ライフサイエンスコーパス: protein A

1 CBU0077 MceA (mitochondrial Coxiellaeffector protein A).

2 substrate is now termed ElpA (ER-localizing protein A).

3 alently modified by Protein-A (Glass/ZnO-NRs/Protein-A).

4 odel protein, the B domain of staphylococcal protein A.

5 g with elongation factor G and BPI-inducible protein A.

6 lpha toxin and the increased accumulation of protein A.

7 exposure to surfactant lipids and surfactant protein A.

8 ntaining multifunctional FHV RNA replication protein A.

9 The isolated protein, a 45-kDa monomer, lacks catalytic activity but

10 purification, we developed a high throughput protein A affinity capture step coupled to inline mass s

11 On an industrial scale, replacing fouled Protein A affinity chromatography resin accounts for a l

12 led to form BsAbs that were purified through protein A affinity chromatography to demonstrate industr

13 ally alter the pH at which a mAb elutes from protein A affinity resin.

14 demonstrate that A. marginale outer membrane protein A (AmOmpA; AM854) contributes to the invasion of

15 ase rapidly hydrolyzes Staphylococcus aureus protein A, an important S. aureus virulence factor invol

16 CARDS TX binds to human surfactant protein A and annexin A2 on airway epithelial cells and

17 rmed within the colloidal suspensions (i.e., Protein A and antibody binding) for tailored and specifi

18 stable VipA-VipB (named for ClpV-interacting protein A and B) heterodimers.

19 A and MoaC (molybdenum cofactor biosynthesis protein A and C, respectively).

20 MHC class I chain-related proteins A and B (MICA and MICB) and UL16-binding protei

21 ic Thermus thermophilus multidrug resistance proteins A and B (TmrAB), which not only shares structur

22 report that the ER-resident VAMP-associated proteins A and B (VAPA and VAPB) interact with the perox

23 ins, the fibrinogen- and fibronectin-binding proteins A and B, were found to bind plasminogen, and on

24 variants of the diverse pneumococcal surface proteins A and C (PspA and PspC) and zinc metalloproteas

25 says that combined monoclonal (outer surface protein A) and polyclonal antibodies were performed on a

26 nd nucleotide excision repair is replication protein A, and we find that its accumulation on UVB-dama

27 od specificity for XPA over RPA (replication protein A), another DNA-binding protein that participate

28 ors selectivity the surface of Glass/ZnO-NRs/Protein-A/Anti-OTA was additionally blocked by BSA.

29 energy for the interaction of Glass/ZnO-NRs/Protein-A/Anti-OTA with OTA were calculated, analyzed an

30 r to form OTA-selective layer (Glass/ZnO-NRs/Protein-A/Anti-OTA).

31 sicle-associated membrane protein-associated proteins A/B) and ACBD5 (acyl Co-A binding protein 5).

32 this general model to study assembly of FtsZ protein, a basic element in the division process of prok

33 by combining interface exchange, asymmetric Protein A binding, and the scFv x Fab format.

34 quantitative detection of Galectin-1 (Gal-1) protein, a biomarker for the onset of multiple oncologic

35 BPI-inducible protein A (BipA) is a member of the family of ribosome-d

36 For both proteins, a broad, gradual transition from the native, f

37 Formed Glass/ZnO-NRs/Protein-A/BSA&Anti-OTA structures were integrated within

38 rameshifting (-1 PRF) to synthesize the NS1' protein, a C terminally extended version of its non-stru

39 mbinant mouse FH and three FHR proteins (FHR proteins A-C).

40 lly when visualizing glial fibrillary acidic protein, a canonical marker for astrocytes.

41 NLR family CARD-containing 3 (NLRC3) protein, a caspase recruitment domain (CARD)-containing

42 TPCN2 encodes the two-pore channel 2 (TPC2) protein, a cation channel.

43 ys identified features on the surface of the protein-a cationic patch and a unique hydrophobic loop-t

44 Curved DNA binding protein A (CbpA) is a co-chaperone and nucleoid associat

45 s (CME) and independently of choline binding protein A (CbpA)/laminin receptor, CbpA/polymeric immuno

46 Catabolite control protein A (CcpA) is a highly conserved, master regulator

47 Chromatin assembled with centromere protein A (CENP-A) is the epigenetic mark of centromere

48 tes are epigenetically defined by centromere protein A (CENP-A), a centromere-specific histone H3 var

49 ovided by the histone H3 variant, centromere protein A (CENP-A), but the molecular mechanisms that un

50 A histone H3 variant, centromere protein A (CENP-A), is essential for epigenetically mark

51 mere-specific H3 histone variant, centromere protein A (CENP-A), shares about 50% amino acid sequence

52 e centromere-specific H3 variant, centromere protein A (CENP-A).

53 lutions make high-resolution studies of this protein a challenging task.

54 MOylation' alters the behavior of the target protein, a change that is utilized to regulate diverse c

55 -based assay by stably expressing 2 reporter proteins (a chimeric coagulation factor and MGP) in HEK2

56 observed a substantially reduced replication protein A- chromatin immunoprecipitation signal at origi

57 t concentration for assessing performance of protein A chromatography resin during purification of mo

58 est increases in concentration of C-reactive protein, a circulating marker of inflammation, have been

59 evealed that the highly surface-expressed M1 protein, a classical GAS virulence factor, was required

60 Biochemical analysis of the encoded proteins, a cobalamin (Cbl)-dependent S-adenosylmethioni

61 n IgG1 monoclonal antibody (mAb) purified by Protein A column elution, cation exchange chromatography

62 Despite the variable nature of this protein, a common major histocompatibility complex class

63 rotein signaling homology domain-interacting protein), a component of the LUBAC (linear ubiquitin cha

64 tes hypoxia responses by demethylating RACK1 protein, a component of hypoxia-inducible factor (HIF) u

65 id surfactants, including phospholipids, and proteins, a composition similar to pulmonary surfactants

66 Suppressor-of-cytokine-2 (SOCS2) protein, a conserved program transcript, is expressed by

67 ounted a CD4(+) T-cell response to the H5 HA protein, a correlation not observed for NP-specific resp

68 ophosphate (cAMP) responsive-element-binding protein, a crucial mediator in long-term memory formatio

69 d between PP1c and PPP1R7, cold-shock domain protein A (CSDA), and phosphodiesterase type-5A (PDE5A)

70 Although well-studied cold-shock protein A (CspA) family members are induced and function

71 outputs included an immunogenic cell-surface protein, a cytokine, a chemokine, and a checkpoint inhib

72 tingly, FACIN is a nonclassical cell surface protein, a cytosolic enzyme acetylornithine transaminase

73 ition test and stained for amyloid precursor protein, a DAI marker.

74 adhesion was mediated by the decorin-binding protein A (DbpA) and DbpB surface molecules of B. garini

75 DNA binding protein A (DbpA) is a member of the human cold shock dom

76 erstand PN activation/detoxification by heme proteins, a definitive assignment of I435 is needed.

77 olves the histone variant CENP-A (centromere protein A), deposited by its chaperone, HJURP (Holliday

78 Although for many of these proteins, a detailed mechanistic understanding for how t

79 of a test protein to a long-lived reference protein, a dihydrofolate reductase (DHFR).

80 to identify potential inhibitors of the PyrD protein, a dihydroorotate dehydrogenase (DHODase) involv

81 Unfolded protein, a disordered structure found before folding of

82 atase domain protein, a putative RNA-binding protein, a DNA methylase, an ATPase-domain protein, and

83 Remarkably, ubiquitinylation of Miro1 protein, a downstream target of the E3 ligase activity o

84 7, which encodes a homolog of disulfide bond protein A (dsbA) of Escherichia coli, is required for l-

85 Results indicated that an arginine based Protein A elution buffer minimized the levels of HCPs id

86 re examined for mAbs purified with different Protein A elution buffers to ensure that the selected bu

87 processing parameters such as harvest time, Protein A elution buffers, and subsequent DSP steps can

88 contaminating parental mAbs by differential protein A elution starting from either a) purified paren

89 quently, surfactant lipids and/or surfactant protein A enhance CD36 transcript and protein levels.

90 et-derived growth factor) and two monovalent proteins (a Fab fragment and the transcription factor TB

91 mportantly, expression of adipose FA binding protein (A-FABP) in macrophages facilitated metabolism o

92 biological function of serine-arginine (SR) proteins, a family of essential regulators of mRNA splic

93 The 14-3-3 proteins, a family of highly conserved scaffolding prote

94 e PF surface, and named it Flagellar-coiling protein A (FcpA).

95 novel interactions with domain 2 of the CTC protein, a feature typical to various Gram-positive bact

96 Yet with a growing number of proteins, a fifth level has been identified: rearrangeme

97 o contain large numbers of often-polymorphic proteins, a finding at odds with many current efforts in

98 e SaeRS-modulated factor fibronectin-binding protein A (FnBPA) also contributed to the fermentative b

99 nchored proteins such as fibronectin-binding protein A (FnBPA) that bind to host ligands (e.g. fibron

100 AB significantly altered the abundance of 76 proteins (a fold change >1.4, or <0.6, p-value <0.05) an

101 xameric coiled-coil bundle and an Fc-binding Protein A fragment, we generated the Hex nanocarrier tha

102 ble light-induced protein dissociation using protein A fragments that bind to the LOV domain only in

103 that reflects IgG binding sites conferred by Protein A/G (pAG) conjugated with the fluorogen malachit

104 he purified protein and their Fc affinity to Protein A/G as a proxy for the FcgammaR receptor.

105 Antibodies were purified with protein A/G columns from nasal polyps (NP), matching pat

106 purification and manufacturing process using protein A/G-based chromatography.

107 ploys neodymium magnetic sticks that capture protein A/G-coated paramagnetic beads bound to antibody-

108 us sequence typing (MLST) and staphylococcal protein A gene (spa) typing results as well as SmaI macr

109 Panton-Valentine leukocidin (PVL) genes, the protein A gene (spa), and arcA and opp3, proxy markers f

110 ty, triglycerides, liver enzymes, C-reactive protein, a genetic score representing insulin resistance

111 Rs were silanized and covalently modified by Protein-A (Glass/ZnO-NRs/Protein-A).

112 orces underlying emergence of beta-propeller proteins, a globular and symmetric fold group with diver

113 jor histocompatibility complex (MHC) class I proteins, a hallmark of early beta-cell inflammation in

114 Protein A has a bimodal P(r) distribution, and the relat

115 stinct enzymatic activities of Sir2 and Top1 proteins, a histone deacetylase and a DNA topoisomerase,

116 Common to both viruses is the M2 protein, a homotetrameric transmembrane proton channel t

117 increased expression of myxovirus resistance protein A in the skin and induction of interferon-stimul

118 and Polycomb Repressive Complex 2-associated protein; a.k.a. C17orf96, esPRC2p48, and E130012A19Rik)

119 rast, CYLD (cylindromatosis tumor-suppressor protein), a K63-specific deubiquitinase enriched in post

120 YAP (yes-associated protein), a key transcriptional co-factor that is negati

121 ting antigenic site II of the RSV fusion (F) protein, a key target in vaccine development.

122 miR-BART16 directly targets CREB-binding protein, a key transcriptional coactivator in IFN signal

123 o leads to increased degradation of the Mfn2 protein, a key ubiquitylation target of Parkin on mitoch

124 module, hipBA, encodes HipA (high persister protein A) kinase, which inhibits glutamyl tRNA syntheta

125 PKCalpha interaction with the PKC-targeting protein A-kinase anchoring protein (AKAP) 79 and interfe

126 ly, of the AMPA-receptor regulatory scaffold protein A-kinase anchoring protein (AKAP) 79/150.

127 coupled receptors coupled by the scaffolding protein A-kinase-anchoring protein (AKAP)79/150.

128 ated T cells, affecting the abundance of Myc protein, a known regulator of ribosome biogenesis.

129 hat EGCG can induce the aggregation of HMGB1 protein, a late mediator of inflammation, which subseque

130 t KRAS have focused on inhibiting the mutant protein; a less explored approach involves targeting KRA

131 t application demonstrates the monitoring of protein A ligand density and foulant concentration for a

132 Our results show that Protein A ligand leached during CIP.

133 umoniae lacking the CBP pneumococcal surface protein A lost its ability to inhibit the IgG anti-cOVA

134 cted to APP (encoding amyloid beta precursor protein), a major player in Alzheimer's disease that is

135 tion protein, and small proline-rich (Sprr2) protein, a major component of cornified envelopes in ker

136 r-interacting amino acid residues in the VP2 protein, a major determinant of viral receptor binding a

137 On the other hand, the ORANGE (OR) protein, a major post-translational regulator of PSY wit

138 the de-repression of thioredoxin-interacting protein, a major redox control molecule, and consequent

139 With <2% of the human genome coding for proteins, a major challenge is to interpret the function

140 yrosine- and serine/threonine-phosphorylated proteins, a marked increase in cellular Tropomyosin-3, p

141 ut remained, after adjustment for C-reactive protein, a marker of low-grade inflammation (mean differ

142 ncreased bronchoalveolar lavage fluid (BALF) protein, a marker of lung permeability, in all genotypes

143 n pumps perturb the membrane surrounding the protein, a mechanism is suggested whereby dipole potenti

144 protective fibrin shields via coagulases and protein A-mediated B cell superantigen activity, are dis

145 chanism wherein membrane binding of a second protein (a membrane interacting chaperone, Hsp27, in thi

146 y reducing postsynaptic KIdney/BRAin (KIBRA) protein, a memory-associated protein.

147 ation between cytoskeletal and actin-binding proteins, a mesenchymal or hybrid EMT phenotype and inva

148 80%, and modified with the antibodies by the Protein A method.

149 tors-the heteromeric macrophage growth locus protein A (MglA)-stringent starvation protein A (SspA) c

150 Here we studied three ORF1 proteins: a modern human one (111p), its resuscitated pr

151 The IFN-induced human myxovirus resistance protein A (MxA) exhibits a broad antiviral activity agai

152 We investigated myxovirus resistance protein A (MxA), viperin, and tripartite-motif 21 (TRIM2

153 global conformational polymorphism of capsid proteins, a network formed by extended N arms, mortise-a

154 utualistic relationship of nucleic acids and proteins, a network known as life's central dogma, is no

155 na) MITOCHONDRIAL TRANSLATION FACTOR1 (MTL1) protein, a new member of the Pentatricopeptide Repeat fa

156 Based on the concept of pseudo proteins, a new predictor, called "dRHP-PseRA", was deve

157 loop-helix (bHLH), Per-Arnt-Sim (PAS) domain protein, a novel type of hormone receptor.

158 median fold changes were SAA (serum amyloid protein A), NPS-PLA2 (secreted phospholipase A2), and CA

159 In these proteins, a nuclear localization signal (NLS) and an int

160 n of XPA with DNA is a core function of this protein; a number of mutations in the DNA-binding domain

161 nding protein (MBP), N-utilisation substance protein A (NusA), human protein disulphide isomerase (PD

162 of the membrane domain of the Outer membrane protein A of Klebsiella pneumoniae (KpOmpA).

163 investigated how Sf6 utilizes outer membrane protein A (OmpA) for infection.

164 testing, sexual history, and outer membrane protein A (OmpA) genotyping of C. trachomatis strains.

165 Outer membrane protein A (OmpA) is a porin involved in Acinetobacter ba

166 l antibodies (MAbs) targeting outer membrane protein A (OmpA) of A. baumannii Five anti-OmpA MAbs wer

167 ous studies demonstrated that outer membrane protein A (OmpA) of E. coli K1 interacts with endothelia

168 An anti-outer membrane protein A (OmpA) polyclonal antibody previously produced

169 transport protein (DppA), and outer membrane protein A (OmpA) were identified as proteolytic substrat

170 Outer surface protein A (OspA) coats the spirochetes from the time the

171 trations of antibodies against outer surface protein A (OspA) were shown to correlate with protection

172 These two proteins, a P-type PPR and a member of a small PPR-DYW s

173 talloproteinase, pregnancy-associated plasma protein-A (PAPP-A), which modulates insulin-like growth

174 talloproteinase, pregnancy-associated plasma protein-A (PAPP-A).

175 phoblast-derived pregnancy-associated plasma protein A (PAPPA) is specifically elevated in pregnant w

176 An interfacial load-bearing protein (A. pectinata foot protein-1, apfp-1) with L-3,4

177 It involves two proteins: a periplasmic one, MsrP, previously named YedY

178 rticular mRNAs to produce plasticity-related protein; a phenomenon exhibited during mGluR-mediated LT

179 Ltn1 results in the aggregation of aberrant proteins, a phenomenon that requires CAT-tail addition t

180 ass III photolyase termed photolyase-related protein A (PhrA) of Agrobacterium tumefaciens at 1.67-A

181 ning, and discovery of (novel) PKA anchoring proteins, a plethora of methodologies is available, incl

182 of CARM1 with post-synaptic density (PSD)-95 protein, a post-synaptic marker.

183 e-binding protein at the Jkappa site (RBP-J) protein, a potent OC inhibitor.

184 an to any of the other isoforms, making this protein a potential candidate for diagnosis and immunoth

185 I-QTOF analysis was employed to identify the proteins, a prerequisite to translate the mass of quanti

186 this ubiquitous family of membrane-spanning proteins a prime target for toxins found in animal venom

187 h functions to clear endogenous mannosylated proteins, a principle used to endow insulin analogs with

188 viruses often inhibit the production of host proteins, a process that is referred to as host shutoff.

189 oteasome system for selective degradation of proteins, a process vital to organismal fitness.

190 immune response to coimmunized heterologous proteins, a property not observed with several other int

191 nstrated using the Hepatitis B virus X (HBx) protein, a protein of unknown function, as a test case.

192 The vaccinia virus (VACV) M1 ankyrin (ANK) protein, a protein with no previously ascribed function,

193 (LOD) and the sensitivity range of anti-OTA/Protein-A/PSi immunosensors were estimated.

194 d by anti-OTA and BSA in this way a anti-OTA/Protein-A/PSi structure sensitive towards OTA was design

195 Interaction of OTA with anti-OTA/Protein-A/PSi surface resulted in the quenching of photo

196 free energy for the interaction of anti-OTA/Protein-A/PSi with OTA were calculated and analyzed usin

197 Response time of the anti-OTA/Protein-A/PSi-based immunosensor toward OTA was in the r

198 The anti-OTA/Protein-A/PSi-based immunosensors were tested in a wide

199 for rapid detection of pneumococcal surface protein A (PspA) peptide and SP lysate from synthetic an

200 In that regard, pneumococcal surface protein A (PspA), a major surface protein of pneumococci

201 oteins (PhtD and PhtE), pneumococcal surface protein A (PspA), plasminogen and fibronectin binding pr

202 orkflow includes an automated, 96-well plate protein A purification step to isolate antibody product

203 s present in monoclonal antibodies following Protein A purification.1 To improve the HCP detection li

204 applied to determine HCP repertoires in the Protein A purified monoclonal antibody (mAb) samples as

205 ike protease, an alkaline phosphatase domain protein, a putative RNA-binding protein, a DNA methylase

206 th the small GTPases Ras-related GTP-binding protein A (RagA) and RagC.

207 ar response is initiated through a signaling protein (a receptor), which interacts with the "signal",

208 dular design consisting of the fusion of two proteins: a recognition protein that binds a triggering

209 For these proteins a regulatory function in bridging the electron

210 ive construction means that, unlike globular proteins, a repeat protein's equilibrium folding and thu

211 ation (Tat) pathway, which transports folded proteins, a requirement for cofactor assembly before tra

212 Protein A resin captures monoclonal antibody (mAb) effec

213 o found that host cell proteins bound to the Protein A resin even more strongly than mAbs and that ty

214 ce (CIP) procedures were developed to extend Protein A resin lifespan, but chromatograms cannot relia

215 ng for Neural retina-specific leucine zipper protein, a rod fate determinant during photoreceptor dev

216 DNA, which are rapidly bound by replication protein A (RPA) and other single-stranded DNA binding pr

217 gle-stranded DNA binding protein replication protein A (RPA) as a regulator of the deposition of newl

218 The replication protein A (RPA) DNA-binding protein has a pivotal role i

219 HCV NS5A(S25-C447) and cellular replication protein A (RPA) functionally cooperate as a processivity

220 CST resembles Replication Protein A (RPA) in that the two complexes harbor compara

221 Replication protein A (RPA) is a highly conserved heterotrimeric sin

222 The replication protein A (RPA) is a single-stranded DNA-binding protein

223 gle-stranded DNA binding protein replication protein A (RPA) on damaged chromatin and severely abroga

224 gle-stranded DNA (ssDNA)-binding replication protein A (RPA) selectively restores XPF-ERCC1 endonucle

225 Here we show that replication protein A (RPA), an essential replisome component that b

226 Here we show that replication protein A (RPA), an ssDNA-binding protein, interacts wit

227 s of the repair complex, such as replication protein A (RPA), is controlled in part by a dynamic acet

228 In the presence of replication protein A (RPA), MRN acts as a processivity factor for E

229 sh2-Msh3), exonuclease 1 (Exo1), replication protein A (RPA), RFC, PCNA, and DNA polymerase delta.

230 interacts with and ubiquitylates replication protein A (RPA), show profound defects in ICL repair.

231 Replication protein A (RPA), the major eukaryotic single-stranded DN

232 Cell Nuclear Antigen (PCNA) and Replication Protein A (RPA), which are critical for DNA replication

233 (CENP-F), allowing ATR to engage replication protein A (RPA)-coated centromeric R loops.

234 interactions of human RAD52 with replication protein A (RPA)-coated ssDNA, and we monitored the fate

235 endent accumulation of (phospho-)replication protein A (RPA)-coated ssDNA.

236 The replication protein A (RPA)-ssDNA complex formed at arrested replica

237 tranded DNA binding heterotrimer replication protein A (RPA).

238 angs, which are quickly bound by replication protein A (RPA).

239 single-stranded DNA, which binds replication protein A (RPA).

240 gle-stranded DNA pre-occupied by replication protein A (RPA).

241 f all DNA metabolic processes is Replication Protein A (RPA).

242 motes DNA end joining, regulates replication protein A (RPA2) phosphorylation and ubiquitination at d

243 rotein [CRP], haptoglobin, and serum amyloid protein A [SAA]), inflammatory markers (matrix metallopr

244 ene encoding the streptococcal collagen-like protein A (SclA) in GAS carrier strains.

245 Recombinant inhibitor-2 protein (a selective PP1 inhibitor) delayed AS160 dephos

246 a binding motif for the quaking RNA binding protein, a sequence we show can significantly regulate m

247 To better understand the activity of this protein a series of mutants, targeted to the NADH co-fac

248 eta signaling pathway and alpha1-antitrypsin protein (a serine protease inhibitor) expression and dow

249 The Akt protein, a serine/threonine kinase, plays important role

250 MenB-FHbp (factor H binding protein), a serogroup B meningococcal (MenB) vaccine, wa

251 peptide A, derived from lactoferrin-binding protein A, showed superior activity in immunogenicity an

252 largest number of genes mapped to ribosomal proteins, a signature hitherto not associated with linez

253 In contrast to globular proteins, a single protein sequence can aggregate into s

254 Salmonella invasion protein A (SipA) is a dual-function effector protein tha

255 uses it to complement its own nuclear export proteins (a site not targeted by current therapy), makin

256 In the lung, surfactant protein A (SP-A) enhanced interleukin-4 (IL-4)-dependent

257 Surfactant protein A (SP-A) is a hydrophilic glycoprotein of the co

258 Surfactant protein A (SP-A) modulates host responses to infectious

259 Surfactant protein A (SP-A) plays a critical role in the clearance

260 Lung surfactant protein A (SP-A) plays an important function in modulati

261 The staphylococcal protein A (spa) gene was sequenced for all isolates to d

262 Staphylococcal protein A (SpA) is an important virulence factor from St

263 ptibility, biofilm formation, Staphylococcal protein A (spa) typing, SCCmec typing, and PCR-based ass

264 Staphylococcal protein A (SPA) was used to modify the silanized fiber s

265 ntation to CD4(+) T cells and staphylococcal protein A (SpA), a cell wall-anchored surface molecule t

266 esponse through expression of staphylococcus protein A (SpA), a surface protein that drives polyclona

267 etic beads, specific antibodies against IL-8 protein, a specific hairpin DNA sequence for IL-8 mRNA a

268 locus protein A (MglA)-stringent starvation protein A (SspA) complex and the DNA-binding protein pat

269 showed that the E. coli stringent starvation protein A (SspA) shares sequence and structural homology

270 screened against three human galectin (hGal) proteins (a stable mutant of hGal1 (hGal-1), a C-termina

271 gosaccharides (HMOs) for four human galectin proteins, a stable mutant of hGal1 (hGal-1), a C-termina

272 VP24 protein, a structural protein present in all family memb

273 e has demonstrated that polycomb group (PcG) proteins, a subset of histone-modifying enzymes known to

274 a tissue-specific reduction of the IKAP/ELP1 protein, a subunit of the Elongator complex.

275 The known viral replication proteins, a telomere binding protein, and a protein kina

276 c behaviour is closer to that of Replication Protein A than to Escherichia coli SSB; a feature that m

277 metry data for chicken egg lysozyme, mutated Protein A, three wild-types of haloalkane dehalogenases,

278 combinant p17 (rp17) and treponemal membrane protein A (TmpA) treponemal antigens.

279 echanisms ensure that the mRNA encoding Hac1 protein, a transcription factor involved in the unfolded

280 UPF1 promotes the decay of MYOD protein, a transcription factor that is a master regulat

281 asmic polyadenylation element binding (CPEB) protein, a translational regulator that recruits mRNAs a

282 Anthrax toxin is composed of three proteins, a translocase channel-forming subunit, called

283 The SAS6-like (SAS6L) protein, a truncated paralogue of the ubiquitous basal b

284 Tail tubular protein A (TTPA) is a structural tail protein of Klebsie

285 rylating and inactivating the retinoblastoma protein, a tumor suppressor that restrains G1- to S-phas

286 nce of specific antibodies against the GTF2b protein, a tumor-associate antigen (TAA) related to colo

287 CHIP (carboxyl terminus of Hsc70-interacting protein), a U-box E3 ligase, suppresses tumor progressio

288 r with other tumor biomarkers and C-reactive protein, a universal biomarker for infection and inflamm

289 ice and amongst the differentially expressed proteins a V-ATPase and a 14-3-3 protein were down-regul

290 ide context, such as with the erythropoietin protein, a V3 polypeptide derived from HIV-1 gp120, or a

291 sicle-associated membrane protein-associated protein A (VAP-A).

292 ui is the surface bound virulence associated protein A (VapA).

293 of the proteoglycan versican and its linking protein, a vertebrate hyaluronan and proteoglycan link p

294 specifically interacts with RPA (Replication protein A) via two conserved RPA-binding domains and is

295 ional groups-carboxyl groups of Alb NPs, p19 protein, a viral protein that can bind and sequester sho

296 nant HSV-1 with a mutation in the gamma134.5 protein, a virulence factor, stimulates dendritic cell (

297 Protein A was covalently immobilized on the surface of P

298 omposite) was developed for detection of p53 protein, a well-known tumor suppressor.

299 of human IgG1 which disrupt interaction with protein A while enhancing interaction with FcRn.

300 ons of unfolded and intrinsically disordered proteins: A wide range of experimental techniques sugges