共 51 条
Progress and challenges in protein structure prediction
被引:358
作者:

Zhang, Yang
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Kansas, Ctr Bioinformat, Lawrence, KS 66047 USA
Univ Kansas, Dept Mol Biosci, Lawrence, KS 66047 USA Univ Kansas, Ctr Bioinformat, Lawrence, KS 66047 USA
机构:
[1] Univ Kansas, Ctr Bioinformat, Lawrence, KS 66047 USA
[2] Univ Kansas, Dept Mol Biosci, Lawrence, KS 66047 USA
关键词:
D O I:
10.1016/j.sbi.2008.02.004
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Depending on whether similar structures are found in the PDB library, the protein structure prediction can be categorized into template-based modeling and free modeling. Although threading is an efficient tool to detect the structural analogs, the advancements in methodology development have come to a steady state. Encouraging progress is observed in structure refinement which aims at drawing template structures closer to the native; this has been mainly driven by the use of multiple structure templates and the development of hybrid knowledge-based and physics-based force fields. For free modeling, exciting examples have been witnessed in folding small proteins to atomic resolutions. However, predicting structures for proteins larger than 150 residues still remains a challenge, with bottlenecks from both force field and conformational search.
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页码:342 / 348
页数:7
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