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
[21]   Complete sequence analysis of the genome of the bacterium Mycoplasma pneumoniae [J].
Himmelreich, R ;
Hilbert, H ;
Plagens, H ;
Pirkl, E ;
Li, BC ;
Herrmann, R .
NUCLEIC ACIDS RESEARCH, 1996, 24 (22) :4420-4449
[22]  
HOBOHM U, 1992, PROTEIN SCI, V1, P409
[23]   STRUCTURE AT 2.8-ANGSTROM RESOLUTION OF CYTOCHROME-C-OXIDASE FROM PARACOCCUS-DENITRIFICANS [J].
IWATA, S ;
OSTERMEIER, C ;
LUDWIG, B ;
MICHEL, H .
NATURE, 1995, 376 (6542) :660-669
[24]   A MODEL RECOGNITION APPROACH TO THE PREDICTION OF ALL-HELICAL MEMBRANE-PROTEIN STRUCTURE AND TOPOLOGY [J].
JONES, DT ;
TAYLOR, WR ;
THORTON, JM .
BIOCHEMISTRY, 1994, 33 (10) :3038-3049
[25]  
Kaneko T, 1996, DNA Res, V3, P109
[26]   Negatively charged amino acid residues play an active role in orienting the Sec-independent Pf3 coat protein in the Escherichia coli inner membrane [J].
Kiefer, D ;
Hu, XT ;
Dalbey, R ;
Kuhn, A .
EMBO JOURNAL, 1997, 16 (09) :2197-2204
[27]   The complete genome sequence of the hyperthermophilic, sulphate-reducing archaeon Archaeoglobus fulgidus [J].
Klenk, HP ;
Clayton, RA ;
Tomb, JF ;
White, O ;
Nelson, KE ;
Ketchum, KA ;
Dodson, RJ ;
Gwinn, M ;
Hickey, EK ;
Peterson, JD ;
Richardson, DL ;
Kerlavage, AR ;
Graham, DE ;
Kyrpides, NC ;
Fleischmann, RD ;
Quackenbush, J ;
Lee, NH ;
Sutton, GG ;
Gill, S ;
Kirkness, EF ;
Dougherty, BA ;
McKenney, K ;
Adams, MD ;
Loftus, B ;
Peterson, S ;
Reich, CI ;
McNeil, LK ;
Badger, JH ;
Glodek, A ;
Zhou, LX ;
Overbeek, R ;
Gocayne, JD ;
Weidman, JF ;
McDonald, L ;
Utterback, T ;
Cotton, MD ;
Spriggs, T ;
Artiach, P ;
Kaine, BP ;
Sykes, SM ;
Sadow, PW ;
DAndrea, KP ;
Bowman, C ;
Fujii, C ;
Garland, SA ;
Mason, TM ;
Olsen, GJ ;
Fraser, CM ;
Smith, HO ;
Woese, CR .
NATURE, 1997, 390 (6658) :364-&
[28]   The complete genome sequence of the Gram-positive bacterium Bacillus subtilis [J].
Kunst, F ;
Ogasawara, N ;
Moszer, I ;
Albertini, AM ;
Alloni, G ;
Azevedo, V ;
Bertero, MG ;
Bessieres, P ;
Bolotin, A ;
Borchert, S ;
Borriss, R ;
Boursier, L ;
Brans, A ;
Braun, M ;
Brignell, SC ;
Bron, S ;
Brouillet, S ;
Bruschi, CV ;
Caldwell, B ;
Capuano, V ;
Carter, NM ;
Choi, SK ;
Codani, JJ ;
Connerton, IF ;
Cummings, NJ ;
Daniel, RA ;
Denizot, F ;
Devine, KM ;
Dusterhoft, A ;
Ehrlich, SD ;
Emmerson, PT ;
Entian, KD ;
Errington, J ;
Fabret, C ;
Ferrari, E ;
Foulger, D ;
Fritz, C ;
Fujita, M ;
Fujita, Y ;
Fuma, S ;
Galizzi, A ;
Galleron, N ;
Ghim, SY ;
Glaser, P ;
Goffeau, A ;
Golightly, EJ ;
Grandi, G ;
Guiseppi, G ;
Guy, BJ ;
Haga, K .
NATURE, 1997, 390 (6657) :249-256
[29]   TRANSPORT ROUTE FOR SYNAPTOBREVIN VIA A NOVEL PATHWAY OF INSERTION INTO THE ENDOPLASMIC-RETICULUM MEMBRANE [J].
KUTAY, U ;
AHNERTHILGER, G ;
HARTMANN, E ;
WIEDENMANN, B ;
RAPOPORT, TA .
EMBO JOURNAL, 1995, 14 (02) :217-223
[30]   Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites [J].
Nielsen, H ;
Engelbrecht, J ;
Brunak, S ;
vonHeijne, G .
PROTEIN ENGINEERING, 1997, 10 (01) :1-6