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Chemical Shift: Internal References and Solvent Effects01:17

Chemical Shift: Internal References and Solvent Effects

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In an NMR sample, precise measurement of the absolute absorption frequencies of nuclei is difficult. A standard internal reference compound is added, and the frequency difference between the reference signal and sample signals is measured.
The internal reference compound generally used in NMR spectroscopy is tetramethylsilane (TMS). TMS is preferred because it is chemically inert, soluble in NMR solvents, and easily removable. Also, the highly shielded methyl protons in TMS yield an intense...
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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...
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Proteins are dynamic macromolecules that carry out a wide variety of essential processes; however, the activities of most proteins depend on their interactions with other molecules or ions, known as ligands.
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Allosteric proteins have more than one ligand binding site; the binding of a ligand to any of these sites influences the binding of ligands to the other sites. When a protein is allosteric, its binding sites are called coupled or linked.  In the case of enzymes, the site that binds to the substrate is known as the active site and the other site is known as the regulatory site. When a ligand binds to the regulatory site, this leads to conformational changes in the protein that can influence...
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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.
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溶剂可访问性在用主要侧链预测程序进行蛋白质建模时促进旋转器错误.

Tareq Hameduh1, Michal Mokry1, Andrew D Miller1,2,3

  • 1Department of Chemistry and Biochemistry, Mendel University in Brno, Zemědělská 1665/1, CZ-613 00 Brno, Czech Republic.

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概括

蛋白质建模中的关键旋转器预测错误与溶剂可访问性有关,特别是对于极性和带电氨基酸. 了解这种相关性对于提高蛋白质结构准确性至关重要.

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科学领域:

  • 计算生物学 计算生物学
  • 结构生物学 结构生物学
  • 生物化学 生物化学

背景情况:

  • 侧链旋转器预测是蛋白质3D结构构建的关键步骤.
  • 先进的算法利用旋转器库,组合式搜索和评分函数进行优化.

研究的目的:

  • 在蛋白质建模中识别关键旋转器错误的来源.
  • 为纠正和改善蛋白质建模精度提供基础.

主要方法:

  • 使用2496个高质量,单链,全原子,过的蛋白质3D结构的蛋白质建模程序的评估.
  • 离散的旋转分析来比较原始和计算的蛋白质结构.
  • 分析了513,024个过的残留物记录.

主要成果:

  • 旋转器错误取决于氨基酸残留物,极性和带电残留物 (例如,氨酸,氨酸,谷氨酸) 显示出更多的错误.
  • 这些错误与氨基酸残留溶剂可访问性增加有关.
  • 在具有高溶剂可访问性的残留物中观察到对非正规离旋体的倾向,这给预测带来了挑战.

结论:

  • 溶剂可访问性显著影响侧链预测的准确性.
  • 了解溶剂可访问性的作用是提高蛋白质建模精度的关键.
  • 蛋白质建模的未来改进应该集中在解决与溶剂暴露残留物相关的旋转预测挑战上.