Prediction of membrane proteins based on classification of transmembrane segments

被引:36
作者
Kihara, D
Shimizu, T
Kanehisa, M [1 ]
机构
[1] Kyoto Univ, Inst Chem Res, Kyoto 6060011, Japan
[2] Hirosaki Univ, Fac Sci, Dept Informat Sci, Hirosaki, Aomori 0368244, Japan
来源
PROTEIN ENGINEERING | 1998年 / 11卷 / 11期
关键词
discriminant analysis; Mahalanobis distance; membrane protein class; protein structure prediction; compatibility score;
D O I
10.1093/protein/11.11.961
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The number of transmembrane segments often corresponds to a structural or functional class of membrane proteins such as to seven-transmembrane receptors and six-transmembrane ion channels. We have developed a new prediction method to detect the membrane protein class that is defined by the number of transmembrane segments, as well as to locate the transmembrane segments in the amino acid sequence. Each membrane protein class is represented by a model of ordering different types of transmembrane segments. Specifically, we have classified the transmembrane segments in known membrane proteins into five groups (types) using the Mahalanobis distance with the average hydrophobicity and the periodicity of hydrophobicity as a measure of similarity. The discriminant functions derived for these groups were then used to detect transmembrane segments and to match with the models for one- to fourteen-spanning membrane proteins and for globular proteins. Using the test data set of 89 membrane proteins whose transmembrane positions are known by experimental evidence, 61.8% of the proteins and 85.1% of the transmembrane segments were correctly predicted. Because of the new feature to predict membrane protein classes, the method should be useful in the functional assignment of genomic sequences.
引用
收藏
页码:961 / 970
页数:10
相关论文
共 37 条
[1]  
[Anonymous], 1976, ADV THEORY STAT
[2]   The SWISS-PROT protein sequence data bank and its supplement TrEMBL [J].
Bairoch, A ;
Apweller, R .
NUCLEIC ACIDS RESEARCH, 1997, 25 (01) :31-36
[3]   Reconstruction of amino acid biosynthesis pathways from the complete genome sequence [J].
Bono, H ;
Ogata, H ;
Goto, S ;
Kanehisa, M .
GENOME RESEARCH, 1998, 8 (03) :203-210
[4]  
CLAROS MG, 1994, COMPUT APPL BIOSCI, V10, P685
[5]   The first genome from the third domain of life [J].
Clayton, RA ;
White, O ;
Ketchum, KA ;
Venter, JC .
NATURE, 1997, 387 (6632) :459-462
[6]   STRUCTURE OF THE PROTEIN SUBUNITS IN THE PHOTOSYNTHETIC REACTION CENTER OF RHODOPSEUDOMONAS-VIRIDIS AT 3A RESOLUTION [J].
DEISENHOFER, J ;
EPP, O ;
MIKI, K ;
HUBER, R ;
MICHEL, H .
NATURE, 1985, 318 (6047) :618-624
[7]  
DONNELLY D, 1993, PROTEIN SCI, V2, P55
[8]   ANALYSIS OF MEMBRANE AND SURFACE PROTEIN SEQUENCES WITH THE HYDROPHOBIC MOMENT PLOT [J].
EISENBERG, D ;
SCHWARZ, E ;
KOMAROMY, M ;
WALL, R .
JOURNAL OF MOLECULAR BIOLOGY, 1984, 179 (01) :125-142
[9]  
ESPOSTI MD, 1989, ITAL J BIOCHEM, V38, P1
[10]  
GOMETSCHELNOKOW U, 1994, EMBO J, V13, P338