ライフサイエンスコーパス: coat protein

1 an be composed of either 90 or 120 dimers of coat protein.

2 ter enzymes covalently attached to the pVIII coat protein.

3 movement of RNA-CP, which encodes the virus coat protein.

4 Here, we identify partners in coat protein.

5 that is more conserved than the rest of the coat protein.

6 e conferred by single point mutations in the coat protein.

7 mposed of the well-studied MS2 bacteriophage coat protein.

8 lical arrangements of thousands of identical coat proteins.

9 ay presents polypeptides as fusions to phage coat proteins.

10 lipid and cholesterol monolayer and specific coat proteins.

11 eplicated genomes be completely protected by coat proteins.

12 preferred curvature in the absence of other coat proteins.

13 resistance motifs on the very numerous pVIII coat proteins.

14 of atALKBH9B to interact (or not) with their coat proteins.

15 or fission, processes that are regulated by coat proteins.

16 of perilipin 5 (PLIN5), a lipid droplet (LD) coating protein.

17 revealed prominent roles for subunits of the coat protein 1 (COPI)-vesicle coatomer, which regulates

18 t allows them to bind specific antibodies on coat protein 3 (p3) and multiple biotin groups on coat p

19 protein 3 (p3) and multiple biotin groups on coat protein 8 (p8) to bind to avidin-conjugated enzymes

20 er peptide expression on the p3 or on the p8 coat proteins, a corresponding density of 5 up to more t

21 y expressed, we observed a reduction in BaMV coat protein accumulation to 47% and 27% that of the wil

22 rticles (146 S; 8200 kDa) or pentameric FMDV coat protein aggregates (12 S; 282 kDa) was detected, a

23 nd postfusion states of the HIV-1 gp41 viral coat protein, although very different from one another,

24 hering system based on the MS2 bacteriophage coat protein and a reporter construct containing an MS2-

25 mes (ORF1 and ORF2), which encode a putative coat protein and an RNA-dependent RNA polymerase (RdRp),

26 The coat protein and NIa-Pro encoded by these two viruses, w

27 nome packaging triggers rearrangement of the coat protein and release of scaffolding protein, resulti

28 l-associated box (KRAB)-are fused to the MS2 coat protein and subsequently recruited by gRNA aptamer

29 and by polar virions that contain the minor coat protein and TGB1 attached to one extremity.

30 NA, termed "packaging signals" (PS), contact coat proteins and facilitate efficient capsid assembly.

31 formation by interacting with its cargo and coat proteins and has significant implications in VLDL s

32 uding several extracellular proteins, as egg coat proteins and inner ear tectorins.

33 operative supramolecular process between the coat proteins and the nucleic acids, which is based on r

34 They control the recruitment of coat proteins, and modulate the structure of actin filam

35 in the absence of coat protein, whereas the coat protein appears to control fidelity.

36 We showed how different coat proteins are distributed within the coat structure

37 Their binding sites on the coat proteins are evolutionarily conserved across the Pa

38 zed for Bacillus sp., but Bacillus sp. spore coat proteins are poorly conserved in Clostridium sp.

39 These internalized coat proteins are the most asymmetrically arranged major

40 , single-stranded RNA viruses assemble their coat proteins around their genomes via extensive nucleot

41 Using the membrane-bound form of the fd coat protein as a model membrane protein and its experim

42 'full virus vector strategy' with the viral coat protein as fusion partner for the designed antimicr

43 of D302A are perpetuated in the full-length coat protein as shown by a higher sensitivity to proteas

44 F-pilus, has a T = 3 icosahedral lattice of coat proteins assembled around its 4,217 nucleotides of

45 proteins that are functional analogs of the coat protein assemblies that mediate intracellular vesic

46 e by tethering biotin ligase (BirA*) via MS2 coat protein at the 3' UTR of endogenous MS2-tagged beta

47 e of alpha-helices and replaces one dimer of coat proteins at a twofold axis.

48 na pollen-borne CRPs, the PCP-Bs (for pollen coat protein B-class) that are related to embryo surroun

49 l design for a self-assembling minimal viral coat protein based on simple polypeptide domains.

50 The structure and function of coat proteins based on the HK97 fold are often embellish

51 otein disulfide isomerase (PDI) and the COPI coat protein beta-COP.

52 By recording how many coat proteins bind to each of many individual RNA strand

53 ith the modified BaMV RNA containing the MS2 coat protein binding sequence.

54 The results show that p37, the viral coat protein, blocks RNA silencing.

55 oteomics studies reveal that VLPs lack viral coat proteins but possess a pharmacopoeia of (1) the euk

56 ant virions, peptides were released from the coat protein by chemical cleavage.

57 (ARF-GEFs), resulting in the recruitment of coat proteins by GTP-bound ARFs.

58 ne proteins termed caveolins and cytoplasmic coat proteins called cavins.

59 ntigen binding, the approximately 4000 other coat proteins can be augmented-by either chemical functi

60 ese viruses, when modified by changing their coat protein, can infect axolotl cells only when they ha

61 s of the plasma membrane-associated caveolar coat proteins caveolin3 and cavin1 were both not reduced

62 or expression of specific peptides on phage coat proteins, characterization of engineered phages in

63 ets an endocytic mechanism that involves the coat protein clathrin, because SA interfered with the cl

64 are both largely free of the classical Golgi coat proteins coatomer (COPI) and clathrin.

65 xes originated from vesicle coats similar to coat protein complex (COP) I, COPII, and clathrin.

66 further demonstrate that TRAPPIII binds the coat protein complex (COP) II coat subunit Sec23.

67 y SNX3-retromer is a minimally concentrative coat protein complex adapted to bulk membrane traffickin

68 The ADP ribosylation factor (Arf) and the coat protein complex I (COPI) are involved in vesicle tr

69 Unexpectedly, coat protein complex I (COPI) is required for lipid drop

70 n ERManI and gamma-COP, the gamma subunit of coat protein complex I (COPI) that is responsible for Go

71 ads to defective intracellular transport via coat protein complex I (COPI), we show that COPA variant

72 We found that knockdown of the coat protein complex I (COPI)-Arf79F (also known as Arf1

73 We have shown that coat protein complex I (COPI)-dependent trafficking, an

74 We investigated the relevance to AD of coat protein complex I (COPI)-dependent trafficking, an

75 resident proteins for retrieval to the ER in coat protein complex I-formed transport carriers.

76 Vesicles that are coated by coat protein complex II (COPII) are the primary mediator

77 Furthermore, knockdown of coat protein complex II (COPII) component SEC24D, which

78 coincides with an up-regulation of the inner coat protein complex II (COPII) components SEC23B, SEC24

79 les from the endoplasmic reticulum (ER), the coat protein complex II (COPII) is also responsible for

80 The coat protein complex II (COPII) is essential for the tra

81 The conserved coat protein complex II (COPII) mediates the initial ste

82 ticulum (ER), but we find, using a cell-free coat protein complex II (COPII) vesicle budding reaction

83 hat CUPS lack Golgi enzymes, but contain the coat protein complex II (COPII) vesicle tethering protei

84 During the budding of coat protein complex II (COPII) vesicles from transition

85 ediates the packaging of collagen into large coat protein complex II (COPII) vesicles that move from

86 23 homolog B (S. cerevisiae), a component of coat protein complex II (COPII), which transports protei

87 ramolecular cargo procollagen is loaded into coat protein complex II (COPII)-coated carriers at endop

88 nd vesicles that are formed by the cytosolic coat protein complex II (COPII).

89 y Randy Schekman led to the discovery of the coat protein complex II (COPII).

90 SERT relies exclusively on the coat protein complex II component SEC24C for endoplasmic

91 hesis with upregulation of secretory pathway coat protein complex II components.

92 of HSP90 is required prior to recruitment of coat protein complex II components.

93 s are consistent with the proposed chaperone/coat protein complex II exchange model.

94 o be recognized by distinct sites within the coat protein complex II machinery.

95 of the endoplasmic reticulum/Golgi transport coat protein complex II Sec proteins.

96 ulates the association between CREBH and the coat protein complex II transport vesicle and thus contr

97 isingly, the mutated gene, SEC24A, encodes a coat protein complex II vesicle coat subunit involved in

98 e protein Atg9 (autophagy-related 9), COPII (coat protein complex II) vesicles, and possibly other so

99 The SEC23 protein is a core component of coat protein complex II-coated vesicles, which transport

100 ein is inhibited indicating its transport in coat protein complex II-coated vesicles.

101 iana tabacum) initially involves a canonical coat protein complex II-dependent endoplasmic reticulum-

102 erone calnexin, altered association with the coat-protein complex II component Sec24D, and thereby im

103 Cytoplasmic coat protein complexes perform central roles in sorting

104 Cargo adaptor subunits of vesicle coat protein complexes sort transmembrane proteins to di

105 rafficking between organelles is achieved by coat protein complexes, coat protomers, that bud vesicle

106 inations is mediated by a number of distinct coat protein complexes, including adaptor protein 1 (AP-

107 cific lipid environment that likely promotes coat protein complexI-mediated retrograde transport, thu

108 articular, we show that the increasing viral coat protein concentration that occurs in infected cells

109 nternal scaffolding protein and three in the coat protein constitute the core of the B protein bindin

110 the analyses demonstrated that the asbestos coating proteins contain high levels of beta-sheet struc

111 [packaging signals (PSs)] that bind cognate coat proteins cooperatively.

112 Coat protein (COP) I and COP II complexes are involved i

113 to dock the I-domains with their respective coat protein core partners, and in sequence motifs displ

114 in B. subtilis led us to identify two spore coat proteins, CotB and CotG, as CotH substrates.

115 We show that another coat protein, CotG, with a central serine-repeat region,

116 B. subtilis coat proteins (CotY, CotE, CotV and CotW) expressed in E

117 by using BSMV silencing vectors defective in coat protein coupled with introducing fungal gene sequen

118 sing Pfs25 fused to the Alfalfa mosaic virus coat protein (CP) and produced these non-enveloped hybri

119 oding for the replication protein (Rep), the coat protein (cp) and the movement protein (mp), as well

120 ons is unknown, since 180 copies of the same coat protein (CP) encapsidate each of the BMV genomic RN

121 receptor for pea enation mosaic virus (PEMV) coat protein (CP) in the gut of the pea aphid, Acyrthosi

122 We have examined the roles of RNA-coat protein (CP) interactions in the assembly of satell

123 In this study, we demonstrated that the coat protein (CP) of Wheat streak mosaic virus (WSMV; ge

124 y upstream of the Turnip crinkle virus (TCV) coat protein (CP) open reading frame (ORF) has been foun

125 everal hundred copies of a helically arrayed coat protein (CP) protecting a (+)ssRNA.

126 etion of the first eight residues of the BMV coat protein (CP) resulted in the RNA1-containing partic

127 fected with TriMV expressing WSMV NIa-Pro or coat protein (CP) substantially excluded superinfection

128 Its genome encodes only its coat protein (CP) subunit, relying on the polymerase of

129 Coat protein (CP)- transgenic papaya lines resistant to

130 The results suggest that the same coat protein (CP)-RNA and maturation protein (MP)-RNA in

131 on the 5 end confers affinity for the Qbeta coat protein (CP).

132 fected cells contained very small amounts of coat protein despite an abundance of RNA2.

133 ss the model proteins and bacteriophage MS2 (coat protein), differing widely in structure, methionine

134 This coat protein dimer binds to the gRNA and interacts with

135 Unexpectedly, we found a coat protein dimer sequestered in the interior of the vi

136 d with one maturation protein monomer and 89 coat protein dimers arranged in a T = 3 icosahedral latt

137 rms a genome-delivery apparatus and joins 89 coat protein dimers to form a capsid.

138 Using novel genetically-fused coat protein dimers, we have been able to trap higher-or

139 s with a stronger response against the PopMV coat protein due to enhanced activation sensitivity.

140 The coat protein E-loops of these viruses are involved in bo

141 type vaccines engineered to direct the HIV-1 coat protein Env to dendritic cells.

142 hanisms coupling pH transitions to endosomal coat protein exchange; discovery of distinct pH threshol

143 al capsids are a prototypical example, where coat proteins exhibit not only self-interactions but als

144 Our coat protein features precise control over the cooperati

145 ssembly mutations, which act on the level of coat protein flexibility.

146 of these common features include a conserved coat protein fold, an internal lipid membrane, and a DNA

147 into a lattice, suggesting that it acts as a coat protein for AP-3 in formation of the regulated secr

148 otein such as a plant lectin or a luteovirus coat protein for transcytosis across the gut epithelium,

149 ette of synonymous MS2 RNA motifs and tandem coat proteins for RNA imaging and showed a dramatic impr

150 y to immobilize sodium dodecyl sulfate (SDS)-coated proteins for fully integrated microfluidic Wester

151 Viral coat proteins function in virion assembly and virus biol

152 tected by co-expression of bacteriophage MS2 coat protein fused with EGFP.

153 rs then recruit the corresponding MS2 or PP7 coat proteins fused with different fluorescent proteins

154 His-154 of the coat protein Gag forms an m(7)Gp adduct, and the H154R m

155 PA technique was standardized to amplify the coat protein gene of CTV (CTV-p25) and detect double lab

156 In cultured neurons, we found that the HIV coat protein gp120 increased the transcriptional express

157 ntify the molecular events evoked by the HIV coat protein gp120 that facilitate the intraneuronal acc

158 In bacteriophage P22, only coat protein (gp5) and scaffolding protein (gp8) are nee

159 ved low levels of identity between the spore coat protein H (CotH), and the Fam20C-related secretory

160 The bacteriophage P22 coat protein has the common HK97-like fold but with a ge

161 Coat proteins have a central role in vesicular transport

162 vesicles derived from subcomplexes of COPII coat proteins have a role in the specialized trafficking

163 teins), also known as SCP superfamily (sperm-coating proteins), have been implicated in many physiolo

164 These procapsids are assembled from a coat protein having the HK97 fold in a reaction driven b

165 ancement, as well as directly coding for the coat protein, highlighting the density of encoded functi

166 otein 27 (FSP27, CIDEC in humans) is a lipid-coating protein highly expressed in mature white adipocy

167 Here we determined that spore coat protein homologs (CotH) of Mucorales act as fungal

168 Studies on vesicle formation by the Coat Protein I (COPI) complex have contributed to a basi

169 Here we show that the coat protein I (COPI) complex sorts anterograde cargoes

170 Studying vesicle formation by the Coat Protein I (COPI) complex, we elucidate that NADH ge

171 hich identified at least two subunits of the coat protein I (COPI) complex.

172 e simplest known MTC, which is essential for coat protein I (COPI) mediated transport from the Golgi

173 In contrast, cytosolic coat protein I (COPI) vesicle coat mutations in sey1Delt

174 COPBI is the beta subunit of the coat protein I (COPI), which is involved in Golgi to end

175 c reticulum (ER) and the Golgi apparatus via Coat Protein I (COPI)- and COPII-coated vesicles.

176 ane recruitment of coatomer and formation of coat protein I (COPI)-coated vesicles is crucial to home

177 Coat protein I (COPI)-coated vesicles mediate retrograde

178 iated by clathrin-coated vesicles, while the COat Protein I and II (COPI and COPII) routes stand for

179 ic reticulum to the Golgi is mediated by the coat protein II (COPII) complex comprising a Sec23-Sec24

180 The coat protein II (COPII)-coated vesicular system transpor

181 ere glycoprotein cargo concentrates prior to coat protein II vesicle-mediated transport to the Golgi.

182 /cTAGE5 receptor can bind multiple copies of coat protein in a close-packed array.

183 Perilipin 1, the most abundant lipid-coat protein in adipocytes, plays a key role in regulati

184 structure of the membrane-bound form of Pf1 coat protein in explicit lipid bilayers using the recent

185 niformly doubly ((15) N, (13) C)-labeled Pf1 coat protein in magnetically aligned DMPC/DHPC bicelles.

186 ional changes of uniformly (15)N-labeled Pf1 coat protein in native-like bilayers.

187 ES activity and produces low levels of viral coat protein in vitro and in vivo Our findings may be ap

188 ics that these RNA segments are bound to the coat proteins in a sequence-specific manner.

189 make important intersubunit contacts between coat proteins in adjacent capsomers.

190 posed, which facilitates assembly by binding coat proteins in such a way that they promote the protei

191 highlights the important function of surface coat proteins in the interplay between complement regula

192 Vesicle coat proteins, including coatomer-I subunits, localize t

193 Four of the five LD coat proteins, including perilipins 2, 3, 4, and 5, were

194 oating of the sensor polymers by recombinant coat proteins induces their stretching due to steric hin

195 Luteovirid coat protein-insect neurotoxin fusions represent a promi

196 and identified three conserved motifs of RNA-coat protein interactions among 15 of these stem-loops w

197 In this system, coat protein interacts with an internal scaffolding prot

198 elevating the protein levels with which the coat protein interacts, were used to elucidate pleiotrop

199 TGB1 mediated insertion of the viral coat protein into PD, probably by its interaction with t

200 y as a guiding principle for the assembly of coat proteins into a capsid shell.

201 proteins with similar features to eukaryotic coat proteins involved in vesicle biogenesis.

202 One LD coat protein is caveolin-1 (Cav-1), an essential compone

203 rosine residues precisely fused to the major coat protein is converted into a photo-responsive organi

204 The luteovirid coat protein is sufficient for delivery of fused protein

205 midgut homeostasis by the mammalian parasite coat proteins is a novel function and indicates that VSG

206 ces parallel to the membrane that buckle the coat protein layer, generated by an actomyosin contracti

207 he center; 2), the inherent curvature of the coat-protein layer; and 3), forces parallel to the membr

208 and Ubp7 resulted in elongation of endocytic coat protein lifetimes at the plasma membrane and recrui

209 ained and tunable release, while the surface-coated protein ligands (e.g., transferrin) were demonstr

210 ecruit fusion proteins consisting of the MS2 coat protein linked to transcription activation domains,

211 that the respective roles of scaffolding and coat proteins may have been redistributed during the evo

212 to coexpress a fluorescent MS2 bacteriophage coat protein (MCP) and an RNA of interest tagged with mu

213 rt-lived mRNAs, the tight binding of the MS2 coat protein (MCP) to the MS2 binding sites (MBS) protec

214 This mode of dual signal binding to a single coat protein might serve as a general mechanism to trigg

215 ons that abolish the salt bridge destabilize coat protein monomers and impair capsid self-assembly, b

216 was achieved by the stepwise acquisition of coat protein mutations.

217 esis of genes 5 and 8, we show that changing coat protein N-arm residue 14 from aspartic acid to alan

218 To a lesser extent, coat protein N-arm residue E18 is also implicated in the

219 periplasm requires binding between the minor coat protein named pIII and a bacterial inner-membrane r

220 A lattice of coat protein nucleates at each of the 5-fold vertices, b

221 Here we use the coat protein of a luteovirus, an aphid-vectored plant vi

222 noparticles (PapMV), self-assembled from the coat protein of a plant virus and a noncoding ssRNA mole

223 that the I domain that is inserted into the coat protein of bacteriophage P22 is important in the pr

224 CAV1, the principal coat protein of caveolae, has been associated with the r

225 blocking its binding to Caveolin-1, the main coat protein of caveolae, using a highly specific peptid

226 The coat protein of each phage has an inserted domain (I-dom

227 VP1 is the major coat protein of murine polyomavirus and forms virus-like

228 virtually complete de novo assignment of the coat protein of Pf1 virus.

229 gnate pathogen-derived effector protein, the coat protein of potato virus X.

230 The major coat proteins of dsDNA tailed phages (order Caudovirales

231 r protein (AP) complexes are the predominant coat proteins of membrane vesicles in post-Golgi traffic

232 ted several second-site mutations in the p38 coat protein open reading frame (ORF) that arose in resp

233 m, through fusion of various epitopes to the coat protein or as adjuvant to enhance humoral immune re

234 FLAG-tag antibody binding peptides on their coat protein outer surfaces, making them selective biose

235 ent genetically encoded ligands on the major coat protein, P8.

236 During morphogenesis, varphiX174 coat protein participates in at least four well-defined

237 t of members of the Brassicaceae, the pollen coat proteins (PCPs), are emerging as important signalli

238 The detected PRSV coat protein PCR product was sequenced and the nucleotid

239 ng elements including a newly developed PRSV coat protein PCR.

240 otein interactions between CGI-58 and the LD coating protein perilipin 1 restrain the ability of CGI-

241 CTXphi uses its minor coat protein pIII, located in multiple copies at the pha

242 mors, we found an increased expression of LD coat protein PLIN2 compared with normal colonic epitheli

243 y transiently coexpressing the RNA-2-encoded coat protein precursor (VP60) with the RNA-1-encoded 24,

244 Perilipin 1 is a lipid droplet coat protein predominantly expressed in adipocytes, wher

245 -scaffolding-protein virus assembly systems, coat proteins promiscuously interact to form heterogeneo

246 Disruption of either the RNA coat protein recognition motif or its contact amino acid

247 We show that the sequences of coat protein recognition motifs within multiple, dispers

248 with ARF1-dependent trafficking but not with coat protein recruitment.

249 Coat protein residue D14 is shown by cross-linking to in

250 MSEs) of 1.3 kcal/mol on high-throughput MS2 coat protein-RNA measurements and 1.5 kcal/mol on an ind

251 distinctive helical array of the COPII inner coat protein Sec23/24*Sar1; the helical arrangement is a

252 ecognition of cytosolic signals by the COPII coat protein, Sec24.

253 ermore, we show that PPP motifs in the outer coat protein Sec31 also bind to Sec23, suggesting that s

254 intrinsically disordered region in the outer coat protein, Sec31, drives binding with an inner coat l

255 the external scaffolding protein acts like a coat protein, self-associating into large aberrant spher

256 which asymmetrically expands the surrounding coat protein shell to potentially facilitate RNA release

257 fold is a structural motif used to form the coat protein shells that encapsidate the genomes of many

258 The core coat protein shows a pronounced folding defect.

259 protein with acidic residues in the N-arm of coat protein, since this interaction has been shown to b

260 s thermodynamic stability to the full-length coat protein so that it can fold reasonably efficiently

261 TANCE Similarities in assembly reactions and coat protein structures of the dsDNA tailed phages and h

262 a comparison of particle morphologies, major coat protein structures, and gene content among the five

263 A) wrapped by thousands of copies of a major coat protein subunit (the capsid).

264 es reveal the C-terminal region of the small coat protein subunit, which is essential for virus assem

265 The coat protein subunits are mostly alpha-helical and curve

266 phage P22, hydrophobic interactions peg the coat protein subunits together within a capsomer, where

267 g polymerized actin and curvature-generating coat proteins such as clathrin.

268 in this process, although other adaptors and coat proteins, such as AP-4, ARH, Numb, exomer, and retr

269 previously developed a method that relies on coating protein surfaces with small-molecule dyes to dis

270 Interchanging the coat protein switched host range.

271 ding capacity of B2 somehow played a role in coat protein synthesis.

272 main is a genetic insertion in the phage P22 coat protein that chaperones its folding and stability.

273 an insertion domain of the bacteriophage P22 coat protein that drives rapid folding and accounts for

274 utively associated cytoplasmic lipid droplet coat protein that has been implicated in fatty liver for

275 n the test fragment, encodes a region of the coat protein that undergoes a conformational change upon

276 ily of plant-specific, LD surface-associated coat proteins that are required for proper biogenesis of

277 mbrane determinants for assembly of clathrin coat proteins that drive formation of clathrin-coated ve

278 d herpesviruses assemble their capsids using coat proteins that have the ubiquitous HK97 fold.

279 ved a structural rearrangement in the capsid coat proteins that is required to package the viral gRNA

280 Owing to extensive cross-linking among coat proteins, this structure has been recalcitrant to d

281 manipulated to express the receptor for that coat protein, thus allowing for the possibility of targe

282 d sigma(K) control the adherence of the CotB coat protein to C. difficile spores, indicating that the

283 ANGO1/cTAGE5 promotes the accretion of inner coat proteins to the helical lattice.

284 nes and Myzus persicae-feed on a recombinant coat protein-toxin fusion, either in an experimental mem

285 type lectin-like domain (CTLD) and the sperm-coating protein/Tpx-1/Ag5/PR-1/Sc7 (SCP/TAPS) domain, al

286 tacyclic variant surface glycoprotein (mVSG) coat protein transcripts identified.

287 Mutations in siRNAs derived from a PRSV coat protein transgene in the absence of virus replicati

288 reveal the crystal structures of mollusk egg coat protein, VERL, complexed with cognate sperm protein

289 Adenovirus minor coat protein VI contains a membrane-disrupting peptide t

290 om an integer multiple of 60 viral capsid or coat protein (VP) monomers.

291 this family are those that lack the internal coat protein, VP4.

292 t and pantropic infectivity, mediated by its coat protein, VSV-G.

293 rison, a molecular dynamics simulation of fd coat protein was also performed without any restraints.

294 Studying the MS2 coat protein, we decompose the binding energy contributi

295 hat clathrin heavy chain (CHC-1), a membrane coat protein well known for its role in receptor-mediate

296 rrant spherical structures in the absence of coat protein, whereas the coat protein appears to contro

297 mino-acid accessory domain inserted into its coat protein, which has the canonical HK97 protein fold.

298 1 hydrogenase prior to expression of the P22 coat protein, which subsequently self assembles.

299 ed the interaction of NLS-GFP-MS2 (phage MS2 coat protein) with the modified BaMV RNA containing the

300 r of RNA directly contacts every copy of the coat protein, with one-third of the interactions occurri