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8URK

Crystal structure of DNA N6-Adenine Methyltransferase M.BceJIV from Burkholderia cenocepacia in complex with duplex DNA substrates

Summary for 8URK
Entry DOI10.2210/pdb8urk/pdb
Related PRD IDPRD_900003
DescriptorMethyltransferase, DNA1, DNA2, ... (7 entities in total)
Functional Keywordsdna n6-adenine methyltransferase, m.bcejiv, burkholderia cenocepacia, dna binding protein
Biological sourceBurkholderia cenocepacia
More
Total number of polymer chains12
Total formula weight162645.53
Authors
Kottur, J.,Quintana-Feliciano, R.,Aggarwal, A.K. (deposition date: 2023-10-26, release date: 2024-09-11, Last modification date: 2024-09-25)
Primary citationQuintana-Feliciano, R.,Kottur, J.,Ni, M.,Ghosh, R.,Salas-Estrada, L.,Ahlsen, G.,Rechkoblit, O.,Shapiro, L.,Filizola, M.,Fang, G.,Aggarwal, A.K.
Burkholderia cenocepacia epigenetic regulator M.BceJIV simultaneously engages two DNA recognition sequences for methylation.
Nat Commun, 15:7839-7839, 2024
Cited by
PubMed Abstract: Burkholderia cenocepacia is an opportunistic and infective bacterium containing an orphan DNA methyltransferase called M.BceJIV with roles in regulating gene expression and motility of the bacterium. M.BceJIV recognizes a GTWWAC motif (where W can be an adenine or a thymine) and methylates N6 of the adenine at the fifth base position. Here, we present crystal structures of M.BceJIV/DNA/sinefungin ternary complex and allied biochemical, computational, and thermodynamic analyses. Remarkably, the structures show not one, but two DNA substrates bound to the M.BceJIV dimer, with each monomer contributing to the recognition of two recognition sequences. We also show that methylation at the two recognition sequences occurs independently, and that the GTWWAC motifs are enriched in intergenic regions in the genomes of B. cenocepacia strains. We further computationally assess the interactions underlying the affinities of different ligands (SAM, SAH, and sinefungin) for M.BceJIV, as a step towards developing selective inhibitors for limiting B. cenocepacia infection.
PubMed: 39244607
DOI: 10.1038/s41467-024-52130-x
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.11 Å)
Structure validation

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건을2024-11-13부터공개중

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