ライフサイエンスコーパス: receptor complex

1 (MHC class I-like located near the leukocyte receptor complex).

2 interaction of a Tat substrate with the Tat receptor complex.

3 tegral signaling components of the B cell Ag receptor complex.

4 e activated FLAGELLIN-SENSING2 (FLS2) immune receptor complex.

5 al signaling events downstream of the T-cell receptor complex.

6 ion of Tat precursor proteins with the TatBC receptor complex.

7 recruits IL-4Ralpha to form a heterodimeric receptor complex.

8 on molecular-dynamics simulations of a micro-receptor complex.

9 obivalent ligands interact with the putative receptor complex.

10 ction of a viral surface protein with a host receptor complex.

11 the process by reducing the stability of the receptor complex.

12 ts of 7DHC on the formation of an active Wnt receptor complex.

13 subsequent activation of the OsBRI1-OsSERK1 receptor complex.

14 , which can orient and stabilize the peptide-receptor complex.

15 components of the same multimolecular T-cell receptor complex.

16 of the TSHR, its ligand TSH, and the hormone-receptor complex.

17 te the internalization of the Tf-TfR1 ligand-receptor complex.

18 helial cells express constituents of the IL2 receptor complex.

19 f the tyrosine phosphatase SHP-1 to the CD16 receptor complex.

20 Tyk2 deficiency can be rescued via the IL-22 receptor complex.

21 ion of a heterotypic, oligomeric, active Eph receptor complex.

22 ges to appropriately activate or inhibit the receptor complex.

23 /MD-2 and antagonize activation of the human receptor complex.

24 for recognition by the Crm1-Ran(GTP) nuclear receptor complex.

25 uggesting that Miro is also part of a Parkin receptor complex.

26 ferentiation occurs through the NgR1/Lingo-1 receptor complex.

27 effects through activation of the TLR4/MD-2 receptor complex.

28 so detected using flow cytometry, as was its receptor complex.

29 4+ neurons expressing the GFRalpha1-RET GDNF receptor complex.

30 ons, and an integral component of the Sema3F receptor complex.

31 treatments, all of which target the hormone-receptor complex.

32 tner CD19 are core subunits of the B cell co-receptor complex.

33 despite accounting for half of the antibody-receptor complex.

34 phorylation upon Axin recruitment to the Wnt receptor complex.

35 ate oligomerization of TatB within the TatBC receptor complex.

36 2) and LLG3, as co-receptors in the BUPS-ANX receptor complex.

37 and structure of NAM binding pockets in the receptor complex.

38 that mediates IL-37 binding to the TGF-beta receptor complex.

39 rtion of a Tat signal peptide into the TatBC receptor complex.

40 f membrane proteins GPR124 and RECK with Wnt receptor complexes.

41 eded efforts aimed at crystallizing cytokine-receptor complexes.

42 with constant formation and dissociation of receptor complexes.

43 s the alphaIIbbeta3 and alphavbeta3 integrin receptor complexes.

44 ical for the signaling functions of multiple receptor complexes.

45 able and conformationally homogeneous ligand-receptor complexes.

46 BAK1 activation in surface-localized immune receptor complexes.

47 occurs upon cocaine binding to sigma1-D1-H3 receptor complexes.

48 merging treatments that target TH2-promoting receptor complexes.

49 eath receptors through formation heteromeric receptor complexes.

50 rimer) not previously observed for other HAd-receptor complexes.

51 olution structures of the ligand/co-receptor/receptor complexes.

52 reserved responses to ligands of a series of receptor complexes.

53 ), defined in terms of stability of an anion-receptor complex (1 + X(-)) against its disintegration,

54 lexes on chromatin is, similar to activating receptor complexes, a highly dynamic process.

55 mode and that the respective covalent ligand-receptor complexes activate G proteins comparable to the

56 This receptor complex acutely sensitizes nonmalignant breast

57 ighlights the key components of the estrogen receptor complex alongside a novel interaction with GRHL

58 Pattern recognition receptor complexes also have roles in cell death control

59 zation of the MSD in its native, full-length receptor complex and a recombinant, unglycosylated MSD i

60 tionally crucial for the formation of ligand-receptor complex and as they replaced evolutionarily hig

61 ritical link between the pattern-recognition receptor complex and calcium-dependent immunity programs

62 that MYCs acting downstream of the jasmonate receptor complex and calmodulin-binding transcription ac

63 ibitor that interferes with the KCTD/GABA(B) receptor complex and efficiently isolates endogenous KCT

64 Endoglin is part of the TGF-beta receptor complex and has a crucial role in fibrogenesis

65 precise mechanisms by which HCV exploits the receptor complex and host machinery to enter the cell re

66 on, PACRG was recruited to the activated TNF receptor complex and interacted with LUBAC components.

67 on of ATF-2 by separately inhibiting the TNF receptor complex and JNK pathway through a negative feed

68 e-directed mutagenesis analysis of the CD16A receptor complex and now report that the association of

69 component and substrate organization in the receptor complex and on the structure of the pore comple

70 TROY is a component of the Nogo receptor complex and plays the key role in neuronal surv

71 iated stronger signaling through the IL-2/15 receptor complex and provided cell function advantages.

72 s, express a functional interleukin-1 (IL-1) receptor complex and respond with NF-kappaB activation a

73 caffolding function of Jak2 within the IFNGR receptor complex and reveal that Jak1 can mediate a semi

74 These results elucidate the receptor complex and signaling hierarchy of downstream k

75 TSC1 interacts with the TGF-beta receptor complex and Smad2/3 and is required for their a

76 IL-26 increased gene expression of the IL-26 receptor complex and STAT1 plus STAT3.

77 receptor encoded within the human leukocyte receptor complex and syntenic region of mouse chromosome

78 what enables the recruitment of Dvl-2 to the receptor complex and the initiation of the Wnt pathway.

79 oss-of-function mutation of the TGF-beta/BMP receptor complex and the second to increased signaling s

80 the cell regulate formation of the arrestin-receptor complex and thereby G protein-independent signa

81 ucose-dependent manner, through the TLR4/MD2 receptor complex and TLR2.

82 of the TatB and TatC units within the TatBC receptor complex and with TatA entering the interior Tat

83 artition between two discrete populations of receptor complexes and approximately 1.5 MDa supercomple

84 sosomal degradation, and recycling of ligand-receptor complexes and cell adhesion molecules from the

85 gand-gated ion channel and G protein-coupled receptor complexes and discuss strategies for their phar

86 These GTPases promote internalization of Wnt receptor complexes and play a critical role in intestina

87 We describe structures of select adhesion receptor complexes and their assembly into larger interc

88 he glycan effect extended to RAMP-CTR amylin receptor complexes and was also conserved in the related

89 le required for the stability of the TGFbeta receptor complex, and a new mechanism by which the extra

90 TatBC comprise the substrate receptor complex, and active Tat translocases are formed

91 L-12 signals via the IL-12Rbeta1.IL-12Rbeta2 receptor complex, and IL-23 uses also IL-12Rbeta1 but en

92 ED KINASE1 (BIK1) of the pattern-recognition receptor complex, and this triggers an increase in the c

93 identified a functional IL-10R2 homodimeric receptor complex, and uncovered broad receptor cross-tal

94 interaction and functional modulation of the receptor complex are currently unclear.

95 Receptor complexes are composed of core receptor protein

96 (MD-2), the coreceptor within the TLR4/MD-2 receptor complex, as the high-affinity sCD83 binding par

97 of endocrine fibroblast growth factor (FGF) receptor complexes, as they are required for the high-af

98 naling occurs via distinctive mechanisms for receptor complex assembly in mice.

99 This work reveals a specificity in AMPA receptor complex assembly that is dynamic in both space

100 We detail the mechanisms of receptor complex assembly, the interrelated nature of th

101 L-6 signaling adopt different mechanisms for receptor complex assembly.

102 coactivator activities to engage the nuclear receptor complex at different steps of transcription.

103 ensional tracking of epidermal growth factor receptor complexes at a depth of approximately 100 mum i

104 ivation through differential partitioning of receptor complexes at the cell surface.

105 , leading to sustained, functional chemokine/receptor complexes at the surface.

106 ng the putative heteromeric 5-HT(2A)/mGlu(2) receptor complex, based on the 5-HT(2A) antagonist MDL-1

107 This receptor complex binds Hh and enhances signalling activa

108 -acting antidepressants that act at the NMDA receptor complex, but without dissociative and psychotom

109 redoxin 6 (PRDX6) is recruited to the opioid receptor complex by c-Jun N-terminal kinase (JNK) phosph

110 2 of CXCR4 and depletion of the heteromeric receptor complexes by CXCR4 knockdown inhibit alpha1-AR-

111 TRAIL responses involves clustering of death receptor complexes by E-cadherin and the actin cytoskele

112 te the structures of 10 distinct native AMPA receptor complexes by single-particle cryo-electron micr

113 most receptor complexes, they exemplify how receptor complexes can be drugged, and lay the groundwor

114 se that this concept may explain why agonist.receptor complexes can be inactive and that adopting mul

115 r mutagenesis, we show that inactive agonist.receptor complexes can result from agonist binding to th

116 k by which local upregulation of MIF and its receptor complex CD74/CD44 mediate glomerular injury and

117 In colder/ambient temperatures, the receptor complex CLAVATA2/CORYNE (CLV2/CRN) is necessary

118 Tat operates by a cycle in which the receptor complex combines with the pore-forming componen

119 isms, initiated by distinct ligand-activated receptor complexes, complement Smad signaling and thus c

120 this process, a pollen tube surface-located receptor complex composed of ANXUR1/2 (ANX1/2) and Buddh

121 acellular protein mediators and the synaptic receptor complex composed of cellular prion protein (PrP

122 IL-31-induced signaling is mediated by a receptor complex composed of oncostatin M receptor beta

123 (IFN-lambdas) signal through a heterodimeric receptor complex composed of the IFN-lambdaR1 subunit, s

124 amino acid isoleucine and perceived by a co-receptor complex composed of the Jasmonate ZIM-domain (J

125 Interleukin (IL)-6 signals via a receptor complex composed of the signal-transducing beta

126 ctionality, and architecture of internalized receptor complexes composed of a single GPCR, beta-arres

127 aleimide sensitive factor attachment protein receptor) complex, composed of synaptobrevin, syntaxin,

128 An evolutionarily ancient plant hormone receptor complex comprising the alpha/beta-fold hydrolas

129 Rab7, and its effector, PLEKHM1; and a SNAP receptor complex consisting of Syntaxin 13, Snap29, and

130 S development and kidney morphogenesis via a receptor complex consisting of the glycerophosphatidylin

131 luble alpha receptor subunit p40, binds to a receptor complex consisting of the IL-23 receptor (IL-23

132 CNTF binds to high or low affinity receptor complexes consisting of CNTFR.gp130.LIFR or IL-

133 ed through interactions with a multi-subunit receptor complex containing IL2Ralpha, IL2Rbeta, and IL2

134 ated to the shoot where they bind to a shoot receptor complex containing the leucine-rich repeat rece

135 explored whether the stability of the IL-10 receptor complex contributes to the immunomodulatory pot

136 he gradual accumulation of long-lived active receptor complexes contributes to the increased intrinsi

137 cific structural rearrangements in the virus-receptor complex could help to trigger the irreversible

138 ergent signaling output from multifunctional receptor complexes critically depends on distinct signal

139 docytic machinery, composed of the scavenger receptor complex Cubilin/Amnionless and Dab2, that is re

140 g link by showing that a pattern recognition receptor complex directly associates with and activates

141 pha secretion, and inhibited macrophage TLR4 receptor complex expression.

142 blockade of mu opioid receptor or Toll-like receptors complex failed to alter, while blockade of per

143 was unexpectedly found to not depend on such receptor complexes for its activity, which was induced w

144 We built structural models of TARP-AMPA receptor complexes for TARPs gamma2 and gamma8, combinin

145 of PAMP-triggered immunity by limiting BAK1-receptor complex formation in the absence of ligands.

146 ffered in their ligand specificities, ligand-receptor complex formation in tissues, and receptor shed

147 found that Daam2 promotes Wnt signaling and receptor complex formation through PIP5K-PIP2.

148 strom crystal structure of the Vif substrate receptor complex from simian immunodeficiency virus isol

149 y that clears negative regulators of the WNT-receptor complex from the membrane.

150 Our data suggest that the antibody/Fc-receptor complex functionally mimics viral receptor in m

151 ate genes that encode for a ligand (NDP) and receptor complex (FZD4, LRP5 and TSPAN12) in the Norrin

152 are found within four genes that encode the receptor complex (FZD4, LRP5, and TSPAN12) and ligand (N

153 platelets via interactions with the platelet receptor complex glycoprotein Ib (GPIb).

154 R gamma-chain, and the von Willebrand factor receptor complex GPIb-IX-V, which are essential for thro

155 e-based activation motif-containing collagen receptor complex GPVI-FcR gamma-chain, and the von Wille

156 In platelets, glycoprotein (GP)Ib-IX receptor complex has been long suggested to be a shear s

157 GF19 signaling through the FGFR4/beta-klotho receptor complex has been shown to be a key driver of gr

158 r, very few structures of a native chemokine-receptor complex have been solved.

159 receptor genes encoded within the leukocyte receptor complex have both been expanded and diversified

160 In addition, heteromeric receptor complexes have been identified.

161 mation and function of the endogenous ligand-receptor complex IL-37-IL-1R8-IL-18Ralpha.

162 ecruitment to a high-affinity heterotrimeric receptor complex (IL-2Ralpha/IL-2Rbeta/gamma(c)).

163 diately after the recruitment of RIP1 to the receptor complex, impairing IkappaB kinase (IKK) recruit

164 e region of each molecule likely targets the receptor complex in ligand-selective modes.

165 analyses to examine expression of the amylin receptor complex in rat LDTg tissue.

166 ling data indicate a role for the quaternary receptor complex in regulating the balance between TGF-b

167 ction analyses show expression of the amylin receptor complex in the LDTg.

168 er function by catalysing the formation of a receptor complex in the plasma membrane consisting of va

169 he formation of the PLP-alphav integrin-AMPA receptor complex in vivo and whether complex formation i

170 w reports new strategies and tools to obtain receptor complexes in a near-native state, revealing ins

171 resolve the differential composition of AMPA receptor complexes in brain regions and through developm

172 Artemin through specific activation of their receptor complexes in distinct subsets of lumbar motor n

173 ling pathways, the formation of higher order receptor complexes in lipid rafts is an equally importan

174 Here, we studied the role of these receptor complexes in mediating the oncogenic activity o

175 with the RFA4 E3 ligase and forms UBC26-RFA4-receptor complexes in nuclear speckles.

176 of NMDA receptors as MK-801 binding and NMDA receptor complexes in postsynaptic density (PSD) were in

177 recruitment and the stability of arrestin-3 receptor complexes in real time using fluorescence reson

178 However, many AMPA and kainate receptor complexes in vivo are heteromers composed of di

179 vior of CD3zeta, a subunit of the CD3 T cell receptor complex, in resting and activated primary human

180 5a regulates the subcellular localization of receptor complexes, including Ror2 homodimers, Ror2/Fzd7

181 he epithelial cells via the IL-22RA1-IL-10R2 receptor complex inducing changes in the expression of g

182 on by CAP-PEs includes assembly of TLR2/TLR1 receptor complex, induction of downstream signaling via

183 tion of Lck kinase, PLC-gamma1 or the T cell receptor complex inhibits light-evoked Ca(2+) transients

184 This ligand/receptor complex initiates survival pathways and cell pr

185 iphery require the translocation of the GDNF receptor complex into lipid rafts.

186 ation and induces internalization of the NDP receptor complex into the endo-lysosomal compartment.

187 ciated with ATG8 proteins that recruit cargo-receptor complexes into autophagosomes.

188 e introgression signatures include olfactory receptor complexes into both species, hypertension resis

189 as a BMP2/BMP4 co-receptor, recruits the BMP receptor complexes into raft microdomains, and positivel

190 uch as lipid rafts, protein-lipid complexes, receptor complexes, invadopodia, and other cellular stru

191 ase, that is a component of an intracellular receptor complex involved in the detection of the smoke

192 hat mediates inflammation by engagement of a receptor complex involving the components CD74, CD44, CX

193 C G protein-coupled receptor T1R1/T1R3 taste receptor complex is an early amino acid sensor in MIN6 p

194 In CLV signaling, the CLV1 receptor complex is bound by CLV3, a secreted peptide mo

195 However, how these modulators target the receptor complex is currently unknown.

196 ormation for how activins assemble a ternary receptor complex is lacking.

197 ore a measure of the average time the ligand-receptor complex is present and is quantified using the

198 rotein 5-6 (LRP5-6)/tetraspanin 12 (TSPAN12) receptor complex is required for developmental vasculari

199 .myeloid differentiation factor 2 (MD-2) LPS receptor complex is strongly activated by hexa-acylated

200 Cell-cell communication mediated by ligand-receptor complexes is critical to coordinating diverse b

201 ontinues, an innovative approach - targeting receptor complexes - is emerging.

202 CD19, a signaling component of the B cell receptor complex, is one of multiple regulators driving

203 signaling inhibits PP2C activity through ABA-receptor complex, it remains unknown if other mechanisms

204 Second, the formation of the receptor complex leading to cis- and trans-signaling bio

205 n we established that signaling through this receptor complex leads to activation of the transcriptio

206 rmone-dependent formation of the COI1-JAZ co-receptor complex leads to ubiquitination and proteasome-

207 obile signal, which triggers SAR through its receptor complex LecRK-VI.2/BAK1 in Arabidopsis thaliana

208 ttern, allowing interaction with the elastin receptor complex located at the surface of cells.

209 The human leukocyte receptor complex (LRC) encompasses several sets of genes

210 An important question is thus how these receptor complexes maintain signalling specificity.

211 Abnormal regulation of the FGFR1-Klotho receptor complex may cause a resistance to the phosphatu

212 ion of a serine protease-pattern recognition receptor complex, MBL-associated serine protease (MASP)-

213 Although the role of the megalin-cubilin receptor complex (MCRC) in this process is unequivocal,

214 ng, structural and mechanistic insights into receptor complexes mediated by IL-23, and by IL-12 famil

215 inding, the environment of 3-I-Tyr(B26) in a receptor complex must differ from that in the free hormo

216 antibodies for components of the Semaphorin receptor complex Nrp1, Chl1, or L1cam.

217 dentify the target of NS1 as the mRNA export receptor complex, nuclear RNA export factor 1-nuclear tr

218 hizobium LCOs are perceived by a heteromeric receptor complex of distinct Lys motif (LysM)-type trans

219 as proNGF induces apoptosis via binding to a receptor complex of the common neurotrophin receptor (p7

220 Heteromeric receptor complexes of P2X7A and P2X7L are predicted to h

221 l presentation and activation of heteromeric receptor complexes of transmembrane, dual-specificity ki

222 stence and function of such inactive agonist.receptor complexes on a molecular level.

223 horins signal through neuropilin-2/plexin-A1 receptor complexes on post-crossing commissural axons to

224 nes exert their function by binding specific receptor complexes on the surface of immune cells and ac

225 inhibitors can interact with either the Nogo receptor complex or paired immunoglobulin-like receptor

226 N-induced T cell activation, and that direct receptor complex-particle interactions are permitted bot

227 interaction of Tat signal peptides with the receptor complex plays a critical role in the transport

228 ranged Igh allele assembles into a PreB cell receptor complex (PreBCR) to generate signals to initiat

229 wo different receptor subunits in a cytokine-receptor complex, precisely as the receptors are dispose

230 esting that endocytosis of non-canonical Wnt/receptor complexes preferentially takes place at the api

231 ody coupling leads to a fully active ternary receptor complex present in amounts correlating directly

232 1,25(OH)2D3 binds the vitamin D receptor complex present in many immune populations and

233 ting key protein-protein interactions within receptor complexes provides an opportunity to develop mo

234 Targeting multiprotein receptor complexes, rather than receptors directly, is a

235 ponses, the mechanism by which the TLR4-MD-2 receptor complex recognizes these changes is not well un

236 her, we have demonstrated that the TLR4-MD-2 receptor complex recognizes variation in lipid A molecul

237 We discovered that the activated IFN receptor complex recruits TNK1 from the cytoplasm.

238 Endocytosis of ligand-receptor complexes regulates signal transduction during

239 Act1 preferentially bound to IL-17 receptor complex, releasing its suppressive effect on FG

240 Hh to the Patched-Interference Hh (Ptc-Ihog) receptor complex relieves Ptc inhibition on Smoothened (

241 Here, we characterize the ligand-receptor complex responsible for substrate anchoring in

242 rovide a template for modulating the GABA(B) receptor complex, revealing a fundamentally novel approa

243 SMONATE-ZIM DOMAIN [JAZ] proteins) by an SCF receptor complex (SCF(COI1)/JAZ).

244 In platelets, the glycoprotein (GP) Ib-IX receptor complex senses blood shear flow and transmits t

245 drophobic pocket of MD-2, inducing an active receptor complex similar to that induced by lipid A.

246 Our study provides insights into how IL-10 receptor complex stability fine-tunes IL-10 biology and

247 CR-triggering models invoke an alteration in receptor complex structure as the initiating event, but

248 In addition to these ligand-receptor complex structures, we report the discovery of

249 with in vitro stabilities of ternary ligand.receptor complexes, suggesting a threshold mean lifetime

250 link between BCL9/B9L, PYGO2 and nuclear co-receptor complexes suggests that these beta-catenin co-f

251 daptor protein MyD88 into an oligomeric post receptor complex termed the Myddosome.

252 atB and TatC form an oligomeric, multivalent receptor complex that binds Tat substrates, while multip

253 structural organization effect of the anion receptor complex that changes the nature of the combined

254 These results reveal a novel ligand-receptor complex that drives the formation of BCSCs and

255 a multigene family encoded by the leukocyte receptor complex that encodes a variety of receptors tha

256 ltiprotein intracellular pattern recognition receptor complex that facilitates the cleavage and secre

257 aemia inhibitory factor (LIF) signal through receptor complexes that are critically dependent on gp13

258 th other G-protein-coupled receptors to form receptor complexes that can amplify or decrease the sign

259 an be attributed to binding of galectin-8 to receptor complexes that positively (uPAR and MRC2) and n

260 d by combinatorial interactions with dynamic receptor complexes that vary more than initially thought

261 In the TatBC receptor complex the transmembrane helix of each TatB mo

262 RBPJ, as well as the interleukin-15 (IL-15) receptor complex, the latter enhancing IL-15 autocrine s

263 In the VEGF165-bound receptor complex, the NCD promotes ABL kinase activation

264 COI1 is an essential component of the JA co-receptor complex, the null coi1-1 mutant is male sterile

265 y protein-protein interaction of the GABA(B) receptor complex-the interaction with KCTD proteins.

266 hese include differences between the antigen receptor complexes themselves and the spatial separation

267 re still in preclinical development for most receptor complexes, they exemplify how receptor complexe

268 cell wall is integrated at the level of the receptor complex through interaction with RECEPTOR-LIKE

269 es the binding affinity of IL-37 to the ALK1 receptor complex, thus allowing IL-37 to signal through

270 ants needed to bind to a functional cytokine receptor complex to constitutively activate STAT5, JAK3(

271 ld to facilitate assembly of the HJV.BMP.BMP receptor complex to induce hepcidin expression.

272 gs are proposed to form a heteromeric netrin-receptor complex to mediate a chemorepellent response.

273 tributions of proximal regulators of the Wnt receptor complex to these processes remain undefined.

274 iased agonist that selectively engages these receptor complexes to activate Galphaq and thus phosphol

275 Furthermore, p52ShcA sequestered TGF-beta receptor complexes to caveolin-associated membrane compa

276 ormational change that ultimately allows the receptor-complex to be recognized by the COPI system.

277 e also interacts with the immunosurveillance receptor complex, Toll-like receptor 4 (TLR4), on microg

278 ipid rafts) influence the assembly of ligand-receptor complexes, too.

279 Here, we show that the receptor complex transmembrane (TM) domains form an inti

280 Moreover, perception of flg22 by its cognate receptor complex triggers actin remodeling through the a

281 The IL-26 receptor complex was detected in neutrophils and IL-26 d

282 role in transmitting signals to the Integrin receptor complex, we conducted genetic studies in Drosop

283 To identify the functional receptor complex, we evaluated its oligomerization in vi

284 le most studies focus on its role in the TNF-receptor complex, we here identify a novel component in

285 Based on the recent structure of a "micro-receptor" complex, we predict that 3-I-Tyr(B26) engages

286 cytosolic effector proteins recruited to the receptor complex were unambiguously quantified by fluore

287 capable of binding and activating the T cell receptor complex), were either immobilized or able to di

288 at Nephrin transmits signals to the Integrin receptor complex, which mediates podocyte adhesion to th

289 This is particularly relevant to the GABA(B) receptor complex, which plays a prominent role in many b

290 ptor regulatory proteins (TARPs), yielding a receptor complex with altered gating kinetics, pharmacol

291 lose paralogue Brother of Ihog (Boi) forms a receptor complex with Patched to mediate intracellular H

292 terminal WRKY DNA binding domain and forms a receptor complex with RPS4, another NB-LRR protein.

293 JAZ proteins form a co-receptor complex with the F-box protein coronatine insen

294 Structures of the stabilized mGlu5 receptor complexed with 25 and another molecule in the s

295 e overlap with that seen for the neonatal Fc receptor complexed with enterovirus E6 but is larger and

296 esent crystal structures of a mammalian P2X7 receptor complexed with five structurally-unrelated anta

297 ers of TatB and TatC form circular substrate-receptor complexes with a central binding cavity for twi

298 tion assay, CXCR7 was found to engage in MIF receptor complexes with CXCR4 and CD74, both after ectop

299 and on the frictional coupling of the ligand-receptor complexes with the actin cytoskeleton, the memb

300 ologic functional impact of this cross-class receptor complex without interfering with the function o