Nucleocytoplasmic transport

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UNIPROT ID/AC

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Metabolite Name

Behenate (1)
1-Nonadecanoyl-2-eicosanoyl-glycero-3-phosphate (1)
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[2-[(4E,7E,10E,13E,16E,19E)-docosa-4,7,10,13,16,19-hexaenoyl]oxy-3-hexadecoxypropyl] 2-(trimethylazaniumyl)ethyl phosphate (1)
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(2R,4S)-2,4-diaminopentanoic acid (1)
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4-(5-Hydroxy-2-methyl-2-azabicyclo[2.2.2]octan-5-yl)-3-methylbutanoic acid (1)
(1E,6R,11R,13R,14S,15S,19E,21E,23S,27R)-27-hydroxy-23-[(1S)-1-hydroxyethyl]-9,15-dimethylspiro[4,12,17,24-tetraoxapentacyclo[21.3.1.113,16.06,11.06,15]octacosa-1,9,19,21-tetraene-14,2'-oxirane]-3,18-dione (1)
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4-Bromophenylacetic acid (1)
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Modelling Approach

Ordinary differential equation model (1)

Lab affiliation

Proteomics and Metabolomics Core Facility, Biomedical Research Institute, Seoul National University Hospital (2)
Izabela Sumara, Institute of Genetics and Molecular and Cellular Biology (IGBMC), Illkirch, France (1)
State Key Laboratory of Virology and Hubei Province Key Laboratory of Allergy and Immunology, Institute of Medical Virology, TaiKang Center for Life and Medical Sciences, TaiKang Medical School, Wuhan University (1)
Department of Biochemistry, Institute of Chemistry, University of São Paulo, 05508-000, São Paulo, SP, Brazil. (1)
Hubrecht Institute - Royal Academy of Arts and Sciences and University Medical Centre Utrecht, Utrecht, the Netherlands (1)
Department of Biochemistry and Pharmacology, The University of Melbourne, VIC 3010. Australia; Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, VIC 3010. Australia (1)
Université catholique de Louvain, de Duve Institute, 74 avenue Hippocrate (VIRO-B1.74.07), B-1200 Brussels, Belgium (1)
1Departments of Biomolecular Sciences and Molecular Neuroscience, Weizmann Institute of Science, 7610001 Rehovot, Israel (1)
Structural and Computational Biology Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstr. 1, 69117 Heidelberg, Germany (1)
Max Perutz Labs, University of Vienna and Medical University of Vienna, Vienna Biocenter Campus (VBC), Dr. Bohr-Gasse 9/3, 1030 Vienna, Austria (1)
Leibniz Institute on Aging – Fritz Lipmann Institute (FLI), Jena, Germany (1)
Georgia State University (1)
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Centre for Medical Genetics, Institute of Reproductive Genetics, University of Münster, Vesaliusweg 12-14, 48149 Münster, Germany. (1)
University Medical Center Göttingen, Department of Molecular Biology, Germany (1)
Biotechnology and Bioengineering Center, Deptartment of Microbiology, Medical College of Wisconsin (1)
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Department of Oncology, University of Oxford, Oxford, Oxfordshire, OX3 7DQ, UK (1)
UNIVERSITY OF CALIFORNIA-RIVERSIDE (1)
Uppsala University (1)
Guizhou University (1)
CSIRO Biomedical Manufacturing Biology R&D Group (1)
Protein Analysis and Proteomics The Francis Crick Institute Mass Spectrometry STP (1)
Cellular Dynamics Laboratory, RIKEN, Japan (1)
University of Virginia (1)
Department of Biological Sciences Wayne state University (1)
Medical Proteomics Unit, Research Department, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand (1)
Structural and Computational Biology Unit European Molecular Biology Laboratory (EMBL) Meyerhofstr. 1 69117 Heidelberg Germany (1)
Centre for Medical Genetics, Institute of Reproductive Genetics, University of Münster, Vesaliusweg 12-14, 48149, Münster, Germany. (1)
Department of Medical Mycology, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, China. (1)

IsPrivate

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Classification

protozoa (3)

Modification

N6-dimethyl-L-lysine (1)
Not available (1)

Study type

RNA-seq of coding RNA (8)
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Unknown experiment type (1)
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ATAC-seq (1)
Other (1)
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Methylation profiling by array (1)
CUT&RUN (1)
RNA-seq of non coding RNA (1)

Release Date

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2015 (32)
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2005 (6)
2000 (5)
2001 (4)
2002 (3)
1999 (1)
1998 (1)

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TMEM63B Regulates Nucleocytoplasmic Transport and Placental Development

PRJNA1226629 | ENA

NEAT1 Regulates BMSCs Aging Through Disruption of FGF2 Nuclear Transport

Background: The aging of bone marrow mesenchymal stem cells (BMSCs) impairs bone tissue regeneration, contributing to skeletal disorders. LncRNA NEAT1 is considered as a proliferative inhibitory role during cellular senescence, but the relevant mechanisms remain insufficient. This study aims to eluc...

ORGANISM(S): Homo Sapiens

2025-01-16 | PXD059860 |

Nucleocytoplasmic transport and membrane growth control nuclear size

How cells control the overall size of membrane-bound organelles is an important unanswered question of cell biology. Fission yeast cells maintain a nuclear size that is proportional to cellular size, resulting in a constant ratio between the nuclear and cellular volumes (N/C ratio). To shed light on...

ORGANISM(S): Schizosaccharomyces pombe

2017-06-05 | PXD004530 | Pride

Nucleocytoplasmic Transport of RNA-Binding Proteins Regulates Neural Stem Cell Fates

PRJNA687227 | ENA

SILAC-Tp (12 importins)

Importin-beta family proteins are nucleocytoplasmic transport receptors (NTRs), and they transport most nuclear proteins as their cargoes into and out of the nuclei. Human cells have 20 species of importin-beta family NTRs, of which 10 (importin-beta, transportin-1, -2, -SR, importin-4, -5, -7, -8, ...

ORGANISM(S): Homo Sapiens (ncbitaxon:9606)

2017-03-30 | MSV000080815 | MassIVE

Stress Granule Assembly Disrupts Nucleocytoplasmic Transport.

Not available

S-EPMC6083872 | biostudies-literature

TMEM63B Regulates Nucleocytoplasmic Transport and Placental Development

The placenta is critical for embryonic development, orchestrating nutrient exchange, hormone production, and immune protection. Trophoblast proliferation and differentiation, governed by precise cell cycle regulation, are fundamental to placental development. Here, we identify TMEM63B, an osmo/mecha...

ORGANISM(S): Homo sapiens

2026-05-11 | GSE290233 | GEO

Arsenic binds to nuclear transport factors and disrupts nucleocytoplasmic transport.

Not available

S-EPMC12401540 | biostudies-literature

Quantitative Nucleocytoplasmic Transport Assays in Cellular Models of Neurodegeneration.

Not available

S-EPMC7842572 | biostudies-literature

Cellular Stress Induces Nucleocytoplasmic Transport Deficits Independent of Stress Granules.

Not available

S-EPMC9138870 | biostudies-literature

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