JASSA: a comprehensive tool for prediction of SUMOylation sites and SIMs

被引:161
作者
Beauclair, Guillaume [1 ,2 ,3 ]
Bridier-Nahmias, Antoine [1 ,2 ,3 ,4 ]
Zagury, Jean-Francois [5 ]
Saib, Ali [1 ,2 ,3 ,4 ]
Zamborlini, Alessia [1 ,2 ,3 ,4 ]
机构
[1] Hop St Louis, CNRS UMR7212, Paris, France
[2] Hop St Louis, Inst Univ Hematol, Inserm U944, Paris, France
[3] Univ Paris Diderot, Sorbonne Paris Cite, Hop St Louis, Paris, France
[4] Cnam, Lab PVM, Paris, France
[5] Cnam, Chaire Bioinformat, EA4627, Lab Genom Bioinformat & Applicat, Paris, France
关键词
SUMO MODIFICATION; MOTIF; BINDING; PHOSPHORYLATION; IDENTIFICATION; CONJUGATION; PROTEINS; PROTEOME; DOMAIN;
D O I
10.1093/bioinformatics/btv403
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Motivation: Post-translational modification by the Small Ubiquitin-like Modifier (SUMO) proteins, a process termed SUMOylation, is involved in many fundamental cellular processes. SUMO proteins are conjugated to a protein substrate, creating an interface for the recruitment of cofactors harboring SUMO-interacting motifs (SIMs). Mapping both SUMO-conjugation sites and SIMs is required to study the functional consequence of SUMOylation. To define the best candidate sites for experimental validation we designed JASSA, a Joint Analyzer of SUMOylation site and SIMs. Results: JASSA is a predictor that uses a scoring system based on a Position Frequency Matrix derived from the alignment of experimental SUMOylation sites or SIMs. Compared with existing web-tools, JASSA displays on par or better performances. Novel features were implemented towards a better evaluation of the prediction, including identification of database hits matching the query sequence and representation of candidate sites within the secondary structural elements and/or the 3D fold of the protein of interest, retrievable from deposited PDB files.
引用
收藏
页码:3483 / 3491
页数:9
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