ライフサイエンスコーパス: nucleocapsid protein

1 on between the coronavirus M protein and the nucleocapsid protein.

2 thin the 65 C-terminal amino acids of the MV nucleocapsid protein.

3 ZBDs, such as those that occur in the HIV-1 nucleocapsid protein.

4 fect levels of S segment RNAs or the encoded nucleocapsid protein.

5 erminal domain of the SARS coronavirus (CoV) nucleocapsid protein.

6 S1 fragment and T-cell responses against the nucleocapsid protein.

7 enomic RNA tightly encapsidated by the viral nucleocapsid protein.

8 ated RNase H, R sequence homology, and viral nucleocapsid protein.

9 iption, E10G, prevented interaction with the nucleocapsid protein.

10 lso prevented M2-1 from interacting with the nucleocapsid protein.

11 inc knuckle of the Mason-Pfizer monkey virus nucleocapsid protein.

12 ssay and were specific for the measles virus nucleocapsid protein.

13 The M2-1 protein also interacts with the nucleocapsid protein.

14 RNA genome tightly encapsidated by the viral nucleocapsid protein.

15 prior to the gene encoding the measles virus nucleocapsid protein.

16 ites to produce sgmRNA 7, encoding the viral nucleocapsid protein.

17 usion to cells, protease, integrase, and the nucleocapsid protein.

18 gag, either to the matrix protein or to the nucleocapsid protein.

19 the carboxyl-terminal 120 amino acids of the nucleocapsid protein.

20 ells specific for influenza hemagglutinin or nucleocapsid protein.

21 ial cleavage occurs between the viral p2 and nucleocapsid proteins.

22 ackaging ability between the HIV-1 and HIV-2 nucleocapsid proteins.

23 BV or inoculated with a DNA plasmid encoding nucleocapsid proteins.

24 tions with the large and middle envelope and nucleocapsid proteins.

25 th wild-type virus or an SFV vector encoding nucleocapsid proteins.

26 terminal zinc-binding peptide from the HIV-1 nucleocapsid protein (10(-8)M</=K(d)(Co)</=10(-7)M; 10(-

27 benzamides (DISeBAs) as novel HIV retroviral nucleocapsid protein 7 (NCp7) inhibitors.

28 HIV-1 nucleocapsid protein, a domain of Gag, can bind to oligo

29 We also show that the hantavirus nucleocapsid protein accumulates in P bodies, where it s

30 The nucleocapsid protein amino acid sequence variability amo

31 manner, as did human immunodeficiency virus nucleocapsid protein, an established chaperone.

32 oth IgM and IgG antibodies against the viral nucleocapsid protein and (2) a neutralizing antibody res

33 region of the MuLV genome which encodes the nucleocapsid protein and a portion of the viral protease

34 ments, suggesting a relationship between the nucleocapsid protein and activation of the SL1 dimerizat

35 This influence was augmented by viral nucleocapsid protein and additional reverse transcriptas

36 Vimentin bound to PRRSV nucleocapsid protein and anti-vimentin antibodies showed

37 Interestingly, if nucleocapsid protein and APO3G are present in the same r

38 mic RNA completely encapsidated by the viral nucleocapsid protein and associated with the viral polym

39 s of the human immunodeficiency virus type 1 nucleocapsid protein and for the moloney murine leukemia

40 The TSWV nucleocapsid protein and human cytomegalovirus glycoprot

41 vestigation and characterization of the PEDV nucleocapsid protein and its possible link to cell cultu

42 ted in cytoplasmic bodies that contain viral nucleocapsid protein and nucleic acids.

43 fied forms of the deltaAg, and even with HIV nucleocapsid protein and polylysine, was unacceptable; t

44 generation of CTL to limited epitopes on the nucleocapsid protein and that infection also results in

45 Recognition between the nucleocapsid protein and the E2 protein was explored in

46 cle and provide signals for encapsidation by nucleocapsid protein and the promoters for RNA transcrip

47 -strand RNA virus is assembled with a single nucleocapsid protein and the viral genomic RNA.

48 xed with an MHV polymerase gene product, the nucleocapsid protein and the viral RNA.

49 roteins on their surface, but do not contain nucleocapsid protein and viral nucleic acids.

50 e of both truncated and mutant Sindbis virus nucleocapsid proteins and a variety of cross-linking rea

51 The core is composed of a complex of the NC (nucleocapsid) protein and genomic RNA, surrounded by a s

52 e salt concentration, presence or absence of nucleocapsid protein, and nature of the blunt-ended dupl

53 to that seen in mice immunized with the SARS nucleocapsid protein, and poor protection against a nonl

54 ore, which consists of the RNA segments, the nucleocapsid protein, and the RNA-dependent RNA polymera

55 leic acid binding/chaperone functions of the nucleocapsid protein, and thus may in principle help reg

56 er fluorescent proteins along with filovirus nucleocapsid proteins, and may suggest that a general in

57 mobilized antigens for SNV and a recombinant nucleocapsid protein antigen of Seoul hantavirus (SEOV)

58 ing cells specific for the hemagglutinin and nucleocapsid proteins appeared in circulation in multipl

59 studies reported here establish a hantavirus nucleocapsid protein as a new PKR inhibitor.

60 s that a helix structural element in the MuV nucleocapsid protein becomes open when the sequestered R

61 trand, and the interaction is independent of nucleocapsid protein binding.

62 Here we show that the hantavirus nucleocapsid protein binds with high affinity to the 5'

63 sequence polymorphism in an RNA encoding the nucleocapsid protein but not in the additional genomic R

64 psid motifs similar to retrovirus capsid and nucleocapsid proteins, but Ty3 lacks a matrix-like struc

65 derived from either the PIV5 or Nipah virus nucleocapsid protein C-terminal ends are sufficient to d

66 ag proteins consisting of the capsid protein-nucleocapsid protein (CA-NC) domains with short N-termin

67 We also show that the HIV-1 nucleocapsid protein can increase synthesis through the

68 Incubation with nucleocapsid protein causes this form to refold to a the

69 Here, we demonstrate that CCHFV nucleocapsid protein (CCHFV-NP) augments mRNA translatio

70 ell clones recognized the measles virus (MV) nucleocapsid protein, confirming that the antibody respo

71 brary to determine if epitopes within the MV nucleocapsid protein could be identified with SSPE brain

72 ies reported here reveal that the hantavirus nucleocapsid protein counteracts the PKR antiviral respo

73 onal Abs specific for the spike, matrix, and nucleocapsid proteins did not prevent recrudescence, dem

74 ICs through several steps whereas capsid and nucleocapsid proteins dissociated.

75 ers the cleavage specificity of RT; however, nucleocapsid protein does not appear to enhance PPT prim

76 tes in a critical interaction with the viral nucleocapsid protein early in infection.

77 Nucleocapsid protein enhanced the overall efficiency of

78 Nevertheless, the viral nucleocapsid protein, expressed as a GFP:N fusion, co-lo

79 human immunodeficiency virus type 1 (HIV-1) nucleocapsid protein flanked by Gag sequences (r-preNC)

80 virus replicons (VRPs) expressing spike and nucleocapsid proteins from MERS-CoV and other human and

81 yplex of a siRNA against the influenza viral nucleocapsid protein gene and PEI87 resulted in a 94% dr

82 The results showed that moving the nucleocapsid protein gene away from the single transcrip

83 Translocation of the promoter-proximal nucleocapsid protein gene N, whose product is required s

84 the promoter-proximal position preceding the nucleocapsid protein gene.

85 Both the amino and carboxy termini of the nucleocapsid protein had been predicted to form trimers

86 We suggest that hantaviral nucleocapsid protein has an active role in hantaviral re

87 The HIV-1 nucleocapsid protein has been shown to participate in ca

88 diate contact between the virus envelope and nucleocapsid protein (HBcAg).

89 Five nucleocapsid protein homologues, the tegument protein ho

90 re, we found that MOV10 interacts with HIV-1 nucleocapsid protein in an RNA-dependent manner and is p

91 model is warranted to include a role for the nucleocapsid protein in cap acquisition and storage.

92 Although structures are available for the nucleocapsid protein in complex with RNA, and also for p

93 d single-stranded nucleic acids, such as the nucleocapsid protein in HIV and the RecA DNA repair prot

94 Here, we have investigated the role of the nucleocapsid protein in MHV-induced disease.

95 t M2-1 does not require interaction with the nucleocapsid protein in order to function during transcr

96 erization at 37 degrees C in the presence of nucleocapsid protein increased the yield of SL1-mediated

97 M-MuLV nucleocapsid protein increases the rates of RNA and DNA

98 sence of cell nuclear proteins and the viral nucleocapsid protein increases virus amplification effic

99 Further studies revealed that Andes virus nucleocapsid protein inhibited PKR dimerization, a criti

100 s between the packaging domain RNA and viral nucleocapsid protein inside virion particles, and identi

101 of paramyxovirus particles depends on matrix-nucleocapsid protein interactions which enable efficient

102 The multifunctional nucleocapsid protein is complexed with the genomic RNA,

103 approximately 10(5) M(-1), implying that the nucleocapsid protein is important in promoting dimerizat

104 Thus, the amino-terminal part of the nucleocapsid protein is probably insufficient to initiat

105 s(2)HisCys) ZBD of Mouse Mammary Tumor Virus nucleocapsid protein (MMTV NCp10) were resistant to reac

106 nucleotides targeted to the 5' end of the MV nucleocapsid protein mRNA.

107 ts with PD and determined that measles virus nucleocapsid protein (MVNP) was expressed in 70% of thes

108 n absence of S, expression of M and E or the nucleocapsid protein N did not induce a detectable serum

109 monstrated that moving the gene encoding the nucleocapsid protein N to successively more promoter-dis

110 in the presence of transcripts encoding the nucleocapsid protein N.

111 As expected, the four nucleocapsid proteins N, P, L, and M2-1 failed to direct

112 enomic and antigenomic) to interact with the nucleocapsid protein (N protein) and the location of thi

113 Here we show that hantavirus nucleocapsid protein (N protein) interacts with RdRp in

114 rotein or M protein was colocalized with VSV nucleocapsid protein (N protein) outside the budding sit

115 The hantavirus nucleocapsid protein (N protein), which is encoded by th

116 nsists of the RNA genome encapsidated by the nucleocapsid protein (N protein).

117 Recombinant polymerase (L), nucleocapsid protein (N) and a reporter minigenome expre

118 e-sense genomic RNA completely coated by the nucleocapsid protein (N) and associated by a phosphoprot

119 otein complex of the genomic RNA coated by a nucleocapsid protein (N) and associated with polymerase.

120 lex L-P and encapsidation complex (N-P) with nucleocapsid protein (N) and binding to N protein-encaps

121 ne the relationship of helicase to the viral nucleocapsid protein (N) and to sites of viral RNA synth

122 Hantavirus nucleocapsid protein (N) binds to host mRNA caps and req

123 highly conserved hydrophobic domains in the nucleocapsid protein (N) C terminus of Edmonston MV.

124 Hantavirus nucleocapsid protein (N) can replace the cellular cap-bi

125 antaviruses do not have matrix proteins, the nucleocapsid protein (N) has been proposed to play a key

126 VFV infection, we measured the production of nucleocapsid protein (N) in cells transfected with small

127 virus (VSV), is completely enwrapped by the nucleocapsid protein (N) in every stage of virus infecti

128 Hantavirus nucleocapsid protein (N) is encoded by the smallest S se

129 The nucleocapsid protein (N) of vesicular stomatitis virus a

130 e interpret to reflect the lack of the viral nucleocapsid protein (N) on the template.

131 The coronavirus nucleocapsid protein (N) plays an essential structural r

132 anded RNA genome that is encapsidated by the nucleocapsid protein (N) to form a helical ribonucleopro

133 -sense RNA genomes that are sequestered by a nucleocapsid protein (N) to form ribonucleoprotein (RNP)

134 rovirus genome are encapsidated by the viral nucleocapsid protein (N) to form ribonucleoprotein (RNP)

135 anded RNA genome that is encapsidated by the nucleocapsid protein (N) to form the nucleocapsid (NC).

136 Interaction of viral nucleocapsid protein (N) with this conserved sequence fa

137 the human respiratory syncytial virus (hRSV) nucleocapsid protein (N) with viral genomic RNA (gRNA).

138 tal structure of the CCHFV strain Baghdad-12 nucleocapsid protein (N), a potential therapeutic target

139 the large viral polymerase protein (L), the nucleocapsid protein (N), and the assembled nucleocapsid

140 and ORF7 had significant similarities to the nucleocapsid protein (N), glycoprotein (G), and polymera

141 he nonstructural proteins (NSs and NSm), the nucleocapsid protein (N), or the Gn glycoprotein.

142 The coronavirus nucleocapsid protein (N), together with the large, posit

143 ranslation initiation mechanism, operated by nucleocapsid protein (N), which preferentially facilitat

144 through packaging of the genomic RNA by the nucleocapsid protein (N).

145 nted RNA genome of RVFV is encapsidated by a nucleocapsid protein (N).

146 mRNAs by a novel mechanism mediated by viral nucleocapsid protein (N).

147 ses comprises a genomic RNA encased within a nucleocapsid protein (N-RNA), and associated with the RN

148 genome, which resides inside an oligomer of nucleocapsid protein (N-RNA).

149 Viral nucleocapsid proteins (N) function in both genome replic

150 an ambisense coding strategy to express the nucleocapsid protein, N, and the nonstructural protein,

151 the promoter-proximal gene that encodes the nucleocapsid protein, N, moved to the second or fourth p

152 The bunyavirus nucleocapsid protein, N, plays a central role in viral r

153 examined the site of expression of the BCCV nucleocapsid protein (NBCCV) in the absence of BCCV glyc

154 lated by gamma-PAK in the Rous sarcoma virus nucleocapsid protein NC in vivo and in vitro.

155 This interaction is mediated by the Gag nucleocapsid protein NC, and the N-terminal part of NC i

156 HIV-1 nucleocapsid protein (NC) also binds nucleic acids and h

157 human immunodeficiency virus-type 1 (HIV-1) nucleocapsid protein (NC) bound to the SL3 stem-loop rec

158 suppressed by the 71-amino acid form of HIV nucleocapsid protein (NC) but not by the 55-amino acid f

159 vely, the nucleic acid chaperone activity of nucleocapsid protein (NC) can catalyze this destabilizat

160 an T-cell lymphotropic virus type 1 (HTLV-1) nucleocapsid protein (NC) chaperone activity compared to

161 The HIV-1 nucleocapsid protein (NC) contains two CCHC-type zinc kn

162 Here, we show that the HIV-1 nucleocapsid protein (NC) enhances this annealing by app

163 ency virus type 1 minus-strand transfer, the nucleocapsid protein (NC) facilitates annealing of the c

164 HIV-1 (human immunodeficiency virus type 1) nucleocapsid protein (NC) facilitates multiple nucleic a

165 The HIV-1 nucleocapsid protein (NC) facilitates this annealing.

166 The nucleocapsid protein (NC) from the mouse mammary tumor v

167 The HIV-1 nucleocapsid protein (NC) functions as a nucleic acid ch

168 known, previous studies have shown that HIV nucleocapsid protein (NC) greatly accelerates primer/tem

169 In this study we show that virion nucleocapsid protein (NC) has a role in expression of HI

170 the nucleic acid chaperone activity of HIV-1 nucleocapsid protein (NC) in reverse transcription: bloc

171 tion in HIV-1 was used to assess the role of nucleocapsid protein (NC) in strand transfer.

172 s the nucleic acid chaperone activity of the nucleocapsid protein (NC) in the minus-strand transfer s

173 Although nucleocapsid protein (NC) interferes with -sssDNA self-p

174 HIV-1 nucleocapsid protein (NC) is a nucleic acid chaperone pr

175 The human immunodeficiency virus type 1 nucleocapsid protein (NC) is a nucleic acid chaperone th

176 Human immunodeficiency virus type 1 (HIV-1) nucleocapsid protein (NC) is a nucleic acid chaperone th

177 HIV-1 nucleocapsid protein (NC) is a nucleic acid chaperone, w

178 nt retroviral zinc finger motif of the HIV-1 nucleocapsid protein (NC) is an attractive target for dr

179 human immunodeficiency virus type 1 (HIV-1) nucleocapsid protein (NC) is an essential protein for re

180 Nucleocapsid protein (NC) is known to influence primer e

181 Enhancement of strand exchange by nucleocapsid protein (NC) is proposed to occur during re

182 The nucleocapsid protein (NC) of HIV type 1 (HIV-1) is a nuc

183 The nucleocapsid protein (NC) of HIV type 1 is a nucleic aci

184 The nucleocapsid protein (NC) of HIV-1 is 55 amino acids in

185 The nucleocapsid protein (NC) of HIV-1 is a small zinc finge

186 The nucleocapsid protein (NC) of human immunodeficiency viru

187 The nucleocapsid protein (NC) of human immunodeficiency viru

188 The nucleocapsid protein (NC) of retroviruses plays a major

189 The retroviral nucleocapsid protein (NC) originates by cleavage of the

190 human immunodeficiency virus type-1 (HIV-1) nucleocapsid protein (NC) plays an important role in the

191 Human immunodeficiency virus type 1 (HIV-1) nucleocapsid protein (NC) plays several important roles

192 fer step of HIV-1 reverse transcription, the nucleocapsid protein (NC) promotes annealing of the 3' '

193 rized deletion of both Cys-His motifs in RSV nucleocapsid protein (NC) reduced both the efficiency of

194 ng the concentration of dNTPs or addition of nucleocapsid protein (NC) reduced pausing and the genera

195 ons using HIV reverse transcriptase (RT) and nucleocapsid protein (NC) that allowed efficient synthes

196 in vitro, we examined the capability of the nucleocapsid protein (NC) to anneal various tRNA primer

197 The specific binding of HIV-1 nucleocapsid protein (NC) to the different forms assumed

198 ombinant human immunodeficiency virus type 1 nucleocapsid protein (NC) to very short oligonucleotides

199 Ribonuclease H (RNase H) cleavages and nucleocapsid protein (NC) were required for long-distanc

200 Psi is capable of binding to the cognate RSV nucleocapsid protein (NC) with high affinity (dissociati

201 s type 1 (HIV-1) reverse transcriptase (RT), nucleocapsid protein (NC), genomic RNA, and the growing

202 gement steps that are catalyzed by the HIV-1 nucleocapsid protein (NC), including for example, the an

203 rangement steps that are "chaperoned" by the nucleocapsid protein (NC), including minus-strand transf

204 steps that are catalyzed (chaperoned) by the nucleocapsid protein (NC), including the annealing of th

205 DP6-Gag), could bind to matrix protein (MA), nucleocapsid protein (NC), or entire DP6-Gag protein.

206 Interestingly, in the presence of nucleocapsid protein (NC), the 24 downstream bases are d

207 Addition of the HIV-1 nucleocapsid protein (NC), the trans-acting viral factor

208 not only reverse transcriptase but also the nucleocapsid protein (NC), which functions as a nucleic

209 1 reverse transcription is chaperoned by the nucleocapsid protein (NC), which has been shown to facil

210 d rearrangements, which are catalyzed by the nucleocapsid protein (NC).

211 This preference was accentuated by HIV nucleocapsid protein (NC).

212 t to be composed mainly of the viral RNA and nucleocapsid protein (NC).

213 y stable linkage by the viral p7 form of the nucleocapsid protein (NC).

214 ibonucleoprotein (vRNP, composed of vRNA and nucleocapsid protein [NC]) is packaged into a conical ca

215 templates in the presence and absence of HIV nucleocapsid protein (NCp) was investigated.

216 Nucleocapsid protein (NCp), although stimulating strand

217 was enhanced by increasing the ratio of the nucleocapsid protein NCp7 to mini c TAR DNA from 0 to 2.

218 stem-loop structure brought on by the HIV-1 nucleocapsid protein NCp7.

219 uctural rearrangement activated by the HIV-1 nucleocapsid protein (NCp7) and considered to be associa

220 l molecule inhibitors of the interactions of nucleocapsid protein (NCp7) and psi-RNA.

221 uctural rearrangement catalyzed by the HIV-1 nucleocapsid protein (NCp7) and suggested to be associat

222 equires reverse transcriptase (RT) and HIV-1 nucleocapsid protein (NCp7) for proper viral replication

223 HIV-1 nucleocapsid protein (NCp7) is a double zinc-fingered pr

224 The HIV-1 nucleocapsid protein (NCp7) is a small basic protein wit

225 The HIV-1 nucleocapsid protein (NCp7) is a small, highly conserved

226 ty when a zinc ion binds to the highly basic nucleocapsid protein (NCp7) of HIV-1.

227 the nucleic acid chaperone activity of HIV-1 nucleocapsid protein (NCp7).

228 to a more stable extended dimer by the viral nucleocapsid protein (NCp7).

229 The HIV-1 nucleocapsid protein, NCp7, facilitates the use of human

230 e compared with earlier studies of the HIV-1 nucleocapsid protein, NCp7, that contains a single trypt

231 d here an AlloSwitch, binds the mature HIV-1 nucleocapsid protein, NCp7.

232 ven RNA stem-loops bound to the mature HIV-1 nucleocapsid protein, NCp7.

233 lls expressing the NBCCV and La Crosse virus nucleocapsid protein (NLACV) showed different intracellu

234 rotein (GP) alone or in combination with the nucleocapsid protein NP or with the cytokine adjuvant gr

235 duction is inhibited by coexpression of ANDV nucleocapsid protein (NP) and glycoprotein precursor (GP

236 Using the 5' UTR of the influenza virus nucleocapsid protein (NP) mRNA as bait, we identified th

237 The nucleocapsid protein (NP) of mumps virus (MuV), a paramy

238 The nucleocapsid protein (NP) of Sendai virus encapsidates t

239 Hantavirus encodes a nucleocapsid protein (NP) to encapsidate the genome and

240 must require a conformational change in the nucleocapsid protein (NP) to make the RNA accessible by

241 Both regions interact with the nucleocapsid protein (NP), an essential component of the

242 lymerase proteins (PB1, PB2, and PA) and the nucleocapsid protein (NP), is responsible for this stabi

243 viral mRNA synthesis, and requires the viral nucleocapsid protein (NP).

244 ctions of the two RNA-binding domains of the nucleocapsid protein of a model coronavirus, mouse hepat

245 We report that FP25K is a nucleocapsid protein of both the budded virus (BV) and o

246 The nucleocapsid protein of hantaviruses encapsidates viral

247 The mature nucleocapsid protein of HIV-1, NCp7, and the NC domains

248 The binding of NCp7, the nucleocapsid protein of human immunodeficiency virus typ

249 positive clones identified fragments of the nucleocapsid protein of MV, the cause of SSPE.

250 The nucleocapsid protein of simian immunodeficiency virus (S

251 d to investigate the interaction of p10, the nucleocapsid protein of the Moloney murine leukemia viru

252 N protein has a fold similar to that of the nucleocapsid protein of the porcine reproductive and res

253 The binding of p7 nucleocapsid protein of type 1 human immunodeficiency vi

254 array" or "zinc knuckle" motif common to the nucleocapsid proteins of nearly all known retroviruses.

255 The nucleocapsid proteins of Sindbis virus and Ross River vi

256 cursor for the matrix (MA), capsid (CA), and nucleocapsid proteins of the mature virion.

257 d from the nucleotide sequences encoding the nucleocapsid protein--one targeting RSV A and the other

258 lines recognized one of two epitopes on the nucleocapsid protein: one epitope spanning amino acids 1

259 be easily adaptable to binding by the HIV-1 nucleocapsid protein or loop receptors.

260 structure, even in the absence of the HIV-1 nucleocapsid protein or other RNA chaperones.

261 AC141 or VP39, suggesting that either other nucleocapsid proteins or adaptor proteins may be require

262 n of noncovalent complexes between the HIV-1 nucleocapsid protein p7 (NC) and RNA hairpins SL2-SL4 of

263 ackaging signal and their complexes with the nucleocapsid protein p7 (NC) were probed by solvent-acce

264 human immunodeficiency virus type 1 (HIV-1) nucleocapsid protein p7 (NCp7) and Escherichia coli Ada

265 human immunodeficiency virus type 1 (HIV-1) nucleocapsid protein p7 (NCp7) with a variety of electro

266 The nucleocapsid protein polymerizes along the length of the

267 ture particle to form the matrix, capsid and nucleocapsid proteins present in the mature virion.

268 We find that Moloney murine leukemia virus nucleocapsid protein reduces RNase H degradation and sli

269 In the absence of the nucleocapsid protein, relatively weak activity was obser

270 with the nucleophilic sulfur of the HIV-1 p7 nucleocapsid protein's zinc finger assembly to eject the

271 SANS data also demonstrated that the RNA and nucleocapsid protein share a closer interaction in the m

272 tructures of amino-terminal fragments of the nucleocapsid protein showed the formation of intramolecu

273 three proteins bound both the HIV-1 and EIAV nucleocapsid protein specifically in vitro.

274 destly increased (threefold) by inclusion of nucleocapsid protein, suggesting an ancillary role for t

275 ibits relatively poor affinity for the HIV-1 nucleocapsid protein, suggesting that the bulge plays ot

276 ns near the C-terminal ends of paramyxovirus nucleocapsid proteins that are important for matrix prot

277 The nucleocapsid protein, the major RNA-binding domain of Ga

278 e protein S1 fragment, membrane protein, and nucleocapsid protein to induce virus-specific broad immu

279 of the remaining viral glycoproteins or the nucleocapsid protein to the apical membrane.

280 ntribute to N protein trimerization and that nucleocapsid protein trimers are hantavirus particle ass

281 In addition, the nucleocapsid proteins VP39, FP25, and BV/ODV-C42 were al

282 The inclusion of nucleocapsid protein was found to partially relieve both

283 Recombinant nucleocapsid protein was used in conjunction with actino

284 ine antiserum raised against recombinant SNV nucleocapsid protein was utilized to localize viral anti

285 The PIV5 M protein (but not the PIV5 nucleocapsid protein) was found to be targeted for monou

286 ties of SSPE rAbs to these regions of the MV nucleocapsid protein were confirmed by binding to synthe

287 RT and the p7 nucleocapsid protein were released more readily from vif

288 Modifications to envelope and nucleocapsid proteins were detected by changes in their

289 hed in HIV-1, and viral RNA, RT, matrix, and nucleocapsid proteins were retained in HIV-1 but to a mu

290 bs specific for the viral spike, matrix, and nucleocapsid proteins were transferred into infected B-c

291 two RNA 3 consensus sequences, encoding the nucleocapsid protein, were found with 12.5% sequence div

292 a cavity between two globular domains of the nucleocapsid protein where the viral RNA is sequestered.

293 These guanines may be recognized by the nucleocapsid protein, which binds tightly to the G-bulge

294 Nucleocapsid protein, which can improve cDNA-acceptor in

295 sequences to initiate encapsidation with the nucleocapsid protein, which is a prerequisite for replic

296 The presence of HIV-1 nucleocapsid protein, which promotes strand exchange, ha

297 iruses demonstrated that the viral spike and nucleocapsid proteins, which play important roles in MHV

298 istep event requiring the association of the nucleocapsid protein with nucleic acid and the subsequen

299 ranscriptase, protease, virus attachment, or nucleocapsid protein zinc fingers.

300 al agents that selectively target retroviral nucleocapsid protein Zn fingers.