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1 d with storage chaperone proteins, including nucleoplasmin.
2 0) are removed from erythrocyte chromatin by nucleoplasmin.
3 osome remains intact even in the presence of nucleoplasmin.
4 e T antigen or the standard bipartite NLS of nucleoplasmin.
5 chromatin, a process that can be mediated by nucleoplasmin.
6 C causes it to dissociate from nucleophosmin/nucleoplasmin.
7 oocyte extracts or hypophosphorylated oocyte nucleoplasmin.
8 hts into the mechanism of histone binding by nucleoplasmins.
9 not form a decamer, unlike certain classical nucleoplasmins.
10                           In Xenopus laevis, nucleoplasmin 2 (NPM2) decondenses sperm DNA in vitro.
11                  Here, oocytes obtained from nucleoplasmin 2 knockout (Npm2-/-) mice were used to inv
12 mplementary DNA for a highly acidic protein, nucleoplasmin 3 (NPM3), was found in multiple positive c
13 nced homology to the histone binding site of nucleoplasmin, a chromatin remodeling protein found in X
14 blocks nuclear import of RPA but not that of nucleoplasmin, a classical import substrate.
15 for this reaction, and have shown that it is nucleoplasmin, a previously known chromatin remodelling
16    On the basis of the similarity of Npm3 to nucleoplasmin and nucleophosmin in amino acid sequence,
17 ed to the nuclear chaperone phosphoproteins, nucleoplasmin and nucleophosmin.
18 the nuclear localization sequences (NLSs) of nucleoplasmin and the tumor suppressor p53 in human cell
19        This protein resembles Xenopus laevis nucleoplasmin, and it has therefore been termed dNLP, fo
20 depletion of importin alpha blocks import of nucleoplasmin but not that of RPA.
21 luster downstream of the bipartite signal of nucleoplasmin can be directed to the nucleus by flanking
22                                              Nucleoplasmin class of histone chaperones perform histon
23                We propose that nucleophosmin/nucleoplasmin complexes serve as chaperones that negativ
24 extracts or purified hyperphosphorylated egg nucleoplasmin decondense sperm chromatin and remove sper
25                                              Nucleoplasmin decondenses the sperm chromatin by removin
26                 We also find that Drosophila Nucleoplasmin (dNlp) is present in regions of active tra
27 additional A2 acidic tract C-terminal to the nucleoplasmin domain for interaction with histone H3/H4
28 her characterization revealed the N-terminal nucleoplasmin domain to interact with H2A/H2B and H3/H4
29 aracterization of HDTs, revealing them to be nucleoplasmin family histone chaperones.
30                                          The nucleoplasmin family of histone chaperones is identified
31 re with a central pore, is only found in the nucleoplasmin family.
32                              The NTDs form a nucleoplasmin fold, exist as pentamers in solution, and
33       The N-terminal domain had a pentameric nucleoplasmin-fold; making this the first report of a pl
34 s of loop mutations support the premise that nucleoplasmins form decamers when they bind H2A-H2B dime
35                RanGTP caused accumulation of nucleoplasmin-gold along the length of extended cytoplas
36                                              Nucleoplasmin is a histone chaperone that consists of a
37                                              Nucleoplasmin is able to partially relieve this repressi
38 re shown in bold; [4,5]), whereas the NLS of nucleoplasmin is bipartite.
39     We conclude that hyperphosphorylation of nucleoplasmin is used to modulate the rapid changes in c
40 ructure confirmed that Pf indeed possesses a nucleoplasmin isoform (PfNPM), and the N-terminal core d
41 ly discovered that consists of an N-terminal nucleoplasmin-like (NPL) domain and a C-terminal FKBP pe
42     Here, we report the first structure of a nucleoplasmin-like domain (NPL) from the unrelated Droso
43 family of proteins that share the pentameric nucleoplasmin-like NPL domain and are found in protists,
44 tin assembly system comprises the Drosophila nucleoplasmin-like protein (dNLP) histone chaperone, the
45 l transcription regulator, which resembles a nucleoplasmin-like protein (NLP) with an AT-hook motif.
46                Surprisingly, one of these is nucleoplasmin-like protein (NLP), which we had previousl
47 s therefore been termed dNLP, for Drosophila nucleoplasmin-like protein.
48  The experimental confirmation that HDTs are nucleoplasmins may spark new interest in this enigmatic
49     Addition of the histone binding protein, nucleoplasmin, mediated the displacement of the core his
50                         We show that H2A and nucleoplasmin methylation appears late in oogenesis and
51 ibe a bipartite NLS in p50/p65, analogous to nucleoplasmin NLS but exposed in trans.
52 ure, and sequence analysis revealed that the nucleoplasmin NLS coding sequence was deleted from the g
53                     Gag proteins bearing the nucleoplasmin NLS insertion displayed an assembly defect
54                                          The nucleoplasmin NLS requires two essential clusters of bas
55                                              Nucleoplasmin (NP) is a pentameric histone chaperone tha
56         Human Npm2 is an ortholog of Xenopus nucleoplasmin (Np), a chaperone that binds histones.
57 ent the structure of an N-terminal domain of nucleoplasmin (Np-core) at 2.3 A resolution.
58                                              Nucleoplasmin (Npm) is a highly conserved histone chaper
59                          We demonstrate that nucleoplasmin (Npm), an exceedingly abundant maternally
60 ts with egg-type histones by the egg protein nucleoplasmin (Npm).
61 e also resolved the 3D cryo-EM structures of nucleoplasmin NPM2 co-isolated with the linker histone H
62 structures to enhance protamine dismissal by nucleoplasmin (NPM2) and enable the recruitment of HIRA
63 onation, we identified the histone chaperone nucleoplasmin (Npm2) as a putative nuclear size effector
64  of, and may share basic functions with, the nucleoplasmin/ nucleophosmin family of molecular chapero
65 H2A/H2A.X-F and H4 and the histone chaperone nucleoplasmin on a conserved motif (GRGXK).
66 udies showed that the nuclear phosphoprotein nucleoplasmin performs the first stage of chromatin deco
67 r localization signal (NLS) derived from the nucleoplasmin protein was inserted into the Myr1E Gag se
68 sphorylated CPC interacts with nucleophosmin/nucleoplasmin proteins, which are known to oligomerize i
69 m nuclei can be licensed by a combination of nucleoplasmin, RLF-M and a partially purified fraction t
70 hether the nuclear targeting activity of the nucleoplasmin sequence was responsible for the infectivi
71        Furthermore, dephosphorylation of egg nucleoplasmin slows sperm decondensation and prevents ba
72 old; making this the first report of a plant nucleoplasmin structure.
73 activity, SW1-SNF, or the histone chaperone, nucleoplasmin, suggesting that the binding of these fact
74 tional nucleolar protein and a member of the nucleoplasmin superfamily of acidic histone chaperones.
75 nds upon the massive hyperphosphorylation of nucleoplasmin that occurs when oocytes mature into eggs.
76        HDTs show some sequence similarity to nucleoplasmins, the histone chaperones that aid in bindi
77                 A bipartite NLS derived from nucleoplasmin was inserted into a region of the MA domai
78 ls an increased association of the chaperone nucleoplasmin with ribonucleoprotein particles dependent