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Bifunctional Acyltransferase/Decarboxylase LnmK as the Missing Link for β-Alkylation in Polyketide Biosynthesis

机译:双功能酰基转移酶/脱羧酶LnmK是聚酮化合物生物合成中β-烷基化的缺失环节

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摘要

Both a- and β-alkylations contribute to the vast structural diversity displayed by polyketide natural products (Figure 1A). While the a-alkyl branches are typically derived from extender units, the choice of which is dictated by the acyltransferase (AT) domain of modular polyketide synthases (PKSs), the β-alkyl branches often result from the activities of hydroxymethylglutaryl-CoA (HMG-CoA) synthase homologues (HCSs).
机译:α-和β-烷基化都有助于聚酮化合物天然产物显示出巨大的结构多样性(图1A)。虽然α-烷基分支通常衍生自增量剂单元,但其选择取决于模块化聚酮化合物合酶(PKS)的酰基转移酶(AT)域,而β-烷基分支通常是由羟甲基戊二酰辅酶A(HMG)的活性产生的-CoA)合酶同源物(HCS)。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2009年第20期|6900-6901|共2页
  • 作者

    Tao Liu; Yong Huang; Ben Shen;

  • 作者单位

    Division of Pharmaceutical Sciences, University of Wisconsin National Cooperative Drug Discovery Group;

    Division of Pharmaceutical Sciences, University of Wisconsin National Cooperative Drug Discovery Group;

    Division of Pharmaceutical Sciences, University of Wisconsin National Cooperative Drug Discovery Group Department of Chemistry, University of Wisconsin-Madison, Madison, Wisconsin 53705-2222 Department of Chemistry, University of Wisconsin-Madison;

  • 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
  • 中图分类
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  • 入库时间 2022-08-18 03:16:56

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