Rethinking what pLDDT really tells us about protein flexibility
Jakob R Riccabona1, Johannes R Loeffler2, Clara T Schoeder1
1Institute for Drug Discovery, Faculty of Medicine, Leipzig University, Leipzig, Germany; Center for Scalable Data Analytics and Artificial Intelligence ScaDS.AI, Dresden/Leipzig, Germany.
Structure (London, England : 1993)
|December 5, 2025
Summary
Deep learning accurately predicts protein structures. However, the study questions if predicted local confidence scores reflect true protein flexibility, crucial for understanding dynamics.
Area of Science:
- Structural biology
- Computational biology
- Biophysics
Background:
- Deep learning models have revolutionized protein 3D structure prediction.
- Confidence metrics like predicted local distance difference test (pLDDT) estimate prediction uncertainty.
Purpose of the Study:
- To investigate whether pLDDT accurately reflects intrinsic protein flexibility.
- To advance the understanding of protein dynamics and conformational changes.
Main Methods:
- Analysis of deep learning model outputs (pLDDT).
- Comparison of pLDDT with experimental and computational measures of protein flexibility.
Main Results:
- The relationship between pLDDT and intrinsic protein flexibility requires further investigation.
- pLDDT's ability to capture true protein dynamics is not fully established.
Conclusions:
- Clarifying the link between pLDDT and protein flexibility is essential.
- Accurate quantification of protein dynamics is key for modeling conformational changes across timescales.
Related Concept Videos
Intrinsically Disordered Proteins
19.2K
Intrinsically disordered proteins are a group of proteins that do not fold into specific three-dimensional structures. Their structural flexibility allows them to complement ordered proteins to perform functions that are inaccessible to rigid structures. They are more common in eukaryotes than prokaryotes and may either be exclusively intrinsically disordered or hybrid proteins, consisting of a mix of ordered and disordered regions. The absence of a rigid structure in these proteins can be...
19.2K
Intrinsically Disordered Proteins
2.7K
2.7K
Protein Folding
125.8K
Overview
125.8K
Protein Folding
10.9K
Proteins are chains of amino acids linked together by peptide bonds. Upon synthesis, a protein folds into a three-dimensional conformation, critical to its biological function. Interactions between its constituent amino acids guide protein folding, and hence the protein structure is primarily dependent on its amino acid sequence.
Protein Structure Is Critical to Its Biological Function
Proteins perform a wide range of biological functions such as catalyzing chemical reactions, providing...
Protein Structure Is Critical to Its Biological Function
Proteins perform a wide range of biological functions such as catalyzing chemical reactions, providing...
10.9K
Covalently Linked Protein Regulators
8.6K
Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein....
These groups modify specific amino acids in a protein....
8.6K
Ligand Binding and Linkage
5.4K
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...
5.4K


