نتایج جستجو برای: ژنهای importin

تعداد نتایج: 2350  

Journal: :The EMBO journal 2004
Toshihiro Sekimoto Masahiro Fukumoto Yoshihiro Yoneda

p27(Kip1) (p27), a CDK inhibitor, migrates into the nucleus, where it controls cyclin-CDK complex activity for proper cell cycle progression. We report here that the classical bipartite-type basic amino-acid cluster and the two downstream amino acids of the C-terminal region of p27 function as a nuclear localization signal (NLS) for its full nuclear import activity. Importin alpha3 and alpha5, ...

Journal: :The Journal of Cell Biology 1999
Efrosyni Paraskeva Elisa Izaurralde F. Ralf Bischoff Jochen Huber Ulrike Kutay Enno Hartmann Reinhard Lührmann Dirk Görlich

Importin beta is a major mediator of import into the cell nucleus. Importin beta binds cargo molecules either directly or via two types of adapter molecules, importin alpha, for import of proteins with a classical nuclear localization signal (NLS), or snurportin 1, for import of m3G-capped U snRNPs. Both adapters have an NH2-terminal importin beta-binding domain for binding to, and import by, i...

2010
Yutaka Ogawa Yoichi Miyamoto Munehiro Asally Masahiro Oka Yoshinari Yasuda Yoshihiro Yoneda

Npap60 (Nup50) is a nucleoporin that binds directly to importin alpha. In humans, there are two Npap60 isoforms: the long (Npap60L) and short (Npap60S) forms. In this study, we provide both in vitro and in vivo evidence that Npap60L and Npap60S function differently in nuclear protein import. In vitro binding assays revealed that Npap60S stabilizes the binding of importin alpha to classical NLS-...

Journal: :Journal of cell science 2002
Gyula Timinszky László Tirián Ferenc T Nagy Gábor Tóth András Perczel Zsuzsanna Kiss-László Imre Boros Paul R Clarke János Szabad

Three of the four independently induced Ketel(D) dominantnegative female sterile mutations that identify the Drosophila importin-beta gene, originated from a C4114--> T transition and the concurrent replacement of Pro446 by Leu (P446L). CD spectroscopy of representative peptides with Pro or Leu in the crucial position revealed that upon the Pro-->Leu exchange the P446L mutant protein loses flex...

Journal: :EMBO reports 2001
P Mühlhäusser E C Müller A Otto U Kutay

Nuclear import of the four core histones H2A, H2B, H3 and H4 is one of the main nuclear import activities during S-phase of the cell cycle. However, the molecular machinery facilitating nuclear import of core histones has not been elucidated. Here, we investigated the pathways by which histone import can occur. First, we show that core histone import can be competed by the BIB (beta-like import...

Journal: :Journal of cell science 2011
Toby W Hurd Shuling Fan Ben L Margolis

Ciliopathies represent a newly emerging group of human diseases that share a common etiology resulting from dysfunction of the cilium or centrosome. The gene encoding the retinitis pigmentosa 2 protein (RP2) is mutated in X-linked retinitis pigmentosa. RP2 localizes to the ciliary base and this requires the dual acylation of the N-terminus, but the precise mechanism by which RP2 is trafficked t...

Journal: :Cell 2014
Min Lu Jaroslav Zak Shuo Chen Luis Sanchez-Pulido David T. Severson Jane Endicott Chris P. Ponting Christopher J. Schofield Xin Lu

Regulation of nuclear import is fundamental to eukaryotic biology. The majority of nuclear import pathways are mediated by importin-cargo interactions. Yet not all nuclear proteins interact with importins, necessitating the identification of a general importin-independent nuclear import pathway. Here, we identify a code that determines importin-independent nuclear import of ankyrin repeats (ARs...

Journal: :Cell 2007
Steffen Frey Dirk Görlich

The permeability barrier of nuclear pore complexes (NPCs) controls the exchange between nucleus and cytoplasm. It suppresses the flux of inert macromolecules > or = 30 kDa but allows rapid passage of even very large cargoes, provided these are bound to appropriate nuclear transport receptors. We show here that a saturated hydrogel formed by a single nucleoporin FG-repeat domain is sufficient to...

Journal: :Molecular Systems Biology 2007
Greg Riddick Ian G Macara

Although there exists a large family of nuclear transport receptors (Karyopherins), the majority of known import cargoes use an adapter protein, Importin-alpha (Impalpha), which links the cargo to a karyopherin, Importin-beta (Impbeta). The reason for the existence of transport adapters is unknown. One hypothesis is that, as Impalpha re-export is coupled to GTP hydrolysis, it can drive a higher...

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