PREDICTING OLIGOMERIZATION STATES OF COILED COILS

被引:199
作者
WOOLFSON, DN [1 ]
ALBER, T [1 ]
机构
[1] UNIV CALIF BERKELEY, DEPT MOLEC & CELL BIOL, BERKELEY, CA 94720 USA
关键词
AMINO ACID PROFILE; COILED COIL; HEPTAD REPEAT; PROFILE ANALYSIS; PROTEIN FOLDING; PROTEIN STRUCTURE PREDICTION;
D O I
10.1002/pro.5560040818
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
An algorithm based on the profile method was developed that faithfully distinguishes between the amino acid sequences of dimeric and trimeric coiled coils. Normalized sequence profiles derived from nonhomologous, two- and three-stranded, coiled-coil sequences with unambiguous registers were used to assign dimer and trimer propensities to test sequences. The difference between the dimer and trimer profile scores accurately reflected the preferred oligomerization state. The method relied on two strategies that may be generally applicable to profile calculations-profile values of solvent-exposed residues and of amino acids that were underrepresented in the database were given zero weight. Differences between the dimer and trimer profiles revealed sequence patterns that match and extend experimental studies of oligomer specification.
引用
收藏
页码:1596 / 1607
页数:12
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