Predicting substrate specificity of adenylation domains of nonribosomal peptide synthetases and other protein properties by latent semantic indexing

被引:40
作者
Baranasic, Damir [1 ,2 ]
Zucko, Jurica [1 ]
Diminic, Janko [1 ]
Gacesa, Ranko [1 ]
Long, Paul F. [3 ,4 ]
Cullum, John [2 ]
Hranueli, Daslav [1 ]
Starcevic, Antonio [1 ]
机构
[1] Univ Zagreb, Fac Food Technol & Biotechnol, Zagreb 10000, Croatia
[2] Univ Kaiserslautern, Dept Genet, D-67653 Kaiserslautern, Germany
[3] Kings Coll London, Inst Pharmaceut Sci, London SE1 9NH, England
[4] Kings Coll London, Dept Chem, London SE1 9NH, England
关键词
LSI; NRPS; Adenylation domains; Protein tokenization; Functional subtype; ALIGNMENTS;
D O I
10.1007/s10295-013-1322-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Successful genome mining is dependent on accurate prediction of protein function from sequence. This often involves dividing protein families into functional subtypes (e.g., with different substrates). In many cases, there are only a small number of known functional subtypes, but in the case of the adenylation domains of nonribosomal peptide synthetases (NRPS), there are > 500 known substrates. Latent semantic indexing (LSI) was originally developed for text processing but has also been used to assign proteins to families. Proteins are treated as ''documents'' and it is necessary to encode properties of the amino acid sequence as ''terms'' in order to construct a term-document matrix, which counts the terms in each document. This matrix is then processed to produce a document-concept matrix, where each protein is represented as a row vector. A standard measure of the closeness of vectors to each other (cosines of the angle between them) provides a measure of protein similarity. Previous work encoded proteins as oligopeptide terms, i.e. counted oligopeptides, but used no information regarding location of oligopeptides in the proteins. A novel tokenization method was developed to analyze information from multiple alignments. LSI successfully distinguished between two functional subtypes in five well-characterized families. Visualization of different ''concept'' dimensions allows exploration of the structure of protein families. LSI was also used to predict the amino acid substrate of adenylation domains of NRPS. Better results were obtained when selected residues from multiple alignments were used rather than the total sequence of the adenylation domains. Using ten residues from the substrate binding pocket performed better than using 34 residues within 8 of the active site. Prediction efficiency was somewhat better than that of the best published method using a support vector machine.
引用
收藏
页码:461 / 467
页数:7
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