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Liang J: Order independent structural alignment of circularly permuted proteins (2008)

Abstract
Abstract–Circular permutation connects the N and C termini of a protein and concurrently cleaves elsewhere in the chain, providing an important mechanism for generating novel protein fold and functions. However, their in genomes is unknown because current detection methods can miss many occurances, mistaking random repeats as circular permutation. Here we develop a method for detecting circularly permuted proteins from structural comparison. Sequence order independent alignment of protein structures can be regarded as a special case of the maximum-weight independent set problem, which is known to be computationally hard. We develop an efficient approximation algorithm by repeatedly solving relaxations of an appropriate intermediate integer programming formulation, we show that the approximation ratio is much better then the theoretical worst case ratio of ¦ § © � �. Circularly permuted proteins reported in literature can be identified rapidly with our method, while they escape the detection by publicly available servers for structural alignment. Keywords–circular permuations, integer programming, linear programming, protein structure alignment

Publication details
Download http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.76.7473
Source http://crab.rutgers.edu/~bhaskar/resume/publ/papers/jliang-align.pdf
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Repository CiteSeerX - Scientific Literature Digital Library and Search Engine (United States)
Type text
Language English
Relation 10.1.1.75.341, 10.1.1.77.4296