5YZE
Crystal structure of the [Co2+-(chromomycin A3)2]-d(CCG)3 complex
5YZE の概要
| エントリーDOI | 10.2210/pdb5yze/pdb |
| 分子名称 | DNA (5'-D(*TP*CP*CP*GP*CP*CP*GP*CP*CP*GP*A)-3'), 3-C-methyl-4-O-acetyl-alpha-L-Olivopyranose-(1-3)-(2R,5S,6R)-6-methyltetrahydro-2H-pyran-2,5-diol-(1-3)-(2R,5S,6R)-6-methyltetrahydro-2H-pyran-2,5-diol, 2,6-dideoxy-4-O-methyl-alpha-D-galactopyranose-(1-3)-(2R,3R,6R)-6-hydroxy-2-methyltetrahydro-2H-pyran-3-yl acetate, ... (6 entities in total) |
| 機能のキーワード | drug-dna complex, chromomycin a3, ccg repeats, i-motif, flipout, dna, antibiotics-dna complex, antibiotics/dna |
| 由来する生物種 | synthetic construct |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 9109.66 |
| 構造登録者 | |
| 主引用文献 | Chen, Y.W.,Satange, R.,Wu, P.C.,Jhan, C.R.,Chang, C.K.,Chung, K.R.,Waring, M.J.,Lin, S.W.,Hsieh, L.C.,Hou, M.H. CoII(Chromomycin)2 Complex Induces a Conformational Change of CCG Repeats from i-Motif to Base-Extruded DNA Duplex Int J Mol Sci, 19:-, 2018 Cited by PubMed Abstract: We have reported the propensity of a DNA sequence containing CCG repeats to form a stable i-motif tetraplex structure in the absence of ligands. Here we show that an i-motif DNA sequence may transition to a base-extruded duplex structure with a GGCC tetranucleotide tract when bound to the (Co)-mediated dimer of chromomycin A3, Co(Chro)₂. Biophysical experiments reveal that CCG trinucleotide repeats provide favorable binding sites for Co(Chro)₂. In addition, water hydration and divalent metal ion (Co) interactions also play a crucial role in the stabilization of CCG trinucleotide repeats (TNRs). Our data furnish useful structural information for the design of novel therapeutic strategies to treat neurological diseases caused by repeat expansions. PubMed: 30227633DOI: 10.3390/ijms19092796 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.87 Å) |
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