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首页> 外文期刊>Chemistry: A European journal >Anion-π Interactions in Flavoproteins Involve a Substantial Charge-Transfer Component
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Anion-π Interactions in Flavoproteins Involve a Substantial Charge-Transfer Component

机译:黄曲霉素中的阴离子-π相互作用涉及大量电荷转移组分

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摘要

Anion-π interactions have been shown to stabilize flavoproteins and to regulate the redox potential of the flavin cofactor. They are commonly attributed to electrostatic forces. Herein we show that anion-flavin interactions can have a substantial charge-transfer component. Our conclusion emanates from a multi-approach theoretical analysis and is backed by previously reported observations of absorption bands, originating from charge transfer between oxidized flavin and proximate cysteine thiolate groups. This partial covalency of anion-flavin contacts renders classical simulations of flavoproteins questionable.
机译:已经显示阴离子-π相互作用以稳定黄酮蛋白并调节黄蛋白辅因子的氧化还原电位。 它们通常归因于静电力。 在此表明阴离子 - 黄素相互作用可以具有大量电荷转移组分。 我们的结论从多方法的理论分析中散发出来,通过先前报道的吸收带的观察来支持,来自氧化的黄素和近半胱氨酸硫酸盐基团之间的电荷转移。 阴离子 - 黄素接触的这种部分共价使黄酮蛋白的典型模拟可疑。

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