TY - GEN
T1 - Extension of Partial Atom-To-Atom Maps
T2 - 25th International Conference on Algorithms for Bioinformatics, WABI 2025
AU - González Laffitte, Marcos E.
AU - Phan, Tieu Long
AU - Stadler, Peter F.
PY - 2025/8/15
Y1 - 2025/8/15
N2 - Chemical reaction databases typically report the molecular structures of reactant and product compounds, as well as their stoichiometry, but lack information, in particular, on the correspondence of reactant and product atoms. These atom-to-atom maps (AAM), however, are crucial for applications including chemical synthesis planning in organic chemistry and the analysis of isotope labeling experiments in modern metabolomics. AAMs therefore need to be reconstructed computationally. This situation is aggravated, furthermore, by the fact that chemically correct AAMs are, fundamentally, determined by quantum-mechanical phenomena and thus cannot be reliably computed by solving graph-theoretical optimization problems defined by the reactant and product structures. A viable solution for this problem is to shift the focus into first identifying a partial AAM containing the reaction center, i.e., covering the atoms incident with all bonds that change during a reaction. This then leads to the problem of extending the partial map to the full reaction. The AAM of a reaction is faithfully represented by the Imaginary Transition State (ITS) graph, providing a convenient graph-theoretic framework to address the questions of when and how a partial AAM can be extended. We show that an unique extension exists whenever, and only if, these partial AAMs cover the reaction center. In this case their extension can be computed by solving a constrained graph-isomorphism search between specific subgraphs of ITS graphs. We close by benchmarking different tools for this task.
AB - Chemical reaction databases typically report the molecular structures of reactant and product compounds, as well as their stoichiometry, but lack information, in particular, on the correspondence of reactant and product atoms. These atom-to-atom maps (AAM), however, are crucial for applications including chemical synthesis planning in organic chemistry and the analysis of isotope labeling experiments in modern metabolomics. AAMs therefore need to be reconstructed computationally. This situation is aggravated, furthermore, by the fact that chemically correct AAMs are, fundamentally, determined by quantum-mechanical phenomena and thus cannot be reliably computed by solving graph-theoretical optimization problems defined by the reactant and product structures. A viable solution for this problem is to shift the focus into first identifying a partial AAM containing the reaction center, i.e., covering the atoms incident with all bonds that change during a reaction. This then leads to the problem of extending the partial map to the full reaction. The AAM of a reaction is faithfully represented by the Imaginary Transition State (ITS) graph, providing a convenient graph-theoretic framework to address the questions of when and how a partial AAM can be extended. We show that an unique extension exists whenever, and only if, these partial AAMs cover the reaction center. In this case their extension can be computed by solving a constrained graph-isomorphism search between specific subgraphs of ITS graphs. We close by benchmarking different tools for this task.
KW - atom-to-atom maps
KW - chemical reaction mechanisms
KW - chemical synthesis planning
KW - condensed graph of the reaction (CGR)
KW - constrained graph isomorphism
KW - imaginary transition state (ITS) graphs
KW - metabolic networks
KW - molecular graphs
U2 - 10.4230/LIPIcs.WABI.2025.12
DO - 10.4230/LIPIcs.WABI.2025.12
M3 - Article in proceedings
AN - SCOPUS:105013842436
T3 - Leibniz International Proceedings in Informatics
BT - 25th International Conference on Algorithms for Bioinformatics, WABI 2025
A2 - Brejova, Brona
A2 - Patro, Rob
PB - Schloss Dagstuhl- Leibniz-Zentrum fur Informatik GmbH, Dagstuhl Publishing
Y2 - 20 August 2025 through 22 August 2025
ER -