Data on the kinetics of in vitro assembled chromatin.

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This system allows easy manipulation of distinct aspects of chromatin assembly such as post-translational histone modifications, the levels of histone chaperones and the concentration of distinct DNA binding factors. In total, 480 proteins have been quantified as chromatin enriched factors and their binding kinetics have been monitored in the time course of 15 min, 1 h and 4 h of chromatin assembly. The data accompanying the manuscript on this approach, Völker-Albert et al., 2016 \"A quantitative proteomic analysis of in vitro assembled chromatin\" [1], has been deposited to the ProteomeXchange Consortium (http://www.proteomexchange.org) via the PRIDE partner repository with the dataset identifier submission number PRIDE: PXD002537 and PRIDE: PXD003445.", "claims": [{"id": "claim-method", "statement": "Data were searched against a combined forward/reversed database (special amino acids: KR) including common contaminants for false-discovery rate filtering of peptide and protein identifications (Dmel_all translation r5.57, 30305 entries).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:27331114", "locator": "sections[12] \"Data analysis of data-dependent LC–MS experiments\" paragraph 2", "quote": "Data were searched against a combined forward/reversed database (special amino acids: KR) including common contaminants for false-discovery rate filtering of peptide and protein identifications (Dmel_all translation r5.57, 30305 entries)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Data is within this article and uploaded to the ProteomeXchange Consortium webpage. 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