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A chemical biology approach to decipher chromatin ubiquitylation by RNF168

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A chemical biology approach to decipher chromatin ubiquitylation by RNF168

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Histone monoubiquitylation position determines specificity and direction of enzymatic cross-talk with histone methyltransferases Dot1L and PRC2

The Size of the Proteasomal Substrate Determines Whether Its Degradation Will Be Mediated by Mono- or Polyubiquitylation

Stability of Nucleosomes Containing Homogenously Ubiquitylated H2A and H2B Prepared Using Semisynthesis

Rad51 paralogues Rad55-Rad57 balance the antirecombinase Srs2 in Rad51 filament formation

Histone H2B ubiquitylation disrupts local and higher-order chromatin compaction