INO80 and SWR complexes: relating structure to function in chromatin remodeling
Trends in Cell Biology, ISSN: 0962-8924, Vol: 24, Issue: 11, Page: 619-631
2014
- 89Citations
- 222Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations89
- Citation Indexes89
- 89
- CrossRef85
- Captures222
- Readers222
- 222
- Mentions1
- Blog Mentions1
- Blog1
Review Description
Virtually all DNA-dependent processes require selective and controlled access to the DNA sequence. Governing this access are sophisticated molecular machines, nucleosome remodelers, which regulate the composition and structure of chromatin, allowing conversion from open to closed states. In most cases these multisubunit remodelers operate in concert to organize chromatin structure by depositing, moving, evicting, or selectively altering nucleosomes in an ATP-dependent manner. Despite sharing a conserved domain architecture, chromatin remodelers differ significantly in how they bind to their nucleosomal substrates. Recent structural studies link specific interactions between nucleosomes and remodelers to the diverse tasks they carry out. We review here insights into the modular organization of the INO80 family of nucleosome remodelers. Understanding their structural diversity will help to shed light on how these related ATPases modify their nucleosomal substrates.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0962892414001019; http://dx.doi.org/10.1016/j.tcb.2014.06.004; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84925397108&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/25088669; https://linkinghub.elsevier.com/retrieve/pii/S0962892414001019; https://dx.doi.org/10.1016/j.tcb.2014.06.004
Elsevier BV
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