6M4T
U shaped head to head four-way junction in d(TTCTGCTGCTGAA) sequence
Summary for 6M4T
| Entry DOI | 10.2210/pdb6m4t/pdb |
| Descriptor | DNA (5'-D(P*(UD)P*TP*CP*TP*GP*CP*TP*GP*CP*TP*GP*AP*A)-3'), COBALT (II) ION, N4-[4-[(6-chloranyl-2-methoxy-acridin-9-yl)amino]butyl]-1,3,5-triazine-2,4,6-triamine, ... (4 entities in total) |
| Functional Keywords | t:t mismatch, ctg repeat, four-way junction, triaminotriazine-acridine conjugate, dna |
| Biological source | synthetic construct |
| Total number of polymer chains | 4 |
| Total formula weight | 18081.20 |
| Authors | Hou, M.H.,Chien, C.M.,Satange, R.B.,Wu, P.C. (deposition date: 2020-03-09, release date: 2020-07-15, Last modification date: 2024-03-27) |
| Primary citation | Chien, C.M.,Wu, P.C.,Satange, R.,Chang, C.C.,Lai, Z.L.,Hagler, L.D.,Zimmerman, S.C.,Hou, M.H. Structural Basis for Targeting T:T Mismatch with Triaminotriazine-Acridine Conjugate Induces a U-Shaped Head-to-Head Four-Way Junction in CTG Repeat DNA. J.Am.Chem.Soc., 142:11165-11172, 2020 Cited by PubMed Abstract: The potent DNA-binding compound triaminotriazine-acridine conjugate (Z1) functions by targeting T:T mismatches in CTG trinucleotide repeats that are responsible for causing neurological diseases such as myotonic dystrophy type 1, but its binding mechanism remains unclear. We solved a crystal structure of Z1 in a complex with DNA containing three consecutive CTG repeats with three T:T mismatches. Crystallographic studies revealed that direct intercalation of two Z1 molecules at both ends of the CTG repeat induces thymine base flipping and DNA backbone deformation to form a four-way junction. The core of the complex unexpectedly adopts a U-shaped head-to-head topology to form a crossover of each chain at the junction site. The crossover junction is held together by two stacked G:C pairs at the central core that rotate with respect to each other in an X-shape to form two nonplanar minor-groove-aligned G·C·G·C tetrads. Two stacked G:C pairs on both sides of the center core are involved in the formation of pseudo-continuous duplex DNA. Four metal-mediated base pairs are observed between the N7 atoms of G and Co, an interaction that strongly preserves the central junction site. Beyond revealing a new type of ligand-induced, four-way junction, these observations enhance our understanding of the specific supramolecular chemistry of Z1 that is essential for the formation of a noncanonical DNA superstructure. The structural features described here serve as a foundation for the design of new sequence-specific ligands targeting mismatches in the repeat-associated structures. PubMed: 32478511DOI: 10.1021/jacs.0c03591 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.55 Å) |
Structure validation
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