ライフサイエンスコーパス: heterotetrameric

1 n, causing it to accumulate in a membrane as heterotetrameric 2RI-2T complex.

2 aryl hydrocarbon receptor (AhR) exists in a heterotetrameric 9S core complex consisting of the AhR l

3 Genes encoding the alpha2beta2 heterotetrameric ACAD structures are present in multiple

4 GIRK1 and GIRK4 subunits combine to form the heterotetrameric acetylcholine-activated potassium curre

5 of overlapping hot spots of dynamin and the heterotetrameric adaptor 2 complex in Drosophila nerve t

6 lasmically exposed sorting signals to either heterotetrameric adaptor AP-1 or AP-3.

7 with distinct endocytic adaptors such as the heterotetrameric adaptor AP3 influence the trafficking o

8 The heterotetrameric adaptor complex 1 (AP-1) and the monome

9 Expression of the epithelial cell-specific heterotetrameric adaptor complex AP-1B is required for t

10 biogenesis from endosomes that requires the heterotetrameric adaptor complex AP3.

11 is a chaperone governing the assembly of the heterotetrameric adaptor complexes 1 and 2 (AP1 and AP2)

12 Heterotetrameric adaptor complexes and SNAREs play key r

13 Heterotetrameric adaptor complexes vesiculate donor memb

14 targeting and are recognized by a family of heterotetrameric adaptor complexes, which then recruit c

15 investigated the interaction of PACS-1 with heterotetrameric adaptor complexes.

16 AP-3 is a heterotetrameric adaptor involved in the biogenesis of l

17 AP-4 is a member of the heterotetrameric adaptor protein (AP) complex family inv

18 t well-characterized member of the family of heterotetrameric adaptor protein (AP) complexes that med

19 AP-4 is a member of the family of heterotetrameric adaptor protein (AP) complexes that med

20 The clathrin-associated, heterotetrameric adaptor protein (AP) complexes, AP-1, A

21 if and mediate sorting via interactions with heterotetrameric adaptor protein (AP) complexes.

22 AP1B1, the gene encoding the beta subunit of heterotetrameric adaptor protein 1 (AP-1) complexes, whi

23 by interaction with the clathrin-associated, heterotetrameric adaptor protein 2 (AP-2) complex.

24 Heterotetrameric adaptor protein 2 (AP2) complexes, whic

25 of genes, including several subunits of the heterotetrameric adaptor protein AP-3, which are require

26 g and vesiculation process that requires the heterotetrameric adaptor protein AP3 and a small molecul

27 The heterotetrameric adaptor protein complex 4 (AP-4) is a c

28 The heterotetrameric adaptor protein complex AP-3 has been s

29 that hVPS41 requires both a functional AP-3 (heterotetrameric adaptor protein complex) and HOPS (homo

30 Here, we report that both the AP-3 (heterotetrameric adaptor protein complex) interaction do

31 tifs within their cytoplasmic domains by the heterotetrameric adaptor protein complex, AP-2.

32 In mammals, the heterotetrameric adaptor protein complex-2 (AP-2) is req

33 In mammals, the heterotetrameric adaptor protein complex-2 (AP-2) sorts

34 Heterotetrameric adaptor protein complexes are important

35 The heterotetrameric adaptor proteins (AP complexes) link th

36 olutionarily ancient member of the family of heterotetrameric adaptor proteins (AP complexes).

37 itment onto membranes are not dependent upon heterotetrameric adaptors or AP180 homologs in yeast.

38 In the heterotetrameric ADP-Glc PPase from potato (Solanum tube

39 The heterotetrameric, allosterically regulated enzyme, adeno

40 , Cep63 and Cep152, cooperatively generate a heterotetrameric alpha-helical bundle that functions in

41 sferase (E2) decorated with 60 copies of the heterotetrameric (alpha(2)beta(2)) 153-kDa pyruvate deca

42 lution temperatures (28 to ~40 degrees C), a heterotetrameric (alpha(2)beta(2)) complex is the most a

43 Dinitrogenase is a heterotetrameric (alpha(2)beta(2)) enzyme that catalyzes

44 acid decarboxylase/dehydrogenase (BCKD) is a heterotetrameric (alpha(2)beta(2)) thiamine diphosphate

45 nt of subunits closely resembles that of the heterotetrameric (alphabeta)(2) phenylalanyl-tRNA synthe

46 Tryptophan synthase (TS) is a heterotetrameric alphabetabetaalpha complex.

47 Heterotetrameric (alphabetagammadelta) sarcosine oxidase

48 coccus furiosus contains an NADPH-utilizing, heterotetrameric (alphabetagammadelta), cytoplasmic hydr

49 homotetrameric recombinant GluR2, the native heterotetrameric AMPA-R adopted various conformations, w

50 in solution as a dynamic equilibrium between heterotetrameric and heterohexameric complexes.

51 motility and ATP hydrolysis of recombinant, heterotetrameric and homodimeric conventional Drosophila

52 Sera of camelids contain both conventional heterotetrameric antibodies and unique functional heavy

53 The heterotetrameric AP and F-COPI complexes help to define

54 iae, there are 13 genes encoding homologs of heterotetrameric AP subunits and two genes encoding AP18

55 The heterotetrameric AP-1 adaptor complex is involved in the

56 high-affinity membrane-binding sites for the heterotetrameric AP-1 adaptor complex.

57 AP-4, a novel protein complex related to the heterotetrameric AP-1, AP-2, and AP-3 adaptors that medi

58 Accordingly, the heterotetrameric AP-2 adaptor complex binds not only to

59 in 1, the so-called DPW domain, binds to the heterotetrameric AP-2 adaptor complex by associating dir

60 lpha-subunit appendage that projects off the heterotetrameric AP-2 adaptor core.

61 ors is either directly or indirectly via the heterotetrameric AP-2 complex [5].

62 A heterotetrameric AP-3 adaptor complex has been implicate

63 with mutations in the beta 3A subunit of the heterotetrameric AP-3 complex.

64 The heterotetrameric AP2 adaptor (alpha, beta 2, mu 2 and si

65 to endocytosis is their ability to bind the heterotetrameric AP2 complex via their C2B domain.

66 l that clathrin function is dependent on the heterotetrameric APs and/or AP180 homologs, yeast strain

67 23 with an OAP-disrupting mutation indicated heterotetrameric AQP4 association.

68 They are heterotetrameric assemblies of Kv7.2 and Kv7.3 subunits.

69 Adaptor protein (AP) complexes are heterotetrameric assemblies of subunits named adaptins.

70 Furthermore, the contribution of any heterotetrameric assembly to the total water transport t

71 the so-called 'hinge' region of MukB forms a heterotetrameric assembly with a C-terminal DNA binding

72 ich are essential for native alpha(2)beta(2) heterotetrameric assembly.

73 ted vesicles are the clathrin triskelion and heterotetrameric associated protein (AP) complexes.

74 The structure reveals a heterotetrameric association, consisting of a disc-like

75 nd dynamics of plasma membrane OAPs, and the heterotetrameric associations of AQP4, we constructed gr

76 t proteins, the dimeric BchL protein and the heterotetrameric BchN/BchB protein.

77 The heterotetrameric (-beta4-mu4-sigma4) complex adaptor pro

78 This heterotetrameric, C(2)-symmetric bundle, A(His):B(Thr),

79 In this study we identify calpactin I, a heterotetrameric, Ca(2+)- and phospholipid-binding prote

80 Unlike heterotetrameric canonical antibodies that are composed

81 ing of the latter to the beta-subunit of the heterotetrameric channel complex.

82 suggested lessening of amino acid clashes in heterotetrameric channel complexes.

83 wild-type subunits to maintain a functional heterotetrameric channel differed among the four RyR1 mu

84 t one or more subunits of Kv1.1 rendered the heterotetrameric channel sensitive to DTX-K.

85 Hence, the inactivation rate of heterotetrameric channels comprising both N-type and non

86 DTX-K is a specific blocker of Kv1.1 and heterotetrameric channels containing Kv1.1.

87 sly expressed human Kv7.4 and Kv7.5 homo- or heterotetrameric channels in A7r5 cells.

88 P3R monomers are assembled to form homo- and heterotetrameric channels that mediate Ca(2+) release fr

89 Coexpression of WT+T421M-Kv11.1 resulted in heterotetrameric channels that remained partially traffi

90 plasma membrane expression by diverting the heterotetrameric channels to lysosomes.

91 splicing in the alpha subunit, formation of heterotetrameric channels, and combinatorial association

92 ive cation channels that form many homo- and heterotetrameric channels.

93 ing that WT and mutant subunits associate in heterotetrameric channels.

94 s the possibility of interaction between the heterotetrameric chromogranin and heterotetrameric IP3 r

95 analysis and mutagenesis studies reveal that heterotetrameric ChsE1-ChsE2 has only two active sites.

96 AP-2, the heterotetrameric clathrin adaptor protein, has been demo

97 Heterotetrameric clathrin adaptors directly link the cla

98 es containing either homotetrameric (CNGA2), heterotetrameric (CNGA2:CNGA4:CNGB1b), or hyperpolarizat

99 ransglutaminase is the catalytic part of the heterotetrameric coagulation FXIII-A(2)B(2) complex that

100 n diphosphate (ThDP)-dependent enzyme with a heterotetrameric cofactor-binding fold.

101 Lateral association seems to be mediated by heterotetrameric coiled coils between the paired C-termi

102 air interactions that directly stabilize the heterotetrameric coiled-coil state.

103 AMPA receptors (AMPA-Rs) are formed as heterotetrameric combinations of subunits known as GluR1

104 NMDARs, which are heterotetrameric, commonly are composed of two GluN1 sub

105 catalyzing intron removal from pre-tRNA is a heterotetrameric complex (splicing endonuclease [SEN] co

106 ts of this CC MBS.LZ PKG-Ialpha low-affinity heterotetrameric complex and allow reevaluation of the r

107 tructure of a protocadherin-15 + cadherin-23 heterotetrameric complex at 2.9- angstrom resolution, de

108 vate transcription, most likely by forming a heterotetrameric complex at the tcpPH promoter.

109 ystal structure and mutational analysis of a heterotetrameric complex between constitutively active R

110 two homodimers assemble into a high-affinity heterotetrameric complex by virtue of two low-affinity i

111 act in vivo and are predicted to form a core heterotetrameric complex capable of creating higher orde

112 Adaptor protein 2 (AP2), a heterotetrameric complex comprising AP2a, AP2B2, AP2u2 a

113 Centralspindlin, a heterotetrameric complex consisting of kinesin-6 and Rho

114 35 are homologous P-loop NTPases that form a heterotetrameric complex essential for FeS protein matur

115 modeling of the dimer-dimer interface of the heterotetrameric complex exhibits the involvement of non

116 The heterotetrameric complex formed by these two proteins ac

117 d-coil tethers of the golgin family, and the heterotetrameric complex GARP.

118 2)-sFlaF(2) co-crystal structure, define its heterotetrameric complex in solution by small-angle X-ra

119 UB1) and its paralog HUB2 act in a conserved heterotetrameric complex in the chromatin-mediated trans

120 C-1-P-directed invasion, indicating that the heterotetrameric complex is required for C-1-P-mediated

121 We also analyzed binding parameters of a heterotetrameric complex of AnxA2 with its S100A10 prote

122 SCRT-0 indicates that it exists largely as a heterotetrameric complex of its two subunits.

123 isoforms initiate signaling by assembling a heterotetrameric complex of paired type I (TbetaRI) and

124 nvolving only 50S subunits and mediated by a heterotetrameric complex of PurH and aEF2-proteins with

125 This heterotetrameric complex reveals a cyclic arrangement of

126 A heterotetrameric complex termed AP-3 is involved in sign

127 WAVE1 exists in a heterotetrameric complex that includes orthologues of hu

128 ember of the S100 protein family and forms a heterotetrameric complex with annexin 2.

129 Analysis of the reconstituted Rad3-Rad26 heterotetrameric complex with electron microscopy enable

130 iption without directly binding DNA but as a heterotetrameric complex with ETS1, a transcription fact

131 tein core domain and for AnxA2 residing in a heterotetrameric complex with its intracellular binding

132 When Kv1.1 was expressed as a heterotetrameric complex with Kv1.5, block by DTX-K domi

133 These subunits form a heterotetrameric complex with R2H2 stoichiometry.

134 Specifically, annexin A2, found in a heterotetrameric complex with S100A10, not only serves a

135 on is believed to derive from formation of a heterotetrameric complex with target proteases involving

136 The coat is largely made up of the heterotetrameric complex, adaptor protein 3, recently im

137 he hypothesis that the "normal" state in the heterotetrameric complex, in which XerC is catalytically

138 molecular and functional insights into this heterotetrameric complex, we computationally constructed

139 also interacts directly with ExsD to form a heterotetrameric complex.

140 AP-3) is a vesicle-coat protein that forms a heterotetrameric complex.

141 m SNAP-23C, syntaxin-4, and VAMP-3 to form a heterotetrameric complex.

142 romotes formation of the GABPalpha(2)beta(2) heterotetrameric complex.

143 transcriptionally active GABPalpha(2)beta(2) heterotetrameric complex.

144 elative subunit position and number within a heterotetrameric complex.

145 ubunits alpha and beta within an alpha2beta2-heterotetrameric complex.

146 ires TbPRMT1 prozyme (PRO) to form an active heterotetrameric complex.

147 g factor, is a target for the p11/annexin A2 heterotetrameric complex.

148 Cu2+ to facilitate the formation of S100A13 heterotetrameric complexes and these signal peptideless

149 ity, the composition and expression of these heterotetrameric complexes are expected to be tightly re

150 that native channels can be either homo- or heterotetrameric complexes composed of several GIRK subu

151 They form massive heterotetrameric complexes endowed with unique allosteri

152 show that Kv1 channels assembled as homo- or heterotetrameric complexes had distinct surface expressi

153 athrin-associated adaptors AP-1 and AP-2 are heterotetrameric complexes involved in the recognition o

154 he interactions between these motifs and the heterotetrameric complexes is controversial.

155 branes in a distinctive manner by assembling heterotetrameric complexes of structurally related serin

156 ociated recycling protein (EARP) are related heterotetrameric complexes that associate with the cytos

157 Adaptor proteins (AP 1-5) are heterotetrameric complexes that facilitate specialized c

158 uitously expressed, evolutionarily conserved heterotetrameric complexes that mediate different types

159 tly expressed in the brain where it can form heterotetrameric complexes with TRPC1 and TRPC4 channel

160 hat HCN1 and HCN2 readily coassemble to form heterotetrameric complexes.

161 nus of an adjacent subunit in both homo- and heterotetrameric complexes.

162 but are instead associated with DO in tight heterotetrameric complexes.

163 ar homeostasis by the formation of homo- and heterotetrameric complexes.

164 Their heterotetrameric composition generates subtypes with dis

165 Kv2/KvS assembly increases the diversity of heterotetrameric configurations and extends the regulato

166 , the biological properties of the different heterotetrameric configurations formed by PIP1 and PIP2

167 ion (GAIT) complex in human myeloid cells is heterotetrameric, consisting of glutamyl-prolyl-tRNA syn

168 Plant AGPs are heterotetrameric, consisting of two large and two small

169 in Alzheimer disease (AD) and consists of a heterotetrameric core complex that includes the aspartyl

170 as a heterotetramer, resembling the (H3/H4)2 heterotetrameric core of the histone octamer, suggesting

171 al complex consisting of a (Mre11)2/(Rad50)2 heterotetrameric DNA processing head and a double coiled

172 The heterotetrameric Dr1-DRAP1 transcriptional repressor com

173 dues in the E1alpha and E1beta chains of the heterotetrameric E1 (alpha(2)beta(2)) component of the P

174 ears to be conserved in the alpha-subunit of heterotetrameric E1s and multiple sequence alignments su

175 Here, we present a structural model of heterotetrameric ENaC alpha1betaalpha2gamma that is cons

176 a single subunit type, the plant AGPase is a heterotetrameric enzyme (alpha2beta2) with distinct role

177 ne oxidase from Corynebacterium sp. P-1 is a heterotetrameric enzyme (alphabetagammadelta) that conta

178 This heterotetrameric enzyme also used the analogous longer c

179 and small (SS) subunits yielded a functional heterotetrameric enzyme capable of complementing a mutat

180 ant ADP-glucose pyrophosphorylase (AGP) is a heterotetrameric enzyme composed of two large and two sm

181 e relative roles of the conserved Lys in the heterotetrameric enzyme from potato (Solanum tuberosum L

182 Protein kinase CK2 (casein kinase II) is a heterotetrameric enzyme implicated in many essential reg

183 ructure of molybdopterin synthase revealed a heterotetrameric enzyme in which the C terminus of each

184 d with SS and that the net properties of the heterotetrameric enzyme is a product of subunit synergy.

185 tide (FAD) to protein Sdh1, a subunit of the heterotetrameric enzyme succinate dehydrogenase.

186 Pyrococcus furiosus is an NADP(H)-dependent heterotetrameric enzyme that contains a nickel-iron cata

187 for NAD could be measured with the purified heterotetrameric enzyme that possessed just 16-18% activ

188 DNA polymerase delta (Pol delta4) is a heterotetrameric enzyme, whose p12 subunit is degraded i

189 ajor T. brucei PRMT, TbPRMT1, functions as a heterotetrameric enzyme-prozyme pair.

190 make up the large and small subunits of this heterotetrameric enzyme.

191 cter sp. and Pseudomonas sp. show that these heterotetrameric enzymes also contain covalently bound F

192 AP4E1 encodes the epsilon subunit of the heterotetrameric (epsilon-beta4-mu4-sigma4) AP-4 complex

193 The crystal structure of the heterotetrameric ESCRT-I complex reveals a highly asymme

194 inal domain of hVps22p in the formation of a heterotetrameric ESCRTII complex.

195 The heptamer can be dissected into a heterotetrameric F-subcomplex, which displays similariti

196 ome bacteria, archaea, and eukaryotes; and a heterotetrameric form (alpha2beta2) present in most bact

197 lder interface conferred specificity for the heterotetrameric form and the trans-orientation of subun

198 1K.S302N) homotetramer are compared with its heterotetrameric form assembled with S D143N.

199 of the Pol2p.Dpb2p complexes reveals a novel heterotetrameric form, consisting of two heterodimers of

200 est that molecular association of IP3Rs into heterotetrameric forms can contribute to the complexity

201 To allow for the separation of various heterotetrameric forms of the enzyme, surface residues w

202 for this diversity, we designed an A(2)B(2) heterotetrameric four-helix bundle with an active site s

203 heterooctomeric ATP-sensitive K channels and heterotetrameric G-protein-regulated inward rectifier K

204 The mature heterotetrameric GAIT complex binds the 3' UTR GAIT elem

205 The heterotetrameric GAIT complex suppresses translation of

206 tRNA synthetase (EPRS) is a component of the heterotetrameric gamma-interferon-activated inhibitor of

207 (gamma-TuC), in which multiple copies of the heterotetrameric gamma-tubulin small complex (gamma-TuSC

208 handover of TA substrates is mediated by the heterotetrameric Get4/Get5 complex (Get4/5), which tethe

209 led homotetrameric GIRK1 channels and in the heterotetrameric GIRK1/2 channel, the truncation of G1-d

210 Heterotetrameric GIRK1/2 shows a higher Gbetagamma appar

211 ma alone activated homotetrameric GIRK1* and heterotetrameric GIRK1/3 channels, without affecting the

212 we show the crystal structure of the intact heterotetrameric GluN1-GluN2B NMDA receptor ion channel

213 Heterotetrameric glutamate receptors are essential for t

214 he mature insulin receptor is a cell surface heterotetrameric glycoprotein composed of two alpha- and

215 The enzyme is a heterotetrameric glycoprotein comprised of two alpha-sub

216 The heterotetrameric human pol delta complex was reconstitut

217 In alpha2beta2-heterotetrameric human pyruvate dehydrogenase, this cofa

218 es, Interferon-gamma modulates assembly of a heterotetrameric inhibitor of translation.

219 that encode monomeric forms of the normally heterotetrameric insulin receptor and monomeric platelet

220 nstituted receptor shows the alpha(2)beta(2) heterotetrameric insulin receptor to be a three-armed pi

221 SP8 assembly, and interface II mediating the heterotetrameric interaction between the two NSP7-NSP8 d

222 Disulfide bonds observed at the heterotetrameric interfaces in the unliganded IDH hetero

223 TRP proteins assemble into heterotetrameric ion channels and are known to support S

224 N-methyl-d-aspartate receptors (NMDARs) are heterotetrameric ion channels assembled as diheteromeric

225 etween the heterotetrameric chromogranin and heterotetrameric IP3 receptor but also appears to reflec

226 hosphate (IP3) receptor and the existence of heterotetrameric IP3 receptor in the cell, the heterotet

227 Thus, how the subunit composition of heterotetrameric IP3R channels contributes to shaping th

228 In summary, we demonstrate that heterotetrameric IP3R do not necessarily behave as the s

229 ide the first insight into the regulation of heterotetrameric IP3R of defined composition.

230 B/LDHA expression analysis intimated various heterotetrameric isoforms comprising LDHA and LDHB in tu

231 omains bound to two JAK2 molecules, creating heterotetrameric JAK2-(SH2-B)2-JAK2 or JAK2-(APS)2-JAK2

232 ata were compared with [125I]MgTX binding to heterotetrameric K(V) channels in rat brain synaptic pla

233 py to reveal the coiled-coil architecture of heterotetrameric kinesin-1 in its compact state.

234 selectively modulate Kv2 subunits by forming heterotetrameric Kv2/KvS channels.

235 In contrast, exogenously-expressed heterotetrameric Kv7.4/7.5 channels in A7r5 cells or nat

236 yl-D-aspartate (NMDA) receptors are obligate heterotetrameric ligand-gated ion channels that play cri

237 Although the structure of the heterotetrameric maize endosperm AGPase remains unsolved

238 GPIT is a minimally heterotetrameric membrane protein complex composed of Ga

239 In budding yeast, the heterotetrameric MIND complex (Mtw1, Nnf1, Nsl1, Dsn1),

240 ependent isocitrate dehydrogenase (IDH) is a heterotetrameric mitochondrial enzyme with 2alpha:1beta:

241 The second step is catalyzed by the heterotetrameric MPT synthase protein consisting of two

242 etween individual domains of E1p relative to heterotetrameric multienzyme complex E1 components opera

243 Moreover, in silico modeling of heterotetrameric mutant GIRK channels indicates a struct

244 and antibody labeling, demonstrates that the heterotetrameric Ndc80 complex is an approximately 570-A

245 of pore-forming transmembrane helices in the heterotetrameric neuronal channel GluN1a-2B N-methyl-D-a

246 Membrane-associated Hyd-2 is an unusual heterotetrameric [NiFe]-hydrogenase that lacks a typical

247 t dimer dissociation is critical for forming heterotetrameric NMDA-Rs containing GluN2 subunits, defi

248 ive AdoCbl-dependent PCM with an alpha2beta2 heterotetrameric organization similar to that of isobuty

249 The heterotetrameric phosphodiesterase (PDE) 6 complex, made

250 primer strand through the dual action of the heterotetrameric polymerase alpha-primase (pol-prim) enz

251 patients that alter function of Kv2.1/Kv8.2 heterotetrameric potassium channels.

252 sidue in the large and small subunits of the heterotetrameric potato (Solanum tuberosum) tuber enzyme

253 factor XIII (FXIII) exists in circulation as heterotetrameric proenzyme FXIII-A2B2 Effectively all FX

254 t complex (b([0,+])AT1-rBAT) which reveals a heterotetrameric protein assembly composed of two heavy

255 ed by actin-capping protein at one end and a heterotetrameric protein complex containing the p62 subu

256 Assembly of AP2 adaptor, a heterotetrameric protein complex regulating clathrin-med

257 showed that the X. sagittifolium lectin is a heterotetrameric protein composed of four 12-kDa subunit

258 ne oxidase from Corynebacterium sp. P-1 is a heterotetrameric protein containing three different enzy

259 In this report, we identify the heterotetrameric protein kinase, casein kinase 2 (CK2),

260 The A(2)B(2) heterotetrameric protein reflects ligand-directed elemen

261 hetase (PheRS) is a multidomain (alphabeta)2 heterotetrameric protein responsible for synthesizing Ph

262 ing through the extracellular annexin a2-p11 heterotetrameric protein, can mediate vascular endotheli

263 The atrial KACh channels are heterotetrameric proteins that consist of two pore-formi

264 The structure reveals a new heterotetrameric quaternary organization for the Type II

265 rent TGFbeta isoforms induce assembly of the heterotetrameric receptor complex in the same general ma

266 or (GDNF) is a ligand for RET and acts via a heterotetrameric receptor complex that includes GDNF rec

267 he insulin receptor, the IGF-1 receptor is a heterotetrameric receptor tyrosine kinase, whereas the I

268 ors of excitatory synaptic transmission, are heterotetrameric receptors.

269 R) are structurally and functionally related heterotetrameric receptors.

270 The heterotetrameric recombination complex contains two mole

271 NasS and NasT proteins co-purify as a stable heterotetrameric regulatory complex, NasS-NasT.

272 The heterotetrameric sarcoglycan complex, composed of alpha-

273 synthase (GltB2), large subunit of putative heterotetrameric sarcosine oxidase (SoxA) and glutamine

274 The crystal structure of heterotetrameric sarcosine oxidase (TSOX) from Pseudomon

275 Heterotetrameric sarcosine oxidase (TSOX) is a complex b

276 The reaction of heterotetrameric sarcosine oxidase (TSOX) of Arthrobacto

277 homologous but oxygen-unreactive FAD site in heterotetrameric sarcosine oxidase.

278 owledge, the functional properties of single heterotetrameric species having 2:2 stoichiometry.

279 All PIP2-PIP1 heterotetrameric species localize at the plasma membrane

280 Here we used heterotetrameric species of SecB to understand the sourc

281 s dimerization to initially form an inactive heterotetrameric species, followed by conversion to acti

282 -containing tRNAs requires the action of the heterotetrameric splicing endonuclease, which is compose

283 nken2 (Sh2) encodes the large subunit of the heterotetrameric starch synthetic enzyme adenosine dipho

284 nomic locations suggest that the alpha2beta2 heterotetrameric structural motif has evolved to enable

285 The presence of the heterotetrameric structure in the crystals is significan

286 This accounts for the common heterotetrameric structure of native receptor heterocomp

287 In the bacterial GA crystals, we observe a heterotetrameric structure similar to that found in the

288 two MoaE subunits and two MoaD subunits in a heterotetrameric structure with the two MoaE subunits fo

289 y that different TRPC subunits coassemble as heterotetrameric structures to form smooth muscle SOCs.

290 core proteins form homotetrameric (Red1) or heterotetrameric (SYCP2:SYCP3 and ASY3:ASY4) coiled-coil

291 rogrammed arrangement of the subunits in the heterotetrameric synapse.

292 e mammalian immune response is mediated by a heterotetrameric transcriptional control complex, called

293 cells and identify a regulatory role for the heterotetrameric translocon-associated protein (TRAP) co

294 ked SSR4 gene which encodes a protein of the heterotetrameric translocon-associated protein (TRAP) co

295 smooth muscle results from the formation of heterotetrameric TRPC structures in different smooth mus

296 l and adult homeostatic events through their heterotetrameric type I and type II receptor complexes.

297 Thus, a heterotetrameric type II topoisomerase can be converted

298 Gyrase, a prokaryotic heterotetrameric type IIA topo, introduces negative supe

299 sarcoglycan complex in striated muscle is a heterotetrameric unit integrally associated with sarcosp

300 lution are required for the formation of the heterotetrameric Vestigial-Scalloped complex on DNA.