| Literature DB >> 12379844 |
Alba Guarné1, Qinghai Zhao, Rodolfo Ghirlando, Wei Yang.
Abstract
The SeqA protein binds clusters of fully methylated or hemimethylated GATC sequences at oriC and negatively modulates the initiation of DNA replication. We find that SeqA can be proteolytically cleaved into an N-terminal multimerization and a C-terminal DNA-binding domain and have determined the crystal structure of the C-terminal domain in complex with a hemimethylated GATC site. SeqA makes direct hydrogen bonds and van der Waals contacts with the hemimethylated A-T base pair in addition to interactions with the surrounding bases and DNA backbone. The tetrameric protein-DNA complex found in the crystal suggests that SeqA binds multiple GATC sites on separate DNA duplexes, altering the overall DNA topology and sequestering oriC from replication initiation.Entities:
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Year: 2002 PMID: 12379844 DOI: 10.1038/nsb857
Source DB: PubMed Journal: Nat Struct Biol ISSN: 1072-8368