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(Gluco) Amylases, what have we learned so far?

机译:(灰色)淀粉酶,到目前为止我们学到了什么?

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A lot has been learned since information on alpha-amylase structure appeared in 1980, but today close to 500 sequences and 50 crystal structures of amylolytic enzymes do not answer all questions on these enzymes. Major issues are i) long-range enzyme-substrate communication, ii) transglycosylation vs. hydrolysis, iii) attack on macromolecular substrates, iv) domain interplay, and v) relations with other proteins. While traditional structure/function relationship investigations developed enormously thanks to advances in structural biology, protein chemistry and recombinant DNA techniques, the emerging era focuses on i) enzymes with custom-made specificity for substrates and proteinaceous inhibitors, ii) new biophysical methods to depict function, and iii) application of genome, proteome, and PIN analysis. This presentation describes the use of mutagenesis and substrate analogs to gain insight into how amylases operate and can be improved.
机译:已经了解了很多,因为1980年出现了关于α-淀粉酶结构的信息,但今天接近500序列,50个氨基溶解酶的晶体结构不会回答这些酶的所有问题。主要问题是i)远程酶 - 衬底通信,II)胰糖基化与水解,III)对大分子底物,IV)结构域的相互作用和V)与其他蛋白质的关系。虽然传统的结构/功能关系调查非常感谢结构生物学,蛋白质化学和重组DNA技术的进步,但新兴时期侧重于I)酶对底物和蛋白质抑制剂的定制特异性,II)描述功能的新生物物理方法和III)在基因组,蛋白质组和引脚分析中的应用。该介绍描述了使用诱变和衬底类似物,以深入了解淀粉酶如何运行并且可以改善。

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