TranCEP: Predicting the substrate class of transmembrane transport proteins using compositional, evolutionary, and positional information

被引:16
作者
Alballa, Munira [1 ,2 ]
Aplop, Faizah [3 ]
Butler, Gregory [1 ,4 ]
机构
[1] Concordia Univ, Dept Comp Sci & Software Engn, Montreal, PQ, Canada
[2] King Saud Univ, Coll Comp & Informat Sci, Riyadh, Saudi Arabia
[3] Univ Malaysia Terengganu, Sch Informat & Appl Math, Terengganu, Malaysia
[4] Concordia Univ, Ctr Struct & Funct Genom, Montreal, PQ, Canada
关键词
MULTIPLE SEQUENCE ALIGNMENT; CLASSIFICATION DATABASE; MEMBRANE TRANSPORTERS; TOPOLOGY PREDICTION; WEB SERVER; GENOME; ANNOTATION; NETWORKS; TCDB;
D O I
10.1371/journal.pone.0227683
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
Transporters mediate the movement of compounds across the membranes that separate the cell from its environment and across the inner membranes surrounding cellular compartments. It is estimated that one third of a proteome consists of membrane proteins, and many of these are transport proteins. Given the increase in the number of genomes being sequenced, there is a need for computational tools that predict the substrates that are transported by the transmembrane transport proteins. In this paper, we present TranCEP, a predictor of the type of substrate transported by a transmembrane transport protein. TranCEP combines the traditional use of the amino acid composition of the protein, with evolutionary information captured in a multiple sequence alignment (MSA), and restriction to important positions of the alignment that play a role in determining the specificity of the protein. Our experimental results show that TranCEP significantly outperforms the state-of-the-art predictors. The results quantify the contribution made by each type of information used.
引用
收藏
页数:23
相关论文
共 58 条
[1]  
Aplop F., 2017, ARPN J ENG APPL SCI, V12
[2]  
Aplop F., 2016, COMPUTATIONAL APPROA
[3]   Transferring functional annotations of membrane transporters on the basis of sequence similarity and sequence motifs [J].
Barghash, Ahmad ;
Helms, Volkhard .
BMC BIOINFORMATICS, 2013, 14
[4]  
Bekkar M., 2013, J Inf Eng Appl, V3
[5]   The Protein Data Bank [J].
Berman, HM ;
Battistuz, T ;
Bhat, TN ;
Bluhm, WF ;
Bourne, PE ;
Burkhardt, K ;
Iype, L ;
Jain, S ;
Fagan, P ;
Marvin, J ;
Padilla, D ;
Ravichandran, V ;
Schneider, B ;
Thanki, N ;
Weissig, H ;
Westbrook, JD ;
Zardecki, C .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2002, 58 :899-907
[6]   TM-Aligner: Multiple sequence alignment tool for transmembrane proteins with reduced time and improved accuracy [J].
Bhat, Basharat ;
Ganai, Nazir A. ;
Andrabi, Syed Mudasir ;
Shah, Riaz A. ;
Singh, Ashutosh .
SCIENTIFIC REPORTS, 2017, 7
[7]   The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003 [J].
Boeckmann, B ;
Bairoch, A ;
Apweiler, R ;
Blatter, MC ;
Estreicher, A ;
Gasteiger, E ;
Martin, MJ ;
Michoud, K ;
O'Donovan, C ;
Phan, I ;
Pilbout, S ;
Schneider, M .
NUCLEIC ACIDS RESEARCH, 2003, 31 (01) :365-370
[8]  
Buehler L., 2015, STRUCTURE MEMBRANE P
[9]  
Busch Wolfgang, 2003, Methods Mol Biol, V227, P21, DOI 10.1385/1-59259-387-9:21
[10]   A Treatise to Computational Approaches Towards Prediction of Membrane Protein and Its Subtypes [J].
Butt, Ahmad Hassan ;
Rasool, Nouman ;
Khan, Yaser Daanial .
JOURNAL OF MEMBRANE BIOLOGY, 2017, 250 (01) :55-76