Pseudo-periodic partitions of biological sequences

被引:9
作者
Li, LG
Jin, RC
Kok, PL
Wan, HH
机构
[1] Maryland Inst Dynam Gen, Lab Bioinformat, Silver Spring, MD 20906 USA
[2] Second Army Med Univ, Nanjing Army Med Coll, Dept Protect Med, Nanjing 210099, Jiangsu, Peoples R China
[3] Temple Univ, Dept Comp & Informat Sci, Philadelphia, PA 19139 USA
[4] Huazhong Univ Sci & Technol, Sch Comp Sci & Technol, Wuhan 430074, Peoples R China
[5] Natl Ctr Genome Resources, Global Bioinformat Lab, Santa Fe, NM 87505 USA
[6] NIEHS, Natl Ctr Toxicogen, NIH, Res Triangle Pk, NC 27709 USA
关键词
D O I
10.1093/bioinformatics/btg404
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Algorithm development for finding typical patterns in sequences, especially multiple pseudo-repeats (pseudo-periodic regions), is at the core of many problems arising in biological sequence and structure analysis. In fact, one of the most significant features of biological sequences is their high quasi-repetitiveness. Variation in the quasi-repetitiveness of genomic and proteomic texts demonstrates the presence and density of different biologically important information. It is very important to develop sensitive automatic computational methods for the identification of pseudo-periodic regions of sequences through which we can infer, describe and understand biological properties, and seek precise molecular details of biological structures, dynamics, interactions and evolution. Results: We develop a novel, powerful computational tool for partitioning a sequence to pseudo-periodic regions. The pseudo-periodic partition is defined as a partition, which intuitively has the minimal bias to some perfect-periodic partition of the sequence based on the evolutionary distance. We devise a quadratic time and space algorithm for detecting a pseudo-periodic partition for a given sequence, which actually corresponds to the shortest path in the main diagonal of the directed (acyclic) weighted graph constructed by the Smith-Waterman self-alignment of the sequence. We use several typical examples to demonstrate the utilization of our algorithm and software system in detecting functional or structural domains and regions of proteins. A big advantage of our software program is that there is a parameter, the granularity factor, associated with it and we can freely choose a biological sequence family as a training set to determine the best parameter. In general, we choose all repeats (including many pseudo-repeats) in the SWISS-PROT amino acid sequence database as a typical training set. We show that the granularity factor is 0.52 and the average agreement accuracy of pseudo-periodic partitions, detected by our software for all pseudo-repeats in the SWISS-PROT database, is as high as 97.6%.
引用
收藏
页码:295 / 306
页数:12
相关论文
共 28 条
[1]   Three-dimensional structure of tetrahydrodipicolinate N-succinyltransferase [J].
Beaman, TW ;
Binder, DA ;
Blanchard, JS ;
Roderick, SL .
BIOCHEMISTRY, 1997, 36 (03) :489-494
[2]   Tandem repeats finder: a program to analyze DNA sequences [J].
Benson, G .
NUCLEIC ACIDS RESEARCH, 1999, 27 (02) :573-580
[3]   THE 2.9 ANGSTROM CRYSTAL-STRUCTURE OF THERMUS-THERMOPHILUS SERYL-TRANSFER-RNA SYNTHETASE COMPLEXED WITH TRNA(SER) [J].
BIOU, V ;
YAREMCHUK, A ;
TUKALO, M ;
CUSACK, S .
SCIENCE, 1994, 263 (5152) :1404-1410
[4]   THE GENETIC-RELATIONSHIPS BETWEEN THE KRINGLE DOMAINS OF HUMAN-PLASMINOGEN, PROTHROMBIN, TISSUE PLASMINOGEN-ACTIVATOR, UROKINASE, AND COAGULATION FACTOR-XII [J].
CASTELLINO, FJ ;
BEALS, JM .
JOURNAL OF MOLECULAR EVOLUTION, 1987, 26 (04) :358-369
[5]   Detecting periodic patterns in biological sequences [J].
Coward, E ;
Drablos, F .
BIOINFORMATICS, 1998, 14 (06) :498-507
[6]   EVOLUTIONARY ORIGIN OF NUMEROUS KRINGLES IN HUMAN AND SIMIAN APOLIPOPROTEIN(A) [J].
IKEO, K ;
TAKAHASHI, K ;
GOJOBORI, T .
FEBS LETTERS, 1991, 287 (1-2) :146-148
[7]   Amino acid repeat patterns in protein sequences: Their diversity and structural-functional implications [J].
Katti, MV ;
Sami-Subbu, R ;
Ranjekar, PK ;
Gupta, VS .
PROTEIN SCIENCE, 2000, 9 (06) :1203-1209
[8]   CRYSTAL-STRUCTURE OF PORCINE RIBONUCLEASE INHIBITOR, A PROTEIN WITH LEUCINE-RICH REPEATS [J].
KOBE, B ;
DEISENHOFER, J .
NATURE, 1993, 366 (6457) :751-756
[9]   MOLMOL: A program for display and analysis of macromolecular structures [J].
Koradi, R ;
Billeter, M ;
Wuthrich, K .
JOURNAL OF MOLECULAR GRAPHICS, 1996, 14 (01) :51-&
[10]  
Levenshtein V.I., 1966, SOV PHYS DOKL, V10, DOI DOI 10.1109/TVCG.2012.323