new Lamarckian genetic algorithm for flexible ligand-receptor docking

We present a Lamarckian genetic algorithm (LGA) variant for flexible ligand-receptor docking which allows to handle a large number of degrees of freedom. Our hybrid method combines a multi-deme LGA with a recently published gradient-based method for local optimization of molecular complexes. We comp...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Journal of computational chemistry Ročník 31; číslo 9; s. 1911 - 1918
Hlavní autoři: Fuhrmann, Jan, Rurainski, Alexander, Lenhof, Hans-Peter, Neumann, Dirk
Médium: Journal Article
Jazyk:angličtina
Vydáno: Hoboken Wiley Subscription Services, Inc., A Wiley Company 15.07.2010
Wiley Subscription Services, Inc
Témata:
ISSN:0192-8651, 1096-987X, 1096-987X
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Popis
Shrnutí:We present a Lamarckian genetic algorithm (LGA) variant for flexible ligand-receptor docking which allows to handle a large number of degrees of freedom. Our hybrid method combines a multi-deme LGA with a recently published gradient-based method for local optimization of molecular complexes. We compared the performance of our new hybrid method to two non gradient-based search heuristics on the Astex diverse set for flexible ligand-receptor docking. Our results show that the novel approach is clearly superior to other LGAs employing a stochastic optimization method. The new algorithm features a shorter run time and gives substantially better results, especially with increasing complexity of the ligands. Thus, it may be used to dock ligands with many rotatable bonds with high efficiency.
Bibliografie:http://dx.doi.org/10.1002/jcc.21478
ark:/67375/WNG-X9PW1HRB-P
istex:045572FFC2B80D79AB8E2419ADCA5D0302275144
ArticleID:JCC21478
These authors contributed equally to this work.
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 14
ObjectType-Article-1
ObjectType-Feature-2
content type line 23
ISSN:0192-8651
1096-987X
1096-987X
DOI:10.1002/jcc.21478