Characterization of the folding degree of proteins

被引:213
作者
Estrada, E [1 ]
机构
[1] Univ Santiago de Compostela, Dept Organ Chem, Fac Pharm, Santiago De Compostela, Spain
关键词
D O I
10.1093/bioinformatics/18.5.697
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: The characterization of the folding degree of chains is central to the elucidation of structure--function relationships in proteins. Here we present a new index for characterizing the folding degree of a (protein) chain. This index shows a range of features that are desirable for the study of the relation between structure and function in proteins. Results: A novel index characterizing the folding degree of (protein) chains is developed based on the spectral moments of a matrix representing the dihedral angles (phi, omega and epsilon) of the protein main chain. The proposed index is normalized to the chain size, is not correlated to the gyration radius of the backbone chain and is able to distinguish between structures for which the sum of the main-chain dihedral angles is identical. The index is well correlated to the percentages of helix and strand in proteins, shows a linear dependence with temperature changes, and is able to differentiate among protein families.
引用
收藏
页码:697 / 704
页数:8
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