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

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

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

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

6 ges to appropriately activate or inhibit the receptor complex.

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

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

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

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

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

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

13 4+ neurons expressing the GFRalpha1-RET GDNF receptor complex.

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

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

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

17 ding on Tha4 assembly with the cpTatC-Hcf106 receptor complex.

18 ly through interference with the host immune receptor complex.

19 stitute a component of the ligand-perceiving receptor complex.

20 ls, whereas IL1RL1 encodes part of the IL-33 receptor complex.

21 centration and thus intrinsic to the agonist-receptor complex.

22 omain, and exists as a component of the NMDA receptor complex.

23 KCTD12 does not influence maturation of the receptor complex.

24 he stability of the immunoprecipitable TNFR1 receptor complex.

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

26 e Hh signaling through interactions with the receptor complex.

27 omplete conformational model for the peptide-receptor complex.

28 eceptor polypeptide to complete the cytokine-receptor complex.

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

30 ptor (TIR) domain-containing proteins of the receptor complex.

31 at S239 is involved in the formation of a Wg/receptor complex.

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

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

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

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

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

37 subsequent activation of the OsBRI1-OsSERK1 receptor complex.

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

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

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

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

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

43 helial cells express constituents of the IL2 receptor complex.

44 s the alphaIIbbeta3 and alphavbeta3 integrin receptor complexes.

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

46 ical for the signaling functions of multiple receptor complexes.

47 able and conformationally homogeneous ligand-receptor complexes.

48 BAK1 activation in surface-localized immune receptor complexes.

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

50 merging treatments that target TH2-promoting receptor complexes.

51 eath receptors through formation heteromeric receptor complexes.

52 ation, but increased the mobility of GABA(B) receptor complexes.

53 of more general use for studying heteromeric receptor complexes.

54 , and could induce formation of higher-order receptor complexes.

55 eded efforts aimed at crystallizing cytokine-receptor complexes.

56 processes by tethering signaling proteins to receptor complexes.

57 ed to detect the presence of the transporter-receptor complexes.

58 motion, reflecting preassembled heteromeric receptor complexes.

59 ating the intracellular sorting of signaling receptor complexes.

60 with constant formation and dissociation of receptor complexes.

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

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

63 This receptor complex acutely sensitizes nonmalignant breast

64 f receptor subunits among different cytokine receptor complexes adds to the intricate landscape.

65 BMP-Alk3-BMP receptor, type 2 (BMPR2) ligand-receptor complex, along with synthetic organic chemistry

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

67 chains (CD25, CD122, and CD132) of the IL-2 receptor complex and are dependent on IL-2 for survival

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

69 ustering of binding sites on the multivalent receptor complex and explains the ability of Tat to tran

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

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

72 ithin the MLCK promoter that binds the Notch receptor complex and is required for transcriptional act

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 nases (PI3Ks) dissociates from growth factor receptor complexes and increases its interaction with th

89 aleimide-sensitive factor attachment protein receptor) complex and strongly accelerates the fusion ra

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

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

92 ZNRF3 is associated with the Wnt receptor complex, and inhibits Wnt signalling by promoti

93 us physical properties of the lumenal ligand-receptor complex appear to act as key determinants for s

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

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

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

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

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

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

100 proximal regions of cpTatC were defective in receptor complex assembly.

101 d mutants defective in substrate binding and 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 This receptor complex binds Hh and enhances signalling activa

107 l of the type I IFNs signal through the same receptor complex, both quantitative and qualitative diff

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

109 2 of CXCR4 and depletion of the heteromeric receptor complexes by CXCR4 knockdown inhibit alpha1-AR-

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

111 Adrenomedullin (AM) and its receptor complexes, calcitonin receptor-like receptor (C

112 our study demonstrates that cell-specific BR receptor complexes can be assembled to perform different

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

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

115 the interaction of the cellular receptor/co-receptor complex CD4/CXCR4 with the viral envelope compl

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

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

118 The receptor complex, competent for uptake of yolk proteins,

119 ion led to extensive Met1-Ub accumulation on receptor complex components.

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

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

122 The phototaxis receptor complex composed of sensory rhodopsin II (SRII)

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 ved inhibitory molecules, after binding to a receptor complex comprised of the Nogo-66 receptor (NgR1

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

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

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

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

132 They signal through heterodimeric receptor complexes consisting of members of IL-17R famil

133 embranes, cpTatC and Hcf106 comprise a large receptor complex containing an estimated eight cpTatC-Hc

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

135 -17A and IL-17F both preferentially engage a receptor complex containing one molecule of IL-17RA and

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

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

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

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

140 trate that dUTX binds to the nuclear hormone receptor complex Ecdysone Receptor/Ultraspiracle, and is

141 they inhibit endocytosis of crosslinked IgE receptor complexes, evidently by inhibiting pinching off

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

143 well established that FGF19 acts through the receptor complex FGFR4-beta-Klotho (KLB) to regulate bil

144 C-terminal Src kinase to the membrane and/or receptor complex following TCR activation.

145 t in the CD14-TLR4 (toll-like receptor)/MD-2 receptor complex for Der p2 recognition.

146 re drivers of T-ALL and require the cytokine receptor complex for transformation.

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

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

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

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

151 BMP-induced receptor complex formation promotes interaction of the m

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

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

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

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

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

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

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

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

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

163 A-1)) results in the clustering of the toxin.receptor complex in lipid rafts.

164 re, we identify novel components of the BRL3 receptor complex in planta by immunoprecipitation and ma

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 he molecular composition of IR64a-containing receptor complexes in either DC4 or DP1m neurons is not

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

175 stoichiometry, fraction and lifetime of such receptor complexes in living cells remain topics of inte

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

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

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

179 the complex crosstalk and switching between receptor complexes in response to different extracellula

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

181 or downregulation of transmembrane adhesive receptor complexes, including Ecadherin (Ecad) and bindi

182 The size of receptor complexes increased with receptor density as a

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

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

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

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

187 g of components of the semaphorin3A (Sema3A) receptor complex into distinct endosomal compartments in

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

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

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

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

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

193 , and this signaling likely occurs through a receptor complex involving Npn1 and either plexinA1 or p

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

195 e on the gamma-aminobutyric acid A (GABA(A)) receptor complex is altered in an experimental model of

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

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

198 This C-1-P-receptor complex is capable of facilitating cellular inv

199 w that mRNA for all components of the amylin receptor complex is expressed in the ventral tegmental a

200 on and signaling at the plasma membrane, the receptor complex is often rapidly internalized via endoc

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

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

203 The intracellular fate of internalized virus-receptor complexes is suspected of influencing the effic

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

205 he corresponding static bi- and trimolecular receptor complexes, it is evident that the dynamic prope

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

207 onist, TLR4.MD-2 dimerizes to form an active receptor complex, leading to initiation of intracellular

208 ruiting and activating Src kinase within the receptor complex, leading to phosphorylation of the OPRM

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

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

211 ciency protein 2), which encode the ER cargo receptor complex LMAN1-MCFD2.

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

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

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

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

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

217 x and suggests that the NgR1-p75/TROY-AMIGO3 receptor complex mediates myelin-induced inhibition of a

218 essed at the growth cone, is part of the DCC receptor complex mediating netrin-1-dependent axon guida

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

220 rt the identification of a tripartite ligand-receptor complex of membrane adhesion molecules that is

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

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

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

226 1,25(OH)2D3 binds the vitamin D receptor complex present in many immune populations and

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

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

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

230 Endocytosis of ligand-receptor complexes regulates signal transduction during

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

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

233 th high affinity, yet the nature of the TeNT receptor complex remains unknown.

234 The Toll-like receptor 2 (TLR2)/TLR1 receptor complex responds to amyloid fibrils, a common c

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

236 The ligand/receptor complexes reveal two distinct architectures: a

237 The crystal structure of the ligand-receptor complex revealed a glycosylation on the Asn-26

238 te that Daam2 modulates the formation of Wnt receptor complexes, revealing new insight into the funct

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

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

241 A shoot-acting receptor complex, similar to the Arabidopsis (Arabidopsi

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

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

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

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

246 assembling a galectin-3-Dectin-1-FcgammaRIIB receptor complex that activated beta-catenin.

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

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

249 berg et al. now identify a tripartite ligand-receptor complex that conveys cues from the substrate ne

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

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

252 wever, IFN-lambda signals through a distinct receptor complex that is expressed in a cell type-specif

253 ry protein (IL-1RAcP) form a functional IL-1 receptor complex that is thought to mediate most, if not

254 an essential signaling component of the NMDA receptor complex that links NMDA receptor activation to

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

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

257 h constant formation and dissociation of new receptor complexes that can be targeted, in a ligand-reg

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

259 aleimide-sensitive factor attachment protein receptor) complexes that mediate fusion of secretory gra

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

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

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

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

264 structural insight into the insulin-insulin receptor complex, the role of the C terminus of the B-ch

265 action with p62/SQSTM1 to form the autophagy receptor complex, thus accelerating autophagic flux.

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

267 le of a bacterial molecule recognized by the receptor complex TLR4/MD-2 with its lipid A moiety, wher

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

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

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

271 upled to a novel GTPase cycle in the SRP.SRP receptor complex to provide the driving force and enhanc

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

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

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

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

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

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

278 d the neuraminidase-1 subunit of the elastin receptor complex triggered by EDPs.

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

280 e six receptor chains forming four signaling receptor complexes, two decoy receptors (IL-1R2, IL-18BP

281 Depending on the receptor complex, Tyk2 is coactivated with either Jak1 o

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

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

284 Remarkably, within the receptor complex, we observe spontaneous transitions bet

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

286 nding of Qa-1 peptide to the CD8-TCR (T-cell receptor) complex, we show that disruption of immune sup

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

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

289 f the tyrosine phosphatase TCPTP to the IL-2 receptor complex, which resulted in dephosphorylation of

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

291 tivity are observed after stimulation of the receptor complex with different type I IFNs.

292 an empty binding pocket (D3R(APO)), and the receptor complex with dopamine (D3R(Dopa)).

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

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

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

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

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

298 oaches of medicinal chemists to target these receptor complexes with homo- and heterobivalent ligands

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