首页> 外文期刊>Journal of the American Chemical Society >Ground State Destabilization in Uracil DNA Glycosylase: Let's Not Forget 'Tautomeric Strain' in Substrates
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Ground State Destabilization in Uracil DNA Glycosylase: Let's Not Forget 'Tautomeric Strain' in Substrates

机译:尿嘧啶DNA糖基化酶中的基态不稳定:让我们不要忘记底物中的“互变异构株”

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Enzymes like uracil DNA glycosylase (UDG) can achieve ground state destabilization, by polarizing substrates to mimic rare tautomers. On the basis of computed nucleus independent chemical shifts, NICS(1)(zz), and harmonic oscillator model of electron delocalization (HOMED) analyses, of quantum mechanics (QM) and quantum mechanics/molecular mechanics (QM/MM) models of the UDG active site, uracil is strongly polarized when bound to UDG and resembles a tautomer >12 kcal/mol higher in energy. Natural resonance theory (NRT) analyses identified a dominant O2 imidate resonance form for residue bound 1-methyluracil. This "tautomeric strain" raises the energy of uracil, making uracilate a better than expected leaving group. Computed gas-phase S(N)2 reactions of free and hydrogen bonded 1-methyl-uracil demonstrate the relationship between the degree of polarization in uracil and the leaving group ability of uracilate.
机译:诸如尿嘧啶DNA糖基化酶(UDG)之类的酶可以通过极化底物以模拟稀有互变异构体,从而实现基态不稳定。基于计算的原子核独立化学位移,NICS(1)(zz)和电子离域(HOMED)分析的谐波振荡器模型,量子力学(QM)和量子力学/分子力学(QM / MM)模型的谐波振荡器模型在UDG的活性位点,尿嘧啶与UDG结合时强烈极化,并且与互变异构体的能量相似,后者的能量高12 kcal / mol以上。自然共振理论(NRT)分析确定了残基结合的1-甲基尿嘧啶的主要O2亚氨酸酯共振形式。这种“互变异构株”提高了尿嘧啶的能量,使尿嘧啶成为比预期的离去基团更好的物质。游离和氢键合的1-甲基-尿嘧啶的气相S(N)2计算结果表明,尿嘧啶的极化程度与尿嘧啶的离去基团能力之间存在关系。

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