1MHT
COVALENT TERNARY STRUCTURE OF HHAI METHYLTRANSFERASE, DNA AND S-ADENOSYL-L-HOMOCYSTEINE
Summary for 1MHT
Entry DOI | 10.2210/pdb1mht/pdb |
Descriptor | DNA (5'-D(P*GP*AP*TP*AP*GP*(C36)P*GP*CP*TP*AP*TP*C)-3'), DNA (5'-D(*TP*GP*AP*TP*AP*GP*(C36)P*GP*CP*TP*AP*TP*C)-3'), PROTEIN (HHAI METHYLTRANSFERASE), ... (4 entities in total) |
Functional Keywords | protein-dna complex, double helix, overhanging base, flipped-out base, modified, transferase-dna complex, transferase/dna |
Biological source | Haemophilus haemolyticus |
Total number of polymer chains | 3 |
Total formula weight | 45155.68 |
Authors | Cheng, X. (deposition date: 1994-12-08, release date: 1995-06-03, Last modification date: 2018-04-18) |
Primary citation | Klimasauskas, S.,Kumar, S.,Roberts, R.J.,Cheng, X. HhaI methyltransferase flips its target base out of the DNA helix. Cell(Cambridge,Mass.), 76:357-369, 1994 Cited by PubMed Abstract: The crystal structure has been determined at 2.8 A resolution for a chemically-trapped covalent reaction intermediate between the HhaI DNA cytosine-5-methyltransferase, S-adenosyl-L-homocysteine, and a duplex 13-mer DNA oligonucleotide containing methylated 5-fluorocytosine at its target. The DNA is located in a cleft between the two domains of the protein and has the characteristic conformation of B-form DNA, except for a disrupted G-C base pair that contains the target cytosine. The cytosine residue has swung completely out of the DNA helix and is positioned in the active site, which itself has undergone a large conformational change. The DNA is contacted from both the major and the minor grooves, but almost all base-specific interactions between the enzyme and the recognition bases occur in the major groove, through two glycine-rich loops from the small domain. The structure suggests how the active nucleophile reaches its target, directly supports the proposed mechanism for cytosine-5 DNA methylation, and illustrates a novel mode of sequence-specific DNA recognition. PubMed: 8293469DOI: 10.1016/0092-8674(94)90342-5 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.6 Å) |
Structure validation
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