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1 e protein is the primary oncogene product of bovine papillomavirus.
2 nt involving a conserved tyrosine (Y) in the bovine papillomavirus 1 (BPV-1) E2 protein at amino acid
5 UTRs) of human papillomavirus 16 (HPV16) and bovine papillomavirus 1 (BPV1) contain a negative regula
7 f the H+ vacuolar ATPase and cooperates with bovine papillomavirus 1 E5 oncoprotein in cell transform
11 ein Brd4 is implicated in the hitchhiking of bovine papillomavirus-1 (BPV-1), and the viral protein E
12 s by which E2 from the related viral strains bovine papillomavirus-1 and human papillomavirus-16 disc
13 n is similar to the crystal structure of the bovine papillomavirus-1 E2 protein when complexed to DNA
15 or the double-stranded DNA-binding domain of bovine papillomavirus-1 E2 that has a three-dimensional
16 ific for HPV-11, since SIs generated against bovine papillomavirus and HPV-16 VLPs were not generally
17 ene and has features similar to those of the bovine papillomavirus and human papillomavirus E5 genes.
18 ons from electron cryomicroscopy (cryoEM) of bovine papillomavirus at 9 A resolution with coordinates
22 s of diverse papillomavirus types, including bovine papillomavirus (BPV) and human papillomavirus 16
25 We previously showed that expression of the bovine papillomavirus (BPV) E2 gene results in a dramati
29 Transformed bovine fibroblasts expressing bovine papillomavirus (BPV) E5 are highly vacuolated and
33 localization of structural and nonstructural bovine papillomavirus (BPV) proteins in cultured cells t
37 ilize the virion or promote capsid assembly, bovine papillomavirus (BPV) virions were subjected to bu
38 e interaction with E1, we have used chimeric bovine papillomavirus (BPV)/human papillomavirus type 11
44 sist in the rapid and efficient detection of bovine papillomavirus DNA and help in the prevention and
45 2 controls the biochemical activities of the bovine papillomavirus E1 and E2 proteins by modifying th
48 y other cellular proteins that interact with bovine papillomavirus E1, an HeLa cDNA library was scree
49 Mutations, which impair the sumoylation of bovine papillomavirus E1, prevent normal nuclear accumul
55 elicase ChlR1 is required for loading of the bovine papillomavirus E2 protein onto chromatin during D
58 rd4 as the mitotic chromosome anchor for the bovine papillomavirus E2 protein, which tethers the vira
60 hift analyses demonstrate that human but not bovine papillomavirus E2 proteins recognize this sequenc
64 gene in HeLa cervical carcinoma cells by the bovine papillomavirus E2 transcription factor activates
68 ze to cellular endomembranes, cooperate with bovine papillomavirus E5 in transformation, as well as b
71 omodimers of the transmembrane 44-amino acid bovine papillomavirus E5 protein bind the transmembrane
82 us VLPS: Exposure to fully assembled VLPs of bovine papillomavirus, human papillomavirus (HPV)16 or H
90 din that, when conjugated at high density to bovine papillomavirus major capsid protein L1 VLPs, indu
93 ic resolution structures of complexes of the bovine papillomavirus strain 1 (BPV-1) E2 protein and DN
94 man papillomavirus strain 16 (HPV-16) E2 and bovine papillomavirus strain 1 (BPV-1) E2 to discriminat
95 he DNA-binding domain of the E2 protein from bovine papillomavirus strain 1 and its complex with DNA
97 We have found that the E6 oncoprotein of Bovine Papillomavirus Type 1 (BE6) as well as the E6 pro
98 mutants that prevent phosphorylation of the bovine papillomavirus type 1 (BPV) E2 protein are transf
100 milar to previously determined structures of bovine papillomavirus type 1 (BPV-1) and human papilloma
102 nimal DNA-binding and dimerization domain of bovine papillomavirus type 1 (BPV-1) E2 alone or this bi
106 6 oncoproteins of cutaneous papillomaviruses Bovine Papillomavirus Type 1 (BPV-1) E6 and human papill
109 ted bovine fibropapillomas were examined for bovine papillomavirus type 1 (BPV-1) E7 localization.
112 an important mechanism for the regulation of bovine papillomavirus type 1 (BPV-1) gene expression dur
113 an important mechanism for the regulation of bovine papillomavirus type 1 (BPV-1) gene expression dur
114 ing plays an important role in regulation of bovine papillomavirus type 1 (BPV-1) gene expression.
123 ich SE4 element regulates the selection of a bovine papillomavirus type 1 (BPV-1) late-specific splic
126 a model for high-risk type genital HPV, and bovine papillomavirus type 1 (BPV-1), a papillomavirus k
128 he best-characterized E2 protein, encoded by bovine papillomavirus type 1 (BPV-1), has been shown to
133 iologic agent of cervical carcinoma, whereas bovine papillomavirus type 1 (BPV1) causes benign fibrop
134 In addition to viral proteins E1 and E2, bovine papillomavirus type 1 (BPV1) depends heavily on h
136 ly demonstrated that acute expression of the bovine papillomavirus type 1 (BPV1) E2 protein in HeLa a
137 ells, we fused the DNA binding domain of the bovine papillomavirus type 1 (BPV1) E2 protein to the ca
138 structurally more similar to the HPV 18 and bovine papillomavirus type 1 (BPV1) E2 proteins than it
139 Tax1BP1 also interacts with the HPV16 and bovine papillomavirus type 1 (BPV1) E2 proteins, with th
142 E-1 cells harboring autonomously replicating bovine papillomavirus type 1 (BPV1) genomes were infecte
144 that syntaxin 18 colocalizes with infectious bovine papillomavirus type 1 (BPV1) pseudovirions during
145 psidate viral genome and generate infectious bovine papillomavirus type 1 (BPV1) upon coexpression of
146 ues 1 to 88 or 11 to 200 derived from HPV16, bovine papillomavirus type 1 (BPV1), or cottontail rabbi
147 ng mechanism has been best characterized for bovine papillomavirus type 1 (BPV1), where the E2 protei
151 6 proteins of the beta-genus HPVs and of the bovine papillomavirus type 1 associated with cutaneous f
154 e absence of E2, is sufficient for low-level bovine papillomavirus type 1 DNA replication in C-33A ce
155 rthermore, SV40 Tag was able to compete with bovine papillomavirus type 1 E1 for binding to RPA.
157 stablished that it participates in tethering bovine papillomavirus type 1 E2 and viral genomes to hos
159 ces between the activation properties of the bovine papillomavirus type 1 E2 protein and those of eit
175 nding target through which the E2 protein of bovine papillomavirus type 1 links the viral genome to m
176 d trimeric L1 species, whereas the capsid of bovine papillomavirus type 1 matures into more extensive
177 Here we demonstrate that melting of the bovine papillomavirus type 1 ori is a sequence-dependent
180 gene expression of the E6 promoter of BPV-1 (bovine papillomavirus type 1) and HPV types 16 and 18.
181 V), cottontail rabbit papillomavirus (CRPV), bovine papillomavirus type 1, and human papillomavirus t
182 nd HPV-18, wart-causing low risk HPV-11, and bovine papillomavirus type 1, in part through enhancing
183 -interacting protein and, in the case of the bovine papillomavirus type 1, serves to tether E2 and th
184 ts counterpart from the related viral strain bovine papillomavirus type 1, the precise placement of t
186 ion is conserved in HPV-11, -16, and -18 and bovine papillomavirus type 4 (BPV-4) E2 and is also requ
191 es were recently hypothesized to be sites of bovine papillomavirus virion assembly, our observation s
192 transcription after infection with authentic bovine papillomavirus virions was similarly elevated in
193 orporated into an immunodominant site of the bovine papillomavirus virus L1 coat protein, which self-
194 ) effectively bound and rapidly internalized bovine papillomavirus VLPS: Exposure to fully assembled
196 he crystal structure of the E1 helicase from bovine papillomavirus, where asymmetric assembly is for
197 n four viral oncoproteins: the E5 protein of bovine papillomavirus, which activates the platelet-deri
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