Comprehensive analysis of transmembrane topologies in prokaryotic genomes

被引:31
作者
Arai, M
Ikeda, M
Shimizu, T [1 ]
机构
[1] Hirosaki Univ, Fac Sci & Technol, Dept Elect & Informat Syst Engn, Hirosaki, Aomori 0368561, Japan
[2] Iwate Univ, United Grad Sch Agr Sci, Sci Bioresources Program, Morioka, Iwate 0208550, Japan
关键词
transmembrane protein; transmembrane topology; signal peptide; consensus prediction; genome-scale analysis; prokaryotic genome;
D O I
10.1016/S0378-1119(02)01181-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We analysed comprehensively transmembrane (TM) topologies of TM proteins of 50 selected prokaryotic genomes, by discriminating between TM and soluble proteins by using SOSUI, then detecting and removing signal peptides by applying 'DetecSig', and finally predicting TM topologies by employing 'ConPred'. Estimated fraction of TM proteins in proteome averaged over the 50 genomes is similar to22%. About 13% of TM proteins were predicted to have a signal peptide, and the fraction of soluble proteins with signal peptide (secretory proteins) ranges from 8 to 18% for most majority of the genomes. The N-in-type TM proteins with 2-, 4, 6- and 12-tms (number of transmembrane segments) are predominant among multi-spanning TM proteins, and correspondingly, significantly higher fractions of N-out-type TM proteins with 1-, 3-, 5- and 11-tms have a signal peptide. It is also found that the TM proteins with signal peptide tend to have a long N-tail loop. The averaged sequence length of TM proteins increases linearly with the increase of the number of TM segments, with the increasing rate of about 35 residues, suggesting a possibility that TM topologies might have been evolved by the 'internal Gene duplication' mechanism. Datasets of TM topologies predicted in this study are available at http://bioinfo.si.hirosaki-u.ac.jp/ similar to TMPinGS/. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:77 / 86
页数:10
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