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4RTM

Complex of Escherichia coli DNA Adenine Methyltransferase (DAM) with AdoMet and with DNA Containing Distal Pap Regulon Sequence

Summary for 4RTM
Entry DOI10.2210/pdb4rtm/pdb
Related2G1P 2ORE 4RTJ 4RTK 4RTL 4RTN 4RTO 4RTP 4RTQ 4RTR 4RTS
DescriptorDNA adenine methylase, DNA (5'-D(*TP*CP*TP*AP*AP*AP*GP*AP*TP*CP*G)-3'), DNA (5'-D(*AP*CP*GP*AP*TP*CP*TP*TP*TP*AP*G)-3'), ... (5 entities in total)
Functional Keywordsdam methylation, gatc recognition, base flipping, bacterial virulence, methylation-independent transcriptional repressor, transferase-dna complex, transferase/dna
Biological sourceEscherichia coli
More
Total number of polymer chains3
Total formula weight41434.83
Authors
Horton, J.R.,Cheng, X. (deposition date: 2014-11-15, release date: 2015-04-15, Last modification date: 2023-09-20)
Primary citationHorton, J.R.,Zhang, X.,Blumenthal, R.M.,Cheng, X.
Structures of Escherichia coli DNA adenine methyltransferase (Dam) in complex with a non-GATC sequence: potential implications for methylation-independent transcriptional repression.
Nucleic Acids Res., 43:4296-4308, 2015
Cited by
PubMed Abstract: DNA adenine methyltransferase (Dam) is widespread and conserved among the γ-proteobacteria. Methylation of the Ade in GATC sequences regulates diverse bacterial cell functions, including gene expression, mismatch repair and chromosome replication. Dam also controls virulence in many pathogenic Gram-negative bacteria. An unexplained and perplexing observation about Escherichia coli Dam (EcoDam) is that there is no obvious relationship between the genes that are transcriptionally responsive to Dam and the promoter-proximal presence of GATC sequences. Here, we demonstrate that EcoDam interacts with a 5-base pair non-cognate sequence distinct from GATC. The crystal structure of a non-cognate complex allowed us to identify a DNA binding element, GTYTA/TARAC (where Y = C/T and R = A/G). This element immediately flanks GATC sites in some Dam-regulated promoters, including the Pap operon which specifies pyelonephritis-associated pili. In addition, Dam interacts with near-cognate GATC sequences (i.e. 3/4-site ATC and GAT). Taken together, these results imply that Dam, in addition to being responsible for GATC methylation, could also function as a methylation-independent transcriptional repressor.
PubMed: 25845600
DOI: 10.1093/nar/gkv251
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

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