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Experimentally constrained topology models for 51,208 bacterial inner membrane proteins
被引:48
作者:
Granseth, E
Daley, DO
Rapp, M
Melén, K
von Heijne, G
[1
]
机构:
[1] AlbaNova, Stockholm Bioinformat Ctr, SE-10691 Stockholm, Sweden
[2] Stockholm Univ, Dept Biochem & Biophys, SE-10691 Stockholm, Sweden
关键词:
membrane protein;
transmembrane helix;
topology prediction;
bioinformatics;
proteomics;
D O I:
10.1016/j.jmb.2005.07.053
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 used 502 Escherichia coli inner membrane proteins with experimentally determined C-terminal locations (cytoplasmic or periplasmic) from a recently published data set, together with an additional 106 bacterial membrane proteins with known topology, as queries in BLAST searches against a data base of 658,210 bacterial open reading frames from GenBank. We find 51,208 homologs to the query sequences for which we can assign the location of the C terminus or an internal residue to the same side of the membrane as the query's C terminus. These assignments are then used as constraints for topology prediction. The 51,208 much improved topology models derived in this way cover similar to 30% of all predicted bacterial inner membrane proteins in 225 fully sequenced bacterial genomes. (c) 2005 Elsevier Ltd. All rights reserved.
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页码:489 / 494
页数:6
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