An Approach for Visualization of the Active Site of Enzymes with Unknown Three-Dimensional Structures |
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| Authors: | A. V. Veselovsky O. V. Tikhonova V. S. Skvortsov A. E. Medvedev A. S. Ivanov |
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| Affiliation: | 1. Laboratory of Molecular Graphics Drug Design, Institute of Biomedical Chemistry, Russian Academy of Medical Sciences , Pogodinskaya Str. 10, Moscow, 119832, Russia;2. Laboratory of Biochemistry of Amines and Cyclic Nucleotides, Institute of Biomedical Chemistry, Russian Academy of Medical Sciences , Pogodinskaya Str. 10, Moscow, 119832, Russia |
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| Abstract: | Abstract A new approach for virtual characterization of the active site structure of enzymes with unknown three-dimensional (3D) structure has been proposed. It includes analysis of data on enzyme interaction with reversible competitive inhibitors, their 3D structures and moulding of the substrate-binding region. The superposition of ligands in biologically active conformations allows to determine the shape and dimension of the active site cavity accommodating these compounds. Monoamine oxidase A (MAO-A), a “typical” enzyme with unknown spatial organisation, was used to test this method. The correctness of such approach was validated by the analysis of HIV protease interaction with its inhibitors using 3D structures of their complexes. Mould of the substrate/inhibitor binding site can be used for the visualization of this binding site and for searching new ligands in molecular databases. |
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| Keywords: | Computer modeling Active site 3D structure Monoamine oxidase A Reversible inhibitors Molecular databases |
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