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DESCRIPTION (provided by applicant): Rapid changes in cell physiology during cell cycle transitions or in response to changes in external conditions are often mediated by the degradation of regulatory molecules. These changes are typically directed by the modification of protein targets with chains of the small protein ubiquitin. Ubiquitinization is carried out by a series of three enzymes, sometimes referred to as E1, E2 and E3, which function in tandem to transfer ubiquitin to a substrate. Substrate specificity is usually mediated by the E3 complex, also called an ubiquitin ligase. The SCF and the APC represent two highly conserved multi-subunit ubiquitin ligases important for both cell cycle progression and the regulation of many aspects of cellular physiology. We will examine mechanisms of APC regulation, and also identify the substrates other ubiquitin ligases using a biochemical technique that we have recently developed. Finally, we will explore the turnover of one ubiquitin ligase substrate, a G1 cyclin, in greater detail.
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Cdc20, an activator at last.
Cdc20,终于成为激活剂。
DOI: 10.1016/j.molcel.2008.11.006
发表时间: 2008
期刊: Molecular cell
影响因子: 16
作者: [Benanti,JenniferA, Toczyski,DavidP]
通讯作者: Toczyski,DavidP
DOI: 10.1371/journal.pgen.1002851
发表时间: 2012
期刊: PLoS genetics
影响因子: 4.5
作者: [Landry BD, Doyle JP, Toczyski DP, Benanti JA]
通讯作者: Benanti JA
DOI: 10.1016/j.molcel.2013.12.003
发表时间: 2014-01-09
期刊: MOLECULAR CELL
影响因子: 16
作者: [Mark, Kevin G., Simonetta, Marco, Maiolica, Alessio, Seller, Charles A., Toczyski, David P.]
通讯作者: Toczyski, David P.
Characterizing the role of RNF25 in repair of DNA alkylation in blood cancers
Characterizing the role of RNF25 in repair of DNA alkylation in blood cancers
Regulation by post-translation modifications in response to stress
Regulation by post-translation modifications in response to stress
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