CHALLENGES IN MATCHING SECONDARY STRUCTURES IN CRYO-EM: AN EXPLORATION

被引:0
作者
Haslam, Devin [1 ]
Zubair, Mohammad [1 ]
Ranjan, Desh [1 ]
Biswas, Abhishek [2 ]
He, Jing [1 ]
机构
[1] Old Dominion Univ, Dept Comp Sci, Norfolk, VA 23529 USA
[2] Oak Ridge Natl Lab, Oak Ridge, TN 37831 USA
来源
2016 IEEE INTERNATIONAL CONFERENCE ON BIOINFORMATICS AND BIOMEDICINE (BIBM) | 2016年
关键词
protein; algorithms; cryo-electron microscopy; graph; secondary structure; topology; heuristic; STRUCTURE ELEMENTS; PROTEIN-STRUCTURE; IDENTIFICATION;
D O I
暂无
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
Cryo-electron microscopy is a fast emerging biophysical technique for structural determination of large protein complexes. While more atomic structures are being determined using this technique, it is still challenging to derive atomic structures from density maps produced at medium resolution when no suitable templates are available. A critical step in structure determ ination is how a protein chain threads through the 3-dimensional density map. A dynamic programm ing method was previously developed to generate K best matches of secondary structures between the density map and its protein sequence using shortest paths in a related weighted graph. We discuss challenges associated with the creation of the weighted graph and explore heuristic methods to solve the problem of matching secondary structures.
引用
收藏
页码:1714 / 1719
页数:6
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