PMID:12379844: Difference between revisions

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<span style = 'font-size: large'> '''Guarné, A, Zhao, Q, Ghirlando, R and Yang, W'''  (2002) Insights into negative modulation of E. coli replication initiation from the structure of SeqA-hemimethylated DNA complex.''Nat. Struct. Biol.'' '''9''':839-43</span>
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|{{TableHeadingColor}} |'''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.
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'''No author listed'''  (2002) Insights into negative modulation of E. coli replication initiation from the structure of SeqA-hemimethylated DNA complex. ''Nat. Struct. Biol.'' '''9''':839-43
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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.
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12379844 PubMed]
Online version:[http://dx.doi.org/10.1038/nsb857 10.1038/nsb857]
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|{{TableHeadingColor}} nowrap |'''Links''' ||  [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12379844 PubMed]
!align=left  |Keywords
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Bacterial Outer Membrane Proteins; Crystallography, X-Ray; DNA Methylation; DNA Replication/physiology; DNA, Bacterial/biosynthesis; DNA, Bacterial/chemistry; DNA, Bacterial/metabolism; DNA-Binding Proteins; Escherichia coli/genetics; Escherichia coli/physiology; Escherichia coli Proteins/chemistry; Escherichia coli Proteins/metabolism; Models, Molecular; Nucleic Acid Conformation; Protein Binding; Protein Structure, Tertiary; Recombinant Proteins/chemistry; Replication Origin; Transcription Factors/chemistry; Transcription Factors/metabolism
 
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==Significance {{HelpIcon|Help:Literature}} ==
==Significance {{HelpIcon|Help:Literature}} ==
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Revision as of 18:15, 1 September 2013

Citation

No author listed (2002) Insights into negative modulation of E. coli replication initiation from the structure of SeqA-hemimethylated DNA complex. Nat. Struct. Biol. 9:839-43

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.

Links

PubMed Online version:10.1038/nsb857

Keywords

Bacterial Outer Membrane Proteins; Crystallography, X-Ray; DNA Methylation; DNA Replication/physiology; DNA, Bacterial/biosynthesis; DNA, Bacterial/chemistry; DNA, Bacterial/metabolism; DNA-Binding Proteins; Escherichia coli/genetics; Escherichia coli/physiology; Escherichia coli Proteins/chemistry; Escherichia coli Proteins/metabolism; Models, Molecular; Nucleic Acid Conformation; Protein Binding; Protein Structure, Tertiary; Recombinant Proteins/chemistry; Replication Origin; Transcription Factors/chemistry; Transcription Factors/metabolism

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