数学和机器学习方法对蛋白质二次结构元素从Cα坐标进行分类.
Ali Sekmen1, Kamal Al Nasr1, Bahadir Bilgin1,2
1Department of Computer Science, Tennessee State University, Nashville, TN 37209, USA.
Biomolecules
|June 28, 2023
概括
仅使用Cα原子的新方法可以识别蛋白质二次结构元素 (SSEs),即使缺少原子数据. 当结构细节不完整时,这些方法可以替代传统工具.
科学领域:
- 结构生物学 结构生物学
- 生物信息学是一种生物信息学.
- 计算化学计算化学
背景情况:
- 二次结构元素 (SSE) 对于蛋白质三级结构的确定至关重要.
- 传统的SSE识别工具,如DSSP和STRIDE依赖于完整的原子信息.
- 缺少的原子数据对准确的SSE预测构成了重大挑战.
研究的目的:
- 开发和评估新的方法来分类SSEs,仅使用Cα原子信息.
- 在缺少空间原子细节的情况下,解决现有工具的局限性.
- 为了比较基于Cα的新方法的性能,相互和最先进的方法.
主要方法:
- 开发了三种不同的方法:数学模型,深度学习模型和五种机器学习模型组合.
- 使用蛋白质链中的Cα原子坐标作为输入.
- 对PCASSO算法和开发的方法进行比较分析.
主要成果:
- 提出的方法证明了使用Cα原子单独进行SSE预测的可行性.
- 绩效评估表明这些新方法在处理不完整的结构数据方面的有效性.
- 对比结果突出了每个开发的方法的优点和弱点.
结论:
- 当原子数据不完整时,基于Cα原子的方法为SSE识别提供了可行的替代方案.
- 这些新方法提高了结构生物学中二次结构预测的稳定性.
- 该研究为实验三级结构确定工作流提供了宝贵的工具.
相关概念视频
Protein Organization
6.6K
Proteins are polymers of amino acid residues. They are versatile and responsible for different cellular functions, including DNA replication, molecular transport, catalysis, and structural support. Proteins have a hierarchical structure comprising at least three levels of organization: primary, secondary, and tertiary structure. Some large proteins have a quaternary structure where individual protein subunits are linked together.
The primary structure of a protein is its amino acid sequence....
The primary structure of a protein is its amino acid sequence....
6.6K
Protein and Protein Structure
79.8K
Proteins are one of the most abundant organic molecules in living systems and have the most diverse range of functions of all macromolecules. Proteins may be structural, regulatory, contractile, or protective. They may serve in transport, storage, or membranes; or they may be toxins or enzymes. Their structures, like their functions, vary greatly. They are all, however, amino acid polymers arranged in a linear sequence.
A protein's shape is critical to its function. For example, an enzyme...
A protein's shape is critical to its function. For example, an enzyme...
79.8K
Protein Folding
118.5K
Overview
118.5K
Protein and Protein Structures
10.6K
10.6K
Conservation of Protein Domains Over Different Proteins
11.0K
Protein domains are small structurally independent units that are part of a single amino acid chain. Although these domains are often structurally independent, they may rely on synergistic effects to perform their functions as part of a larger protein. Protein domains may be conserved within the same organism, as well as across different organisms.
A limited set of protein domains often duplicate and recombine during evolution. These domains can be organized in different combinations to...
A limited set of protein domains often duplicate and recombine during evolution. These domains can be organized in different combinations to...
11.0K
Conserved Binding Sites
4.2K
Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
4.2K


