Gibbs sampling and helix-cap motifs.
Gibbs sampling and helix-cap motifs.
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DOI:
10.1093/nar/gki842
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发表时间:
2005
影响因子:
14.9
通讯作者:
Wingreen NS
中科院分区:
文献类型:
--
作者:
Kruus E;Thumfort P;Tang C;Wingreen NS
Protein backbones have characteristic secondary structures, including α-helices and β-sheets. Which structure is adopted locally is strongly biased by the local amino acid sequence of the protein. Accurate (probabilistic) mappings from sequence to structure are valuable for both secondary-structure prediction and protein design. For the case of α-helix caps, we test whether the information content of the sequence–structure mapping can be self-consistently improved by using a relaxed definition of the structure. We derive helix-cap sequence motifs using database helix assignments for proteins of known structure. These motifs are refined using Gibbs sampling in competition with a null motif. Then Gibbs sampling is repeated, allowing for frameshifts of ±1 amino acid residue, in order to find sequence motifs of higher total information content. All helix-cap motifs were found to have good generalization capability, as judged by training on a small set of non-redundant proteins and testing on a larger set. For overall prediction purposes, frameshift motifs using all training examples yielded the best results. Frameshift motifs using a fraction of all training examples performed best in terms of true positives among top predictions. However, motifs without frameshifts also performed well, despite a roughly one-third lower total information content.
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影响因子:
14.9
作者:
Ginalski, K;Grishin, NV;Godzik, A;Rychlewski, L
通讯作者:
Rychlewski, L
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作者:
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DOI:
10.1080/07391102.2000.10506570
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通讯作者:
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