ライフサイエンスコーパス: E1B protein

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1 critical for the recognition of the native p-E1b protein.

2 bly due to the presence of the smaller (19K) E1B proteins.

3 agated in cells providing adenovirus E1A and E1B proteins.

4 Adenovirus E1B proteins (19,000-molecular-weight [19K] and 55K prot

5 mutations that impaired nuclear entry of the E1B protein, and consideration of its primary sequence s

6 (CR) 1 and 2, and inhibition of apoptosis by E1B proteins are required for oncogenic transformation.

7 elated with the transforming activity of the E1B protein, but its contribution to viral replication i

8 carry insertions at various positions in the E1B protein coding sequence.

9 n, monkey, or baby hamster kidney cells, the E1B protein colocalized in the nucleus with the E4 prote

10 Simultaneously, the previously cytoplasmic E1B protein colocalized with the E4 protein in both huma

11 A binding, and this motif is conserved among E1B proteins from different Ad serotypes.

12 We have used these properties of the E1B proteins from different viral serotypes to map the p

13 The adenoviral E1B protein has sequential and functional homology to Bc

14 in to direct the nuclear localization of the E1B protein in REF-52 rat cells was overcome by fusion w

15 The larger E1B proteins of both Ad2/5 and Ad12 bind to p53 and inhi

16 nactivation of an endogenous mutant p53 with E1B proteins resulted in an increase in PTHrP expression

17 ddition to high levels of adenovirus E1A and E1B proteins), the pTP deletion mutant virus replicates

18 In the absence of this E1B protein, the p53 transcriptional program is not indu

19 Binding of the E1B protein to the activation domain of p53 inhibits p53

20 y cells, the E4 protein failed to direct the E1B protein to the nucleus in rat and mouse cell lines a

21 ion or the unexpected failure of the altered E1B proteins to enter the nucleus efficiently.

22 ion of several p53-responsive genes when the E1B protein was also absent from infected cells.

23 key, hamster, rat, and mouse cell lines, the E1B protein was predominantly cytoplasmic and typically

24 f the adenovirus type 5 34-kDa E4 and 55-kDa E1B proteins was determined in the absence of other aden

25 A complex of the E4 and E1B proteins was identified by coimmunoprecipitation in

26 xpression specifically in the absence of the E1B protein were identified by consensus k-means cluster

27 nding sites for p53 on both the Ad2 and Ad12 E1B proteins will disrupt the interaction in vivo and in

28 the previously described association of the E1B protein with intranuclear structures that correspond

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