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相关概念视频

Ligand Binding Sites02:40

Ligand Binding Sites

12.7K
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.
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...
12.7K
Conserved Binding Sites01:49

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...
4.2K
Protein-protein Interfaces02:04

Protein-protein Interfaces

12.4K
Many proteins form complexes to carry out their functions, making protein-protein interactions (PPIs) essential for an organism's survival. Most PPIs are stabilized by numerous weak noncovalent chemical forces. The physical shape of the interfaces determines the way two proteins interact. Many globular proteins have closely-matching shapes on their surfaces, which form a large number of weak bonds. Additionally, many PPIs occur between two helices or between a surface cleft and a...
12.4K
The Equilibrium Binding Constant and Binding Strength02:18

The Equilibrium Binding Constant and Binding Strength

12.8K
The equilibrium binding constant (Kb) quantifies the strength of a protein-ligand interaction. Kb can be calculated as follows when the reaction is at equilibrium:
12.8K
Ligand Binding and Linkage00:49

Ligand Binding and Linkage

4.8K
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...
4.8K

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相关实验视频

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Author Spotlight: Streamlining Protein Target Prediction and Validation via Molecular Docking and CETSA
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Author Spotlight: Streamlining Protein Target Prediction and Validation via Molecular Docking and CETSA

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PPDock:以口袋预测为基础的蛋白质 - 连接体盲对接

Jie Du1,2, Mingzhi Yuan1,2, Ao Shen1,2

  • 1Digital Medical Research Center, School of Basic Medical Sciences, Fudan University, Shanghai 200032, P. R. China.

Journal of chemical information and modeling
|January 15, 2025
PubMed
概括

我们开发了PPDock,这是一种新的深度学习方法,用于蛋白质 - 配体对接. 它通过在对接之前首先预测绑定口袋来提高准确性和效率,优于现有的盲目对接技术.

科学领域:

  • 计算化学是一种计算化学.
  • 药物发现 药物发现
  • 生物信息学是一种生物信息学.

背景情况:

  • 蛋白质-连接体对接对于药物发现至关重要,但传统方法在准确性和速度方面扎,特别是在盲目对接中.
  • 深度学习提高了效率,但经常使用整个蛋白质,阻碍了口袋识别和概括.

研究的目的:

  • 提出一种新的两阶段对接范式,以改进蛋白质-连接体对接.
  • 推出PPDock,一种新的盲目对接方法,结合口袋预测.

主要方法:

  • 一个两阶段的方法:首先预测蛋白质结合口袋,然后执行基于口袋的对接.
  • 开发PPDock,一种基于深度学习的盲目对接方法,利用口袋预测阶段.

主要成果:

  • 在基准数据集上,PPDock在多个评估指标上表现出卓越的表现.
  • 该方法实现了高的对接精度,增强了概括能力,并与现有技术相比提高了计算效率.

结论:

  • 在PPDock中实施的拟议的两阶段对接范式有效地解决了当前盲目对接方法的局限性.
  • 在药物发现中,PPDock为准确和高效的蛋白质-连接体对接提供了有前途的进步.

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