• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

使用最小割树分析和表示蛋白质界面的热点及其网络。

Analysis and network representation of hotspots in protein interfaces using minimum cut trees.

机构信息

Center for Computational Biology and Bioinformatics and College of Engineering, Koc University, Istanbul, Turkey.

出版信息

Proteins. 2010 Aug 1;78(10):2283-94. doi: 10.1002/prot.22741.

DOI:10.1002/prot.22741
PMID:20544964
Abstract

We propose a novel approach to analyze and visualize residue contact networks of protein interfaces by graph-based algorithms using a minimum cut tree (mincut tree). Edges in the network are weighted according to an energy function derived from knowledge-based potentials. The mincut tree, which is constructed from the weighted residue network, simplifies and summarizes the complex structure of the contact network by an efficient and informative representation. This representation offers a comprehensible view of critical residues and facilitates the inspection of their organization. We observed, on a nonredundant data set of 38 protein complexes with experimental hotspots that the highest degree node in the mincut tree usually corresponds to an experimental hotspot. Further, hotspots are found in a few paths in the mincut tree. In addition, we examine the organization of hotspots (hot regions) using an iterative clustering algorithm on two different case studies. We find that distinct hot regions are located on specific sites of the mincut tree and some critical residues hold these clusters together. Clustering of the interface residues provides information about the relation of hot regions with each other. Our new approach is useful at the molecular level for both identification of critical paths in the protein interfaces and extraction of hot regions by clustering of the interface residues.

摘要

我们提出了一种新的方法,通过基于图的算法和最小割树(mincut tree)来分析和可视化蛋白质界面残基接触网络。网络中的边根据基于知识的势能导出的能量函数进行加权。最小割树是从加权残基网络构建的,通过有效且信息丰富的表示形式简化和总结了接触网络的复杂结构。这种表示形式提供了对关键残基的可理解视图,并方便了对它们组织的检查。我们在具有实验热点的 38 个蛋白质复合物的非冗余数据集上观察到,mincut 树中的最高度节点通常对应于实验热点。此外,热点存在于 mincut 树中的几条路径中。此外,我们使用迭代聚类算法在两个不同的案例研究中检查热点(热区)的组织。我们发现,不同的热点位于 mincut 树的特定位置,一些关键残基将这些簇连接在一起。界面残基的聚类提供了有关热点区域彼此之间关系的信息。我们的新方法在分子水平上对于识别蛋白质界面中的关键路径以及通过界面残基聚类提取热点区域都非常有用。

相似文献

1
Analysis and network representation of hotspots in protein interfaces using minimum cut trees.使用最小割树分析和表示蛋白质界面的热点及其网络。
Proteins. 2010 Aug 1;78(10):2283-94. doi: 10.1002/prot.22741.
2
Exploring the charge space of protein-protein association: a proteomic study.探索蛋白质-蛋白质相互作用的电荷空间:一项蛋白质组学研究。
Proteins. 2005 Aug 15;60(3):341-52. doi: 10.1002/prot.20489.
3
Small-world network approach to identify key residues in protein-protein interaction.用小世界网络方法识别蛋白质-蛋白质相互作用中的关键残基。
Proteins. 2005 Feb 15;58(3):672-82. doi: 10.1002/prot.20348.
4
Prediction of the interaction site on the surface of an isolated protein structure by analysis of side chain energy scores.通过分析侧链能量得分预测孤立蛋白质结构表面的相互作用位点。
Proteins. 2004 Nov 15;57(3):548-57. doi: 10.1002/prot.20238.
5
Identification of computational hot spots in protein interfaces: combining solvent accessibility and inter-residue potentials improves the accuracy.蛋白质界面中计算热点的识别:结合溶剂可及性和残基间势能可提高准确性。
Bioinformatics. 2009 Jun 15;25(12):1513-20. doi: 10.1093/bioinformatics/btp240. Epub 2009 Apr 8.
6
Statistical analysis and prediction of protein-protein interfaces.蛋白质-蛋白质相互作用界面的统计分析与预测
Proteins. 2005 Aug 15;60(3):353-66. doi: 10.1002/prot.20433.
7
ProMate: a structure based prediction program to identify the location of protein-protein binding sites.ProMate:一个基于结构的预测程序,用于识别蛋白质-蛋白质结合位点的位置。
J Mol Biol. 2004 Apr 16;338(1):181-99. doi: 10.1016/j.jmb.2004.02.040.
8
Network analysis of protein structures identifies functional residues.蛋白质结构的网络分析可识别功能残基。
J Mol Biol. 2004 Dec 3;344(4):1135-46. doi: 10.1016/j.jmb.2004.10.055.
9
MIAX: a new paradigm for modeling biomacromolecular interactions and complex formation in condensed phases.MIAX:一种用于模拟凝聚相中生物大分子相互作用和复合物形成的新范式。
Proteins. 2002 Sep 1;48(4):696-732. doi: 10.1002/prot.10122.
10
Optimal protein-RNA area, OPRA: a propensity-based method to identify RNA-binding sites on proteins.最优蛋白-核酸面积(OPRA):一种基于倾向的方法,用于识别蛋白质上的 RNA 结合位点。
Proteins. 2010 Jan;78(1):25-35. doi: 10.1002/prot.22527.

引用本文的文献

1
Predicting interacting hotspots for nanobodies' binding using triplets of residues.利用残基三联体预测纳米抗体结合的相互作用热点。
Protein Sci. 2025 Aug;34(8):e70220. doi: 10.1002/pro.70220.
2
Densest subgraph-based methods for protein-protein interaction hot spot prediction.基于最稠密子图的蛋白质-蛋白质相互作用热点预测方法。
BMC Bioinformatics. 2022 Oct 31;23(1):451. doi: 10.1186/s12859-022-04996-1.
3
Computational analysis of hot spots and binding mechanism in the PD-1/PD-L1 interaction.PD-1/PD-L1相互作用中热点及结合机制的计算分析
RSC Adv. 2019 May 14;9(26):14944-14956. doi: 10.1039/c9ra01369e. eCollection 2019 May 9.
4
Weighted protein residue networks based on joint recurrences between residues.基于残基间联合递归的加权蛋白质残基网络。
BMC Bioinformatics. 2015 May 26;16:173. doi: 10.1186/s12859-015-0621-1.
5
Prediction of hot spots in protein interfaces using extreme learning machines with the information of spatial neighbour residues.利用具有空间相邻残基信息的极限学习机预测蛋白质界面中的热点。
IET Syst Biol. 2014 Aug;8(4):184-90. doi: 10.1049/iet-syb.2013.0049.
6
Boosting prediction performance of protein-protein interaction hot spots by using structural neighborhood properties.利用结构邻域特性提高蛋白质-蛋白质相互作用热点的预测性能。
J Comput Biol. 2013 Nov;20(11):878-91. doi: 10.1089/cmb.2013.0083. Epub 2013 Oct 17.