ライフサイエンスコーパス: HMGB protein

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1 alized by comparison of solved structures of HMGB proteins.

2 ecific and non-sequence-specific families of HMGB proteins.

3 ctural proteins such as high mobility group (HMGB) proteins.

4 tural factors such as high mobility group B (HMGB) proteins.

5 ively identified as high mobility group box (HMGB) proteins 1 and 3, and a 70-kDa band was identified

6 e chromatin protein high mobility group box (HMGB) protein 2 is restricted to the SZ in articular car

7 e chromatin protein high-mobility group box (HMGB) protein 2 is uniquely expressed in the superficial

8 Eukaryotic High-Mobility Group B (HMGB) proteins alter DNA elasticity while facilitating t

9 E. coli cells to explore the extent to which HMGB proteins and derivatives can complement a DNA loopi

10 nds are only moderately discriminated by the HMGB proteins and TBP, but the recognition of dsTG*G*A i

11 HMO1 is one of 10 Saccharomyces cerevisiae HMGB proteins, and it is required for normal growth and

12 HMGB proteins are abundant non-histone components of euk

13 High mobility group box (HMGB) proteins are architectural proteins whose HMG DNA

14 While all of the HMGB proteins bend DNA to preferred angles, Nhp6A promot

15 HMGB proteins bind preferentially to DNA that is bent or

16 High-mobility group B (HMGB) proteins bind duplex DNA without sequence specific

17 two eukaryotic high-mobility group class B (HMGB) proteins binding to approximately 200-bp DNA molec

18 ed proteins, of which high-mobility group B (HMGB) proteins consistently cofractionated by cation-exc

19 Surprisingly, HMGB proteins constrain DNA winding, and this torsional

20 Group B (HMGB) proteins contain HMG box domains known to bind to

21 High mobility group B (HMGB) proteins contain two HMG box domains known to bind

22 Therefore, the mechanism by which HMGB proteins enhance the flexibility of DNA must differ

23 ic recognition of DNA kinks, we propose that HMGB proteins facilitate RAG1/2-RSS interactions by reco

24 There is evidence that HMGB proteins facilitate, while linker histones inhibit

25 ein is an essential high mobility group box (HMGB) protein facilitating Pol I transcription in T. bru

26 e (HU) and eukaryotic high-mobility group B (HMGB) proteins fall into this category.

27 HMGB4, a new member of the mammalian HMGB protein family expressed preferentially in the test

28 accharomyces cerevisiae which belongs to the HMGB protein family.

29 The single-domain HMGB protein from Saccharomyces cerevisiae, Nhp6A, effic

30 ows that linker histones and the chromosomal HMGB proteins, HMG-D and HMG-Z, have opposite effects on

31 show here that the Saccharomyces cerevisiae HMGB protein HMO1 stabilizes chromatin as evidenced by f

32 s features with the Saccharomyces cerevisiae HMGB protein Hmo1, but it is the first architectural chr

33 logical function of DNA sequence-nonspecific HMGB proteins is obscure.

34 cterial DNA-binding protein HU and the yeast HMGB protein NHP6A display the same phenomenon of protei

35 Here, we show that derivatives of the yeast HMGB protein Nhp6A rescue DNA looping in E. coli lacking

36 We also show data for the yeast HMGB protein NHP6A showing a similar DNA-concentration-d

37 o a specific site to determine the effect of HMGB proteins on recognition of these lesions.

38 Our observations support a model in which HMGB proteins soften DNA through random dynamic binding

39 Our previous work suggests that the Nhp6 HMGB protein stimulates RNA polymerase II transcription

40 HMGB4 is a new member in the family of HMGB proteins that has been characterized in sperm cells

41 (h-mtTFA) is a dual high mobility group box (HMGB) protein that binds site-specifically to the mitoch

42 results show that HMO1 shares with mammalian HMGB proteins the ability to promote DNA association.

43 linker histones and high-mobility group box (HMGB) proteins--to DDR and their potential significance

44 ne the nature of this behavior for different HMGB proteins, we used atomic force microscopy to quanti

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