| Literature DB >> 28665599 |
Xavier García-LLinás1, Antonio Bauzá1, Saikat K Seth1,2, Antonio Frontera1.
Abstract
In this article, ab initio calculations have been combined with a search in the Protein Data Bank (PDB) to demonstrate the importance of σ-hole tetrel bonding interactions in biological systems. In particular, we focus our attention on the ability of the -CF3 group to participate in noncovalent interactions as Lewis acids, and we show the importance of this interaction in the inhibition mechanism of a NADP+-dependent isocitrate dehydrogenase (IDH) enzyme that converts isocitrate to α-ketoglutarate. IDH mutations are found in multiple hematologic and solid tumors, inducing premalignant disorders. A potent triazine-based inhibitor of the mutant IDH (enasidenib) presents two -CF3 groups in the structure. One establishes a tetrel bonding interaction with an aspartate residue that contributes to the binding and selectivity of the inhibitor to the active site.Entities:
Year: 2017 PMID: 28665599 DOI: 10.1021/acs.jpca.7b06052
Source DB: PubMed Journal: J Phys Chem A ISSN: 1089-5639 Impact factor: 2.781