Prediction of presynaptic and postsynaptic neurotoxins by combining various Chou's pseudo components

被引:26
作者
Huo, Haiyan [1 ]
Li, Tao [2 ]
Wang, Shiyuan [3 ]
Lv, Yingli [3 ]
Zuo, Yongchun [4 ]
Yang, Lei [3 ]
机构
[1] Hohhot Univ Nationalities, Dept Environm Engn, Hohhot 010051, Peoples R China
[2] Inner Mongolia Agr Univ, Coll Life Sc, Hohhot 010018, Peoples R China
[3] Harbin Med Univ, Coll Bioinformat Sci & Technol, Harbin 150081, Heilongjiang, Peoples R China
[4] Inner Mongolia Univ, Key Lab Mammalian Reprod Biol & Biotechnol, Minist Educ, Hohhot 010021, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
AMINO-ACID-COMPOSITION; SUPPORT VECTOR MACHINES; NAJA-NAJA-SPUTATRIX; CONOTOXIN SUPERFAMILY; PROTEIN-SEQUENCE; NEUROMUSCULAR ACTIVITY; FEATURE-SELECTION; DIFFERENT MODES; CDNA CLONING; WEB SERVER;
D O I
10.1038/s41598-017-06195-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Presynaptic and postsynaptic neurotoxins are two groups of neurotoxins. Identification of presynaptic and postsynaptic neurotoxins is an important work for numerous newly found toxins. It is both costly and time consuming to determine these two neurotoxins by experimental methods. As a complement, using computational methods for predicting presynaptic and postsynaptic neurotoxins could provide some useful information in a timely manner. In this study, we described four algorithms for predicting presynaptic and postsynaptic neurotoxins from sequence driven features by using Increment of Diversity (ID), Multinomial Naive Bayes Classifier (MNBC), Random Forest (RF), and K-nearest Neighbours Classifier (IBK). Each protein sequence was encoded by pseudo amino acid (PseAA) compositions and three biological motif features, including MEME, Prosite and InterPro motif features. The Maximum Relevance Minimum Redundancy (MRMR) feature selection method was used to rank the PseAA compositions and the 50 top ranked features were selected to improve the prediction accuracy. The PseAA compositions and three kinds of biological motif features were combined and 12 different parameters that defined as P1-P12 were selected as the input parameters of ID, MNBC, RF, and IBK. The prediction results obtained in this study were significantly better than those of previously developed methods.
引用
收藏
页数:10
相关论文
共 81 条
[1]   Four new postsynaptic neurotoxins from Naja naja sputatrix venom:: cDNA cloning, protein expression, and phylogenetic analysis [J].
Afifiyan, F ;
Armugam, A ;
Gopalakrishnakone, P ;
Tan, NH ;
Tan, CH ;
Jeyaseelan, K .
TOXICON, 1998, 36 (12) :1871-1885
[2]  
Afifiyan F, 1999, GENOME RES, V9, P259
[3]   MEME: discovering and analyzing DNA and protein sequence motifs [J].
Bailey, Timothy L. ;
Williams, Nadya ;
Misleh, Chris ;
Li, Wilfred W. .
NUCLEIC ACIDS RESEARCH, 2006, 34 :W369-W373
[4]   dRHP-PseRA: detecting remote homology proteins using profile-based pseudo protein sequence and rank aggregation [J].
Chen, Junjie ;
Long, Ren ;
Wang, Xiao-long ;
Liu, Bin ;
Chou, Kuo-Chen .
SCIENTIFIC REPORTS, 2016, 6
[5]   iRNA-AI: identifying the adenosine to inosine editing sites in RNA sequences [J].
Chen, Wei ;
Feng, Pengmian ;
Yang, Hui ;
Ding, Hui ;
Lin, Hao ;
Chou, Kuo-Chen .
ONCOTARGET, 2017, 8 (03) :4208-4217
[6]   iRNA-PseU: Identifying RNA pseudouridine sites [J].
Chen, Wei ;
Tang, Hua ;
Ye, Jing ;
Lin, Hao ;
Chou, Kuo-Chen .
MOLECULAR THERAPY-NUCLEIC ACIDS, 2016, 5 :e332
[7]   IACP: a sequence-based tool for identifying anticancer peptides [J].
Chen, Wei ;
Ding, Hui ;
Feng, Pengmian ;
Lin, Hao ;
Chou, Kuo-Chen .
ONCOTARGET, 2016, 7 (13) :16895-16909
[8]   Using deformation energy to analyze nucleosome positioning in genomes [J].
Chen, Wei ;
Feng, Pengmian ;
Ding, Hui ;
Lin, Hao ;
Chou, Kuo-Chen .
GENOMICS, 2016, 107 (2-3) :69-75
[9]   iRSpot-PseDNC: identify recombination spots with pseudo dinucleotide composition [J].
Chen, Wei ;
Feng, Peng-Mian ;
Lin, Hao ;
Chou, Kuo-Chen .
NUCLEIC ACIDS RESEARCH, 2013, 41 (06) :e68
[10]   iATC-mISF: a multi-label classifier for predicting the classes of anatomical therapeutic chemicals [J].
Cheng, Xiang ;
Zhao, Shu-Guang ;
Xiao, Xuan ;
Chou, Kuo-Chen .
BIOINFORMATICS, 2017, 33 (03) :341-346