4XPE
Crystal structure of 5'-CTTATGGGCCCATAAG in a host-guest complex
4XPE の概要
エントリーDOI | 10.2210/pdb4xpe/pdb |
関連するPDBエントリー | 4XNO 4XO0 4XPC |
分子名称 | reverse transcriptase, DNA (5'-D(*CP*TP*TP*AP*TP*GP*GP*G)-3'), DNA (5'-D(P*CP*CP*CP*AP*TP*AP*AP*G)-3'), ... (5 entities in total) |
機能のキーワード | host-guest complex, b-dna, non-natural nucleobase pair, synthetic biology, transferase-dna complex, transferase/dna |
由来する生物種 | Moloney murine leukemia virus (isolate Shinnick) (MoMLV) 詳細 |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 34325.12 |
構造登録者 | |
主引用文献 | Georgiadis, M.M.,Singh, I.,Kellett, W.F.,Hoshika, S.,Benner, S.A.,Richards, N.G. Structural basis for a six nucleotide genetic alphabet. J. Am. Chem. Soc., 137:6947-6955, 2015 Cited by PubMed Abstract: Expanded genetic systems are most likely to work with natural enzymes if the added nucleotides pair with geometries that are similar to those displayed by standard duplex DNA. Here, we present crystal structures of 16-mer duplexes showing this to be the case with two nonstandard nucleobases (Z, 6-amino-5-nitro-2(1H)-pyridone and P, 2-amino-imidazo[1,2-a]-1,3,5-triazin-4(8H)one) that were designed to form a Z:P pair with a standard "edge on" Watson-Crick geometry, but joined by rearranged hydrogen bond donor and acceptor groups. One duplex, with four Z:P pairs, was crystallized with a reverse transcriptase host and adopts primarily a B-form. Another contained six consecutive Z:P pairs; it crystallized without a host in an A-form. In both structures, Z:P pairs fit canonical nucleobase hydrogen-bonding parameters and known DNA helical forms. Unique features include stacking of the nitro group on Z with the adjacent nucleobase ring in the A-form duplex. In both B- and A-duplexes, major groove widths for the Z:P pairs are approximately 1 Å wider than those of comparable G:C pairs, perhaps to accommodate the large nitro group on Z. Otherwise, ZP-rich DNA had many of the same properties as CG-rich DNA, a conclusion supported by circular dichroism studies in solution. The ability of standard duplexes to accommodate multiple and consecutive Z:P pairs is consistent with the ability of natural polymerases to biosynthesize those pairs. This, in turn, implies that the GACTZP synthetic genetic system can explore the entire expanded sequence space that additional nucleotides create, a major step forward in this area of synthetic biology. PubMed: 25961938DOI: 10.1021/jacs.5b03482 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.78 Å) |
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