Nucleic Acids ResearchBioinformaticsPeer-reviewed journal article
AlphaFind v2: Similarity Search in AlphaFold DB and TED Domains across Structural Contexts
Terézia SlaninákováiD, Adrián RošineciD, Jakub ČillíkiD, Aleš KřenekiD, Katarína GrešováiD, Jana PorubskáiD, Eva MarsalkovaiD, Jaroslav OľhaiD, David ProcházkaiD, Lukáš HejtmánekiD, Vlastislav DohnaliD, Karel BerkaiD, Radka Svobodová VařekováiD, Matej AntoliD
Abstract
The availability of large-scale protein structure collections enables structure-based analysis of their function and evolution beyond what is possible from sequence alone. However, applying three-dimensional structure comparison at scale remains computationally demanding and limits practical exploration of large experimental and predicted collections. This creates a need for fast, structure-based search methods that retain biological relevance while enabling large-scale exploration. In this paper, we present AlphaFind v2, an application for finding structurally similar proteins in the AlphaFold Database (https://alphafold.ebi.ac.uk/) of predicted structures. AlphaFind v2 uses fast pre-filtering via state-of-the-art protein embeddings that preserve structural information, followed by refinement with US-align. The application presents multiple complementary search modes, including (i) search over full protein chains, (ii) search aware of the AlphaFold pLDDT metric, restricting similarity computation to the most stable and structurally relevant regions, (iii) search over protein domains from the TED database (https://ted.cathdb.info/), and (iv) a multidomain search mode, combining multiple chain-level domain matches within a single score and alignment. The application accepts protein identifiers and returns similar proteins with metrics, rich metadata, and interactive superpositions. AlphaFind v2 additionally allows searching within an organism or CATH label and matches the proteins with experimental structures. AlphaFind v2 is accessible at https://alphafind.ics.muni.cz/. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=79 SRC="FIGDIR/small/710735v1_ufig1.gif" ALT="Figure 1"> View larger version (22K): org.highwire.dtl.DTLVardef@5e7ce7org.highwire.dtl.DTLVardef@15a3458org.highwire.dtl.DTLVardef@12299ccorg.highwire.dtl.DTLVardef@9f21af_HPS_FORMAT_FIGEXP M_FIG C_FIG
- assay: protein structure
- research focus: database / resource
- research focus: benchmarking
- research focus: software / tool
- research focus: sequence-to-function modeling
- approach: deep learning
- approach: statistical model
- Citations
- 2
- FWCI
- 4.10
- Field percentile
- top 6%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- AlphaFind: Discover structure similarity across the entire known proteome
David Procházka, Terézia Slanináková, … Matej Antol·bioRxiv·Feb 15, 2024
- An interpretable alphabet for local protein structure search based on amino acid neighborhoods
Saba Zerefa, Jesse Cool, … Samantha Petti·BioinformaticsPeer-reviewed·Aug 23, 2025
- Foldseek: fast and accurate protein structure search
Michel van Kempen, Stephanie S. Kim, … Martin Steinegger·Nature BiotechnologyPeer-reviewed·May 8, 2023
- Reciprocal Best Structure Hits: Using AlphaFold models to discover distant homologues
Vivian Monzon, Typhaine Paysan‐Lafosse, … Alex G. Bateman·Bioinformatics AdvancesPeer-reviewed·Jan 1, 2022
- Foldclass and Merizo-search: embedding-based deep learning tools for protein domain segmentation, fold recognition and comparison
Shaun M. Kandathil, Andy M C Lau, … David T. Jones·bioRxiv·Mar 25, 2024
- Rapid and accurate protein structure database search using inverse folding model and contrastive learning
Qiuyi Lyu, Hong Wei, … Jianyi Yang·Journal of Chemical Information and ModelingPeer-reviewed·Nov 26, 2025