2LBY
G-quadruplex structure formed at the 5'-end of NHEIII_1 element in human c-MYC promoter
Summary for 2LBY
| Entry DOI | 10.2210/pdb2lby/pdb |
| Related | 1XAV 2F8U 2L7V 2M27 |
| NMR Information | BMRB: 17580 |
| Descriptor | DNA (5'-D(*TP*AP*GP*GP*GP*AP*GP*GP*GP*TP*AP*GP*GP*GP*AP*GP*GP*GP*T)-3') (1 entity in total) |
| Functional Keywords | dna, g-quadruplex, c-myc |
| Total number of polymer chains | 1 |
| Total formula weight | 6070.92 |
| Authors | Mathad, R.,Hatzakis, E.,Yang, D. (deposition date: 2011-04-07, release date: 2012-02-22, Last modification date: 2024-05-15) |
| Primary citation | Mathad, R.I.,Hatzakis, E.,Dai, J.,Yang, D. c-MYC promoter G-quadruplex formed at the 5'-end of NHE III1 element: insights into biological relevance and parallel-stranded G-quadruplex stability. Nucleic Acids Res., 39:9023-9033, 2011 Cited by PubMed Abstract: We studied the structures and stabilities of G-quadruplexes formed in Myc1234, the region containing the four consecutive 5' runs of guanines of c-MYC promoter NHE III(1,) which have recently been shown to form in a supercoiled plasmid system in aqueous solution. We determined the NMR solution structure of the 1:2:1 parallel-stranded loop isomer, one of the two major loop isomers formed in Myc1234 in K(+) solution. This major loop isomer, although sharing the same folding structure, appears to be markedly less stable than the major loop isomer formed in the single-stranded c-MYC NHE III(1) oligonucleotide, the Myc2345 G-quadruplex. Our NMR structures indicated that the different thermostabilities of the two 1:2:1 parallel c-MYC G-quadruplexes are likely caused by the different base conformations of the single nucleotide loops. The observation of the formation of the Myc1234 G-quadruplex in the supercoiled plasmid thus points to the potential role of supercoiling in the G-quadruplex formation in promoter sequences. We also performed a systematic thermodynamic analysis of modified c-MYC NHE III(1) sequences, which provided quantitative measure of the contributions of various loop sequences to the thermostabilities of parallel-stranded G-quadruplexes. This information is important for understanding the equilibrium of promoter G-quadruplex loop isomers and for their drug targeting. PubMed: 21795379DOI: 10.1093/nar/gkr612 PDB entries with the same primary citation |
| Experimental method | SOLUTION NMR |
Structure validation
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