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Related Concept Videos

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,...
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Protein-protein Interfaces02:04

Protein-protein Interfaces

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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...
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Conserved Binding Sites01:49

Conserved Binding Sites

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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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Ligand Binding Sites02:40

Ligand Binding Sites

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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.
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...
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G Protein-coupled Receptors01:15

G Protein-coupled Receptors

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G Protein-Coupled Receptors or GPCRs are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to sensory stimuli such as light, odors, hormones, cytokines, or neurotransmitters.
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
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Ligand Binding and Linkage00:49

Ligand Binding and Linkage

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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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A Knowledge Graph Approach to Elucidate the Role of Organellar Pathways in Disease via Biomedical Reports
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Predicting Protein Functions Based on Heterogeneous Graph Attention Technique.

Yingwen Zhao, Zhihao Yang, Lei Wang

    IEEE Journal of Biomedical and Health Informatics
    |February 6, 2024
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    Summary
    This summary is machine-generated.

    This study introduces a novel deep learning method for protein function prediction. By incorporating negative annotations into a heterogeneous graph, it enhances prediction accuracy for biological research and drug discovery.

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    Area of Science:

    • Bioinformatics
    • Computational Biology
    • Genomics

    Background:

    • Protein function prediction is vital for drug discovery and understanding disease mechanisms.
    • Current methods often overlook negative experimental annotations, limiting prediction precision.
    • Existing databases primarily contain positive protein function annotations.

    Purpose of the Study:

    • To develop an advanced deep learning method for accurate protein function prediction.
    • To address the underestimation of precision caused by ignoring negative annotations.
    • To improve the prediction of unobserved functional annotations.

    Main Methods:

    • Constructing a heterogeneous graph integrating protein-protein interactions, ontology structure, and negative annotations.
    • Utilizing a heterogeneous graph attention technique to learn protein and ontology term embeddings.
    • Reconstructing positive protein-term associations and scoring unobserved annotations.

    Main Results:

    • The proposed method demonstrated superior performance in predicting new protein annotations across Human, Mouse, and Arabidopsis.
    • Incorporating limited negative annotations significantly enhanced predictive performance.
    • The approach outperformed existing state-of-the-art methods in protein function prediction.

    Conclusions:

    • The novel deep learning method effectively leverages negative annotations for improved protein function prediction.
    • This approach offers a significant advancement for bioinformatics research and applications.
    • Accurate protein function prediction is crucial for biological discovery and therapeutic development.