• 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

恶性疟原虫线粒体转运肽的特性与预测

Properties and prediction of mitochondrial transit peptides from Plasmodium falciparum.

作者信息

Bender Andreas, van Dooren Giel G, Ralph Stuart A, McFadden Geoffrey I, Schneider Gisbert

机构信息

Johann Wolfgang Goethe-Universität Frankfurt, Institut für Organische Chemie und Chemische Biologie, Marie-Curie-Strasse 11, D-60439, Frankfurt, Germany.

出版信息

Mol Biochem Parasitol. 2003 Dec;132(2):59-66. doi: 10.1016/j.molbiopara.2003.07.001.

DOI:10.1016/j.molbiopara.2003.07.001
PMID:14599665
Abstract

A neural network approach for the prediction of mitochondrial transit peptides (mTPs) from the malaria-causing parasite Plasmodium falciparum is presented. Nuclear-encoded mitochondrial protein precursors of P. falciparum were analyzed by statistical methods, principal component analysis and supervised neural networks, and were compared to those of other eukaryotes. A distinct amino acid usage pattern has been found in protein encoding regions of P. falciparum: glycine, alanine, tryptophan and arginine are under-represented, whereas isoleucine, tyrosine, asparagine and lysine are over-represented compared to the SwissProt average. Similar patterns were observed in mTPs of P. falciparum. Using principal component analysis (PCA), mTPs from P. falciparum were shown to differ considerably from those of other organisms. A neural network system (PlasMit) for prediction of mTPs in P. falciparum sequences was developed, based on the relative amino acid frequency in the first 24 N-terminal amino acids, yielding a Matthews correlation coefficient of 0.74 (90% correct prediction) in a 20-fold cross-validation study. This system predicted 1177 (22%) mitochondrial genes, based on 5334 annotated genes in the P. falciparum genome. A second network with the same topology was trained to give more conservative estimate. This more stringent network yielded a Matthews correlation coefficient of 0.51 (84% correct prediction) in a 10-fold cross-validation study. It predicted 381 (7.1%) mitochondrial genes, based on 5334 annotated genes in the P. falciparum genome.

摘要

本文提出了一种用于预测疟原虫(恶性疟原虫)线粒体转运肽(mTPs)的神经网络方法。通过统计方法、主成分分析和监督神经网络对恶性疟原虫的核编码线粒体蛋白前体进行了分析,并与其他真核生物的进行了比较。在恶性疟原虫的蛋白质编码区域发现了一种独特的氨基酸使用模式:与SwissProt平均值相比,甘氨酸、丙氨酸、色氨酸和精氨酸的含量较低,而异亮氨酸、酪氨酸、天冬酰胺和赖氨酸的含量较高。在恶性疟原虫的mTPs中也观察到了类似的模式。使用主成分分析(PCA)表明,恶性疟原虫的mTPs与其他生物的mTPs有很大差异。基于前24个N端氨基酸的相对氨基酸频率,开发了一种用于预测恶性疟原虫序列中mTPs的神经网络系统(PlasMit),在20倍交叉验证研究中,马修斯相关系数为0.74(正确预测率为90%)。基于恶性疟原虫基因组中的5334个注释基因,该系统预测了1177个(22%)线粒体基因。训练了一个具有相同拓扑结构的第二个网络,以给出更保守的估计。在10倍交叉验证研究中,这个更严格的网络马修斯相关系数为0.51(正确预测率为84%)。基于恶性疟原虫基因组中的5334个注释基因,它预测了381个(7.1%)线粒体基因。

相似文献

1
Properties and prediction of mitochondrial transit peptides from Plasmodium falciparum.恶性疟原虫线粒体转运肽的特性与预测
Mol Biochem Parasitol. 2003 Dec;132(2):59-66. doi: 10.1016/j.molbiopara.2003.07.001.
2
Deciphering apicoplast targeting signals--feature extraction from nuclear-encoded precursors of Plasmodium falciparum apicoplast proteins.解析顶质体靶向信号——从恶性疟原虫顶质体蛋白的核编码前体中提取特征
Gene. 2001 Dec 12;280(1-2):19-26. doi: 10.1016/s0378-1119(01)00776-4.
3
A Prioritized and Validated Resource of Mitochondrial Proteins in Identifies Unique Biology.在 中鉴定出的线粒体蛋白质的优先和验证资源。
mSphere. 2021 Oct 27;6(5):e0061421. doi: 10.1128/mSphere.00614-21. Epub 2021 Sep 8.
4
Using increment of diversity to predict mitochondrial proteins of malaria parasite: integrating pseudo-amino acid composition and structural alphabet.利用多样性增量预测疟原虫的线粒体蛋白:整合伪氨基酸组成和结构字母。
Amino Acids. 2012 Apr;42(4):1309-16. doi: 10.1007/s00726-010-0825-7. Epub 2010 Dec 30.
5
Identification of mitochondrial proteins of malaria parasite using analysis of variance.利用方差分析鉴定疟原虫的线粒体蛋白
Amino Acids. 2015 Feb;47(2):329-33. doi: 10.1007/s00726-014-1862-4. Epub 2014 Nov 11.
6
Dissecting apicoplast targeting in the malaria parasite Plasmodium falciparum.剖析恶性疟原虫中顶质体靶向机制
Science. 2003 Jan 31;299(5607):705-8. doi: 10.1126/science.1078599.
7
Genome-Wide Collation of the Plasmodium falciparum WDR Protein Superfamily Reveals Malarial Parasite-Specific Features.恶性疟原虫WD重复蛋白超家族的全基因组比对揭示疟原虫特异性特征。
PLoS One. 2015 Jun 4;10(6):e0128507. doi: 10.1371/journal.pone.0128507. eCollection 2015.
8
[Analysis of polymorphism of 2 gene in from falciparum malaria patients in Yunnan Province].[云南省恶性疟患者中2个基因的多态性分析]
Zhongguo Xue Xi Chong Bing Fang Zhi Za Zhi. 2016 Jul 18;28(4):411-417. doi: 10.16250/j.32.1374.2016113.
9
Proteome composition in Plasmodium falciparum: higher usage of GC-rich nonsynonymous codons in highly expressed genes.恶性疟原虫的蛋白质组组成:高表达基因中富含GC的非同义密码子的使用频率更高。
J Mol Evol. 2005 Oct;61(4):513-23. doi: 10.1007/s00239-005-0023-5. Epub 2005 Jul 21.
10
MitProt-Pred: Predicting mitochondrial proteins of Plasmodium falciparum parasite using diverse physiochemical properties and ensemble classification.MitProt-Pred:利用多种物理化学性质和集成分类预测疟原虫寄生虫的线粒体蛋白。
Comput Biol Med. 2013 Oct;43(10):1502-11. doi: 10.1016/j.compbiomed.2013.07.024. Epub 2013 Aug 2.

引用本文的文献

1
Characterization of signal and transit peptides based on motif composition and taxon-specific patterns.基于模体组成和分类群特异性模式的信号肽和转运肽特征分析。
Sci Rep. 2023 Sep 21;13(1):15751. doi: 10.1038/s41598-023-42987-1.
2
A novel deep learning-assisted hybrid network for plasmodium falciparum parasite mitochondrial proteins classification.一种新型深度学习辅助混合网络用于疟原虫寄生虫线粒体蛋白分类。
PLoS One. 2022 Oct 6;17(10):e0275195. doi: 10.1371/journal.pone.0275195. eCollection 2022.
3
Mitochondrially targeted proximity biotinylation and proteomic analysis in Plasmodium falciparum.
疟原虫中线粒体靶向邻近生物素化和蛋白质组学分析。
PLoS One. 2022 Aug 19;17(8):e0273357. doi: 10.1371/journal.pone.0273357. eCollection 2022.
4
Functional genomics of RAP proteins and their role in mitoribosome regulation in Plasmodium falciparum.RAP 蛋白的功能基因组学及其在疟原虫线粒体核糖体调控中的作用。
Nat Commun. 2022 Mar 11;13(1):1275. doi: 10.1038/s41467-022-28981-7.
5
A Prioritized and Validated Resource of Mitochondrial Proteins in Identifies Unique Biology.在 中鉴定出的线粒体蛋白质的优先和验证资源。
mSphere. 2021 Oct 27;6(5):e0061421. doi: 10.1128/mSphere.00614-21. Epub 2021 Sep 8.
6
Recognition of Mitochondrial Proteins in Plasmodium Based on the Tripeptide Composition.基于三肽组成对疟原虫线粒体蛋白质的识别
Front Cell Dev Biol. 2020 Sep 16;8:578901. doi: 10.3389/fcell.2020.578901. eCollection 2020.
7
An essential pentatricopeptide repeat protein in the apicomplexan remnant chloroplast.质体中必需的五肽重复蛋白在顶复门类生物的残余叶绿体中。
Cell Microbiol. 2019 Dec;21(12):e13108. doi: 10.1111/cmi.13108. Epub 2019 Sep 16.
8
Biochemical characterization and essentiality of fumarate hydratase.延胡索酸水合酶的生化特性及必需性。
J Biol Chem. 2018 Apr 20;293(16):5878-5894. doi: 10.1074/jbc.M117.816298. Epub 2018 Feb 15.
9
Prokaryotic ancestry and gene fusion of a dual localized peroxiredoxin in malaria parasites.疟原虫中一种双定位过氧化物还原酶的原核生物起源和基因融合
Microb Cell. 2015 Jan 5;2(1):5-13. doi: 10.15698/mic2015.01.182.
10
Plasmodium vivax Tryptophan Rich Antigen PvTRAg36.6 Interacts with PvETRAMP and PvTRAg56.6 Interacts with PvMSP7 during Erythrocytic Stages of the Parasite.间日疟原虫富含色氨酸抗原PvTRAg36.6在疟原虫红细胞期与PvETRAMP相互作用,PvTRAg56.6与PvMSP7相互作用。
PLoS One. 2016 Mar 8;11(3):e0151065. doi: 10.1371/journal.pone.0151065. eCollection 2016.