Retention of enzyme gene duplicates by subfunctionalization
被引:8
作者:
Braun, FN
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机构:
Stockholm Univ, Dept Biochem & Biophys, Stockholm Bioinformat Ctr, S-10691 Stockholm, SwedenStockholm Univ, Dept Biochem & Biophys, Stockholm Bioinformat Ctr, S-10691 Stockholm, Sweden
Braun, FN
[1
]
Liberles, DA
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机构:Stockholm Univ, Dept Biochem & Biophys, Stockholm Bioinformat Ctr, S-10691 Stockholm, Sweden
Liberles, DA
机构:
[1] Stockholm Univ, Dept Biochem & Biophys, Stockholm Bioinformat Ctr, S-10691 Stockholm, Sweden
[2] Univ Bergen, BCCS, Computat Biol Unit, N-5020 Bergen, Norway
gene duplication;
sequence-structure-function correlation;
enzyme specificity;
protein evolution;
D O I:
10.1016/S0141-8130(03)00059-X
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:
Duplication-degeneration-complementation (DDC) describes a process by which evolving duplicates of a pleiotropic ancestral gene divide up the multiple functions of the ancestor between them (i.e. subfunctionalize), and this ultimately frustrates the rate of pseudogene formation. Focusing explicitly on enzyme-like pleiotropic function, we model DDC driven by sequence divergence between duplicates. The model incorporates an idealized sequence-function mapping in which enzyme-substrate binding affinity is related to hydrophobic versus polar (HP) amino-acid composition of tertiary structure about the binding pocket. In this sense, a transparent coupling between physical-chemical function of an enzyme and sequence evolution is presented. (C) 2003 Elsevier B.V. All rights reserved.