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iLoc-Euk: A Multi-Label Classifier for Predicting the Subcellular Localization of Singleplex and Multiplex Eukaryotic Proteins

机译:iLoc-Euk:预测单重和多重真核蛋白亚细胞定位的多标签分类器

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摘要

Predicting protein subcellular localization is an important and difficult problem, particularly when query proteins may have the multiplex character, i.e., simultaneously exist at, or move between, two or more different subcellular location sites. Most of the existing protein subcellular location predictor can only be used to deal with the single-location or “singleplex” proteins. Actually, multiple-location or “multiplex” proteins should not be ignored because they usually posses some unique biological functions worthy of our special notice. By introducing the “multi-labeled learning” and “accumulation-layer scale”, a new predictor, called >iLoc-Euk, has been developed that can be used to deal with the systems containing both singleplex and multiplex proteins. As a demonstration, the jackknife cross-validation was performed with >iLoc-Euk on a benchmark dataset of eukaryotic proteins classified into the following 22 location sites: (1) acrosome, (2) cell membrane, (3) cell wall, (4) centriole, (5) chloroplast, (6) cyanelle, (7) cytoplasm, (8) cytoskeleton, (9) endoplasmic reticulum, (10) endosome, (11) extracellular, (12) Golgi apparatus, (13) hydrogenosome, (14) lysosome, (15) melanosome, (16) microsome (17) mitochondrion, (18) nucleus, (19) peroxisome, (20) spindle pole body, (21) synapse, and (22) vacuole, where none of proteins included has pairwise sequence identity to any other in a same subset. The overall success rate thus obtained by >iLoc-Euk was 79%, which is significantly higher than that by any of the existing predictors that also have the capacity to deal with such a complicated and stringent system. As a user-friendly web-server, >iLoc-Euk is freely accessible to the public at the web-site . It is anticipated that >iLoc-Euk may become a useful bioinformatics tool for Molecular Cell Biology, Proteomics, System Biology, and Drug Development Also, its novel approach will further stimulate the development of predicting other protein attributes.
机译:预测蛋白质亚细胞定位是一个重要且困难的问题,尤其是当查询蛋白质可能具有多重特征时,即同时存在于两个或多个不同的亚细胞定位位点或在两个或多个不同的亚细胞定位位点之间移动时,尤其如此。现有的大多数蛋白质亚细胞定位预测子只能用于处理单定位或“单重”蛋白。实际上,不应忽略多位置或“多重”蛋白质,因为它们通常具有一些独特的生物学功能,值得我们特别注意。通过引入“多标签学习”和“积累层规模”,已开发出一种名为> iLoc-Euk 的新预测变量,可用于处理包含单重和多重的系统蛋白质。作为演示,用> iLoc-Euk 对真核蛋白的基准数据集进行了折刀交叉验证,真核蛋白分为以下22个位置位点:(1)顶体,(2)细胞膜,(3 )细胞壁,(4)中心粒,(5)叶绿体,(6)氰腈,(7)细胞质,(8)细胞骨架,(9)内质网,(10)内体,(11)细胞外,(12)高尔基体,(13)氢氧体,(14)溶酶体,(15)黑素体,(16)微粒体(17)线粒体,(18)核,(19)过氧化物酶体,(20)纺锤体,(21)突触和(22)液泡,其中所含蛋白质均不与同一亚组中的任何其他蛋白质具有成对的序列同一性。因此,> iLoc-Euk 所获得的总体成功率为79%,大大高于任何也有能力应对这种复杂而严格的系统的现有预测指标。作为用户友好的Web服务器,> iLoc-Euk 在网站上可供公众免费访问。预计> iLoc-Euk 可能会成为分子细胞生物学,蛋白质组学,系统生物学和药物开发的有用的生物信息学工具。此外,其新颖的方法将进一步刺激预测其他蛋白质属性的发展。

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