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III类腺苷酸环化酶和鸟苷酸环化酶的底物选择

Substrate selection by class III adenylyl cyclases and guanylyl cyclases.

作者信息

Linder Jürgen U

机构信息

Abteilung Pharmazeutische Biochemie, Fakultät für Chemie und Pharmazie, Universität Tübingen, Tübingen, Germany.

出版信息

IUBMB Life. 2005 Dec;57(12):797-803. doi: 10.1080/15216540500415636.

Abstract

The second messengers cAMP and cGMP are of central importance in signal transduction pathways. To assure pathway specificity adenylyl and guanylyl cyclases are highly selective for their substrates, ATP and GTP, respectively. The universal class III cyclases are equipped with a variety of purine-binding modes, which have been identified by structure determination and mutagenesis. Most selection mechanisms rely on a pair of residues which form hydrogen bonds to N1 and the N(6)-amino or O(6)-keto group of adenine and guanine, respectively. Furthermore, selection is supported by hydrogen bonds involving the peptide backbone and by constraints imposed by hydrophobic side-chains.

摘要

第二信使环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)在信号转导途径中至关重要。为确保途径特异性,腺苷酸环化酶和鸟苷酸环化酶分别对其底物三磷酸腺苷(ATP)和三磷酸鸟苷(GTP)具有高度选择性。通用的III类环化酶具有多种嘌呤结合模式,这些模式已通过结构测定和诱变得以确定。大多数选择机制依赖于一对残基,它们分别与腺嘌呤和鸟嘌呤的N1以及N(6)-氨基或O(6)-酮基形成氢键。此外,肽主链形成的氢键以及疏水侧链施加的限制也有助于进行选择。

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