SPOT-Peptide: Template-Based Prediction of Peptide-Binding Proteins and Peptide-Binding Sites

被引:15
|
作者
Litfin, Thomas [1 ]
Yang, Yuedong [2 ]
Zhou, Yaoqi [1 ,3 ]
机构
[1] Griffith Univ, Sch Informat & Commun Technol, Southport, Qld 4222, Australia
[2] Sun Yat Sen Univ, Sch Data & Comp Sci, Guangzhou 510006, Guangdong, Peoples R China
[3] Griffith Univ, Inst Glyc, Southport, Qld 4222, Australia
基金
英国医学研究理事会; 中国国家自然科学基金; 澳大利亚研究理事会;
关键词
HUMAN-DISEASE; MEAN FORCE; LIGAND; DATABASE; SEQUENCE; DOCKING; SIMILARITY; ALIGNMENT; SURFACES; COFACTOR;
D O I
10.1021/acs.jcim.8b00777
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Peptide-binding domains have been successfully targeted in therapeutic applications. However, many peptide-binding proteins (PBPs) remain uncharacterized. Computational prediction of peptide-domain interfaces is challenging due to short lengths, lack of well-defined structures, and limited conservation of peptide motifs. Here we present SPOT-peptide, a template-based protocol for the simultaneous prediction of peptide-binding domains and peptide binding sites independent of specific peptide composition. SPOT-peptide leverages the dogmatic relationship between protein structure and function to predict peptide-binding characteristics for an unknown target based on remote structural homologues. In a leave-homologue out benchmark evaluation, PBPs are discriminated with a Matthews correlation coefficient (MCC) of 0.420 and the correct binding sites are identified in 80% of the predicted PBPs. Furthermore, replacing the holo target structures with equivalent structures in the apo conformation only marginally diminished PBP recovery. The method is available as a web server at http://sparks-lab.org/tom/SPOT-peptide.
引用
收藏
页码:924 / 930
页数:7
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