Evidence map›Paper›PMID 39630291›Full record

ArticleJournal of computer-aided molecular design2024

Combining crystallographic and binding affinity data towards a novel dataset of small molecule overlays.

Sophia M N Hönig, Torben Gutermuth, Christiane Ehrt, Christian Lemmen, Matthias Rarey

Abstract read
In one paragraph

Article in Journal of computer-aided molecular design, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Sophia M N HönigBioSolveIT, An der Ziegelei 79, 53757, Sankt Augustin, Germany.ORCID 0000-0003-4742-7899
Torben GutermuthUniversity of Hamburg, ZBH - Center for Bioinformatics, Albert-Einstein-Ring 8-10, 22761, Hamburg, Germany.ORCID 0000-0002-9304-8251
Christiane EhrtUniversity of Hamburg, ZBH - Center for Bioinformatics, Albert-Einstein-Ring 8-10, 22761, Hamburg, Germany.ORCID 0000-0003-1428-0042
Christian LemmenBioSolveIT, An der Ziegelei 79, 53757, Sankt Augustin, Germany.ORCID 0000-0002-4264-6657
Matthias RareyUniversity of Hamburg, ZBH - Center for Bioinformatics, Albert-Einstein-Ring 8-10, 22761, Hamburg, Germany. matthias.rarey@uni-hamburg.de.ORCID 0000-0002-9553-6531

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although small molecule superposition is a standard technique in drug discovery, a rigorous performance assessment of the corresponding methods is currently challenging. Datasets in this field are sparse, small, tailored to specific applications, unavailable, or outdated. The newly developed LOBSTER set described herein offers a publicly available and method-independent dataset for benchmarking and method optimization. LOBSTER stands for "Ligand Overlays from Binding SiTe Ensemble Representatives". All ligands were derived from the PDB in a fully automated workflow, including a ligand efficiency filter. So-called ligand ensembles were assembled by aligning identical binding sites. Thus, the ligands within the ensembles are superimposed according to their experimentally determined binding orientation and conformation. Overall, 671 representative ligand ensembles comprise 3583 ligands from 3521 proteins. Altogether, 72,734 ligand pairs based on the ensembles were grouped into ten distinct subsets based on their volume overlap, for the benefit of introducing different degrees of difficulty for evaluating superposition methods. Statistics on the physicochemical properties of the compounds indicate that the dataset represents drug-like compounds. Consensus Diversity Plots show predominantly high Bemis-Murcko scaffold diversity and low median MACCS fingerprint similarity for each ensemble. An analysis of the underlying protein classes further demonstrates the heterogeneity within our dataset. The LOBSTER set offers a variety of applications like benchmarking multiple as well as pairwise alignments, generating training and test sets, for example based on time splits, or empirical software performance evaluation studies. The LOBSTER set is publicly available at https://doi.org/10.5281/zenodo.12658320 , representing a stable and versioned data resource. The Python scripts are available at https://github.com/rareylab/LOBSTER , open-source, and allow for updating or recreating superposition sets with different data sources.

Indexed as

Databases, ProteinProtein BindingProteinsSmall Molecule LibrariesBinding SitesCrystallography, X-RayDrug DesignDrug DiscoveryHumansLigandsModels, MolecularProtein ConformationSoftwareLigandsProteinsSmall Molecule Libraries

Identifiers

PMID39630291
PMCPMC11618164

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.