Details

Autor(en) / Beteiligte

• Pereira, Andreia T.
• Ribeiro, António J. M.
• Fernandes, Pedro A.
• Ramos, Maria J.

Titel

Benchmarking of density functionals for the kinetics and thermodynamics of the hydrolysis of glycosidic bonds catalyzed by glycosidases

Ist Teil von

• International journal of quantum chemistry, 2017-09, Vol.117 (18), p.n/a

Ort / Verlag

Hoboken: Wiley Subscription Services, Inc

Erscheinungsjahr

2017

Link zum Volltext

Quelle

Wiley Online Library - AutoHoldings Journals

Beschreibungen/Notizen

• In recent years, there has been an increased interest in understanding the enzymatic mechanism of glycosidases resorting mostly to DFT and DFT/MM calculations. However, the performance of density functionals (DFs) is well known to be system and property dependent. Trends drawn from general studies, despite important to evaluate the quality of the DFs and to pave the way for the development of new DFs, may be misleading when applied to a single specific system/property. To overcome this issue, we carried out a benchmarking study of 40 DFs applied to the geometry optimization and to the electronic barrier height (EBarrier) and electronic energy of reaction (ER) of prototypical glycosidase‐catalyzed reactions. Additionally, we report calculations with SCC‐DFTB and four semiempirical MO methods applied to the same problem. We have used a universal molecular model for retaining glycosidases, comprising only a 22‐atoms system that mimics the active site and substrate. High accuracy reference geometries and energies were calculated at the CCSD(T)/CBS//MP2/aug‐cc‐pVTZ level of theory. Most DFs reproduce the reference geometries extremely well, with mean unsigned errors (MUE) smaller than 0.05 Å for bond lengths and 3° for bond angles. Among the DFs, wB97X‐D, CAM‐B3LYP, B3P86, and PBE1PBE have the best performance in geometry optimizations (MUE = 0.02 Å). Conversely, semiempirical MO and SCC‐DFTB methods yielded less accurate geometries (MUE between 0.09 and 0.17 Å). The inclusion of D3 correction has a small, but still relevant, influence in the geometry predicted by some DFs. Regarding EBarrier, 11 DFs (MPW1B95, CAM‐B3LYP, M06 ‐ 2X, PBE1PBE, wB97X ‐ D, B1B95, BMK, MN12 – SX, M05, M06, and M11) presented errors below 1 kcal.mol−1, in relation to the reference energy. Most of these functionals belong to the family of hybrid functionals (H‐GGA, HH‐GGA, and HM‐GGA), which shows a positive influence of HF exchange in the determination of EBarrier. The inclusion of D3 correction has not affected significantly the EBarrier and ER. The use of geometries at the accurate but expensive MP2/aug‐cc‐pVTZ level of theory has a small, albeit not insignificant, influence in the EBarrier when compared with energies calculated with geometries determined with the DFs (usually a few tenths of kcal.mol−1, with exceptions). In general, semiempirical MO methods and DFTB are associated with larger errors in the determination of EBarrier, with unsigned errors from 6.9 to 24.7 kcal.mol−1. Despite the large number of density functional (DF) in existence, a universally optimal DF is still missing. DFs performances are dependent on the specific model/reaction/property under study. This work evaluates the performance of DFs, semiempirical, and SCC‐DFTB methods for the determination of geometries and the electronic barrier height and energy of reaction of the reactions catalyzed by glycosidases. This will help researchers making appropriate choices in the method selection for computational studies of glycosidase reactions.