinase (AMPK) is a heterotrimeric enzyme that senses and governs changes in

35 The heterotrimeric Escherichia coli RecBCD enzyme comprises

36 as the Werner syndrome protein (WRN) and the heterotrimeric eukaryotic ss-DNA binding protein RPA.

37 hibitor of B55alpha- and B56delta-containing heterotrimeric forms of PP2A.

38 ortex during mitosis by the alpha subunit of heterotrimeric G protein (Galpha)/mammalian homologue of

39 G protein-coupled receptor-mediated heterotrimeric G protein activation is a major mode of s

40 eptide agonist permitting receptor-dependent heterotrimeric G protein activation.

41 8 (Ric-8) proteins regulate an early step of heterotrimeric G protein alpha (Galpha) subunit biosynth

42 ty and is a chaperone for several classes of heterotrimeric G protein alpha subunits in vertebrates.

43 ne nucleotide exchange (GEF) activity toward heterotrimeric G protein alpha subunits of the i, q, and

44 GNAQ and GNA11 are heterotrimeric G protein alpha subunits, which are mutat

45 ial genes that encode positive regulators of heterotrimeric G protein alpha subunits.

46 nctional scaffolding protein that integrates heterotrimeric G protein and H-Ras signaling pathways.

47 A role for heterotrimeric G protein betagamma subunits was shown by

48 and phosphorylates the alpha subunit of the heterotrimeric G protein complex, Galphaq, resulting in

49 The manner in which the heterotrimeric G protein complexes Gbeta1gamma2 and Galp

50 Plants and some protists have heterotrimeric G protein complexes that activate spontan

51 GDD and provide insights how perturbation in heterotrimeric G protein function contributes to the dis

52 Clearly, Ric-8 has a profound influence on heterotrimeric G protein function.

53 Heterotrimeric G protein Galpha13 is known to transmit G

54 The heterotrimeric G protein Galpha13 transduces signals fro

55 Pharmacological inhibition of heterotrimeric G protein Galphai or PI3K signaling and s

56 e B lymphocyte surface receptors, triggering heterotrimeric G protein Galphai subunit guanine nucleot

57 ta is the canonical downstream target of the heterotrimeric G protein Galphaq.

58 red an interaction between PP1calpha and the heterotrimeric G protein Gbeta1 subunit.

59 showed that interactions between APP and the heterotrimeric G protein Goalpha-regulated Goalpha activ

60 ivative, was validated using cell-free aGPCR/heterotrimeric G protein guanosine 5'-3-O-(thio)triphosp

61 TAS1R taste receptors and their associated heterotrimeric G protein gustducin are involved in sugar

62 aces and on stimulation forms a complex with heterotrimeric G protein in 2:1 stoichiometry.

63 f the C terminus of the alpha subunit of the heterotrimeric G protein in G protein-coupled receptor (

64 A long-held tenet of heterotrimeric G protein signal transduction is that it

65 les in G protein-coupled receptor (GPCR) and heterotrimeric G protein signal transduction.

66 on of chemoattractant sensing occurs between heterotrimeric G protein signaling and Ras activation.

67 Heterotrimeric G protein signaling cascades are one of t

68 ne nucleotide exchange factor that activates heterotrimeric G protein signaling downstream of RTKs an

69 intermediate molecule(s) that could activate heterotrimeric G protein signaling in a calcium-dependen

70 integrin activation in platelets is through heterotrimeric G protein signaling regulating hemostasis

71 ts and reveal a higher level of diversity in heterotrimeric G protein signaling.

72 Galpha12/13 but not representatives of other heterotrimeric G protein subfamilies, such as Galphai1,

73 cible sequestration system to inactivate the heterotrimeric G protein subunit Gbeta and find that thi

74 re we report that signal transduction by the heterotrimeric G protein subunit Gbeta1 is essential for

75 onfirmation of expected interactions such as heterotrimeric G protein subunit interactions and aquapo

76 C-beta (PLC-beta) isoforms are stimulated by heterotrimeric G protein subunits and members of the Rho

77 elial cell adhesion molecule-1 (PECAM-1) and heterotrimeric G protein subunits Galphaq and 11 (Galpha

78 of the AC NT for mechanisms of regulation by heterotrimeric G protein subunits is isoform-specific.

79 its own spectrum of activators that includes heterotrimeric G protein subunits, protein tyrosine kina

80 rect control over the activity of endogenous heterotrimeric G protein subunits.

81 pled receptor (GPCR) rhodopsin activates the heterotrimeric G protein transducin (Gt) to transmit the

82 atalyzing the exchange of GDP for GTP on the heterotrimeric G protein transducin (GT).

83 o examine the role of Galpha13, a G12 family heterotrimeric G protein, in regulating cellular invasio

84 dissociation of the Galpha subunit from the heterotrimeric G protein, leading to downstream signalin

85 ere the very first genes for agonist-binding heterotrimeric G protein-coupled receptors (GPCRs) to be

86 rs and also direct receptor signaling toward heterotrimeric G protein-independent signaling pathways.

87 activation of MMP14 and identify MMP14 as a heterotrimeric G protein-regulated effector.

88 naling triad analogous to the core triad for heterotrimeric G proteins (GEF + G proteins + effector).

89 ed to both members of the Galpha12 family of heterotrimeric G proteins alpha subunits, Galpha12 and G

90 spective inhibitors of the Galpha subunit of heterotrimeric G proteins and adenylyl cyclases.

91 ies in plant immunity provide a link between heterotrimeric G proteins and an MAPK cascade via the RA

92 -protein-coupled receptors (GPCRs) activates heterotrimeric G proteins and downstream signaling.

93 rs (GPCRs) and the interaction of GPCRs with heterotrimeric G proteins and effector molecules.

94 ich agonist stimulation leads to coupling of heterotrimeric G proteins and generation of second messe

95 Heterotrimeric G proteins and other regulators are impor

96 These signaling pathways are modulated by heterotrimeric G proteins and the scaffold proteins beta

97 iple waves of signaling that are mediated by heterotrimeric G proteins and the scaffolding proteins b

98 ed receptors (GPCRs) allosterically activate heterotrimeric G proteins and trigger GDP release.

99 Heterotrimeric G proteins are activated by exchange of G

100 Heterotrimeric G proteins are conformational switches th

101 Heterotrimeric G proteins are crucial for the perception

102 Heterotrimeric G proteins are localized to the plasma me

103 Heterotrimeric G proteins are molecular switches that re

104 Heterotrimeric G proteins are quintessential signalling

105 Although small and heterotrimeric G proteins are subjects of intensive stud

106 Although most heterotrimeric G proteins are thought to dissociate into

107 Heterotrimeric G proteins are usually activated by the g

108 Heterotrimeric G proteins are well known to transmit sig

109 ggers signal transduction cascades involving heterotrimeric G proteins as key players.

110 Activation of heterotrimeric G proteins by cytoplasmic nonreceptor pro

111 Heterotrimeric G proteins composed of alpha, beta, and g

112 Heterotrimeric G proteins comprising Galpha, Gbeta, and

113 Heterotrimeric G proteins couple external signals to the

114 ivates several signaling pathways, including heterotrimeric G proteins Gq and G12, as well as the ext

115 R40 is known to signal predominantly via the heterotrimeric G proteins Gq/11.

116 versity of functions and phenotypes in which heterotrimeric G proteins have been implicated.

117 Accordingly, XLGs expand the repertoire of heterotrimeric G proteins in plants and reveal a higher

118 receptors (GPCRs), in addition to activating heterotrimeric G proteins in the plasma membrane, appear

119 Additionally, we studied the role of heterotrimeric G proteins in Wnt-5a-dependent synaptic d

120 studies have questioned the idea that plant heterotrimeric G proteins interact with canonical GPCRs,

121 -protein-coupled receptor (GPCR) coupling to heterotrimeric G proteins is confined to the plasma memb

122 its activation depends on integrin beta1 and heterotrimeric G proteins of the G12/13 family.

123 Heterotrimeric G proteins of the Galpha(i) family have b

124 not essential for the initial activation of heterotrimeric G proteins or Ras by uniform chemoattract

125 Heterotrimeric G proteins play a pivotal role in the sig

126 Heterotrimeric G proteins play an essential role in cell

127 Heterotrimeric G proteins play an essential role in the

128 Our findings reveal that FZD9 and heterotrimeric G proteins regulate Wnt-5a signaling and

129 mediated activation of the Galpha subunit of heterotrimeric G proteins requires allosteric communicat

130 Heterotrimeric G proteins signal at a variety of endomem

131 tein Signaling (RGS) promote deactivation of heterotrimeric G proteins thus controlling the magnitude

132 oupling to any of the four major subtypes of heterotrimeric G proteins was found.

133 investigated the inactive-state assembly of heterotrimeric G proteins with FZD4, a receptor importan

134 Gsalpha, the stimulatory subunit of heterotrimeric G proteins, activates downstream signalin

135 , (ii) binding of the Gbetagamma subunits of heterotrimeric G proteins, and (iii) phosphorylation of

136 GPCRs signal through heterotrimeric G proteins, and among the different types

137 ghly homologous alpha subunits of Galphaq/11 heterotrimeric G proteins, and in PLCB4 (phospholipase C

138 1 matrix metalloprotease (MMP14, MT1-MMP) by heterotrimeric G proteins, and in turn, the generation o

139 to promote arrestin binding, decoupling from heterotrimeric G proteins, and internalization.

140 Arrestin recruitment uncouples GPCRs from heterotrimeric G proteins, and targets the proteins for

141 e structure of Smo implies interactions with heterotrimeric G proteins, but the degree to which G pro

142 cells by catalyzing nucleotide release from heterotrimeric G proteins, but the mechanism underlying

143 Heterotrimeric G proteins, composed of alpha, beta, and

144 In animals, heterotrimeric G proteins, comprising Ga, Gb, and Gg sub

145 The G12/13 class of heterotrimeric G proteins, comprising the alpha-subunits

146 Heterotrimeric G proteins, consisting of Galpha, Gbeta,

147 ins, which form the alpha subunit of certain heterotrimeric G proteins, drive uveal melanoma oncogene

148 agonist-promoted interactions of GPCRs with heterotrimeric G proteins, GPCR kinases (GRKs), and arre

149 (GNB1) gene, encoding the Gbeta1 subunit of heterotrimeric G proteins, have recently been identified

150 Heterotrimeric G proteins, including combinations believ

151 is transient (<10 minutes) and initiated by heterotrimeric G proteins, is followed by a second wave

152 modulated by three families of proteins: the heterotrimeric G proteins, the G-protein-coupled recepto

153 between receptor tyrosine kinases (RTKs) and heterotrimeric G proteins, two major and distinct signal

154 PKA and upstream of the Galphai component of heterotrimeric G proteins, which itself localizes to cil

155 cterized based on their ability to couple to heterotrimeric G proteins.

156 ontrol bundle polarity cell-autonomously via heterotrimeric G proteins.

157 hosphorylated GPCRs and uncoupling them from heterotrimeric G proteins.

158 ong binding affinities observed for multiple heterotrimeric G proteins.

159 ange of GDP for GTP on the Galpha subunit of heterotrimeric G proteins.

160 nal and posttranslational suppression of rod heterotrimeric G proteins.

161 efficiently regulate the cellular levels of heterotrimeric G proteins.

162 signal transduction processes by activating heterotrimeric G proteins.

163 ross-linking did not require the presence of heterotrimeric G proteins.

164 ling by receptors coupled to the Gq/11 class heterotrimeric G proteins.

165 es through Galphai2- and Galphai3-containing heterotrimeric G proteins.

166 d GNAQ, genes that encode Galpha subunits of heterotrimeric G proteins.

167 aARs) become desensitized and uncoupled from heterotrimeric G proteins.

168 mpounds are available that directly modulate heterotrimeric G proteins.

169 The loss of heterotrimeric G(o) signaling through the expression of

170 Mutations that increase heterotrimeric G-protein activity expand the bending-gro

171 ype that resembles the one described for the heterotrimeric G-protein alpha subunit (GPA1) null mutan

172 s dynein recruitment to the cell cortex by a heterotrimeric G-protein alpha subunit in complex with a

173 s Columbia accession (Col) wild type and the heterotrimeric G-protein alpha subunit mutant, gpa1, whi

174 suggesting a role for Bni1 downstream of the heterotrimeric G-protein and Cdc42 during gradient sensi

175 T based sensor for detecting activation of a heterotrimeric G-protein by G-protein coupled receptors.

176 d Ggamma proteins of a soybean (Glycine max) heterotrimeric G-protein complex are involved in regulat

177 1 Gbeta and 3 Ggamma proteins represent the heterotrimeric G-protein complex in Arabidopsis, and a s

178 Arabidopsis heterotrimeric G-protein complex modulates pathogen-asso

179 B2 encodes the beta2 subunit (Gbeta2) of the heterotrimeric G-protein complex that is being released

180 for the signaling processes mediated by the heterotrimeric G-protein complex.

181 Signaling pathways mediated by heterotrimeric G-protein complexes comprising Galpha, Gb

182 ng the Galpha, Gbeta, and Ggamma subunits of heterotrimeric G-protein complexes, which function upstr

183 a signaling cascade, which is mediated by a heterotrimeric G-protein consisting of alpha, beta, and

184 e therefore diagnoses in the group of mosaic heterotrimeric G-protein disorders, joining McCune-Albri

185 applications to dihydrofolate reductase and heterotrimeric G-protein families along with a discussio

186 he histamine receptor subtypes for different heterotrimeric G-protein families with single-cell resol

187 t chemoattractants rely on activation of the heterotrimeric G-protein Galphai to regulate directional

188 opic glutamate receptor mGluR6 activates the heterotrimeric G-protein Galphaobeta3gamma13, and this l

189 ortholog [APPL (APP-Like)] directly bind the heterotrimeric G-protein Goalpha, supporting the model t

190 The lack of heterotrimeric G-protein homologs in the sequenced genom

191 RGS4, a heterotrimeric G-protein inhibitor, localizes to plasma

192 Heterotrimeric G-protein signal transduction initiated b

193 Our studies demonstrate that targeting heterotrimeric G-protein signaling offers opportunities

194 oxygen species, cytosolic Ca2+ (Ca2+c), and heterotrimeric G-protein signaling.

195 ling (RGS) proteins are potent inhibitors of heterotrimeric G-protein signaling.

196 city, in which it is functionally coupled to heterotrimeric G-protein signaling.

197 PAR1 is promiscuous and couples to multiple heterotrimeric G-protein subtypes in the same cell and p

198 Putative functions of the heterotrimeric G-protein subunit Galphai2-dependent sign

199 ulin-like (CML) protein, and by showing that heterotrimeric G-protein subunits Galpha (GPA1) and Gbet

200 hat Galphaolf exclusively forms a functional heterotrimeric G-protein with Gbeta1 and Ggamma13 in OSN

201 -gated channel via a cascade that includes a heterotrimeric G-protein, cone transducin, comprising Ga

202 eIF2, a heterotrimeric G-protein, is activated by guanine nucleo

203 gand histamine by activating three canonical heterotrimeric G-protein-mediated signaling pathways wit

204 ive Fus3 binding to the alpha-subunit of the heterotrimeric G-protein.

205 moting neurons, and likely couples to a Gi/o heterotrimeric G-protein.

206 Heterotrimeric G-proteins (comprising Galpha and Gbetaga

207 tem to drive expression of dominant-negative heterotrimeric G-proteins (DNG) in retinal ganglion cell

208 GPCRs) relay extracellular signals mainly to heterotrimeric G-proteins (Galphabetagamma) and they are

209 proteins that bind the betagamma subunits of heterotrimeric G-proteins (Gbetagamma).

210 We examine the possible roles of heterotrimeric G-proteins activated by the PPR.

211 Heterotrimeric G-proteins are essential cellular signal

212 Heterotrimeric G-proteins are implicated in several plan

213 Heterotrimeric G-proteins comprised of Galpha, Gbeta and

214 Signaling pathways regulated by heterotrimeric G-proteins exist in all eukaryotes.

215 we report the functional characterization of heterotrimeric G-proteins from a nonvascular plant, the

216 The basic schemes of heterotrimeric G-proteins have been outlined.

217 s (Rac1, RhoA/B/C, and Cdc42) as well as for heterotrimeric G-proteins in a series of live-cell imagi

218 Heterotrimeric G-proteins play a crucial role in the con

219 Heterotrimeric G-proteins, comprising Galpha, Gbeta, and

220 coupled receptors and Galpha subunits of the heterotrimeric G-proteins, induce contraction of smooth

221 or-activating protein receptors (SNAREs) and heterotrimeric G-proteins.

222 ed glutamine residue in the alpha subunit of heterotrimeric G-proteins.

223 PR126 directly increases cAMP by coupling to heterotrimeric G-proteins.

224 juana component (9)-tetrahydrocannabinol, to heterotrimeric G12/G13 proteins that triggers rapid and

225 GPCRs signal via the canonical heterotrimeric Galpha and Gbetagamma subunits.

226 and Gbetagamma independently of the classic heterotrimeric Galphabetagamma.

227 Both of these require heterotrimeric Galphai protein signaling, whose intensit

228 ns in the GNAQ and GNA11 oncogenes, encoding heterotrimeric Galphaq family members, have been identif

229 receptor, in complex with peptide ligand and heterotrimeric Galphasbetagamma protein determined by Vo

230 oupled receptors that predominantly activate heterotrimeric Gi proteins and are involved in immune ce

231 sic G protein-coupled receptor by activating heterotrimeric Gi/Go proteins resulting in adenylyl cycl

232 show that activation of receptors coupled to heterotrimeric Gi/o proteins inhibits TRPM3 channels.

233 These enzymes are regulated by stimulatory heterotrimeric Gs proteins; however, the presence of Gs

234 es the predicted alpha-subunit (Galpha) of a heterotrimeric GTP binding protein.

235 FLJ00018 is regulated by the interaction of heterotrimeric GTP-binding protein Gbetagamma subunits o

236 lpha7 nAChRs bind signaling proteins such as heterotrimeric GTP-binding proteins (G proteins).

237 GNB5 encodes an atypical beta subunit of the heterotrimeric GTP-binding proteins (Gbeta5).

238 Heterotrimeric GTP-binding proteins are membrane-associa

239 translation initiation factor 2 (eIF2) is a heterotrimeric GTPase, which plays a critical role in pr

240 TPases, nuclear lamins, the gamma-subunit of heterotrimeric GTPases, and several protein kinases and

241 specifically with the alpha subunits of G12 heterotrimeric GTPases.

242 GPR56 encodes a heterotrimeric guanine nucleotide-binding protein (G pro

243 GPR15, an orphan heterotrimeric guanine nucleotide-binding protein (G pro

244 ocalization signal and reversible G protein (heterotrimeric guanine nucleotide-binding protein)-coupl

245 Heterotrimeric guanine-nucleotide-binding regulatory pro

246 which are transcribed and replicated by the heterotrimeric IAV RNA-dependent RNA-polymerase (RdRp).

247 ock IL-15 action in cells that expressed the heterotrimeric IL-15 receptor in cis.

248 The heterotrimeric influenza virus polymerase performs repli

249 channels (ASICs) form both homotrimeric and heterotrimeric ion channels that are activated by extrac

250 ASIC proteins can form both homotrimeric and heterotrimeric ion channels.

251 7, osmotic avoidance abnormal-3 (OSM-3)] and heterotrimeric (KIF3) kinesin-2 motors are required to e

252 Homodimeric KIF17 and heterotrimeric KIF3AB are processive, kinesin-2 family m

253 The heterotrimeric kinase AMPK acts as an energy sensor to c

254 Mammalian KIF3AC is classified as a heterotrimeric kinesin-2 that is best known for organell

255 for shorter run lengths observed for another heterotrimeric kinesin-2, KIF3AB.

256 strate unexpected new roles for both ciliary heterotrimeric kinesins and IFT particle genes and clari

257 Here, the full heterotrimeric MBH of Ralstonia eutropha, including the

258 f bacteria is mediated by a highly conserved heterotrimeric membrane protein complex denoted Sec61 in

259 to a protein-conducting channel formed by a heterotrimeric membrane protein complex, the prokaryotic

260 Intracellularly, heterotrimeric molecules associate to form dimers and te

261 The mammalian kinesin-2, KIF3A/B, is a heterotrimeric motor involved in intraflagellar transpor

262 Because of the heterotrimeric nature of the PCNA clamp in some archaea,

263 A C subunit of the heterotrimeric nuclear factor Y (NF-YC1) was shown to pl

264 factor C (RFC) is sufficient for loading the heterotrimeric PCNA123 [proliferating cell nuclear antig

265 ae isolate NCTC13129 produces three distinct heterotrimeric pili that contain SpaA, SpaD, and SpaH, m

266 tochondrial DNA (mtDNA) is replicated by the heterotrimeric Pol gamma comprised of a single catalytic

267 virus PB1 protein is the core subunit of the heterotrimeric polymerase complex (PA, PB1 and PB2) in w

268 tes in the cell nucleus and assembles into a heterotrimeric polymerase with PB1 and PA.

269 is superior in predicting heterodimeric and heterotrimeric protein assemblies.

270 mma of eukaryotes is a universally conserved heterotrimeric protein channel complex that accommodates

271 Replication Protein A (RPA) is a heterotrimeric protein complex that binds single-strande

272 eonine phosphatase in eukaryotic cells, is a heterotrimeric protein composed of structural, catalytic

273 s in many organisms secrete laminin, a large heterotrimeric protein consisting of an alpha, beta, and

274 LE: AMPK (AMP-activated protein kinase) is a heterotrimeric protein that plays an important role in e

275 Laminin, an approximately 800-kDa heterotrimeric protein, is a major functional component

276 representative of its structure in the viral heterotrimeric protein.

277 Here, we show that formation of the heterotrimeric RCC1/Ran/RanBP1 complex in M phase Xenopu

278 has been well studied as a component of the heterotrimeric RecBCD helicase-nuclease enzyme important

279 mere DNA-binding protein Teb1, paralogous to heterotrimeric replication protein A (RPA).

280 The heterotrimeric RES complex is organized around the Snu17

281 The PB2 subunit of the viral heterotrimeric RNA polymerase binds the cap structure of

282 hemical fluorophore onto a single subunit of heterotrimeric RPA.

283 Here, we describe a stimulus-inducible, heterotrimeric S-nitrosylase complex consisting of induc

284 dynamic polypeptide-conducting channel, the heterotrimeric Sec61 complex.

285 annel SecYEG, the motor ATPase SecA, and the heterotrimeric SecDFyajC membrane protein complex.

286 The heterotrimeric SecY translocon complex is required for t

287 tes with the protein-conducting channel, the heterotrimeric SecYEG complex, in a so-called posttransl

288 Protein phosphatase 2A (PP2A) is a heterotrimeric serine/threonine phosphatase involved in

289 AMP kinase is a heterotrimeric serine/threonine protein kinase that regu

290 was expressed as individual subunits or as a heterotrimeric single-chain SPT fusion protein.

291 BTR-mediated dHJ dissolution reaction by the heterotrimeric single-stranded DNA binding protein repli

292 cation protein A (RPA) is a highly conserved heterotrimeric single-stranded DNA-binding protein invol

293 the beta-adrenergic receptors coupled to the heterotrimeric stimulatory Gs protein, followed by subse

294 nal ensemble of the alpha subunit Galphas of heterotrimeric stimulatory protein Gs exhibits structura

295 heds light on the process whereby an ancient heterotrimeric TF mainly controlling cell division in an

296 Here we describe a heterotrimeric TFIID subcomplex consisting of the TAF2,

297 Nuclear Factor Y (NF-Y) is a heterotrimeric transcription factor that binds CCAAT ele

298 binding protein contains twice the number of heterotrimeric units of SecYEG as does that for the prec

299 In this context, heterotrimeric viral PA/PB1/PB2 RNA-dependent RNA polyme

300 Mutants of the heterotrimeric viral polymerase components, particularly