ライフサイエンスコーパス: beta subunit

1 ound in Mtb infected patients (S456>L of the beta subunit).

2 cond highly conserved His residue within the beta subunit.

3 rodimer by various isoforms of its alpha and beta subunit.

4 membrane by virtue of the membrane-embedded beta subunit.

5 ed of an alpha subunit and a heme-containing beta subunit.

6 orce takes when applied through the integrin beta-subunit.

7 to transfer PEB to the host phycobiliprotein beta-subunit.

8 ERA1), that encodes the farnesyl transferase beta-subunit.

9 e opening, with conformational change in the beta-subunit.

10 unit and a protein disulfide isomerase (PDI) beta-subunit.

11 eceptors with the reverse ratio of alpha and beta subunits.

12 ated by RNF138 and auxiliary alpha2delta and beta subunits.

13 l surface as pentamers composed of alpha and beta subunits.

14 ors (GlyRs) composed primarily of alpha1 and beta subunits.

15 (sGC) is a heterodimer composed of alpha and beta subunits.

16 ransmembrane receptors composed of alpha and beta subunits.

17 d upon depletion of other integrin alpha and beta subunits.

18 nsist of different combinations of alpha and beta subunits.

19 in are heterotrimeric complexes of alpha and beta subunits.

20 scription factor TFIIE consists of alpha and beta subunits.

21 ore-forming alpha subunit and two associated beta subunits.

22 DELSEED loop in the C-terminal domain of the beta subunits.

23 s, which occur at the catalytic sites in the beta subunits.

24 body (nb.F3) that binds auxiliary HVACC Ca(V)beta subunits.

25 pha1A subunit with auxiliary alpha2delta and beta subunits.

26 an Actinobacteria-unique insert of the RNAP beta' subunit.

27 pecifically to the coiled-coil region of the beta' subunit.

28 cate to the interface between the alpha- and beta-subunits.

29 plication that generated distinct alpha- and beta-subunits.

30 ive alpha-subunit and one or more associated beta-subunits.

31 ecies, depending on the presence of distinct beta-subunits.

32 s ablating interaction between alpha(1C) and beta-subunits, (2) flexibility-inducing polyglycine subs

33 o our knowledge, GNB3 encoding the G-protein beta subunit 3 (Gbeta3) has not previously been implicat

34 erase reporter construct containing the AChR beta-subunit 3'UTR, caused an increase in luciferase act

35 GNB5 encodes the G protein beta subunit 5 and is involved in inhibitory G protein s

36 subunit) to the NDP-binding site (within the beta subunit), a distance of 51 A has to be bridged.

37 on heat exposure postautocatalysis, Psd1(ts) beta subunits accumulate in protein aggregates that are

38 ionic/quinonoid intermediate analogue in the beta-subunit active site of the PLP-requiring enzyme try

39 (Hb) tetramer dissociates into the alpha and beta subunits (alpha- and beta-Hb), which are then separ

40 Ca(V)2 knockout impaired the localization of beta subunits, alpha2delta-1 localized normally.

41 g a carbohydrate-binding module (CBM) in the beta-subunit (AMPKbeta) capable of attaching AMPK to gly

42 Ancestral beta-subunit (Anbu) is homologous to HslV and 20S protea

43 eptors composed of one alpha subunit and one beta subunit and are involved in cellular growth, differ

44 result suggests that the ATP binding in one beta subunit and the adenosine 5'-diphosphate (ADP) rele

45 ese activities are strictly dependent on the beta subunit and the promoter sequence.

46 ed in Escherichia coli in the absence of the beta subunit and the protein displayed F-actin capping a

47 examining both the iron loading into the RNR beta subunit and the RNR catalytic activity in yeast mut

48 al spectrin cytoskeletons consist of diverse beta subunits and alphaII spectrin.

49 pha) form dimers with their stably expressed beta subunits and control the transcription of downstrea

50 a2 was homogenously distributed, and the two beta subunits and gamma2 showed faint immunostaining.

51 e residues on Rad decreases its affinity for beta subunits and relieves constitutive inhibition of Ca

52 ation of KCNQ1 with different accessory KCNE beta-subunits and different modulators, but also seems l

53 tase), FARSB (phenylalanine-tRNA synthetase, beta-subunit), and NPC2 (Niemann-Pick disease type C2);

54 th other binding partners, such as alpha and beta subunits, and further assemble into pentameric rece

55 oes an endoproteolytic cleavage into a large beta-subunit, and a smaller alpha-subunit, which harbors

56 ce that lack all four specialized proteasome beta-subunits, and therefore express only constitutive p

57 s into the main channel, prying the beta and beta' subunits apart and, aided by delta, dislodging DNA

58 coassembly of these alpha subunits with the beta subunit appears to occur to a lesser extent than in

59 ng a dioxidation modification mapping to the beta subunit are observed.

60 Mutations in the genes encoding beta subunits are linked to a number of diseases, includ

61 Our data demonstrate that beta subunits are required for beta-adrenergic regulatio

62 potassium (BK) channels and their modulatory beta-subunits are able to dampen or stop excitatory stim

63 Regulatory beta-subunits are one of the mechanisms responsible for

64 he ligand-binding pocket, and the alpha- and beta-subunits are well separated with their cytoplasmic

65 GluClR assemblies having three alpha and two beta subunits arranged in a counterclockwise beta-alpha-

66 teasome by virtue of its different catalytic beta-subunits, as well as the proteasome activator 28 re

67 KCNE beta-subunits assemble with and modulate the properties

68 CNE4, a voltage-gated potassium (Kv) channel beta subunit associated with human atrial fibrillation,

69 biophysical properties of the skeletal DHPR beta subunit beta1a Removal of the intrinsically disorde

70 th a sequence analysis showing that the AP-2 beta subunit (beta2) of higher fungi lacks a clathrin-bi

71 rmed by the alpha-subunit beta-propeller and beta-subunit betaI domains.

72 requires an intact rigid linker between the beta-subunit binding site in the I-II loop and the chann

73 ugh NMR and bioforce-probe analyses that the beta-subunit binds pMHC using Vbeta complementarity-dete

74 hin the hydrophobic core of individual cross-beta subunits but has a clear effect on the motions at t

75 the metal ion-dependent adhesion site in the beta-subunit can be sufficient for binding the receptors

76 roteins bind to voltage-gated Ca(2+) channel beta subunit (Cavbeta) subunits in vitro, but the necess

77 Expression of the beta-subunit (CaVbeta) is required for normal function o

78 ked to a compromised expression of the IL-2R beta subunit (CD122) by old CD8+ T cells.

79 alpha-subunit common to gonadotropins, and a beta-subunit conferring hormone specificity.

80 recordings, indicates that heteromeric alpha/beta subunit-containing receptors underlie both synaptic

81 nsmembrane receptors consisting of alpha and beta subunits; crucial integrins in the kidney collectin

82 sed by activation and thiol deprotonation of beta-subunit cysteines.

83 initiation of separation between alpha- and beta-subunit cytoplasmic regions, headpiece extension, a

84 ive selection express specialized proteasome beta-subunits different from those expressed by all othe

85 The beta subunit differentially regulates maturation, traffi

86 d, and enabled identification of a "missing" beta' subunit domain.

87 ed with Kv4.3 (or Kv4.2), KChIP2 and another beta-subunit, DPP6-L (long isoform).

88 hibitor of apoptosis) or COP (COPI coatomer, beta subunit) dsRNA silenced their target genes and caus

89 The 5 human (h)KCNE beta subunits each regulate various cation channels and

90 cation and characterization of ETF alpha and beta subunit encoding genes (ETFA and ETFB) and ETFDH en

91 rmline deletion in mice of potassium channel beta subunit-encoding Kcne2 (Kcne2(CS-/-) ) causes dilat

92 anched-chain alpha-ketoacid dehydrogenase E1 beta-subunit-encoding gene (NaBCKDE1B) in the trichomes

93 isolates, and deletion of the only G-protein beta-subunit-encoding gene of A. oligospora nearly aboli

94 demonstration of S-palmitoylation of a VGSC beta subunit, establishing precedence for this post-tran

95 line deletion of the KCNE2 potassium channel beta subunit exhibited NAFLD as early as postnatal day 7

96 of the interaction of this segment with the beta subunit explain the necessity for a second highly c

97 eptogenic variants and involves differential beta subunit expression of GABA(A)R populations, which p

98 The first contained a redox-active Tyr in beta subunits (F41Y), a substitution present in Hb Mequo

99 ted Na(+) channel complex) that includes the beta subunit family.

100 te (the VGSC complex) that includes the VGSC beta subunit family.

101 of the complex, Fas2, when its partner, the beta-subunit Fas1, is absent.

102 ltaneously to facilitate the assembly of the beta subunits for forming immunoproteasomes.

103 In all CPs characterized to date, alpha and beta subunits form the active heterodimer.

104 In the class I-c beta subunit from Chlamydia trachomatis, a heterodinucle

105 f which are heterodimers specified by unique beta subunits (FSHbeta/LHbeta).

106 beta subunits function in VGSC and potassium channel mod

107 as rich in alpha1, alpha2, alpha5, all three beta-subunits, gamma2, and delta.

108 Here, we report that G protein beta subunits (Gbeta) bind to DDB1 and that Gbeta2 targe

109 complex consisting of the atypical G protein beta subunit Gbeta5 and a regulator of G protein signali

110 nding of a TF, using the luteinizing hormone beta subunit gene (Lhb) promoter and Egr-1 as a model sy

111 ion of the geranylgeranyltransferase type I, beta subunit gene (Pggt1b), called Pggt1b(DeltaCD4) mice

112 e knocked out the mitochondrial ATP synthase beta subunit gene in the rodent malaria parasite, Plasmo

113 Parasites lacking the beta subunit gene of the ATP synthase generated viable g

114 Ookinetes lacking the beta subunit gene of the ATP synthase had normal motilit

115 Disruption of the beta subunit gene of the ATP synthase only marginally re

116 rin to the mitochondrion, where it binds the beta-subunit (HADHB) of the mitochondrial trifunctional

117 The stoichiometry between alpha and beta-subunits has been controversial with studies report

118 e oxidoreductase domain(8,9) of Shaker's K(V)beta subunit, Hyperkinetic(10,11).

119 The IL-2 receptor beta subunit (IL-2Rbeta) serves in this capacity and is

120 ic alpha subunit complexes with glycosylated beta subunit in the ER to proceed through Golgi and post

121 s regulate the hormone-specific gonadotropin beta subunits in vivo, we deleted Dicer in gonadotropes

122 or enhancing the catalytic efficiency of the beta-subunit in the absence of its binding partner.

123 -terminal region of predominantly one of the beta-subunits in the most closed of the three catalytic

124 Kv4 pore-forming subunits co-assemble with beta-subunits including KChIP2 and DPP6 and the resultan

125 effects are influenced by the type of alpha/beta subunits incorporated into the functional receptor.

126 f-chaperone refolding mechanism, whereby the beta-subunits independently refold, thereby templating t

127 To investigate the mechanisms by which beta-subunits influence Nav channel function, we solved

128 Co-expression of its beta subunit inhibits misfolding and thus allows secreti

129 ment of Nun interacts with the RNAP beta and beta' subunits inside the RNAP active site cleft as well

130 show no significant opening of the ATP-bound beta subunit; instead, we observe that mechanical energy

131 of disulfide-bonding capability at the Na(V)beta subunit-interaction sites.

132 Ca2+ channel beta-subunit interactions with pore-forming alpha-subuni

133 btained from molecular modeling of the alpha-beta subunit interface and suggests that in alpha3betaGl

134 he photooxidation of FnY356 within the alpha/beta subunit interface occurs within the Marcus inverted

135 binding sites and at the noncanonical delta-beta subunit interface.

136 ne domain with high affinity to the gamma(+)-beta(-) subunit interface site with negative energetic c

137 that its binding site may be at the alpha + beta- subunit interface.

138 B3(D120N, E180G, Y302C) mutations located at beta+ subunit interfaces reduced whole cell currents by

139 GABRB3(N110D) and GABRB1(F246S) mutations at beta- subunit interfaces produced minor changes in whole

140 acellular protease treatment, which suggests beta subunit involvement.

141 31 of Escherichia coli RNA polymerase (RNAP) beta subunit is a part of RNA binding domain in transcri

142 In affected keratinocytes the AP-1 beta subunit is lost, and the gamma subunit is greatly r

143 The KCNE2 potassium channel beta subunit is required for normal lung function and re

144 The Cys(93) residue of the beta subunit is the primary site of dioxidation.

145 nning voltage-gated potassium (K(v)) channel beta subunit is ubiquitously expressed and essential for

146 chondrial BK(Ca) channel (mitoBK(Ca) ) by BK-beta subunits is not established.

147 oprecipitates with hsp60 indicating that the beta-subunit is likely a substrate for the chaperonin.

148 that the KPNB1, a key member of Karyopherin beta subunits, is highly expressed in advanced prostate

149 s in the KCNE2-encoded voltage-gated channel beta-subunit, is limited.

150 ha2, or alpha3) associated with an auxiliary beta-subunit isoform (beta1 or beta2).

151 and (75)Cys, a unique feature among the four beta-subunit isoforms.

152 fold, recruiting both vFLIP and the IKKalpha/beta subunits, it has been proposed that binding of vFLI

153 Kv4.2 and Kv4.3; co-expression of cytosolic beta subunit KChIP2, which regulates Kv4 channels in car

154 transfected with cloned Kv4.3 (or Kv4.2) and beta-subunit KChIP2, NS5806 significantly increased the

155 Kv4.2 and Kv4.3, together with the accessory beta-subunit KChIP2.

156 sue-specific manner through co-assembly with beta subunits KCNE1-5.

157 Kv7.1 and the beta-subunit KCNE1 form the cardiac IKs channel that is

158 d potassium channel that is modulated by the beta-subunit KCNE1 to generate IKs, the slow delayed rec

159 ic voltage-gated ion channel, KCNQ1, and its beta-subunit, KCNE1.

160 We crossed the self-infertile ATP synthase beta subunit knockout parasites with a male-deficient, s

161 f the voltage-gated potassium (K(+)) channel beta-subunit (Kvbeta) Hyperkinetic (Hk).

162 ripheral glia results in accumulation of the beta subunit (LanB1), leading to distended endoplasmic r

163 ically associates with channel proteins in a beta-subunit-like fashion.

164 ork will help to form a model reflecting the beta-subunit location in a Nav channel complex.

165 amino acids near the cytoplasmic end of the beta subunit M4 (beta3Pro-415, beta3Leu-417, and beta3Th

166 The two beta-subunits make a tightly bound homodimer at the cent

167 in the 3'-untranslated region (UTR) of AChR beta-subunit mRNA.

168 As, predicted in silico to bind gonadotropin beta subunit mRNAs, were suppressed in purified gonadotr

169 causes an increase in the stability of AChR beta-subunit mRNAs in denervated muscle.

170 -transcriptional events indeed regulate AChR beta-subunit mRNAs in response to denervation.

171 y assays revealed that the half-life of AChR beta-subunit mRNAs was increased in the presence of dene

172 hosphorylation by ULK1 was dependent on AMPK beta-subunit myristoylation, metabolic stress associated

173 ne 5'-diphosphate (ADP) release from another beta subunit occur via a transient whose lifetime is ~10

174 rtially unstructured until assembly with its beta-subunit occurs and identify a major site of incompl

175 f-function mutation in atp1b1a, encoding the beta subunit of a Na,K-ATPase pump, causes edema and epi

176 enzyme strikingly resembles the ring-shaped beta subunit of a vertebrate ion channel.

177 gm, the signal peptide of ruminant CD18, the beta subunit of beta2 integrins, is not cleaved and henc

178 ions by means of retrograde transport of the beta subunit of cholera toxin.

179 tilocus sequence analysis of gyrase B of the beta subunit of DNA topoisomerase (gyrB), and 16S rRNA a

180 of a consensus pentapeptide motif toward the beta subunit of Escherichia coli DNA polymerase III holo

181 cl-xL), leading to its dissociation from the beta subunit of F1Fo-ATP synthase.

182 GNB3 encodes the beta subunit of G protein heterotrimer (Galphabetagamma)

183 Hepatocystin functions as the noncatalytic beta subunit of Glucosidase II, an endoplasmic reticulum

184 t serve as a structural subunit, much like a beta subunit of heteromeric nAChRs, providing only compl

185 ic mutations in AP1B1, the gene encoding the beta subunit of heterotetrameric adaptor protein 1 (AP-1

186 CYP11A1, PTGS2, EREG, and the intracellular beta subunit of human chorionic gonadotropin (hCGbeta) a

187 3)(-) regulatory T cells in vitro, such that beta subunit of IL-27 (Ebi)(-/-) (ie, IL-27-incompetent)

188 on encoding the rifampin binding site on the beta subunit of RNA polymerase (rpoB).

189 lar function for Sequence Insertion 1 in the beta subunit of RNA polymerase and significantly advance

190 h encodes the canonical rifampin target, the beta subunit of RNA polymerase.

191 for understanding how a mutation within the beta subunit of RNAP (G1249D), which is far removed from

192 s null variants in AP1B1, encoding the large beta subunit of the AP-1 complex.

193 COPBI is the beta subunit of the coat protein I (COPI), which is invo

194 These genes encode the beta subunit of the G-protein complex (STE4), the pherom

195 consequence of the activation of the common beta subunit of the granulocyte-macrophage colony-stimul

196 GNB5 encodes an atypical beta subunit of the heterotrimeric GTP-binding proteins

197 , HPV11 and HPV16 directly interact with the beta subunit of the mitochondrial ATP-synthase (ATP5B),

198 It encodes the beta subunit of the non-classical major histocompatibili

199 ro] and c.559G>T [p.Asp187Tyr]) encoding the beta subunit of transcription factor IIE (TFIIEbeta).

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

201 solved, it is clear that both the alpha1 and beta subunits of DHPR are essential for this process.

202 4 (CHD4) physically interacts with alpha and beta subunits of HIF1 and HIF2 and enhances HIF-driven t

203 pin beta (CGB) genes, which encode alpha and beta subunits of human chorionic gonadotrophin (hCG), a

204 identify GNPTAB, which encodes the alpha and beta subunits of N-acetylglucosamine-1-phosphate transfe

205 two putative alpha subunits and two putative beta subunits of Rab-GGTs have been annotated in the Ara

206 Although the alpha and beta subunits of the GPCRs are the first intracellular m

207 t with protein kinase CK2: (a) the alpha and beta subunits of the nicotinic acetylcholine receptors w

208 ains of topoisomerase I (TopoI-CTDs) and the beta' subunit of RNA polymerase of M. smegmatis in the a

209 genome encodes distant homologs of beta and beta' subunits of bacterial RNA polymerase (RNAP).

210 de of Caudovirales that encodes the beta and beta' subunits of multi-subunit RNA polymerase (RNAP), a

211 The identification of the beta-subunit of archaeal TFE enabled us to reconstruct t

212 albumin, malate dehydrogenase (MDH), and the beta-subunit of ATP synthase in in-vitro protein-folding

213 lfurylase accumulated very low levels of the beta-subunit of beta-conglycinin.

214 n to two cysteine residues (C50, C61) on the beta-subunit of both PEI (CpeB) and PEII (MpeB).

215 The beta-subunit of core binding factor (CBFbeta), that hete

216 ecific methyltransferase that methylates the beta-subunit of electron transfer flavoprotein (ETFbeta)

217 the specific binding of the antibody to the beta-subunit of Fsh to block its action.

218 rase alpha-subunit, PTAR1, and the catalytic beta-subunit of GGTase2, RabGGTB.

219 fluid (CSF) levels of alpha-fetoprotein and beta-subunit of human chorionic gonadotropin are used as

220 involving a positively charged patch on the beta-subunit of MoFeP.

221 Five copies of nrdB, encoding beta-subunit of ribonucleotide reductase (RNR), a critic

222 ated in rpoB, an essential gene encoding the beta-subunit of RNA polymerase.

223 The Cngb1 locus-encoded beta-subunit of rod cGMP-gated cation channel and associ

224 X-ray crystal structures of the unusual beta-subunit of the acyl-CoA carboxylase (YCC) responsib

225 t players in aerobic respiration such as the beta-subunit of the ATP synthase.

226 r HEY2, which uncovered KCNIP2, encoding the beta-subunit of the channel underlying the transient out

227 ligonucleotide-mediated exon skipping of the beta-subunit of the high-affinity IgE receptor (Fcepsilo

228 It is known, is that the beta-subunit of the human mitochondrial ATP synthase co-

229 based purification scheme, we identified the beta-subunit of the mitochondrially localized electron t

230 A polyclonal antibody that targets the beta-subunit of the pituitary hormone follicle-stimulati

231 We previously engineered the beta-subunit of tryptophan synthase (TrpB), which cataly

232 urce of latent catalytic potential using the beta-subunit of tryptophan synthase from Pyrococcus furi

233 cross-links between Psb28 and the alpha- and beta-subunits of cytochrome b559, an essential component

234 alpha-subunit (Cga) and the hormone-specific beta-subunits of gonadotropin.

235 that HCV interacted with both the alpha- and beta-subunits of the mitochondrial trifunctional protein

236 tations locating to the essential alpha- and beta-subunits of tryptophan synthase.

237 lational modification of both the alpha- and beta-subunits of tubulin.

238 dy explored the impact of the CK2 regulatory beta-subunit on platelet biogenesis and activation.

239 The trace activity of the wild-type beta-subunit on this substrate was enhanced more than 10

240 Importantly, ENaC beta-subunit or alpha-subunit silencing or kidney tubule

241 fled border of osteoclasts, CLC-7 requires a beta-subunit, OSTM1, for stability and activity.

242 omposite cytokines, consisting of the common beta subunit p40 and the specific cytokine alpha subunit

243 unit palmitoylation had a dominant role over beta subunit palmitoylation in regulating ENaC.

244 Cs 1, 2, and 14 still activated ENaC lacking beta subunit palmitoylation sites.

245 beta subunit palmitoylation was increased by ENaC co-exp

246 and functional divergence of duplicated TSH beta-subunit paralogs (tshbetaa and tshbetab) in Atlanti

247 to modulating sodium and potassium currents, beta subunits play nonconducting roles as cell adhesion

248 x active Y's, a stable Y radical (Y.) in the beta subunit (position 122 in E. coli), and three transi

249 snorkeling' lysine at the TM/CT interface of beta subunits, previously proposed to regulate alphaIIbb

250 lted in profound suppression of gonadotropin-beta subunit proteins and, consequently, the heterodimer

251 IL-3 shares a common beta subunit receptor with both IL-5 and GM-CSF but, thr

252 surface alpha-receptor, IL-11Ralpha, and the beta-subunit receptor, gp130.

253 stoylated and membrane-associated regulatory beta-subunits restrict nuclear localization and inhibit

254 alpha1 subunit cell surface expression with beta subunits resulting in severely reduced synaptic inh

255 tion in 241, which encodes an RNA polymerase beta subunit, revealed that without this subunit, no oth

256 opsis Rab-GGT alpha subunits RGTA1/RGTA2 and beta subunits RGTB1/RGTB2, but only RGTA1.RGTB1 and RGTA

257 Defected SCS ADP-forming beta subunit (SCS A-beta) is linked to lethal infantile

258 Similarly, viral-mediated expression of a beta-subunit-sequestering peptide sharply curtailed beta

259 n of plasma membrane BK(Ca) channels with BK-beta subunits shapes their biophysical properties and ph

260 Co-expressing KCNQ1 with the KCNE2 beta-subunit shows that both KCNQ1 mutants increase curr

261 Voltage-gated sodium channel (VGSC) beta subunits signal through multiple pathways on multip

262 tion of the succinate-CoA ligase GDP-forming beta subunit (SUCLG2), which regulates succinate metabol

263 chromophores to Cys-155 of phycobiliprotein beta-subunits, suggesting that PhiCpeT may also help ass

264 alpha1(-26') and reciprocal mutations in the beta subunit suggests that this subunit remains relative

265 ially forms encounter complexes on the MoFeP beta-subunit surface en route to the ATP-activated, ET-c

266 s the protein into a large membrane-anchored beta subunit that noncovalently associates with the smal

267 rts expressing mutant Ca(V)1.2 alpha(1C) and beta subunits that can no longer be phosphorylated by pr

268 e have termed mod2B, composed of homodimeric beta subunits that contain amino acid sequences from the

269 tif that separates the enzyme into alpha and beta subunits that remain non-covalently attached and ar

270 eracts with a structural element of the RNAP beta'-subunit that we call the beta'-clamp-toe (beta'CT)

271 otential targets for regulation by auxiliary beta-subunits that are expressed together with the alpha

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

273 the alpha subunit containing the BC and the beta subunit the CT and BCCP domains, and it is believed

274 Unlike the beta subunit, the CP alpha subunit of the apicomplexan p

275 e-TCR alpha (pTalpha) subunit and a variable beta subunit, the latter of which is incorporated into t

276 receptors (nAChRs) assembled from alpha and beta subunits, the alpha9alpha10 receptor is an atypical

277 d in a groove between the integrin alpha and beta-subunits; the basic Lys or Arg side chain hydrogen

278 e actin flow with their cytoskeleton-binding beta-subunits tilted by applied force.

279 s to their cellular destination requires the beta subunit TMEM30A proteins.

280 the Thermotoga maritima tryptophan synthase beta-subunit (TmTrpB) through multi-mutation pathways in

281 he individual contributions of the alpha and beta subunits to the fundamental process of ATP synthesi

282 chemical energy (ATP hydrolysis in the alpha/beta-subunits) to mechanical energy and torque (rotation

283 Importantly, HuR binds to endogenous AChR beta-subunit transcripts in cultured myotubes and in viv

284 ding to an increase in the stability of AChR beta-subunit transcripts.

285 synapses, by stimulus-dependent ATP synthase beta subunit translation; this increases the ratio of AT

286 activation of the alpha-subunit TrpA and the beta-subunit TrpB via a complex allosteric network.

287 set of mutations of the tryptophan synthase beta-subunit (TrpB) from Pyrococcus furiosus, which mimi

288 is a heteropentamer consisting of alpha and beta subunit types, with yet unknown subunit stoichiomet

289 recovered in laboratory-evolved stand-alone beta-subunit variants.

290 C1 sequesters precursors of immunoproteasome beta subunits via PRAS40.

291 A wide array of integrin beta subunits was detected in betaTC3 and NIT-1 insulino

292 Although beta subunits were originally termed auxiliary, we now k

293 of the gamma-subunit, but not the alpha- and beta-subunits, were decreased by injury, an event associ

294 present in luteinizing hormone, and a unique beta subunit, which is transcriptionally regulated by go

295 the hydrophobic interface between the cross-beta subunits, which has been previously found to be wat

296 the hydrophobic interface between the cross-beta subunits, which is defined by Met-35 contacts.

297 on of class I ribonucleotide reductase (RNR) beta subunits, which self-assemble dimetal cofactors wit

298 bind into the open ATP-binding groove of the beta-subunit, which thereafter becomes tightly locked by

299 ur KCNQ1 alpha-subunits and up to four KCNE1 beta-subunits, which are thought to reside within extern

300 chanism limits the association of up to four beta-subunits within the IKs complex.