5HHI
Structure of human DNA polymerase beta Host-Guest complexed with CBZ-platinated N7-G
5HHI の概要
| エントリーDOI | 10.2210/pdb5hhi/pdb |
| 関連するPDBエントリー | 5HHH |
| 分子名称 | DNA polymerase beta, DNA (5'-D(*CP*CP*GP*AP*CP*GP*GP*AP*GP*GP*AP*GP*CP*AP*GP*G)-3'), DNA (5'-D(P*CP*CP*TP*GP*CP*TP*CP*CP*TP*C)-3'), ... (7 entities in total) |
| 機能のキーワード | transferase, lyase-dna complex, lyase/dna |
| 由来する生物種 | Homo sapiens (Human) 詳細 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 47520.79 |
| 構造登録者 | |
| 主引用文献 | Cheun, Y.,Koag, M.C.,Naguib, Y.W.,Ouzon-Shubeita, H.,Cui, Z.,Pakotiprapha, D.,Lee, S. Synthesis, structure, and biological evaluation of a platinum-carbazole conjugate. Chem Biol Drug Des, 91:116-125, 2018 Cited by PubMed Abstract: Cisplatin resistance is caused, in part, by the efficient removal of the helix-distorting cisplatin 1,2-intrastrand cross-links by nucleotide excision repair (NER) machinery. To make a platinum-DNA adduct that causes less helical distortion than the cisplatin 1,2-intrastrand adduct, we designed and synthesized a monofunctional platinum-carbazole conjugate (carbazoplatin). The 2.5 Å crystal structure of carbazoplatin-DNA adduct revealed both the monoplatination of the N7 of a guanine (G) base and the intercalation into two G:C base pairs, while causing a minor distortion of the DNA helix. A 50-mer dsDNA containing a single carbazoplatin lesion was poorly processed by UvrABC endonuclease, the prokaryotic NER machinery that detects helical distortion and performs dual incision around the lesion. Our cell viability assay indicated that the cytotoxic pathways of carbazoplatin might be different from those of cisplatin; carbazoplatin was 5-8 times more cytotoxic than cisplatin against PANC-1 and MDA-MB-231 cancer cell lines. PubMed: 28649747DOI: 10.1111/cbdd.13062 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.517 Å) |
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