| Literature DB >> 29746236 |
Andrey G Baranovskiy1, Hollie M Siebler2, Youri I Pavlov3, Tahir H Tahirov4.
Abstract
Research during the past decade witnessed the discovery of [4Fe-4S] clusters in several members of the eukaryotic DNA replication machinery. The presence of clusters was confirmed by UV-visible absorption, electron paramagnetic resonance spectroscopy, and metal analysis for primase and the B-family DNA polymerases δ and ζ. The crystal structure of primase revealed that the [4Fe-4S] cluster is buried inside the protein and fulfills a structural role. Although [4Fe-4S] clusters are firmly established in the C-terminal domains of catalytic subunits of DNA polymerases δ and ζ, no structures are currently available and their precise roles have not been ascertained. The [4Fe-4S] clusters in the polymerases and primase play a structural role ensuring proper protein folding and stability. In DNA polymerases δ and ζ, they can potentially play regulatory role by sensing hurdles during DNA replication and assisting with DNA polymerase switches by oscillation between oxidized-reduced states.Entities:
Keywords: B-subunit; Crystal structure; DNA polymerase; DNA replication; Iron–sulfur cluster; Primase
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Year: 2017 PMID: 29746236 PMCID: PMC5947875 DOI: 10.1016/bs.mie.2017.09.003
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600