Data · dataset · 2015
Screening of cell cycle fusion proteins to identify kinase signaling networks
Listed in DataCite
Kinase signaling networks are well-established mediators of cell cycle transitions.
Description
However, how kinases interact with the ubiquitin proteasome system (UPS) to elicit protein turnover is not fully understood. We sought a means of identifying kinase-substrate interactions to better understand signaling pathways controlling protein degradation.
Our prior studies used a luciferase fusion protein to uncover kinase networks controlling protein turnover. In this study, we utilized a similar approach to identify pathways controlling the cell cycle protein p27 Kip1 . We generated a p27 Kip1 -luciferase fusion and expressed it in cells incubated with compounds from a library of pharmacologically active compounds.
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We then compared the relative effects of the compounds on p27 Kip1 -luciferase fusion stabilization. This was combined with in silico kinome profiling to identify potential kinases inhibited by each compound. This approach effectively uncovered known kinases regulating p27 Kip1 turnover.
Collectively, our studies suggest that this parallel screening approach is robust and can be applied to fully understand kinase-ubiquitin pathway interactions.
Links
Where it is published
- Repository landing page tandf.figshare.com/articles/dataset/Screening_of_cell_cycle_fusion_proteins_to_id… ↗
landing page · from DataCite
- Repository landing page tandf.figshare.com/articles/dataset/Screening_of_cell_cycle_fusion_proteins_to_id… ↗
landing page · from DataCite
- DOI doi.org/10.6084/m9.figshare.1292440 ↗
DOI / persistent id · from DataCite
- DOI doi.org/10.6084/m9.figshare.1292440.v6 ↗
DOI / persistent id · from DataCite
Documentation and papers
- Creative Commons Attribution 4.0 International creativecommons.org/licenses/by/4.0/legalcode ↗
license · from DataCite
- IsSupplementTo 10.1080/15384101.2015.1006987 doi.org/10.1080/15384101.2015.1006987 ↗
publication · from DataCite
Catalogue records · 4
- DataCite API api.datacite.org/dois/10.6084/m9.figshare.1292440.v6 ↗
metadata API · from DataCite
- DataCite API api.datacite.org/dois/10.6084/m9.figshare.1292440 ↗
metadata API · from DataCite
- DataCite Commons commons.datacite.org/doi.org/10.6084/m9.figshare.1292440.v6 ↗
catalogue entry · from DataCite
- DataCite Commons commons.datacite.org/doi.org/10.6084/m9.figshare.1292440 ↗
catalogue entry · from DataCite
Topics
- Stated by source
- Biological sciences · Biological sciences · Chemical sciences · Chemical sciences · Clinical medicine · Clinical medicine · Computer and information sciences · Computer and information sciences · Health sciences · Health sciences
- From keywords
- Cancer · Cancer · Medicine & Health · Medicine & Health
Related
- Inverse of has versionScreening of cell cycle fusion proteins to identify kinase signaling networks
- Inverse of has versionScreening of cell cycle fusion proteins to identify kinase signaling networks
- Possibly the same asScreening of cell cycle fusion proteins to identify kinase signaling networks
- Inverse of has versionScreening of cell cycle fusion proteins to identify kinase signaling networks
- Possibly the same asScreening of cell cycle fusion proteins to identify kinase signaling networks
- Inverse of has versionScreening of Cell Cycle Fusion Proteins to Identify Kinase Signaling Networks
- Possibly the same asScreening of Cell Cycle Fusion Proteins to Identify Kinase Signaling Networks
- Inverse of has versionScreening of cell cycle fusion proteins to identify kinase signaling networks
- Possibly the same asScreening of cell cycle fusion proteins to identify kinase signaling networks
- Possibly the same asScreening of cell cycle fusion proteins to identify kinase signaling networks
Provenance · 2 source records, 22 field assertions
| Source | Key | Last seen | Raw |
|---|---|---|---|
| DataCite | 10.6084/m9.figshare.1292440 | 12 d ago | JSON v1 |
| DataCite | 10.6084/m9.figshare.1292440.v6 | 12 d ago | JSON v1 |
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