A nonredundant structure dataset for benchmarking protein-RNA computational docking.
A nonredundant structure dataset for benchmarking protein-RNA computational docking.
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DOI:
10.1002/jcc.23149
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发表时间:
2013-02-05
影响因子:
3
通讯作者:
Zou, Xiaoqin
中科院分区:
文献类型:
--
作者:
Huang, Sheng-You;Zou, Xiaoqin
Protein-RNA interactions play an important role in many biological processes. The ability to predict the molecular structures of protein-RNA complexes from docking would be valuable for understanding the underlying chemical mechanisms. We have developed a novel non-redundant benchmark dataset for protein-RNA docking and scoring. The diverse dataset of 72 targets consists of 52 unbound-unbound test complexes, and 20 unbound-bound test complexes. Here, unbound-unbound complexes refer to cases in which both binding partners of the co-crystallized complex are either in apo form or in a conformation taken from a different protein-RNA complex, whereas unbound-bound complexes are cases in which only one of the two binding partners has another experimentally determined conformation. The dataset is classified into three categories according to the interface RMSD and the percentage of native contacts in the unbound structures: 49 easy, 16 medium, and 7 difficult targets. The bound and unbound cases of the benchmark dataset are expected to benefit the development and improvement of docking and scoring algorithms for the docking community. All the easy-to-view structures are freely available to the public at http://zoulab.dalton.missouri.edu/RNAbenchmark/.
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影响因子:
7.7
作者:
Kolb, Peter;Ferreira, Rafaela S.;Irwin, John J.;Shoichet, Brian K.
通讯作者:
Shoichet, Brian K.
影响因子:
2.9
作者:
Huang, Sheng-You;Zou, Xiaoqin
通讯作者:
Zou, Xiaoqin
影响因子:
5.6
作者:
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通讯作者:
Carlson HA
影响因子:
14.9
作者:
Leontis, NB;Stombaugh, J;Westhof, E
通讯作者:
Westhof, E
DOI:
10.1002/prot.10390
发表时间:
2003-07-01
期刊:
PROTEINS-STRUCTURE FUNCTION AND GENETICS
影响因子:
--
作者:
Chen, R;Mintseris, J;Weng, ZP
通讯作者:
Weng, ZP