2A5P
Monomeric parallel-stranded DNA tetraplex with snap-back 3+1 3' G-tetrad, single-residue chain reversal loops, GAG triad in the context of GAAG diagonal loop, NMR, 8 struct.
Summary for 2A5P
Entry DOI | 10.2210/pdb2a5p/pdb |
Related | 1D6D 1EEG 1JJP 1Y8D 2A5R |
Descriptor | 5'-D(*TP*GP*AP*GP*GP*GP*TP*GP*GP*IP*GP*AP*GP*GP*GP*TP*GP*GP*GP*GP*AP*AP*GP*G)-3' (1 entity in total) |
Functional Keywords | monomeric parallel-stranded quadruplex; c-myc promoter 3+1 g-tetrad; single nucleotide chain reversal loop; gag triad; gaag loop, dna |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 7701.93 |
Authors | Phan, A.T.,Kuryavyi, V.V.,Gaw, H.Y.,Patel, D.J. (deposition date: 2005-06-30, release date: 2005-07-26, Last modification date: 2024-05-22) |
Primary citation | Phan, A.T.,Kuryavyi, V.,Gaw, H.Y.,Patel, D.J. Small-molecule interaction with a five-guanine-tract G-quadruplex structure from the human MYC promoter. Nat.Chem.Biol., 1:167-173, 2005 Cited by PubMed Abstract: It has been widely accepted that DNA can adopt other biologically relevant structures beside the Watson-Crick double helix. One recent important example is the guanine-quadruplex (G-quadruplex) structure formed by guanine tracts found in the MYC (or c-myc) promoter region, which regulates the transcription of the MYC oncogene. Stabilization of this G-quadruplex by ligands, such as the cationic porphyrin TMPyP4, decreases the transcriptional level of MYC. Here, we report the first structure of a DNA fragment containing five guanine tracts from this region. An unusual G-quadruplex fold, which was derived from NMR restraints using unambiguous model-independent resonance assignment approaches, involves a core of three stacked guanine tetrads formed by four parallel guanine tracts with all anti guanines and a snapback 3'-end syn guanine. We have determined the structure of the complex formed between this G-quadruplex and TMPyP4. This structural information, combined with details of small-molecule interaction, provides a platform for the design of anticancer drugs targeting multi-guanine-tract sequences that are found in the MYC and other oncogenic promoters, as well as in telomeres. PubMed: 16408022DOI: 10.1038/nchembio723 PDB entries with the same primary citation |
Experimental method | SOLUTION NMR |
Structure validation
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