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本文引用的文献

1
The current Salmonella-host interactome.当前沙门氏菌-宿主相互作用组。
Proteomics Clin Appl. 2012 Jan;6(1-2):117-33. doi: 10.1002/prca.201100083. Epub 2011 Dec 27.
2
Determining confidence of predicted interactions between HIV-1 and human proteins using conformal method.使用共形方法确定HIV-1与人类蛋白质之间预测相互作用的置信度。
Pac Symp Biocomput. 2012:311-22.
3
Predicting protein-protein interactions on a proteome scale by matching evolutionary and structural similarities at interfaces using PRISM.通过使用 PRISM 在界面处匹配进化和结构相似性,在全蛋白质组尺度上预测蛋白质-蛋白质相互作用。
Nat Protoc. 2011 Aug 11;6(9):1341-54. doi: 10.1038/nprot.2011.367.
4
New insights into pathogen recognition.病原体识别的新见解。
Expert Rev Anti Infect Ther. 2011 Aug;9(8):577-9. doi: 10.1586/eri.11.73.
5
Evidence for network evolution in an Arabidopsis interactome map.Arabidopsis 相互作用组图谱中网络进化的证据。
Science. 2011 Jul 29;333(6042):601-7. doi: 10.1126/science.1203877.
6
Prediction of protein-protein interactions between Ralstonia solanacearum and Arabidopsis thaliana.预测青枯雷尔氏菌与拟南芥之间的蛋白质-蛋白质相互作用。
Amino Acids. 2012 Jun;42(6):2363-71. doi: 10.1007/s00726-011-0978-z. Epub 2011 Jul 24.
7
A predicted protein-protein interaction network of the filamentous fungus Neurospora crassa.丝状真菌粗糙脉孢菌的预测蛋白质-蛋白质相互作用网络。
Mol Biosyst. 2011 Jul;7(7):2278-85. doi: 10.1039/c1mb05028a. Epub 2011 May 16.
8
Porcine Toll-like receptors: recognition of Salmonella enterica serovar Choleraesuis and influence of polymorphisms.猪 Toll 样受体:对肠炎沙门氏菌血清型霍乱弧菌的识别及多态性的影响。
Mol Immunol. 2011 May;48(9-10):1114-20. doi: 10.1016/j.molimm.2011.02.004. Epub 2011 Mar 17.
9
TLR signaling is required for Salmonella typhimurium virulence.TLR 信号转导对于鼠伤寒沙门氏菌的毒力是必需的。
Cell. 2011 Mar 4;144(5):675-88. doi: 10.1016/j.cell.2011.01.031.
10
Virus interactions with human signal transduction pathways.病毒与人类信号转导通路的相互作用。
Int J Comput Biol Drug Des. 2011;4(1):83-105. doi: 10.1504/IJCBDD.2011.038658. Epub 2011 Feb 17.

预测和比较沙门氏菌-人类和沙门氏菌-拟南芥互作组。

Prediction and comparison of Salmonella-human and Salmonella-Arabidopsis interactomes.

机构信息

Forschungszentrum Jülich, Institute of Complex Systems (ICS-5), D-52425 Jülich, Germany.

出版信息

Chem Biodivers. 2012 May;9(5):991-1018. doi: 10.1002/cbdv.201100392.

DOI:10.1002/cbdv.201100392
PMID:22589098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3407687/
Abstract

Salmonellosis caused by Salmonella bacteria is a food-borne disease and a worldwide health threat causing millions of infections and thousands of deaths every year. This pathogen infects an unusually broad range of host organisms including human and plants. A better understanding of the mechanisms of communication between Salmonella and its hosts requires identifying the interactions between Salmonella and host proteins. Protein-protein interactions (PPIs) are the fundamental building blocks of communication. Here, we utilize the prediction platform BIANA to obtain the putative Salmonella-human and Salmonella-Arabidopsis interactomes based on sequence and domain similarity to known PPIs. A gold standard list of Salmonella-host PPIs served to validate the quality of the human model. 24,726 and 10,926 PPIs comprising interactions between 38 and 33 Salmonella effectors and virulence factors with 9,740 human and 4,676 Arabidopsis proteins, respectively, were predicted. Putative hub proteins could be identified, and parallels between the two interactomes were discovered. This approach can provide insight into possible biological functions of so far uncharacterized proteins. The predicted interactions are available via a web interface which allows filtering of the database according to parameters provided by the user to narrow down the list of suspected interactions. The interactions are available via a web interface at http://sbi.imim.es/web/SHIPREC.php.

摘要

由沙门氏菌引起的沙门氏菌病是一种食源性疾病,也是一个全球性的健康威胁,每年导致数百万人感染和数千人死亡。这种病原体感染了包括人类和植物在内的异常广泛的宿主生物。更好地了解沙门氏菌与其宿主之间的通讯机制需要确定沙门氏菌与宿主蛋白之间的相互作用。蛋白质-蛋白质相互作用(PPIs)是通讯的基本构建块。在这里,我们利用预测平台 BIANA 基于序列和域相似性来获得基于已知 PPIs 的推定的沙门氏菌-人类和沙门氏菌-拟南芥相互作用组。沙门氏菌-宿主 PPIs 的黄金标准列表用于验证人类模型的质量。预测了分别由 38 个和 33 个沙门氏菌效应子和毒力因子与 9740 个人类和 4676 个拟南芥蛋白之间相互作用的 24726 个和 10926 个 PPI。可以鉴定推定的枢纽蛋白,并发现两个相互作用组之间的平行关系。这种方法可以深入了解迄今为止尚未表征的蛋白质的可能生物学功能。预测的相互作用可通过网络界面获得,该界面允许根据用户提供的参数过滤数据库,以缩小可疑相互作用列表的范围。该相互作用可通过网络界面 http://sbi.imim.es/web/SHIPREC.php 获得。