Jove
Visualize
联系我们

相关概念视频

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
The Equilibrium Binding Constant and Binding Strength02:18

The Equilibrium Binding Constant and Binding Strength

12.9K
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:
12.9K
Ligand Binding Sites02:40

Ligand Binding Sites

12.9K
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...
12.9K
Protein-protein Interfaces02:04

Protein-protein Interfaces

12.5K
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...
12.5K
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
Protein Networks02:26

Protein Networks

4.0K
An organism can have thousands of different proteins, and these proteins must cooperate to ensure the health of an organism. Proteins bind to other proteins and form complexes to carry out their functions. Many proteins interact with multiple other proteins creating a complex network of protein interactions.
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
4.0K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Targeting tumor-associated macrophages in pancreatic cancer.

iLIVER·2026
Same author

Tumor microenvironment remodeling in pancreatic cancer liver metastasis.

iLIVER·2025
Same author

Color and Aroma of Plums: Biosynthesis, Regulation, and Interrelationships.

Journal of agricultural and food chemistry·2025
Same author

<i>CCK</i> * (Convex Closure <i>K</i> *): A Suite of Algorithms for the De Novo Design of L- and D-peptide Binders.

bioRxiv : the preprint server for biology·2025
Same author

A novel protein cPFKFB4 encoded by hsa_circ_0065394 strengthens PKM2-mediated glucose metabolic reprogramming to facilitate pancreatic cancer progression under hypoxia.

Molecular cancer·2025
Same author

Predicting Pose Distribution of Protein Domains Connected by Flexible Linkers Is an Unsolved Problem.

Proteins·2025
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关实验视频

Updated: Jul 9, 2025

Author Spotlight: A Computational Approach to Decipher Amino Acid Preferences in Multispecific Protein-Protein Interactions
06:50

Author Spotlight: A Computational Approach to Decipher Amino Acid Preferences in Multispecific Protein-Protein Interactions

Published on: January 26, 2024

1.9K

通过同类学 (PATH) 预测亲和关系:可解释的绑定亲和关系预测与持久的同类学.

Yuxi Long, Bruce R Donald

    bioRxiv : the preprint server for biology
    |November 28, 2023
    PubMed
    概括

    我们开发了一种新的,可解释的算法,称为PATH,用于使用计算拓学预测蛋白质-连接体结合亲和力. 这种方法比以前的方法快得多,效率更高,在药物设计中提供了可比或更好的性能.

    科学领域:

    • 计算化学和结构生物学
    • 机器学习在药物发现中的作用
    • 对生物分子相互作用的拓数据分析.

    背景情况:

    • 准确的结合亲和力预测对于基于结构的药物设计至关重要.
    • 计算拓学,特别是代数拓学,在表示蛋白质-连接体相互作用方面表现出了前景.
    • 以前的拓方法缺乏解释性,并且具有很高的计算复杂性,限制了它们的应用.

    研究的目的:

    • 开发一种更快,更易于解释的算法,用持久的同类学来预测蛋白质 - 连接体结合亲和力.
    • 引入新的拓特征,核间持久轮 (IPC) 和持久指纹,用于结合亲和力预测.
    • 介绍PATH (通过同质性预测亲和力) 算法,包括PATH+和PATH-,用于增强药物设计.

    主要方法:

    • 开发了最快的已知算法,用于计算蛋白质-连接体复合体的持久同质特征,独立于蛋白质大小.
    • 引入了核间持久轮 (IPC) 和持久指纹,用于可解释的特征表示.
    • 实现了PATH算法,使用持久性指纹 (PATH+) 和IPC (PATH-) 上的浅回归树.

    主要成果:

    • 实现了对计算持久性指纹的时间复杂性的显著改进,独立于蛋白质大小.
    • 证明PATH+实现了与最先进的方法相匹配的性能,使用的功能显著减少,并提供可解释性.

    更多相关视频

    A Protocol for Computer-Based Protein Structure and Function Prediction
    16:41

    A Protocol for Computer-Based Protein Structure and Function Prediction

    Published on: November 3, 2011

    68.7K
    Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules
    10:58

    Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules

    Published on: July 25, 2013

    17.1K

    相关实验视频

    Last Updated: Jul 9, 2025

    Author Spotlight: A Computational Approach to Decipher Amino Acid Preferences in Multispecific Protein-Protein Interactions
    06:50

    Author Spotlight: A Computational Approach to Decipher Amino Acid Preferences in Multispecific Protein-Protein Interactions

    Published on: January 26, 2024

    1.9K
    A Protocol for Computer-Based Protein Structure and Function Prediction
    16:41

    A Protocol for Computer-Based Protein Structure and Function Prediction

    Published on: November 3, 2011

    68.7K
    Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules
    10:58

    Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules

    Published on: July 25, 2013

    17.1K
  • 与已建立的方法进行基准PATH,表现出可比或优越的性能,并减少过度装配.
  • 结论:

    • 开发的拓方法和PATH算法提供了一种高效,可解释和准确的方法来进行绑定亲和力预测.
    • 持久性指纹有效地捕获具有约束力的相关结构信息,在数据集中进行概括.
    • PATH代表了计算药物设计的重大进步,提供了一个开源解决方案.