MODi :: a powerful and convenient web server for identifying multiple post-translational peptide modifications from tandem mass spectra

被引:47
作者
Kim, Sangtae
Na, Seungjin
Sim, Ji Woong
Park, Heejin
Jeong, Jaeho
Kim, Hokeun
Seo, Younghwan
Seo, Jawon
Lee, Kong-Joo
Paek, Eunok [1 ]
机构
[1] Hanyang Univ, Res Ctr Comp Technol, Seoul 133791, South Korea
[2] Univ Seoul, Dept Mech & Informat Engn, Seoul 130743, South Korea
[3] Seoul Natl Univ, Sch Comp Sci & Engn, Seoul 151742, South Korea
[4] Hanyang Univ, Coll Informat & Commun, Seoul 133791, South Korea
[5] Ewha Womans Univ, Ctr Cell Signaling Res, Div Mol Life Sci, Seoul 120750, South Korea
[6] Ewha Womans Univ, Coll Pharm, Div Mol Life Sci, Seoul 120750, South Korea
[7] Korea Inst Sci & Technol, Funct Proteom Ctr, Seoul 136791, South Korea
[8] Lab Frontier Co Ltd, Seoul 120750, South Korea
关键词
D O I
10.1093/nar/gkl245
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
MODi( http://modi.uos.ac.kr/modi/) is a powerful and convenient web service that facilitates the interpretation of tandem mass spectra for identifying post-translational modifications (PTMs) in a peptide. It is powerful in that it can interpret a tandem mass spectrum even when hundreds of modification types are considered and the number of potential PTMs in a peptide is large, in contrast to most of the methods currently available for spectra interpretation that limit the number of PTM sites and types being used for PTM analysis. For example, using MODi, one can consider for analysis both the entire PTM list published on the unimod webpage (http://www.unimod.org) and user-defined PTMs simultaneously, and one can also identify multiple PTM sites in a spectrum. MODi is convenient in that it can take various input file formats such as.mzXML,. dta,. pkl and. mgf files, and it is equipped with a graphical tool called MassPective developed to display MODi's output in a user-friendly manner and helps users understand MODi's output quickly. In addition, one can perform manual de novo sequencing using MassPective.
引用
收藏
页码:W258 / W263
页数:6
相关论文
共 20 条
[1]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[2]  
[Anonymous], 2001, Bioinformatics
[3]   A major step on the road to understanding a unique posttranslational modification and its role in a genetic disease [J].
Baenziger, JU .
CELL, 2003, 113 (04) :421-422
[4]   A dynamic programming approach to de novo peptide sequencing via tandem mass spectrometry [J].
Chen, T ;
Kao, MY ;
Tepel, M ;
Rush, J ;
Church, GM .
JOURNAL OF COMPUTATIONAL BIOLOGY, 2001, 8 (03) :325-337
[5]   A method for reducing the time required to match protein sequences with tandem mass spectra [J].
Craig, R ;
Beavis, RC .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2003, 17 (20) :2310-2316
[6]   AN APPROACH TO CORRELATE TANDEM MASS-SPECTRAL DATA OF PEPTIDES WITH AMINO-ACID-SEQUENCES IN A PROTEIN DATABASE [J].
ENG, JK ;
MCCORMACK, AL ;
YATES, JR .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (11) :976-989
[7]   PepNovo: De novo peptide sequencing via probabilistic network modeling [J].
Frank, A ;
Pevzner, P .
ANALYTICAL CHEMISTRY, 2005, 77 (04) :964-973
[8]   Modification-specific proteomics: characterization of post-translational modifications by mass spectrometry [J].
Jensen, ON .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2004, 8 (01) :33-41
[9]   PEAKS:: powerful software for peptide de novo sequencing by tandem mass spectrometry [J].
Ma, B ;
Zhang, KZ ;
Hendrie, C ;
Liang, CZ ;
Li, M ;
Doherty-Kirby, A ;
Lajoie, G .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2003, 17 (20) :2337-2342
[10]   ERROR TOLERANT IDENTIFICATION OF PEPTIDES IN SEQUENCE DATABASES BY PEPTIDE SEQUENCE TAGS [J].
MANN, M ;
WILM, M .
ANALYTICAL CHEMISTRY, 1994, 66 (24) :4390-4399