scholarly article | Q13442814 |
P2093 | author name string | S R Wente | |
M K Iovine | |||
P2860 | cites work | A nuclear export signal in hnRNP A1: a signal-mediated, temperature-dependent nuclear protein export pathway | Q24309825 |
The peptide repeat domain of nucleoporin Nup98 functions as a docking site in transport across the nuclear pore complex | Q24316128 | ||
Identification of NTF2, a cytosolic factor for nuclear import that interacts with nuclear pore complex protein p62 | Q24317417 | ||
Identification of hSRP1 alpha as a functional receptor for nuclear localization sequences | Q24318457 | ||
Sequence and characterization of cytoplasmic nuclear protein import factor p97 | Q24318868 | ||
Two different subunits of importin cooperate to recognize nuclear localization signals and bind them to the nuclear envelope | Q24320769 | ||
Identification of a novel cellular cofactor for the Rev/Rex class of retroviral regulatory proteins | Q24321880 | ||
A human nucleoporin-like protein that specifically interacts with HIV Rev | Q24322635 | ||
Identification of different roles for RanGDP and RanGTP in nuclear protein import | Q24561933 | ||
Mammalian karyopherin alpha 1 beta and alpha 2 beta heterodimers: alpha 1 or alpha 2 subunit binds nuclear localization signal and beta subunit interacts with peptide repeat-containing nucleoporins | Q24563707 | ||
Previously identified protein of uncertain function is karyopherin alpha and together with karyopherin beta docks import substrate at nuclear pore complexes | Q24563814 | ||
Amphibian transcription factor IIIA proteins contain a sequence element functionally equivalent to the nuclear export signal of human immunodeficiency virus type 1 Rev | Q24568152 | ||
Nuclear export of late HIV-1 mRNAs occurs via a cellular protein export pathway | Q24568233 | ||
Nuclear protein import: Ran-GTP dissociates the karyopherin alphabeta heterodimer by displacing alpha from an overlapping binding site on beta | Q24617416 | ||
Isolation of the yeast nuclear pore complex | Q24651185 | ||
Molecular and functional characterization of the p62 complex, an assembly of nuclear pore complex glycoproteins | Q24671748 | ||
Transformation of intact yeast cells treated with alkali cations | Q24672708 | ||
A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae | Q27860636 | ||
A novel genetic system to detect protein-protein interactions | Q27860915 | ||
NUP145 encodes a novel yeast glycine-leucine-phenylalanine-glycine (GLFG) nucleoporin required for nuclear envelope structure | Q27930563 | ||
The GLFG repetitive region of the nucleoporin Nup116p interacts with Kap95p, an essential yeast nuclear import factor | Q27931303 | ||
Kap104p: a karyopherin involved in the nuclear transport of messenger RNA binding proteins | Q27932702 | ||
Nup120p: a yeast nucleoporin required for NPC distribution and mRNA transport | Q27932741 | ||
GLE2, a Saccharomyces cerevisiae homologue of the Schizosaccharomyces pombe export factor RAE1, is required for nuclear pore complex structure and function | Q27933501 | ||
Identification of a novel nuclear pore-associated protein as a functional target of the HIV-1 Rev protein in yeast | Q27933981 | ||
Identification of a yeast karyopherin heterodimer that targets import substrate to mammalian nuclear pore complexes | Q27934056 | ||
A new family of yeast nuclear pore complex proteins | Q27934086 | ||
Nup145p is required for nuclear export of mRNA and binds homopolymeric RNA in vitro via a novel conserved motif | Q27934225 | ||
Functional interaction of Nic96p with a core nucleoporin complex consisting of Nsp1p, Nup49p and a novel protein Nup57p | Q27934383 | ||
Defining the essential functional regions of the nucleoporin Nup145p. | Q27935376 | ||
Purification of NSP1 reveals complex formation with ‘GLFG’ nucleoporins and a novel nuclear pore protein NIC96 | Q27937202 | ||
The essential yeast nucleoporin NUP159 is located on the cytoplasmic side of the nuclear pore complex and serves in karyopherin-mediated binding of transport substrate | Q27937661 | ||
Characterization of nuclear localizing sequences derived from yeast ribosomal protein L29. | Q27939511 | ||
The HIV-1 Rev activation domain is a nuclear export signal that accesses an export pathway used by specific cellular RNAs | Q28131708 | ||
Protein import into nuclei: association and dissociation reactions involving transport substrate, transport factors, and nucleoporins | Q28131733 | ||
Isolation of a protein that is essential for the first step of nuclear protein import | Q28243173 | ||
Ran binding domains promote the interaction of Ran with p97/beta-karyopherin, linking the docking and translocation steps of nuclear import | Q28274296 | ||
Nucleocytoplasmic transport | Q28275907 | ||
A G protein involved in nucleocytoplasmic transport: the role of Ran | Q28286483 | ||
HIV Rev uses a conserved cellular protein export pathway for the nucleocytoplasmic transport of viral RNAs | Q28289718 | ||
Identification of a protein complex that is required for nuclear protein import and mediates docking of import substrate to distinct nucleoporins | Q28573887 | ||
The HIV-1 Rev trans-activator shuttles between the nucleus and the cytoplasm | Q28646841 | ||
Identification of a signal for rapid export of proteins from the nucleus | Q29547742 | ||
Identification and characterization of a nuclear pore complex protein | Q29616069 | ||
An RNA-export mediator with an essential nuclear export signal | Q29617266 | ||
Regulation of the yeast HO gene | Q29618279 | ||
A temperature-sensitive NUP116 null mutant forms a nuclear envelope seal over the yeast nuclear pore complex thereby blocking nucleocytoplasmic traffic | Q29618710 | ||
Shuttling of pre-mRNA binding proteins between nucleus and cytoplasm | Q29618907 | ||
Distinct functions for the two importin subunits in nuclear protein import | Q29620112 | ||
The GTP-binding protein Ran/TC4 is required for protein import into the nucleus | Q29620192 | ||
Inhibition of nuclear protein import by nonhydrolyzable analogues of GTP and identification of the small GTPase Ran/TC4 as an essential transport factor | Q29620193 | ||
Nuclear protein import in permeabilized mammalian cells requires soluble cytoplasmic factors | Q29620194 | ||
Cytosolic proteins that specifically bind nuclear location signals are receptors for nuclear import | Q29620195 | ||
Components of the yeast spindle and spindle pole body | Q29620925 | ||
Identification of cytosolic factors required for nuclear location sequence-mediated binding to the nuclear envelope | Q29622845 | ||
The yeast nuclear import receptor is required for mitosis | Q33995362 | ||
Nuclear import can be separated into distinct steps in vitro: nuclear pore binding and translocation | Q34175285 | ||
An N-ethylmaleimide-sensitive cytosolic factor necessary for nuclear protein import: requirement in signal-mediated binding to the nuclear pore | Q36222719 | ||
Reconstituted nuclei depleted of a vertebrate GLFG nuclear pore protein, p97, import but are defective in nuclear growth and replication | Q36235386 | ||
Dynamic localization of the nuclear import receptor and its interactions with transport factors | Q36237107 | ||
RanBP1 stabilizes the interaction of Ran with p97 nuclear protein import | Q36237637 | ||
GTP hydrolysis by Ran occurs at the nuclear pore complex in an early step of protein import | Q36685432 | ||
Nucleotide-specific interaction of Ran/TC4 with nuclear transport factors NTF2 and p97. | Q37432537 | ||
The nuclear transport factor karyopherin beta binds stoichiometrically to Ran-GTP and inhibits the Ran GTPase activating protein | Q38360627 | ||
Characterization of an essential Orc2p-associated factor that plays a role in DNA replication | Q40018637 | ||
Nucleocytoplasmic transport: factors and mechanisms | Q40403309 | ||
Nuclear export signals and the fast track to the cytoplasm | Q40459787 | ||
Mechanisms of nuclear protein import. | Q40475438 | ||
Cytosolic factors in nuclear transport: what's importin? | Q40655599 | ||
In vivo evidence for involvement of a 58 kDa component of nuclear pore-targeting complex in nuclear protein import | Q40788934 | ||
A karyophilic protein forms a stable complex with cytoplasmic components prior to nuclear pore binding | Q41350466 | ||
Role of the nuclear transport factor p10 in nuclear import | Q48064951 | ||
The nuclear pore‐targeting complex binds to nuclear pores after association with a karyophile | Q48072038 | ||
The two steps of nuclear import, targeting to the nuclear envelope and translocation through the nuclear pore, require different cytosolic factors | Q49486533 | ||
Nuclear protein migration involves two steps: rapid binding at the nuclear envelope followed by slower translocation through nuclear pores | Q70378768 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 797-811 | |
P577 | publication date | 1997-05-01 | |
P1433 | published in | Journal of Cell Biology | Q1524550 |
P1476 | title | A nuclear export signal in Kap95p is required for both recycling the import factor and interaction with the nucleoporin GLFG repeat regions of Nup116p and Nup100p | |
P478 | volume | 137 |
Q39318117 | A subset of FG-nucleoporins is necessary for efficient Msn5-mediated nuclear protein export |
Q27937963 | Accelerating the rate of disassembly of karyopherin.cargo complexes |
Q33964950 | Assembly and preferential localization of Nup116p on the cytoplasmic face of the nuclear pore complex by interaction with Nup82p |
Q27931219 | Binding of the Mex67p/Mtr2p heterodimer to FXFG, GLFG, and FG repeat nucleoporins is essential for nuclear mRNA export. |
Q36376892 | Calcineurin-dependent nuclear import of the transcription factor Crz1p requires Nmd5p |
Q37813021 | Controlling Subcellular Delivery to Optimize Therapeutic Effect |
Q36592228 | Controlling protein compartmentalization to overcome disease |
Q77323192 | Cse1p functions as the nuclear export receptor for importin alpha in yeast |
Q39576650 | Cse1p is involved in export of yeast importin alpha from the nucleus |
Q27939696 | Exportin 1 (Crm1p) is an essential nuclear export factor |
Q27933306 | Facilitated transport and diffusion take distinct spatial routes through the nuclear pore complex |
Q36932768 | Functional characterization of a Nup159p-containing nuclear pore subcomplex |
Q47926605 | Functions of the GTPase Ran in RNA export from the nucleus |
Q24310348 | GLFG and FxFG nucleoporins bind to overlapping sites on importin-beta |
Q28143781 | GTP hydrolysis links initiation and termination of nuclear import on the nucleoporin nup358 |
Q36816824 | Inhibition of mRNA export in vertebrate cells by nuclear export signal conjugates |
Q27937378 | Interactions between a nuclear transporter and a subset of nuclear pore complex proteins depend on Ran GTPase |
Q27933578 | Karyopherin-mediated import of integral inner nuclear membrane proteins |
Q47721363 | Karyopherins and kissing cousins |
Q24683280 | Major binding sites for the nuclear import receptor are the internal nucleoporin Nup153 and the adjacent nuclear filament protein Tpr |
Q27931250 | Minimal nuclear pore complexes define FG repeat domains essential for transport |
Q27931616 | Mtr10p functions as a nuclear import receptor for the mRNA-binding protein Npl3p |
Q24291848 | Novel vertebrate nucleoporins Nup133 and Nup160 play a role in mRNA export |
Q24644057 | Npp106p, a Schizosaccharomyces pombe nucleoporin similar to Saccharomyces cerevisiae Nic96p, functionally interacts with Rae1p in mRNA export |
Q42792243 | Nuclear envelope irregularity is induced by RET/PTC during interphase |
Q74084072 | Nuclear localization of the Saccharomyces cerevisiae HMG protein NHP6A occurs by a Ran-independent nonclassical pathway |
Q27934517 | Nuclear mRNA export requires complex formation between Mex67p and Mtr2p at the nuclear pores. |
Q27933063 | Nup116p and nup100p are interchangeable through a conserved motif which constitutes a docking site for the mRNA transport factor gle2p. |
Q73763113 | Nup116p associates with the Nup82p-Nsp1p-Nup159p nucleoporin complex |
Q27931388 | Nup2p, a yeast nucleoporin, functions in bidirectional transport of importin alpha |
Q56687975 | Peering through the Pore |
Q42715997 | Purification of the vertebrate nuclear pore complex by biochemical criteria |
Q41075696 | Ran-unassisted nuclear migration of a 97-kD component of nuclear pore-targeting complex |
Q24644181 | RanGTP-mediated nuclear export of karyopherin alpha involves its interaction with the nucleoporin Nup153 |
Q37477637 | Reconstitution of HIV-1 rev nuclear export: independent requirements for nuclear import and export |
Q33937097 | Regulation of nuclear import and export. |
Q52545634 | Role of importin-beta in the control of nuclear envelope assembly by Ran. |
Q44792760 | Separate nuclear import pathways converge on the nucleoporin Nup153 and can be dissected with dominant-negative inhibitors |
Q57809839 | Septin-associated proteins Aim44 and Nis1 traffic between the bud neck and the nucleus in the yeast Saccharomyces cerevisiae |
Q37325778 | Simple rules for passive diffusion through the nuclear pore complex. |
Q41980902 | Size-dependent leak of soluble and membrane proteins through the yeast nuclear pore complex |
Q27931940 | Specific binding of the karyopherin Kap121p to a subunit of the nuclear pore complex containing Nup53p, Nup59p, and Nup170p. |
Q27625995 | Structural basis for the interaction between FxFG nucleoporin repeats and importin-beta in nuclear trafficking |
Q28283466 | The 90-kDa molecular chaperone family: structure, function, and clinical applications. A comprehensive review |
Q27935647 | The GLFG regions of Nup116p and Nup100p serve as binding sites for both Kap95p and Mex67p at the nuclear pore complex |
Q41173696 | The Ty1 integrase protein can exploit the classical nuclear protein import machinery for entry into the nucleus |
Q24323008 | The human homologue of Saccharomyces cerevisiae Gle1p is required for poly(A)+ RNA export |
Q28254641 | The importin-beta family member Crm1p bridges the interaction between Rev and the nuclear pore complex during nuclear export |
Q27939968 | The integral membrane protein snl1p is genetically linked to yeast nuclear pore complex function |
Q27938827 | The karyopherin Kap95 regulates nuclear pore complex assembly into intact nuclear envelopes in vivo |
Q77304445 | The nuclear pore complex |
Q33912881 | The nuclear pore complex: a protein machine bridging the nucleus and cytoplasm |
Q27939919 | The yeast hnRNP-Like proteins Yra1p and Yra2p participate in mRNA export through interaction with Mex67p |
Q27934181 | The yeast nucleoporin rip1p contributes to multiple export pathways with no essential role for its FG-repeat region. |
Q29615611 | Transport into and out of the nucleus |
Q47926615 | Transport routes through the nuclear pore complex |
Q25257693 | Yeast phosphatidylinositol 4-kinase, Pik1, has essential roles at the Golgi and in the nucleus |
Q40975251 | beta-subunit of nuclear pore-targeting complex (importin-beta) can be exported from the nucleus in a Ran-independent manner |
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