Suppr超能文献

具有刚性辅基的蛋白质活性位点三维模板的生成。

Generation of 3D templates of active sites of proteins with rigid prosthetic groups.

作者信息

Nebel Jean-Christophe

机构信息

Faculty of Computing, Information Systems & Mathematics, Kingston University Kingston-upon-Thames, Surrey KT1 2EE, UK.

出版信息

Bioinformatics. 2006 May 15;22(10):1183-9. doi: 10.1093/bioinformatics/btl040. Epub 2006 Feb 10.

Abstract

MOTIVATION

With the increasing availability of protein structures, the generation of biologically meaningful 3D patterns from the simultaneous alignment of several protein structures is an exciting prospect: active sites could be better understood, protein functions and protein 3D structures could be predicted more accurately. Although patterns can already be generated at the fold and topological levels, no system produces high-resolution 3D patterns including atom and cavity positions. To address this challenge, our research focuses on generating patterns from proteins with rigid prosthetic groups. Since these groups are key elements of protein active sites, the generated 3D patterns are expected to be biologically meaningful.

RESULTS

In this paper, we present a new approach which allows the generation of 3D patterns from proteins with rigid prosthetic groups. Using 237 protein chains representing proteins containing porphyrin rings, our method was validated by comparing 3D templates generated from homologues with the 3D structure of the proteins they model. Atom positions were predicted reliably: 93% of them had an accuracy of 1.00 A or less. Moreover, similar results were obtained regarding chemical group and cavity positions. Results also suggested our system could contribute to the validation of 3D protein models. Finally, a 3D template was generated for the active site of human cytochrome P450 CYP17, the 3D structure of which is unknown. Its analysis showed that it is biologically meaningful: our method detected the main patterns of the cytochrome P450 superfamily and the motifs linked to catalytic reactions. The 3D template also suggested the position of a residue, which could be involved in a hydrogen bond with CYP17 substrates and the shape and location of a cavity. Comparisons with independently generated 3D models comforted these hypotheses.

AVAILABILITY

Alignment software (Nestor3D) is available at http://www.kingston.ac.uk/~ku33185/Nestor3D.html

摘要

动机

随着蛋白质结构的可得性不断增加,通过同时比对多个蛋白质结构来生成具有生物学意义的三维模式是一个令人兴奋的前景:活性位点能够得到更好的理解,蛋白质功能和三维结构能够被更准确地预测。尽管已经可以在折叠和拓扑层面生成模式,但尚无系统能够生成包括原子和腔位置的高分辨率三维模式。为应对这一挑战,我们的研究聚焦于从带有刚性辅基的蛋白质生成模式。由于这些基团是蛋白质活性位点的关键要素,所生成的三维模式有望具有生物学意义。

结果

在本文中,我们提出了一种新方法,该方法能够从带有刚性辅基的蛋白质生成三维模式。使用代表含卟啉环蛋白质的237条蛋白质链,我们的方法通过将同源物生成的三维模板与它们所模拟蛋白质的三维结构进行比较而得到验证。原子位置被可靠地预测:其中93%的原子位置精度在1.00埃或更低。此外,在化学基团和腔位置方面也获得了类似结果。结果还表明我们的系统有助于三维蛋白质模型的验证。最后,为人细胞色素P450 CYP17的活性位点生成了一个三维模板,其三维结构未知。对其分析表明它具有生物学意义:我们的方法检测到了细胞色素P450超家族的主要模式以及与催化反应相关的基序。该三维模板还表明了一个残基的位置,它可能参与与CYP17底物的氢键形成以及一个腔的形状和位置。与独立生成的三维模型的比较证实了这些假设。

可用性

比对软件(Nestor3D)可在http://www.kingston.ac.uk/~ku33185/Nestor3D.html获取

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验