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Szklarczyk, D.

Publications and source records attributed to Szklarczyk, D..

8 recordsLinked to original sources

SPACE: STRING proteins as complementary embeddings

Representation learning has revolutionized sequence-based prediction of protein function and subcellular localization. Protein networks are an important source of information complementary to sequences, but the use of protein networks has proven to be challenging in the context of machine learning, especially in a cross-species setting. To address this, we leveraged the STRING database of protein networks and orthology relations for 1,322 eukaryotes to generate network-based cross-species protein embeddings. We did this by first creating species-specific network embeddings and subsequently aligning them based on orthology relations to facilitate direct cross-species comparisons. We show that these aligned network embeddings ensure consistency across species without sacrificing quality compared to species-specific network embeddings. We also show that the aligned network embeddings are complementary to sequence embedding techniques, despite the use of seqeuence-based orthology relations in the alignment process. Finally, we demonstrate the utility and quality of the embeddings by using them for two well-established tasks: subcellular localization prediction and protein function prediction. Training logistic regression classifiers on aligned network embeddings and sequence embeddings improved the accuracy over using sequence alone, reaching performance numbers close to state-of-the-art deep-learning methods. A set of precomputed cross-species network embeddings and ProtT5 embeddings for all eukaryotic proteins have been included in STRING version 12.0.

bioinformatics↗

Clade-wise alignment integration improves co-evolutionary signals for protein-protein interaction prediction

BackgroundProtein-protein interactions play essential roles in almost all biological processes. The binding interfaces between interacting proteins impose evolutionary constraints, leading to co-evolutionary signals that have successfully been employed to predict protein interactions from multiple sequence alignments (MSAs). During the construction of MSAs for this purpose, critical choices have to be made: how to ensure the reliable identification of orthologs, how to deal with paralogs, and how to optimally balance the need for large alignments versus sufficient alignment quality. ResultsHere, we propose a divide-and-conquer strategy for MSA generation: instead of building a single, large alignment for each protein, multiple distinct alignments are constructed, each covering only a single clade in the tree of life. Co-evolutionary signals are searched separately within these clades, and are only subsequently integrated into a final interaction prediction using machine learning. We find that this strategy markedly improves overall prediction performance, concomitant with better alignment quality. Using the popular DCA algorithm to systematically search pairs of such alignments, a genome-wide all-against-all interaction scan in a bacterial genome is demonstrated. ConclusionsGiven the recent successes of AlphaFold in predicting protein-protein interactions at atomic detail, a discover-and-refine approach is proposed: our method could provide a fast and accurate strategy for pre-screening the entire genome, submitting to AlphaFold only promising interaction candidates - thus reducing false positives as well as computation time.

bioinformatics↗

PaxDB 5.0: curated protein quantification data suggests adaptive proteome changes

The "Protein Abundances Across Organisms" database (PaxDB) is an integrative meta-resource dedicated to protein abundance levels, in tissue-specific or whole-organism proteomes. PaxDB focuses on computing best-estimate abundances for proteins in normal/healthy contexts, and expresses abundance values for each protein in "parts per million" (ppm) in relation to all other protein molecules in the cell. The uniform data re-processing, quality scoring, and integrated orthology relations have made PaxDB one of the preferred tools for comparisons between individual datasets, tissues or organisms. In describing the latest version 5.0 of PaxDB, we particularly emphasise the data integration from various types of raw data, and how we expanded the number of organisms and tissue groups as well as the proteome coverage. The current collection of PaxDB includes 831 original datasets from 170 species, including 22 Archaea, 81 Bacteria and 67 Eukaryota. Apart from detailing the data update, we also show a comparative analysis of the human proteome subset of PaxDB against the two most widely-used human proteome data resources: Human Protein Atlas (HPA) and Genotype-Tissue Expression (GTEx). Lastly, we present a use case of PaxDB, showing how protein abundance data can be used to study the evolution of relative amino acid usage in Fungi.

bioinformatics↗

CanIsoNet: A Database to Study the Functional Impact of Isoform Switching Events in Cancer

MotivationAlternative splicing, as an essential regulatory mechanism in normal mammalian cells, is frequently disturbed in cancer and other diseases. Switches in the expression of most dominant alternative isoforms can alter protein interaction networks of associated genes giving rise to a disease or disease progression. Here, we present CanIsoNet (disease-specific isoform interaction network), a database to view, browse and search these isoform switching events. CanIsoNet is the first webserver that incorporates isoform expression data with STRING interaction networks and ClinVar annotations to predict the pathogenic impact of isoform switching events in various diseases. ResultsData in CanIsoNet can be browsed by disease or searched by genes or isoforms in annotation-rich data tables. Various annotations for 11,072 isoforms and 13,531 unique isoform switching events across 28 different tissue types are provided. The network density score for each disease-specific isoform, PFAM domain IDs of disrupted interactions, domain structure visualization of transcripts and expression data of switched isoforms for each sample are given. Additionally, the genes annotated in ClinVar are highlighted in the interactive interaction network. AvailabilityCanIsoNet is freely available at https://caniso.net. The source codes can be found under a Creative Common License at https://github.com/kahramanlab/CanIsoNet_Web. Supplementary InformationSupplementary data are available at Bioinformatics online.

cancer biology↗

GUNC: Detection of Chimerism and Contamination in Prokaryotic Genomes

Genomes are critical units in microbiology, yet ascertaining quality in prokaryotic genomes remains a formidable challenge. We present GUNC (the Genome UNClutterer), a tool that accurately detects and quantifies genome chimerism based on the lineage homogeneity of individual contigs using a genomes full complement of genes. GUNC complements existing approaches by targeting previously underdetected types of contamination: we conservatively estimate that 5.7% of genomes in GenBank, 5.2% in RefSeq, and 15-30% of pre-filtered high quality metagenome-assembled genomes in recent studies are undetected chimeras. GUNC provides a fast and robust tool to substantially improve prokaryotic genome quality. Source code (GPLv3+): https://github.com/grp-bork/gunc

bioinformatics↗

Tree reconciliation combined with subsampling improves large scale inference of orthologous group hierarchies

BackgroundAn orthologous group (OG) comprises a set of orthologous and paralogous genes that share a last common ancestor (LCA). OGs are defined with respect to a chosen taxonomic level, which delimits the position of the LCA in time to a specified speciation event. A hierarchy of OGs expands on this notion, connecting more general OGs, distant in time, to more recent, fine-grained OGs, thereby spanning multiple levels of the tree of life. Large scale inference of OG hierarchies with independently computed taxonomic levels can suffer from inconsistencies between successive levels, such as the position in time of a duplication event. This can be due to confounding genetic signal or algorithmic limitations. Importantly, inconsistencies limit the potential use of OGs for functional annotation and third-party applications.\n\nResultsHere we present a new methodology to ensure hierarchical consistency of OGs across taxonomic levels. To resolve an inconsistency, we subsample the protein space of the OG members and perform gene tree-species tree reconciliation for each sampling. Differently from previous approaches, by subsampling the protein space, we avoid the notoriously diffcult task of accurately building and reconciling very large phylogenies. We implement the method into a high-throughput pipeline and apply it to the eggNOG database. We use independent protein domain definitions to validate its performance.\n\nConclusionThe presented consistency pipeline shows that, contrary to previous limitations, tree reconciliation can be a useful instrument for the construction of OG hierarchies. The key lies in the combination of sampling smaller trees and aggregating their reconciliations for robustness. Results show comparable or greater performance to previous pipelines. The code is available on Github at: https://github.com/meringlab/og_consistency_pipeline

bioinformatics↗

Viruses.STRING: A virus-host protein-protein interaction database

As viruses continue to pose risks to global health, having a better un-derstanding of virus-host protein-protein interactions aids in the development of treatments and vaccines. Here, we introduce Viruses.STRING, a protein-protein interaction database specifically catering to virus-virus and virus-host interactions. This database combines evidence from experimental and text-mining channels to provide combined probabilities for interactions between viral and host proteins. The database contains 177,425 interactions between 239 viruses and 319 hosts. The database is publicly available at viruses.string-db.org, and the interaction data can also be accessed through the latest version of the Cytoscape STRING app.

bioinformatics↗

Analysis of the human kinome and phosphatome reveals diseased signaling networks induced by overexpression

Kinase and phosphatase overexpression drives tumorigenesis and drug resistance in many cancer types. Signaling networks reprogrammed by protein overexpression remain largely uncharacterized, hindering discovery of paths to therapeutic intervention. We previously developed a single cell proteomics approach based on mass cytometry that enables quantitative assessment of overexpression effects on the signaling network. Here we applied this approach in a human kinome- and phosphatome-wide study to assess how 649 individually overexpressed proteins modulate the cancer-related signaling network in HEK293T cells. Based on these data we expanded the functional classification of human kinases and phosphatases and detected 208 novel signaling relationships. In the signaling dynamics analysis, we showed that increased ERK-specific phosphatases sustained proliferative signaling, and using a novel combinatorial overexpression approach, we confirmed this phosphatase-driven mechanism of cancer progression. Finally, we identified 54 proteins that caused ligand-independent ERK activation with potential as biomarkers for drug resistance in cells carrying BRAF mutations.

systems biology↗