• Something wrong with this record ?

Benchmark RI-MP2 database of nucleic acid base trimers: performance of different density functional models for prediction of structures and binding energies

M. Kabeláč, H. Valdés, EC. Sherer, CJ. Cramer, P. Hobza

. 2007 ; 9 (36) : 5000-5008.

Language English Country Great Britain

A new database of nucleic acid base trimers has been developed that includes 141 geometries and stabilization energies obtained at the RI-MP2 level of theory with the TZVPP basis set. Compared to previously compiled biologically oriented databases, this new construct includes considerably more complicated structures; the various intermolecular interactions in the trimers are quite heterogeneous and in particular include simultaneous hydrogen bonding and stacking interactions, which is similar to the situation in actual biopolymers. Validation against these benchmark data is therefore a more demanding task for approximate models, since correct descriptions of all energy terms are unlikely to be accomplished by fortuitous cancellations of systematic errors. The density functionals TPSS (both with and without an empirical dispersion term), PWB6K, M05-2X, and BH&H, and the self-consistent charge density functional tight binding method augmented with an empirical dispersion term (SCC-DFTB-D) were assessed for their abilities accurately to compute structures and energies. The best reproduction of the BSSE corrected RI-MP2 stabilization energies was achieved by the TPSS functional (TZVPP basis set) combined with empirical dispersion; removal of the dispersion correction leads to significantly degraded performance. The M05-2X and PWB6K functionals performed very well in reproducing the RI-MP2 geometries, but showed a systematic moderate underestimation of the magnitude of base stacking interactions. The SCC-DFTB-D method predicts geometries in fair agreement with RI-MP2; given its computational efficiency it represents a good option for initial scanning of analogous biopolymeric potential energy surfaces. BH&H gives geometries of comparable quality to the other functionals but significantly overestimates interaction energies other than stacking.

000      
03265naa 2200301 a 4500
001      
bmc10013233
003      
CZ-PrNML
005      
20120205093336.0
008      
100602s2007 xxk e eng||
009      
AR
040    __
$a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxk
100    1_
$a Kabeláč, Martin. $7 _AN035448
245    10
$a Benchmark RI-MP2 database of nucleic acid base trimers: performance of different density functional models for prediction of structures and binding energies / $c M. Kabeláč, H. Valdés, EC. Sherer, CJ. Cramer, P. Hobza
314    __
$a Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic and Center for Complex Molecular Systems and Biomolecules, Flemingovo nam 2, 166 10, Prague 6, Czech Republic. martin.kabelac@uochb.cas.cz
520    9_
$a A new database of nucleic acid base trimers has been developed that includes 141 geometries and stabilization energies obtained at the RI-MP2 level of theory with the TZVPP basis set. Compared to previously compiled biologically oriented databases, this new construct includes considerably more complicated structures; the various intermolecular interactions in the trimers are quite heterogeneous and in particular include simultaneous hydrogen bonding and stacking interactions, which is similar to the situation in actual biopolymers. Validation against these benchmark data is therefore a more demanding task for approximate models, since correct descriptions of all energy terms are unlikely to be accomplished by fortuitous cancellations of systematic errors. The density functionals TPSS (both with and without an empirical dispersion term), PWB6K, M05-2X, and BH&H, and the self-consistent charge density functional tight binding method augmented with an empirical dispersion term (SCC-DFTB-D) were assessed for their abilities accurately to compute structures and energies. The best reproduction of the BSSE corrected RI-MP2 stabilization energies was achieved by the TPSS functional (TZVPP basis set) combined with empirical dispersion; removal of the dispersion correction leads to significantly degraded performance. The M05-2X and PWB6K functionals performed very well in reproducing the RI-MP2 geometries, but showed a systematic moderate underestimation of the magnitude of base stacking interactions. The SCC-DFTB-D method predicts geometries in fair agreement with RI-MP2; given its computational efficiency it represents a good option for initial scanning of analogous biopolymeric potential energy surfaces. BH&H gives geometries of comparable quality to the other functionals but significantly overestimates interaction energies other than stacking.
650    _2
$a databáze nukleových kyselin $7 D030561
650    _2
$a konformace nukleové kyseliny $7 D009690
650    _2
$a oligonukleotidy $x chemie $7 D009841
650    _2
$a termodynamika $7 D013816
650    _2
$a financování organizované $7 D005381
700    1#
$a Valdés, Haydee. $7 _AN059471
700    1_
$a Sherer, Edward C.
700    1_
$a Cramer, Christopher J.
700    1_
$a Hobza, Pavel, $d 1946- $7 jk01041427
773    0_
$t Physical Chemistry Chemical Physics $w MED00008271 $g Roč. 9, č. 36 (2007), s. 5000-5008 $x 1463-9076
910    __
$a ABA008 $b x $y 7
990    __
$a 20110413111038 $b ABA008
991    __
$a 20120205093323 $b ABA008
999    __
$a ok $b bmc $g 749109 $s 612728
BAS    __
$a 3
BMC    __
$a 2007 $b 9 $c 36 $d 5000-5008 $i 1463-9076 $m PCCP. Physical chemistry chemical physics $n Phys Chem Chem Phys $x MED00008271
LZP    __
$a 2010-B2/ipme

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...