ライフサイエンスコーパス: accessory protein

1 nd a shared subunit, IL-1RAcP (IL-1 receptor accessory protein).

2 antibodies but is prevented by the HIV-1 Nef accessory protein.

3 ly to form a dimer or by interaction with an accessory protein.

4 e RNase L antagonist, murine coronavirus NS2 accessory protein.

5 , serving here as an example of an endocytic accessory protein.

6 o molecular function had been linked to this accessory protein.

7 nism of MERS-CoV open reading frame (ORF) 8b accessory protein.

8 interactions between the DNA helicase and an accessory protein.

9 ing that NAADP regulation is conferred by an accessory protein.

10 and the middle domain interacts with the UL8 accessory protein.

11 polymerase basic protein 1-frame 2 (PB1-F2) accessory protein.

12 homology containing 4 (Lrch4) as a novel TLR accessory protein.

13 1 (ICU11) as a Polycomb Repressive Complex 2 accessory protein.

14 d within the carboxy-terminal domain of this accessory protein.

15 s of the filament, such as the 11 stripes of accessory proteins.

16 y its cellular function, may be modulated by accessory proteins.

17 usion complex, including multiple SNAREs and accessory proteins.

18 h reduced expression of fimbriae lacking all accessory proteins.

19 sely regulated by the assembly of SNAREs and accessory proteins.

20 ent this mechanism is exploited by endocytic accessory proteins.

21 th the replicative DNA polymerases and other accessory proteins.

22 an ion channel formed by MEC-4, MEC-10, and accessory proteins.

23 of zeste 12 (SUZ12), along with a number of accessory proteins.

24 the participation of several nucleus-encoded accessory proteins.

25 e function of Mfa5, one of the Mfa1 fimbrial accessory proteins.

26 unclear, but its properties are modulated by accessory proteins.

27 modulation are complex and involve multiple accessory proteins.

28 t makes dynamic interactions with additional accessory proteins.

29 whose properties are determined by a host of accessory proteins.

30 CO, and contain carbonic anhydrase and other accessory proteins.

31 pore transitions, and to define the role of accessory proteins.

32 ein that requires preactivation by two other accessory proteins.

33 ctivated and regulated by cargo adaptors and accessory proteins.

34 nal domain, which in turn recruits endocytic accessory proteins.

35 n machinery (gD, gH/gL, and gB) and numerous accessory proteins.

36 ounteraction of these host defenses by viral accessory proteins.

37 hanistically, TMEM106B binds vacuolar-ATPase accessory protein 1 (AP1).

38 Using expression cloning, we identified an accessory protein, 17 kDa membrane-associated protein (M

39 ATPase H(+)-transporting lysosomal accessory protein 2 (Atp6ap2), also known as the (pro)re

40 ghout the hypothalamus.Melanocortin receptor accessory protein 2 (MRAP2) is an adaptor protein that c

41 The Melanocortin Receptor Accessory Protein 2 (MRAP2) is an important regulator of

42 The melanocortin receptor accessory protein 2 (MRAP2) plays a pivotal role in the

43 The melanocortin receptor accessory protein 2 (MRAP2) was previously shown to regu

44 ATP6ap2 (ATPase H(+)-transporting lysosomal accessory protein 2) was identified in both mouse and hu

45 esponse of its avian host, and it identifies accessory protein 3a as multifaceted antagonist of the a

46 ant to IFN treatment and identify a role for accessory protein 3a in the resistance against the type

47 state induced by IFN and identify that viral accessory protein 3a is involved in resistance to IFN, a

48 Furthermore, we provide evidence that accessory proteins 3a and 3b of IBV modulate the respons

49 es induce host shutoff, and we find that its accessory protein 5b is indispensable for this function.

50 Furthermore, we demonstrate that accessory protein 5b of IBV plays a crucial role in the

51 gous missense mutations in ATP6AP1, encoding accessory protein Ac45 of the V-ATPase.

52 Both a isoforms associated with accessory protein Ac45, knockdown of which stalled trans

53 nd for understanding the mechanisms by which accessory proteins affect G protein-coupled receptor fun

54 ression of the IL-1 receptors, IL-1 receptor accessory protein and IL-1 receptor type 1 (IL-1R1), and

55 Recent work demonstrates that accessory proteins and post-translational modifications

56 Translation is controlled by numerous accessory proteins and translation factors.

57 tivation, signal transduction, regulation by accessory proteins, and crosstalk with other GPCRs.

58 ctional nature of these HIV-1 regulatory and accessory proteins, and in particular their transcriptio

59 e structural nitrogenase components and many accessory proteins, and occurs both in situ, for the P-c

60 ut their RNA-targeting function, how Type VI accessory proteins are able to modulate Cas13 activity,

61 provide the first evidence that multiple BMP accessory proteins are altered in fibrosis and may play

62 elp with substrate unfolding, and additional accessory proteins are believed to assist with Clp compl

63 y interferes with IFN signaling and that its accessory proteins are dispensable for this activity.

64 hus, second messengers, including Ca(2+), or accessory proteins are not needed for hTRPA1 responses t

65 ion to the catalytic 20S editosome, multiple accessory proteins are required for this conversion.

66 The functions of the accessory proteins are unknown, but the LarB C terminus

67 160 nm) consists of a network of cytokinesis accessory proteins as well as multiple signaling compone

68 Thus, the C protein, rather than being an "accessory" protein as qualified in textbooks so far, is

69 ncluding where MR1 acquires ligands and what accessory proteins assist ligand binding.

70 rolases, 200 membrane proteins, and numerous accessory proteins associated with the cytosolic surface

71 kinetic transitions are tightly regulated by accessory proteins at the synapse.

72 Here, we describe the Arabidopsis thaliana accessory proteins ATG11 and ATG101, which help link the

73 the retina and require association with the accessory protein basigin, encoded by Bsg, for maturatio

74 An MmpL transporter frequently works with an accessory protein, belonging to the MmpS (mycobacterial

75 PRC2.1 and PRC2.2, are defined by the set of accessory proteins bound to the core PRC2 subunits.

76 f ER shaping proteins and potential receptor accessory proteins, but the role of REEP6 in the retina

77 factor 3 (ATF3), which, in association with accessory proteins (c-Jun dimerization protein 2 [JDP2],

78 activity, most lentiviruses express a viral accessory protein called the virion infectivity factor (

79 ngle amino acid replacements in a regulatory accessory protein can affect protein-protein interaction

80 urring polymorphisms in one gene encoding an accessory protein can significantly alter the global tra

81 e, we show that the actin-binding domains of accessory proteins can be sensitive to filament conforma

82 They also show that accessory proteins can bias signaling downstream of GPCR

83 ur results suggest that different classes of accessory proteins can confer sensitive and robust respo

84 t powers cardiac muscle contraction, and its accessory protein, cardiac myosin binding protein C (cMy

85 Two accessory proteins, coactosin-like protein (CLP) and 5-l

86 Numerous endocytic accessory proteins collaborate with clathrin and AP2 to

87 binding to the IL-36 receptor/IL-1 receptor accessory protein complex and functional activation and

88 HypC is an accessory protein conserved in all [NiFe] hydrogenase sy

89 Each accessory protein contributed to Dmc1's activity, with t

90 cterium Rhodospirillum rubrum requires three accessory proteins, CooC, CooT, and CooJ, dedicated to n

91 eric DNA-binding proteins and the telomerase accessory proteins coordinate the recruitment of telomer

92 reaction rates examined are enhanced by the accessory protein cytochrome b5 (b5), but the exact role

93 ounteracting restriction factors by encoding accessory proteins dedicated to neutralizing the antivir

94 ests that it might substitute for the absent accessory protein DNMT3L to recruit DNMT3A in somatic ce

95 monstrating a similar functional role to the accessory protein DNMT3L, which is only expressed in und

96 The accessory protein domains of the oxidative phosphorylati

97 onto DNA by dedicated initiator, loader, and accessory proteins during the initiation of DNA replicat

98 ilient machinery that includes >70 endocytic accessory proteins (EAP).

99 lated process involves a myriad of endocytic accessory proteins (EAPs), many of which are multidomain

100 processive helicase when complexed with two accessory proteins, eIF4G and eIF4B.

101 ed in vivo with PRC2 core components and the accessory proteins, EMBRYONIC FLOWER 1 (EMF1), LIKE HETE

102 PB1-F2 is a small accessory protein encoded by an alternative open reading

103 Viral protein U (Vpu) is an accessory protein encoded by HIV-1 as well as by some si

104 Vpu is an accessory protein encoded by HIV-1 that interferes with

105 t.IMPORTANCE The Vpr and its paralog Vpx are accessory proteins encoded by different human immunodefi

106 /N interference by Vif.IMPORTANCE Of all the accessory proteins encoded by HIV-1 and other primate le

107 structural proteins as well as more diverse accessory proteins, encoded in the 3' ends of their geno

108 which recombinase specificities for meiotic accessory proteins enhance separation of the recombinase

109 secretion of EsaD is dependent on a further accessory protein, EsaE, that does not interact with the

110 romoting the binding of Ccq1 to a telomerase accessory protein Est1.

111 Using conserved motifs, the accessory proteins exploit the cellular machinery to deg

112 Glycosylated Gag (glycoGag) is an accessory protein expressed by most gammaretroviruses, i

113 n-1 and dynein motors either directly or via accessory proteins for bi-directional movement.

114 el for fibrosis, we examined an array of BMP accessory proteins for changes in mRNA expression.

115 nd mammalian uncoordinated18 (Munc18) fusion accessory proteins for membrane fusion.

116 us Nef and the gammaretrovirus glycoGag, the accessory protein from EIAV is an example of a retrovira

117 alyze all 10 (structural, non-structural and accessory) proteins from SARS-CoV-2 using predictive alg

118 viral factors-in particular, HIV subtype and accessory protein function-in modulating viral reservoir

119 expressing LPL with a soluble variant of its accessory protein glycosylphosphatidylinositol-anchored

120 Research into the roles of the accessory proteins has revealed the existence of previou

121 composed of two lipid bilayers and numerous accessory proteins, has evolved to house the genetic mat

122 e ubiquitous SNARE machinery and a number of accessory proteins have been implicated in regulating se

123 In concert with cochaperones and accessory proteins, heat shock proteins mediate essentia

124 ance of IBV to IFN and the potential role of accessory proteins herein.

125 Viral accessory proteins hijack host cell E3 enzymes to antago

126 ted protein severely disrupts binding of the accessory protein, HMGB1.

127 We found that stable expression of an HTLV-1 accessory protein, HTLV-1 bZIP factor (HBZ), in Jurkat T

128 athrin N-terminal domain (TD) and endocyctic accessory proteins (i.e., clathrin inhibition1).

129 to this, we found that independently of its accessory proteins, IBV inhibits IFN-mediated phosphoryl

130 SPR locus integration complex, including the accessory protein IHF (integration host factor).

131 ukin 1 (IL-1) cytokine family, IL-1 receptor accessory protein (IL-1RAcP) is the co-receptor for eigh

132 a heterodimeric IL-33Ralpha (ST2L)/IL-1alpha accessory protein (IL-1RAcP) receptor that coordinates a

133 s (rs4742170 and rs7037276), 1 IL-1 receptor accessory protein (IL1RAP) SNP (rs10513854), and 1 TRAF6

134 arkers such as interleukin-1 (IL-1) receptor accessory protein (IL1RAP), CD99, T-cell immunoglobulin

135 Interleukin-1 receptor accessory protein (IL1RAP; IL1R3) is a coreceptor of int

136 The interleukin 1 receptor accessory protein (IL1RAP; IL1R3) is expressed on candid

137 that can be observed even in the absence of accessory proteins implicated in the formation of the ac

138 e recently identified as targets of an HIV-1 accessory protein important for viral infectivity.

139 terminus that shares homology with NifX, an accessory protein in M cluster biosynthesis.

140 Viral protein R (Vpr), a highly conserved accessory protein in primate lentiviruses, was previousl

141 The presence of the Psb27 accessory protein in these complexes suggests the involv

142 Although this process involves many accessory proteins in cells, in vitro experiments indica

143 This channel is regulated by a number of accessory proteins including fibroblast growth factor 14

144 RAD51 is regulated by many accessory proteins including the highly conserved Shu co

145 yncytial phenotype in the absence of several accessory proteins, including gE, gI, UL16, and UL21, wh

146 The HIV-1 Vpr accessory protein induces ubiquitin/proteasome-dependent

147 Accessory proteins interact with TCSs to fine-tune their

148 sociated mutations are able to impair Na(V) -accessory protein interactions without altering other pr

149 structural and biophysical details of Na(V) -accessory protein interactions.

150 ptor (ST2) and its coreceptor, IL-1 receptor accessory protein, into a single fusion protein.

151 by multiple interactions between enzymes and accessory proteins involved.

152 ow activity in TKO mESCs, indicating that an accessory protein is absolutely required for its functio

153 canonical function of HIV-1 Vif, this viral accessory protein is also known to trigger G(2)/M cell c

154 Moreover, we determine that HIV-1 Nef accessory protein is dispensable in BAFF upregulation as

155 ed DNA, self-assembly or interaction with an accessory protein is needed to activate its helicase act

156 ed by frataxin (FXN), scaffold protein ISCU, accessory protein ISD11, and acyl-carrier protein ACP.

157 uses, especially in regard to the variety of accessory proteins, it is crucial to characterize the sp

158 gent class XIV myosins (MyoA) coordinated by accessory proteins known as light chains.

159 patient skin fibroblasts, CAV1 and caveolar accessory protein levels are reduced, fewer caveolae are

160 and deletions of the interleukin-1 receptor accessory protein like 1 (IL1RAPL1) gene, located on the

161 al disability protein interleukin-1 receptor accessory protein like 1 (IL1RAPL1) regulates dendrite m

162 s consistently most similar to IL-1R9 (IL-1R accessory protein-like 2), another member of the IL-1R f

163 e possibility that natural variation in this accessory protein may contribute to viral pathogenesis a

164 We hypothesized that multiple BMP accessory proteins may be responsible for maintaining th

165 receptors and that heterogeneity of KARs and accessory proteins may contribute to the formation of pa

166 that endogenous abundance of CEBPB and saRNA accessory proteins may dictate efficacy of CEBPA-saRNA w

167 consequence of its interaction with the DSB accessory protein Mei-P22, and localizes to those DSB si

168 ortin type 2 receptor) messenger RNA and its accessory protein (melanocortin type 2 receptor accessor

169 c factor 1, and melanocortin type 2 receptor accessory protein messenger RNAs and steroidogenic acute

170 that Mfa5 affects the incorporation of other accessory proteins, Mfa3 and Mfa4, into fibers and the e

171 f a multicopper oxidase (MCO), MnxG, and two accessory proteins, MnxE and MnxF.

172 requires complex interactions with a host of accessory proteins, most of which remain largely unknown

173 Melanocortin 2 receptor accessory protein (MRAP) is highly expressed in adrenal

174 ceptor acts in concert with the MC2 receptor accessory protein (MRAP) that is absolutely required for

175 lations predict that melanocortin 2 receptor accessory protein (MRAP), needed for MC2R function, bind

176 Here, we showed that the accessory protein MRAP2 altered GHSR1a signaling by inhi

177 The G-protein-coupled receptor accessory protein MRAP2 is implicated in energy control

178 e complex of MukB, the kleisin, MukF, and an accessory protein, MukE.

179 dditionally, viral factors such as the HIV-1 accessory protein Nef can antagonize this antiviral acti

180 The HIV-1 accessory protein Nef controls multiple aspects of the v

181 Since the viral accessory protein Nef has been shown to downregulate MHC

182 The HIV-1 accessory protein Nef is essential for viral pathogenesi

183 The HIV accessory protein Nef modulates key immune evasion and p

184 The accessory protein Nef of human immunodeficiency virus (H

185 fect of SERINC5 is counteracted by the viral accessory protein Nef.

186 cells due to CD4 downregulation by the HIV-1 accessory proteins Nef and Vpu.

187 rus (RSV) is no exception, as it encodes two accessory proteins (NS1 and NS2) which are well establis

188 Nef is an accessory protein of human immunodeficiency viruses that

189 PB1-F2 is a nonstructural accessory protein of Influenza A virus described to enha

190 Nef is an accessory protein of primate lentiviruses that is essent

191 The Nef accessory protein of simian immunodeficiency virus (SIV)

192 Our data suggest that IGF2BP2 is an accessory protein of the argonaute (AGO2)-miR-33a/b-RISC

193 nstrate that FimL, a Chp chemosensory system accessory protein of unknown function, directly links th

194 iral strategies.IMPORTANCE The conserved Vif accessory proteins of primate lentiviruses HIV-1, simian

195 Most of the identified domains in the accessory proteins of the ribosome are also found in euk

196 nvolving HIV-1 exploitation, through its Nef accessory protein, of the interconnectivity among three

197 es enhanced by interactions with calmodulin, accessory proteins, or CaMKII that modulate channel acti

198 t could interact with other domains of CesA, accessory proteins, or other CesA catalytic domains to c

199 Our results demonstrate that the viral accessory protein Orf6 exerts this anti-IFN activity.

200 tivation of nickel enzymes requires specific accessory proteins organized in multiprotein complexes c

201 one and blood pressure (BP), the role of its accessory protein phospholemman has not been characteriz

202 The Kv1.3 accessory protein, potassium voltage-gated channel subfa

203 here that PqqE activity is dependent on the accessory protein PqqD, which was recently shown to bind

204 y interacting with the essential replication accessory protein proliferating cell nuclear antigen (PC

205 pressed in specific neuronal pathways; these accessory proteins provide a new dimension for drug disc

206 verexpression of one such product, the HERVK accessory protein Rec, in a pluripotent cell line is suf

207 ocapsid condensation, RNA encapsidation, and accessory protein recruitment.

208 cript levels of genes for PSI structural and accessory proteins remained unaffected, whereas the leve

209 The HIV-1 Vpr accessory protein reprograms CRL4(DCAF1) E3 to antagoniz

210 ose that PICK1 is a cargo-specific endocytic accessory protein required for efficient, activity-depen

211 he nickel-binding site and the role of three accessory proteins required for its activation remain en

212 Surprisingly, very different patterns of accessory protein requirements were revealed.

213 in replicated DNA or require recruitment of accessory proteins, resulting in significant delays to f

214 y is the CovR/S two-component system and the accessory protein RocA.

215 ns from budding yeast including Dmc1 and its accessory proteins RPA, Rad51, Rdh54/Tid1, Mei5-Sae3 and

216 identified in IL1RAP (interleukin-1 receptor accessory protein; rs12053868-G; P = 1.38 x 10(-9)) and

217 hese results indicate that the GluA1 subunit accessory protein SAP97 may represent a novel target for

218 ed SecYEG protein-conducting channel and the accessory proteins SecDF-YajC and YidC constitute the ba

219 in assembly complex (LUBAC) but not the HOIP accessory protein SHARPIN.

220 As do most FtsZ-accessory proteins, SlmA interacts with the conserved C-

221 on occurred due to the presence of the AMPAR accessory protein stargazin that enhances the AMPAR resp

222 S348A/S409A mutant weakly interacts with the accessory protein STRAP, needed for coordinated translat

223 otein complex denoted as "Mnx" that includes accessory protein subunits MnxE and MnxF, with an estima

224 hyltransferases (DNMT1 and DNMT3A/B) require accessory proteins such as UHRF1 and DNMT3L.

225 brane organelle proteins, whereas translocon accessory proteins, such as ribophorin I, were present i

226 Recruitment of the AP-4 accessory protein tepsin, to the membrane was also aboli

227 n that requires ATP hydrolysis and a host of accessory proteins termed co-chaperones to facilitate th

228 ular interest, deletion of the transcription accessory protein Tex was shown to be highly attenuating

229 Nef is an HIV-encoded accessory protein that enhances pathogenicity by down-re

230 Vpu is a well-studied HIV-1 accessory protein that enhances virus release by antagon

231 ococcus (GAS), regulator of Cov (RocA) is an accessory protein that functions with the control of vir

232 uman immunodeficiency virus type 1 Vpr is an accessory protein that induces G2/M cell cycle arrest.

233 cine-rich repeats (TRIL) is a brain-enriched accessory protein that is important in TLR3 and TLR4 sig

234 he fact that viruses such as HIV-2 encode an accessory protein that is packaged in the virion and is

235 region that expresses a membrane-associated accessory protein that limits AAV production through com

236 CsgE is a periplasmic accessory protein that plays a crucial role in curli bio

237 l component of HIV-1 and show that ASP is an accessory protein that promotes viral replication.

238 Vif is a lentiviral accessory protein that regulates viral infectivity in pa

239 structural elements that modulate them, and accessory proteins that appear to control RNA polymerase

240 ract the restriction by encoding Vpx or Vpr, accessory proteins that are packaged in virions and whic

241 his threat, some primate lentiviruses encode accessory proteins that bind SAMHD1 and induce its degra

242 cellular processes are described, as well as accessory proteins that control their activity, and curr

243 s APOBEC3, SAMHD1 and tetherin and the viral accessory proteins that counteract them.

244 nt silencing is developmentally regulated by accessory proteins that either increase the concentratio

245 Here, genome-wide screening identified accessory proteins that enable reconstitution of human a

246 mall nuclear ribonucleoproteins (snRNPs) and accessory proteins that excises introns from pre-mRNAs.

247 own and what remains to be learned about the accessory proteins that facilitate CuA site maturation.

248 cludes the viral fusion proteins and various accessory proteins that prevent cells from fusing.

249 Recent reports have identified accessory proteins that provide essential support to TLR

250 icated process that requires many associated accessory proteins that supply the requisite cofactors a

251 s of interaction of AP-4 with its only known accessory protein, the ENTH/VHS-domain-containing protei

252 - Pol IV and Pol V - and a growing number of accessory proteins, the functions of which in the RdDM m

253 volved regulator of Cov (RocA), a regulatory accessory protein to CovRS.

254 Thus, we propose that RocA is an accessory protein to the CovRS system that influences th

255 psis thaliana Epsin-like proteins, which are accessory proteins to APs facilitating vesicle biogenesi

256 like HIV-1 and related retroviruses, evolved accessory proteins to counteract these restriction facto

257 be prevented by removing various individual accessory proteins to further disable the machinery.

258 [FeFe]-hydrogenases is synthesized by three accessory proteins, two of which are radical S-adenosylm

259 plants, its activation requires three urease accessory proteins (UAPs), UreD, UreF, and UreG.

260 Previously, the accessory protein UL21 was found to be important for the

261 The HIV-1 accessory protein Vif (virion infectivity factor) enhanc

262 The viral accessory protein Vif counteracts APOBEC3 activity by bi

263 The multifunctional HIV-1 accessory protein Vif counters the antiviral activities

264 ar kinetics to APOBEC3C, and found the viral accessory protein Vif to be necessary and sufficient for

265 Two other HIV-1 accessory proteins, Vif and Vpr, also contribute to the

266 restricts HIV-1 in the absence of the viral accessory protein viral infectivity factor (Vif) by deam

267 The HIV-1 accessory protein viral protein U (Vpu) enhances release

268 osis in transgenic mice expressing the HIV-1 accessory protein Vpr (Vpr-Tg) in liver and adipose tiss

269 human immunodeficiency virus type 1 (HIV-1) accessory protein Vpr enhances viral replication in both

270 Here we show that HIV-1 accessory protein Vpr induces depletion of class I HDACs

271 Accessory protein Vpr, found in all primate lentiviruses

272 Vpx with the evolutionally related HIV-1/SIV accessory protein Vpr.

273 ith the human immunodeficiency virus, type 1 accessory protein Vpr.

274 The HIV-1 accessory protein Vpu counteracts BST-2 by downregulatin

275 hogenesis and/or spread.IMPORTANCE The HIV-1 accessory protein Vpu enhances viral spread by downregul

276 The HIV-1 accessory protein Vpu enhances virus release by countera

277 The HIV-1 accessory protein Vpu has previously been shown to downr

278 zes the restriction factor tetherin with the accessory protein Vpu, while HIV-2 and the filovirus Ebo

279 Novel substrates of the viral accessory proteins Vpu and Nef were sought by use of del

280 Host factors targeted by the viral accessory proteins Vpu or Nef included the amino acid tr

281 me SIVs encode either of two lineages of the accessory protein Vpx that bind the SAMHD1 N or C termin

282 The viral accessory protein Vpx, expressed by certain simian and h

283 and HIV-2 overcome this restriction via the accessory protein Vpx, which targets SAMHD1 for degradat

284 The lentiviral accessory proteins Vpx and Vpr are known to utilize CRL4

285 cterize the products of the HM synthases and accessory proteins, we chose a synthetic biology approac

286 ted to plasmodesmata, while two forms of the accessory protein were differentiated on the basis of th

287 essory protein (melanocortin type 2 receptor accessory protein) were also measured by real-time quant

288 orting mechanism of the BAG6 complex and its accessory proteins which, together, decide the fate of s

289 eceptor but prohibit recruitment of receptor accessory protein, which precludes functional signaling

290 on membranes requires cytosolic adaptors and accessory proteins, which bridge triskeleons with the li

291 Viral protein R (Vpr) is an HIV-1 accessory protein whose function remains poorly understo

292 Lentiviruses such as HIV-1 and HIV-2 encode accessory proteins whose function is to overcome host re

293 text of a Syn variant, removal of a required accessory protein will block cell fusion, again forcing

294 In contrast, removal of individual accessory proteins will block cell-to-cell spread, forci

295 is a homodimeric membrane-binding endocytic accessory protein with a high dimerization affinity.

296 The wide distribution of the accessory proteins without Lar suggests that it may play

297 AP, there is little understanding of how the accessory protein works.

298 striction is overcome by the action of viral accessory protein x (Vpx) or the related viral protein r

299 ated by its anti-sigma factor, YhdL, and the accessory protein YhdK.

300 rial Sec translocon, SecYEG, associates with accessory proteins YidC and the SecDF-YajC subcomplex to