The fragment transformation method to detect the protein structural motifs

Authors

  • Chih-Hao Lu,

    1. Institute of Bioinformatics, National Chiao Tung University, Hsinchu, Taiwan, Republic of China
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  • Yeong-Shin Lin,

    1. Department of Biological Science & Technology, National Chiao Tung University, Hsinchu, Taiwan, Republic of China
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  • Yu-Ching Chen,

    1. Institute of Bioinformatics, National Chiao Tung University, Hsinchu, Taiwan, Republic of China
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  • Chin-Sheng Yu,

    1. Department of Biological Science & Technology, National Chiao Tung University, Hsinchu, Taiwan, Republic of China
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  • Shi-Yu Chang,

    1. Institute of Bioinformatics, National Chiao Tung University, Hsinchu, Taiwan, Republic of China
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  • Jenn-Kang Hwang

    Corresponding author
    1. Institute of Bioinformatics, National Chiao Tung University, Hsinchu, Taiwan, Republic of China
    2. Department of Biological Science & Technology, National Chiao Tung University, Hsinchu, Taiwan, Republic of China
    3. Core Facility for Structural Bioinformatics, National Chiao Tung University, Hsinchu, Taiwan, Republic of China
    • Institute of Bioinformatics, National Chiao Tung University, Hsinchu 30050, Taiwan, ROC
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Abstract

To identify functional structural motifs from protein structures of unknown function becomes increasingly important in recent years due to the progress of the structural genomics initiatives. Although certain structural patterns such as the Asp-His-Ser catalytic triad are easy to detect because of their conserved residues and stringently constrained geometry, it is usually more challenging to detect a general structural motifs like, for example, the ββα-metal binding motif, which has a much more variable conformation and sequence. At present, the identification of these motifs usually relies on manual procedures based on different structure and sequence analysis tools. In this study, we develop a structural alignment algorithm combining both structural and sequence information to identify the local structure motifs. We applied our method to the following examples: the ββα-metal binding motif and the treble clef motif. The ββα-metal binding motif plays an important role in nonspecific DNA interactions and cleavage in host defense and apoptosis. The treble clef motif is a zinc-binding motif adaptable to diverse functions such as the binding of nucleic acid and hydrolysis of phosphodiester bonds. Our results are encouraging, indicating that we can effectively identify these structural motifs in an automatic fashion. Our method may provide a useful means for automatic functional annotation through detecting structural motifs associated with particular functions. Proteins 2006. © 2006 Wiley-Liss, Inc.

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