Query3d: a new method for high-throughput analysis of functional residues in protein structures

被引:35
作者
Ausiello, G [1 ]
Via, A [1 ]
Helmer-Citterich, M [1 ]
机构
[1] Univ Roma Tor Vergata, Dept Biol, Ctr Mol Bioinformat, I-00133 Rome, Italy
来源
BMC BIOINFORMATICS | 2005年 / 6卷
关键词
DATABASE; SITES; SEQUENCE; PATTERNS;
D O I
10.1186/1471-2105-6-S4-S5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: The identification of local similarities between two protein structures can provide clues of a common function. Many different methods exist for searching for similar subsets of residues in proteins of known structure. However, the lack of functional and structural information on single residues, together with the low level of integration of this information in comparison methods, is a limitation that prevents these methods from being fully exploited in high-throughput analyses. Results: Here we describe Query3d, a program that is both a structural DBMS (Database Management System) and a local comparison method. The method conserves a copy of all the residues of the Protein Data Bank annotated with a variety of functional and structural information. New annotations can be easily added from a variety of methods and known databases. The algorithm makes it possible to create complex queries based on the residues' function and then to compare only subsets of the selected residues. Functional information is also essential to speed up the comparison and the analysis of the results. Conclusion: With Query3d, users can easily obtain statistics on how many and which residues share certain properties in all proteins of known structure. At the same time, the method also finds their structural neighbours in the whole PDB. Programs and data can be accessed through the PdbFun web interface.
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收藏
页数:6
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