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The Structure of Human 5-Lipoxygenase

机译:人5-脂氧合酶的结构

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摘要

The synthesis of both proinflammatory leukotrienes and anti-inflammatory lipoxins requires the enzyme 5-lipoxygenase (5-LOX). 5-LOX activity is short-lived, apparently in part because of an intrinsic instability of the enzyme. We identified a 5-LOX-specific destabilizing sequence that is involved in orienting the carboxyl terminus, which binds the catalytic iron. Here, we report the crystal structure at 2.4 angstrom resolution of human 5-LOX stabilized by replacement of this sequence.
机译:促炎性白三烯和抗炎脂蛋白的合成都需要酶5-脂氧合酶(5-LOX)。 5-LOX活性是短暂的,显然部分是由于该酶固有的不稳定性。我们确定了一个5-LOX特定的去稳定序列,该序列与定向结合催化铁的羧基末端有关。在这里,我们报告通过替换此序列稳定的人类5-LOX在2.4埃分辨率的晶体结构。

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  • 来源
    《Science》 |2011年第6014期|p.217-219|共3页
  • 作者单位

    Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA;

    Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA;

    Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA;

    Northeastern Collaborative Access Team, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439, USA;

    Department of Pharmacology, Vanderbilt University School of Medicine,Nashville, TN 37232, USA;

    Department of Pharmacology, Vanderbilt University School of Medicine,Nashville, TN 37232, USA;

    Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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