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

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

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

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

6 nate receptor and then recruiting a receptor accessory protein.

7 us and proposes the existence of a fifth IBV accessory protein.

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

9 brane protein that functions as an endocytic accessory protein.

10 ation of Glycine max UreG (GmUreG), a urease accessory protein.

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

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

13 interactions between the DNA helicase and an accessory protein.

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

15 t makes dynamic interactions with additional accessory proteins.

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

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

18 ein that requires preactivation by two other accessory proteins.

19 NA-ligand interactions, without the need for accessory proteins.

20 ytoskeleton are choreographed by hundreds of accessory proteins.

21 vesicle-vesicle fusion assays for SNAREs and accessory proteins.

22 process involving the participation of many accessory proteins.

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

24 plasma membrane are mediated by adaptor and accessory proteins.

25 segmental expressions of Hox genes and their accessory proteins.

26 signal transduction components with several accessory proteins.

27 h reduced expression of fimbriae lacking all accessory proteins.

28 ent this mechanism is exploited by endocytic accessory proteins.

29 th the replicative DNA polymerases and other accessory proteins.

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

31 the participation of several nucleus-encoded accessory proteins.

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

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

34 We identified a heterozygous receptor accessory protein 1 (REEP1) exon 2 deletion in a patient

35 pe the ER into sheets and tubules - receptor accessory protein 1 (REEP1), atlastin-1 (ATL1), and spas

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

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

38 MC4R interacts with melanocortin receptor accessory protein 2 (MRAP2) in vitro, but its functions

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

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

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

42 e of brain-expressed melanocortin 2 receptor accessory protein 2 (MRAP2), we characterized mice with

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

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

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

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

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

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

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

50 Thus, without an organizing template or accessory proteins, a minimal bundle of actin and myosin

51 ety by alpha-mannosidase and that CD1e is an accessory protein absolutely required for the generation

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

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

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

55 6p/p34 as a novel type of conserved clathrin accessory protein and founding members of a new G protei

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

57 o study the roles of various SNARE proteins, accessory proteins and effects of different lipid compos

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

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

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

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

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

63 Clathrin and endocytic accessory proteins are recruited to receptors by specifi

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

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

66 TSG101 with a tetrapeptide PSAP motif of an accessory protein, arrestin domain-containing protein 1

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

68 eased association with AMPAR protein complex accessory proteins at the end of the third postnatal wee

69 ncrease results in assembly of ESCRT III and accessory proteins at the site of repair.

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

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

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

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

74 domains of CagA and an interaction with the accessory protein CagF.

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

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

77 of endocytosis three components-adaptor and accessory proteins, cargo, and lipids-come together at t

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

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

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

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

82 er membrane lipoprotein CsgG and two soluble accessory proteins, CsgE and CsgF.

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

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

85 The LIS1 accessory protein directly binds dynein, although its pr

86 Cre recombination does not require accessory proteins, DNA supercoiling or particular metal

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

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

89 The accessory protein domains of the oxidative phosphorylati

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

91 s led to the hypothesis that other endocytic accessory proteins (EAPs) generate curvature needed to s

92 Numerous endocytic accessory proteins (EAPs) mediate assembly and maturatio

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

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

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

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

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

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

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

100 The accessory proteins FCHo1/2 are not; instead, they are re

101 G-protein signaling modulator-1, Gpsm1), an accessory protein for G-protein signaling, has functiona

102 that require the action of a TPR-containing accessory protein for the periplasmic transport of a pot

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

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

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

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

107 Hydrogenase accessory proteins from bacteria-synthesizing hydrogenas

108 study, we describe a functional role for the accessory protein, G-protein signaling modulator 1 (GPSM

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

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

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

112 Because these two accessory proteins have distinct structures, and because

113 e report that expression of chloride channel accessory protein hCLCA2 is a characteristic of epitheli

114 We show that the ESCRT accessory protein HD-PTP/PTPN23 associates with EGFR and

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

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

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

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

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

120 IL-1 receptor (IL-1R1) and the IL-1 receptor accessory protein (IL-1RAcP) form a functional IL-1 rece

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

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

123 e newly discovered alternative IL-1 receptor accessory protein, IL-1RAcPb.

124 f IL1beta ligand, the receptor IL1RI and the accessory protein IL1RAcP.

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

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

127 ression of 11 genes, including IL-1 receptor accessory protein (IL1RAP), in all leukemic stem and pro

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

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

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

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

132 enic targets are ion channels, receptors and accessory proteins important in both cellular homeostasi

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

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

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

136 The activation mechanism and roles of each accessory protein in urease maturation are the subject o

137 through interactions with multiple endocytic accessory proteins in a phosphorylation-dependent manner

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

139 idual cells; the roles of ubiquitination and accessory proteins in regulating CaV channel expression;

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

141 n of the pit by binding cargo, clathrin, and accessory proteins, including the Eps-homology (EH) doma

142 hrin-coated vesicles, clathrin and endocytic accessory proteins interact with AP-2 in a temporally an

143 by multiple interactions between enzymes and accessory proteins involved.

144 a molecular description of how a lentiviral accessory protein is able to subvert the cell's normal p

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

146 One essential accessory protein is the GTPase HypB, which is required

147 ur recently characterized peptidases and two accessory proteins is essential for maintaining H. pylor

148 e site cysteine in a manner depending on the accessory protein Isd11.

149 zinc-finger motif of DksA, an RNA polymerase accessory protein known to regulate the stringent respon

150 ires an increasing number of nuclear-encoded accessory proteins known as assembly factors.

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

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

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

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

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

156 und that this is probably attributable to an accessory protein, LRRC26, which is expressed in parotid

157 hemical reactions catalyzed by a plethora of accessory proteins, many of them required to synthesize

158 Inclusion of accessory proteins may be essential in the future develo

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

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

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

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

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

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

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

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

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

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

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

170 Melanocortin receptor accessory proteins (MRAPs) modulate signaling of melanoc

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

172 receptor that functions in complex with its accessory protein myeloid differentiation factor-2 (MD-2

173 yme responsible for urea hydrolysis, and its accessory proteins, necessary for nickel incorporation i

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

175 human immunodeficiency virus type 1 (HIV-1) accessory protein Nef directs virus escape from immune s

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

177 human immunodeficiency virus type 1 (HIV-1) accessory protein Nef is heavily targeted by CD8(+) T ly

178 Finally, we found that the KAR accessory protein, Neto1, is expressed at the base of co

179 We hypothesized that the accessory proteins normally recruited by AP2 may be recr

180 viously showed that murine coronavirus (MHV) accessory protein ns2, a 2H phosphoesterase superfamily

181 The MHV accessory protein, ns2, antagonizes the type I interfero

182 Nef is an accessory protein of human immunodeficiency viruses that

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

184 Myosin-binding protein C (MyBP-C) is an accessory protein of striated muscle thick filaments and

185 We demonstrate that morphine binds to an accessory protein of Toll-like receptor 4 (TLR4), myeloi

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

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

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

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

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

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

192 These accessory proteins orchestrate apoprotein activation by

193 In addition, we ablated expression of the accessory protein ORF5 (rMERS*ORF5) and replaced it with

194 evere acute respiratory syndrome coronavirus accessory protein ORF6 antagonizes interferon signaling

195 It is known to interact with several accessory proteins other than those canonically involved

196 Clathrin coat accessory proteins play key roles in transport mediated

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

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

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

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

201 nd soluble N-ethylmaleimide-sensitive factor accessory protein receptor binding sites of Munc18-2.

202 udy, we examined the effects of two types of accessory proteins, receptor transporting protein 1 shor

203 means to allow AP-2-mediated coordination of accessory protein recruitment and clathrin polymerizatio

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

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

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

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

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

209 alytic subunits on a preassembled complex of accessory proteins retained on DNA during translesion DN

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

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

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

213 Thus, the LRRC26 BK channel accessory protein selectively alters the pharmacology of

214 Actin filaments, with the aid of multiple accessory proteins, self-assemble into a variety of netw

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

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

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

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

219 Although the LRRC26 accessory protein strongly inhibited the ability of MTX

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

221 Required for Transport (ESCRT) apparatus and accessory proteins such as Bro1, which recruits the deub

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

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

224 steine desulfurase SufS (EC 2.8.1.7) and its accessory protein SufE work together to mobilize persulf

225 ere, we characterize the in vivo roles of an accessory protein TapA (TasA anchoring/assembly protein;

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 this, we hypothesized that a number of Hsp90 accessory proteins, termed co-chaperones, could also aff

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

230 1b (suppressor of the G2 allele of SKP1), an accessory protein that associates with SCF-complex, in p

231 aques (SIVmac) encode Vpx, a virion-packaged accessory protein that counteracts SAMHD1 by inducing it

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

233 FIV also encodes a multifunctional OrfA accessory protein that has characteristics similar to HI

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

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

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

237 ions suggest a possible role for SAO-1 as an accessory protein that participates with SEL-10 in downr

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

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

240 arily by recruiting co-repressors, which are accessory proteins that antagonize transcription by modi

241 principal ion-permeating core subunit(s) and accessory proteins that are assembled with the channel c

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

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

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

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

246 related mammalian p34 are putative clathrin accessory proteins that interact with clathrin adaptor c

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

248 We identified one such accessory protein, the F-BAR protein FCH domain only-2 (

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

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

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

252 ting cargo proteins, clathrin triskelia, and accessory proteins to the sites of endocytosis.

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

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

255 The accessory protein UNC93B1 is indispensable for activatio

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

257 eplication when the virus is deprived of its accessory protein Vif (virion infectivity factor).

258 The FIV accessory protein Vif abrogates the inhibition of infect

259 ranscription factor CBFbeta to stabilize its accessory protein Vif and promote APOBEC3G degradation.

260 The viral accessory protein Vif counteracts APOBEC3 activity by bi

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

262 The HIV-1 accessory protein Vif hijacks a cellular Cullin-RING ubi

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

264 onstrated that APOL1 depletes cellular viral accessory protein Vif, which counteracts the host restri

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 Spearman's rho), and evolution of the HIV-1 accessory protein viral protein U (Vpu) during IFN-alpha

268 n immunodeficiency viruses (SIVs) encode the accessory protein viral protein X (Vpx) that counteracts

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

270 The HIV-1 accessory protein Vpr enhances infection of primary macr

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

272 The viral accessory protein Vpr is responsible for SAMHD1 degradat

273 Accessory protein Vpr, found in all primate lentiviruses

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

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

276 The HIV-1 accessory protein Vpu binds to both BST-2 and betaTrCP,

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

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

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

280 IRF3 regulation maps specifically to the HIV accessory protein Vpu.

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

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

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

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

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

286 AMHD1 is counteracted by the virion-packaged accessory protein Vpx.

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

288 the possible sites of interaction with other accessory proteins were investigated.

289 e adapter protein complex AP-2, or endocytic accessory proteins were necessary collectively for Epsin

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

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

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

293 we identify and characterize the first AP-4 accessory protein, which we have named tepsin.

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

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

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

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

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

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

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