ライフサイエンスコーパス: bipartite nuclear localization signal

1 The same region also contains a functional bipartite nuclear localization signal.

2 (Arg(638)-Lys(655)) that closely resembles a bipartite nuclear localization signal.

3 this nuclear targeting represent a classical bipartite nuclear localization signal.

4 An acidic domain, as well as a putative bipartite nuclear localization signal, a nuclear export

5 protein, referred to as pUL31, containing a bipartite nuclear localization signal, an intrinsically

6 , we showed that the Int6 protein contains a bipartite nuclear localization signal and a nuclear expo

7 It has a putative bipartite nuclear localization signal and is located to

8 These results indicate that EBNA-LP has a bipartite nuclear localization signal and that efficient

9 Both proteins contain a consensus bipartite nuclear localization signal and were found in

10 -binding consensus site at the N-terminus, a bipartite nuclear localization signal, and an eps15 homo

11 The carboxyl domain of cry2 bears a basic bipartite nuclear localization signal, and the cry2 prot

12 ns: HMG-14/-17 proteins contain an intrinsic bipartite nuclear localization signal, and their entry i

13 Deletion analysis showed that a bipartite nuclear localization signal at the amino termi

14 this nuclear localization is dependent on a bipartite nuclear localization signal at the C-terminus

15 in the middle portion of the protein, and a bipartite nuclear localization signal at the carboxyl te

16 the MK2 Ile-366-Ala-390, which includes the bipartite nuclear localization signal, binds to the p38a

17 ct in which a kinase substrate is fused to a bipartite nuclear localization signal (bNLS) and nuclear

18 rase reflects the recognition of an atypical bipartite nuclear localization signal by the importin/ka

19 eus, which is dependent on the presence of a bipartite nuclear localization signal in the DEDD2 prote

20 isoforms, B' beta 3 and B' gamma, contain a bipartite nuclear localization signal in their COOH term

21 The longest variant, MAGI-1c, contains three bipartite nuclear localization signals in its unique COO

22 The first is a bipartite nuclear localization signal, indicating that t

23 We demonstrate that the putative bipartite nuclear localization signal is not required, b

24 Although the KRK motif resembles half of a bipartite nuclear localization signal, it appears to fun

25 A bipartite nuclear localization signal motif indicates a

26 Here we identify a bipartite nuclear localization signal (NLS) and a CRM1-d

27 We demonstrate that Nrf2 contains a bipartite nuclear localization signal (NLS) and a leucin

28 We identified a highly conserved putative bipartite nuclear localization signal (NLS) and demonstr

29 ion of Vpr (amino acids 73 to 96) contains a bipartite nuclear localization signal (NLS) composed of

30 using a gain-of-function genetic approach, a bipartite nuclear localization signal (NLS) derived from

31 We have identified a bipartite nuclear localization signal (NLS) in IN requir

32 The bipartite nuclear localization signal (NLS) in the tail

33 leocytoplasmic transport is carried out by a bipartite nuclear localization signal (NLS) located at i

34 Cln3p localization requires a bipartite nuclear localization signal (NLS) located at t

35 onstrated that N contains a carboxy-terminal bipartite nuclear localization signal (NLS) located betw

36 vity by releasing importin alpha/beta from a bipartite nuclear localization signal (NLS) located in t

37 We have identified a putative bipartite nuclear localization signal (NLS) motif in the

38 SAP11 contains a bipartite nuclear localization signal (NLS) that targets

39 We first characterize a bipartite nuclear localization signal (NLS) within Ci.

40 this study, we report that Nurr1 contains a bipartite nuclear localization signal (NLS) within its D

41 tochondrial-targeting signal and an internal bipartite nuclear localization signal (NLS) yet is targe

42 er, we found that the bHLH domain contains a bipartite nuclear localization signal (NLS).

43 e nuclear proteins, each of which contains a bipartite nuclear localization signal (NLS).

44 ntain a tubby signature motif (FXGRVTQ), two bipartite nuclear localization signals (NLSs) at the C-t

45 All steroid receptors possess a bipartite nuclear localization signal sequence (NLS) tha

46 bsolutely dependent on the carboxyl-terminal bipartite nuclear localization signal sequence of VirD2.

47 sis demonstrated that COP1 carries a single, bipartite nuclear localization signal that functions ind

48 Geminin contains a typical bipartite nuclear localization signal that is also requi

49 open reading frame also contains a consensus bipartite nuclear localization signal, though no specifi

50 it is the full-length version of MPP4, has a bipartite nuclear localization signal, two motifs that c

51 terized, hydrophilic protein with a putative bipartite nuclear localization signal, Von Willebrand fa

52 minal domain of cry2 that contains the basic bipartite nuclear localization signal was sufficient to

53 Amino acids 120 to 151 contained an apparent bipartite nuclear localization signal, whereas amino aci

54 H(2)-terminal region of the VRK3s contains a bipartite nuclear localization signal, which directs the

55 Nuclear entry of dreCmas1 was mediated by a bipartite nuclear localization signal, which seemed irre