Genome-wide analysis of integral membrane proteins from eubacterial, archaean, and eukaryotic organisms

被引:1187
作者
Wallin, E [1 ]
von Heijne, G [1 ]
机构
[1] Univ Stockholm, Dept Biochem, S-10691 Stockholm, Sweden
关键词
genomics; membrane protein; topology;
D O I
10.1002/pro.5560070420
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
We have carried out detailed statistical analyses of integral membrane proteins of the helix-bundle class from eubacterial, archaean, and eukaryotic organisms for which genome-wide sequence data are available. Twenty to 30% of all ORFs are predicted to encode membrane proteins, with the larger genomes containing a higher fraction than the smaller ones. Although there is a general tendency that proteins with a smaller number of transmembrane segments are more prevalent than those with many, uni-cellular organisms appear to prefer proteins with 6 and 12 transmembrane segments, whereas Caenorhabditis elegans and Homo sapiens have a slight preference for proteins with seven transmembrane segments. In all organisms, there is a tendency that membrane proteins either have many transmembrane segments with short connecting loops or few transmembrane segments with large extra-membraneous domains. Membrane proteins from all organisms studied, except possibly the archaeon Methanococcus jannaschii, follow the so-called "positive-inside" rule; i.e., they tend to have a higher frequency of positively charged residues in cytoplasmic than in extracytoplasmic segments.
引用
收藏
页码:1029 / 1038
页数:10
相关论文
共 47 条
[31]   FINE-TUNING THE TOPOLOGY OF A POLYTOPIC MEMBRANE-PROTEIN - ROLE OF POSITIVELY AND NEGATIVELY CHARGED AMINO-ACIDS [J].
NILSSON, IM ;
VONHEIJNE, G .
CELL, 1990, 62 (06) :1135-1141
[32]   Prediction of membrane protein topology utilizing multiple sequence alignments [J].
Persson, B ;
Argos, P .
JOURNAL OF PROTEIN CHEMISTRY, 1997, 16 (05) :453-457
[33]  
Persson B, 1996, PROTEIN SCI, V5, P363
[34]  
Rapoport TA, 1996, ANNU REV BIOCHEM, V65, P271
[35]   Topology prediction for helical transmembrane proteins at 86% accuracy [J].
Rost, B ;
Fariselli, P ;
Casadio, R .
PROTEIN SCIENCE, 1996, 5 (08) :1704-1718
[36]   PREDICTING THE TOPOLOGY OF EUKARYOTIC MEMBRANE-PROTEINS [J].
SIPOS, L ;
VONHEIJNE, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 213 (03) :1333-1340
[37]   HEADS OR TAILS - WHAT DETERMINES THE ORIENTATION OF PROTEINS IN THE MEMBRANE [J].
SPIESS, M .
FEBS LETTERS, 1995, 369 (01) :76-79
[38]   CLUSTAL-W - IMPROVING THE SENSITIVITY OF PROGRESSIVE MULTIPLE SEQUENCE ALIGNMENT THROUGH SEQUENCE WEIGHTING, POSITION-SPECIFIC GAP PENALTIES AND WEIGHT MATRIX CHOICE [J].
THOMPSON, JD ;
HIGGINS, DG ;
GIBSON, TJ .
NUCLEIC ACIDS RESEARCH, 1994, 22 (22) :4673-4680
[39]   The complete genome sequence of the gastric pathogen Helicobacter pylori [J].
Tomb, JF ;
White, O ;
Kerlavage, AR ;
Clayton, RA ;
Sutton, GG ;
Fleischmann, RD ;
Ketchum, KA ;
Klenk, HP ;
Gill, S ;
Dougherty, BA ;
Nelson, K ;
Quackenbush, J ;
Zhou, LX ;
Kirkness, EF ;
Peterson, S ;
Loftus, B ;
Richardson, D ;
Dodson, R ;
Khalak, HG ;
Glodek, A ;
McKenney, K ;
Fitzegerald, LM ;
Lee, N ;
Adams, MD ;
Hickey, EK ;
Berg, DE ;
Gocayne, JD ;
Utterback, TR ;
Peterson, JD ;
Kelley, JM ;
Cotton, MD ;
Weldman, JM ;
Fujii, C ;
Bowman, C ;
Watthey, L ;
Wallin, E ;
Hayes, WS ;
Weidman, JM ;
Fujii, C ;
Borodovsky, M ;
Karp, PD ;
Smith, HO ;
Fraser, CM ;
Venter, JC .
NATURE, 1997, 388 (6642) :539-547
[40]   The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 angstrom [J].
Tsukihara, T ;
Aoyama, H ;
Yamashita, E ;
Tomizaki, T ;
Yamaguchi, H ;
ShinzawaItoh, K ;
Nakashima, R ;
Yaono, R ;
Yoshikawa, S .
SCIENCE, 1996, 272 (5265) :1136-1144