xMaP—An Interpretable Alignment-Free Four-Dimensional Quantitative Structure–Activity Relationship Technique Based on Molecular Surface Properties and Conformer Ensembles
| Autor: | Jan Dreher, Josef Scheiber, Knut Baumann, Nikolaus Stiefl |
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| Rok vydání: | 2018 |
| Předmět: |
Models
Molecular 0301 basic medicine Quantitative structure–activity relationship Surface Properties General Chemical Engineering Quantitative Structure-Activity Relationship Library and Information Sciences Topology 01 natural sciences 03 medical and health sciences Molecular descriptor Molecule Invariant (mathematics) Conformational isomerism Mathematics Molecular Structure Reproducibility of Results General Chemistry 0104 chemical sciences Computer Science Applications 010404 medicinal & biomolecular chemistry 030104 developmental biology Fourth Dimension Biological system Hydrophobic and Hydrophilic Interactions Algorithms |
| Zdroj: | Journal of Chemical Information and Modeling. 58:165-181 |
| ISSN: | 1549-960X 1549-9596 |
| DOI: | 10.1021/acs.jcim.7b00419 |
| Popis: | A novel alignment-free molecular descriptor called xMaP (flexible MaP descriptor) is introduced. The descriptor is the advancement of the previously published translationally and rotationally invariant three-dimensional (3D) descriptor MaP (mapping property distributions onto the molecular surface) to the fourth dimension (4D). In addition to MaP, xMaP is independent of the chosen starting conformation of the encoded molecules and is therefore entirely alignment-free. This is achieved by using ensembles of conformers, which are generated by conformational searches. This step of the procedure is similar to Hopfinger's 4D quantitative structure-activity relationship (QSAR). A five-step procedure is used to compute the xMaP descriptor. First, a conformational search for each molecule is carried out. Next, for each of the conformers an approximation to the molecular surface with equally distributed surface points is computed. Third, molecular properties are projected onto this surface. Fourth, areas of identical properties are clustered to so-called patches. Fifth, the spatial distribution of the patches is converted into an alignment-free descriptor that is based on the entire conformer ensemble. The resulting descriptor can be interpreted by superimposing the most important descriptor variables and the molecules of the data set. The most important descriptor variables are identified with chemometric regression tools. The novel descriptor was applied to several benchmark data sets and was compared to other descriptors and QSAR techniques comprising a binary fingerprint, a topological pharmacophore descriptor (Cats2D), and the field-based 3D-QSAR technique GRID/PLS which is alignment-dependent. The use of conformer ensembles renders xMaP very robust. It turns out that xMaP performs very well on (almost) all data sets and that the statistical results are comparable to GRID/PLS. In addition to that, xMaP can also be used to efficiently visualize the derived quantitative structure-activity relationships. |
| Databáze: | OpenAIRE |
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