盒子外:关于P4 atp酶磷脂易位的最新消息。

Journal of Chemical Biology Pub Date : 2012-07-15 Print Date: 2012-10-01 DOI:10.1007/s12154-012-0078-x
Alex Stone, Patrick Williamson
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引用次数: 18

摘要

p型atp酶的P4亚家族包括磷脂转运蛋白。在膜上移动如此庞大的两亲性底物分子会产生独特的机制问题。最近,来自三个不同实验室的三篇论文对其中的一些问题提出了见解。这些实验的一个影响将是点燃一场关于底物通过酶的途径的健康辩论。第二个影响是为关键底物结合位点提出了一个反直觉的模型。通过具体的假设,为研究这些蛋白质的作用机制奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Outside of the box: recent news about phospholipid translocation by P4 ATPases.

The P4 subfamily of P-type ATPases includes phospholipid transporters. Moving such bulky amphipathic substrate molecules across the membrane poses unique mechanistic problems. Recently, three papers from three different laboratories have offered insights into some of these problems. One effect of these experiments will be to ignite a healthy debate about the path through the enzyme taken by the substrate. A second effect is to suggest a counterintuitive model for the critical substrate-binding site. By putting concrete hypotheses into play, these papers finally provide a foundation for investigations of mechanism for these proteins.

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