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Protein Folding Structures: Formation of Folding StructuresBased on Probability Theory

机译:蛋白质折叠结构:折叠结构的形成基于概率论

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摘要

To the best of our knowledge, this is the first study that shows that the X-ray structures of proteins can be dissected into their continuous folding structure units. Each folding structure unit was designed such that both the terminal di- or tri-peptide sequences shared common sequences with the two adjacent folding structure units. To encode the folding structure information of proteins into their amino acid sequences, we proposed 44 kinds of folding elements, which covered all of the amino acids in the protein chains, and defined all folding structure units. The folding element was defined to mean a minimum structural piece, which covered the frame of the main chain of each amino acid in a protein chain. A folding structure unit of a local sequence could be fully characterized by the sequential combination of individual folding elements assigned to each amino acid. The folding structure information showed amino acid preferences in various positions in folding structure units. Folding structure formation proceeded on the basis of probability theory. Strikingly, relative formation ability analysis clearly indicatedthat we can decode the types and the chain length of folding structureunits from the amino acid sequence of a protein.
机译:据我们所知,这是第一项显示蛋白质X射线结构可以分解为连续折叠结构单元的研究。设计每个折叠结构单元,使得末端二肽或三肽序列均与两个相邻的折叠结构单元共享共同序列。为了将蛋白质的折叠结构信息编码成它们的氨基酸序列,我们提出了44种折叠元件,它们覆盖了蛋白质链中的所有氨基酸,并定义了所有折叠结构单元。折叠元件被定义为意指最小的结构片段,其覆盖蛋白质链中每个氨基酸的主链的框架。局部序列的折叠结构单元可以通过分配给每个氨基酸的各个折叠元件的顺序组合来充分表征。折叠结构信息显示了在折叠结构单元中各个位置的氨基酸偏好。折叠结构的形成基于概率论进行。令人惊讶的是,相对形成能力分析清楚地表明我们可以解码折叠结构的类型和链长蛋白质氨基酸序列的最大单位。

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