Ontology highlight
ABSTRACT:
SUBMITTER: Garske AL
PROVIDER: S-EPMC2922993 | biostudies-literature | 2010 Apr
REPOSITORIES: biostudies-literature
Garske Adam L AL Oliver Samuel S SS Wagner Elise K EK Musselman Catherine A CA LeRoy Gary G Garcia Benjamin A BA Kutateladze Tatiana G TG Denu John M JM
Nature chemical biology 20100228 4
Specific interactions between post-translational modifications (PTMs) and chromatin-binding proteins are central to the idea of a 'histone code'. Here, we used a 5,000-member, PTM-randomized, combinatorial peptide library based on the N terminus of histone H3 to interrogate the multisite specificity of six chromatin binding modules, which read the methylation status of Lys4. We found that Thr3 phosphorylation, Arg2 methylation and Thr6 phosphorylation are critical additional PTMs that modulate t ...[more]