Search arXivSearch

arXiv · 1809.06632

Modular decomposition of protein structure using community detection

Abstract

As the number of solved protein structures increases, the opportunities for meta-analysis of this dataset increase too. Protein structures are known to be formed of domains; structural and functional subunits that are often repeated across sets of proteins. These domains generally form compact, globular regions, and are therefore often easily identifiable by inspection, yet the problem of automatically fragmenting the protein into these compact substructures remains computationally challenging. Existing domain classification methods focus on finding subregions of protein structure that are conserved, rather than finding a decomposition which spans the full protein structure. However, such a decomposition would find ready application in coarse-graining molecular dynamics, analysing the protein's topology, in de novo protein design and in fitting electron microscopy maps. Here, we present a tool for performing this modular decomposition using the Infomap community detection algorithm. The protein structure is abstracted into a network in which its amino acids are the nodes, and where the edges are generated using a simple proximity test. Infomap can then be used to identify highly intra-connected regions of the protein. We perform this decomposition systematically across 4000 distinct protein structures, taken from the Protein Data Bank. The decomposition obtained correlates well with existing PFAM sequence classifications, but has the advantage of spanning the full protein, with the potential for novel domains. The coarse-grained network formed by the communities can also be used as a proxy for protein topology at the single-chain level; we demonstrate that grouping these proteins by their coarse-grained network results in a functionally significant classification.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

William P. Grant, Sebastian E. Ahnert. 2018-09-18. Modular decomposition of protein structure using community detection. https://doi.org/10.1093/comnet%2Fcny014

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

SaltyMeta: a curated benchmark and protein language model-informed web tool for salty peptide prediction

Excess sodium intake remains a major public health challenge, while salty and saltiness-enhancing peptides offer a potential route to preserve sensory saltiness in reduced-sodium foods. Machine-learning studies of salty peptides, however, are constrained by small datasets, heterogeneous evidence standards, uncertain negative labels, and sequence similarity leakage. Here we present SaltyMeta, a curated benchmark and web-accessible screening framework for salty or saltiness-enhancing short peptides. The benchmark contains 580 peptides, including 280 positive peptides and 300 negative peptides, all standardized to 2-15 residue one-letter amino-acid sequences. Quality control found no non-standard residues, exact duplicates, or positive-negative overlaps. A similarity-grouped split retained 456 peptides for training and 124 for held-out testing. We evaluated 548 interpretable peptide descriptors, frozen ESM2 embeddings at 8M, 35M, and 150M parameter scales, and descriptor-embedding fusion models under grouped cross-validation. The traditional ExtraTrees baseline selected by training-set grouped cross-validation achieved ROC-AUC=0.693 in cross-validation and ROC-AUC=0.704, PR-AUC=0.702, F1=0.626, and MCC=0.304 on the held-out test set. The best initial protein-language-model fusion was traditional descriptors plus ESM2-8M embeddings, with grouped CV ROC-AUC=0.696 and test ROC-AUC=0.700. Advanced optimization using PCA95 dimensionality reduction and ExtraTrees feature-importance filtering yielded a practical ESM2-8M PCA95 top-300 model with test ROC-AUC=0.715 and PR-AUC=0.703, although repeated-CV gains remained modest. SaltyMeta is a transparent prioritization tool, not a sensory validation substitute. We provide benchmark, models, scripts, GitHub, and Streamlit for reproducible screening of food-derived peptides.

q-bio.BM

Synthesizing State-of-the-Art Structure Predictions from Soup of Co-folding Models

Co-folding models have advanced rapidly, yet no single model consistently performs best across all biomolecular complexes. This raises the question of whether independently trained co-folding models encode complementary information that can be transferred across co-folding models. We introduce SoupFold, which improves co-folding predictions by learning simple mappings between the representation spaces of co-folding models. At inference time, SoupFold transfers and incorporates representations from other co-folding models to update the representation used for structure prediction. Importantly, this does not re-train the co-folding models. We evaluate SoupFold on protein-protein and protein-ligand prediction tasks of FoldBench using AlphaFold3, Protenix, ESMFold2, and OpenDDE. By combining their representations, SoupFold achieves state-of-the-art performance on both protein-protein and protein-ligand structure prediction, showing that independently trained co-folding models encode complementary information that can be effectively transferred across models.

q-bio.BM

Exploring Optimal Parameters for Ligand-Based Virtual Screening in Early Drug Discovery

Ligand-based virtual screening depends on choices that are often treated as implementation details, including the similarity threshold, fingerprint setting and atom-invariant scheme. We examined how these choices altered the composition of ranked searches against the Enamine library for four aminergic reference ligands: atomoxetine, bupropion, mirtazapine and venlafaxine. Candidate sets were evaluated by compound-weighted scaffold novelty, normalized Shannon scaffold diversity and three computational estimates of synthetic accessibility. We first identified ligand-specific operating points along cumulative Tanimoto-ranked searches. We then compared five extended-connectivity fingerprint settings at matched retrieval depths and compared ECFP4 with the feature-class analogue FCSFP4. Finally, 240 records, corresponding to 229 unique structures, were scored independently by three chemists who were blinded to the computational scores. No single Tanimoto cutoff described all four searches. ECFP8 provided the most stable pooled setting, although venlafaxine favored ECFP2. ECFP4 was the stronger primary fingerprint in pooled comparisons, whereas FCSFP4 contributed nonredundant chemical space. Agreement among individual chemists was moderate, and the mean rating was more reliable than a single rating. SCScore showed the highest association with the blinded consensus, but performance varied by ligand. These results support a staged screening design in which a pooled default is followed by ligand-specific calibration and expert review.

q-bio.BM