{"title":"在蛋白质- rna界面中挖掘图形模式","authors":"Wen Cheng, Changhui Yan","doi":"10.1109/BIBM.2015.7359862","DOIUrl":null,"url":null,"abstract":"Protein-RNA interactions play important roles in the biological systems. The goal of this study is to discover structural patterns in the protein-RNA interfaces that contribute the affinity of the interactions. We represented known protein-RNA interfaces using graphs and then identify common subgraphs enriched in the interfaces. Comparison of the discovered graph patterns with UniProt annotations showed that the graph patterns had a significant overlap with residue sites that had been proven by experimental methods to be crucial for RNA bindings. Using 200 patterns as input features, a Support Vector Machine method was able to classify protein surface patches into RNA-binding sites and non-RNA-biding sites with 84.0% accuracy and 88.9% precision. We built a simple scoring function that calculated the total number of the graph patterns that occurred in a protein-RNA interface. That scoring function was able to discriminate near native protein-RNA complexes from docking decoys with a performance comparable with a state-of-the-art complex scoring function.","PeriodicalId":186217,"journal":{"name":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"345 ","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Mining graph patterns in the protein-RNA interfaces\",\"authors\":\"Wen Cheng, Changhui Yan\",\"doi\":\"10.1109/BIBM.2015.7359862\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Protein-RNA interactions play important roles in the biological systems. The goal of this study is to discover structural patterns in the protein-RNA interfaces that contribute the affinity of the interactions. We represented known protein-RNA interfaces using graphs and then identify common subgraphs enriched in the interfaces. Comparison of the discovered graph patterns with UniProt annotations showed that the graph patterns had a significant overlap with residue sites that had been proven by experimental methods to be crucial for RNA bindings. Using 200 patterns as input features, a Support Vector Machine method was able to classify protein surface patches into RNA-binding sites and non-RNA-biding sites with 84.0% accuracy and 88.9% precision. We built a simple scoring function that calculated the total number of the graph patterns that occurred in a protein-RNA interface. That scoring function was able to discriminate near native protein-RNA complexes from docking decoys with a performance comparable with a state-of-the-art complex scoring function.\",\"PeriodicalId\":186217,\"journal\":{\"name\":\"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)\",\"volume\":\"345 \",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-11-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/BIBM.2015.7359862\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/BIBM.2015.7359862","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Mining graph patterns in the protein-RNA interfaces
Protein-RNA interactions play important roles in the biological systems. The goal of this study is to discover structural patterns in the protein-RNA interfaces that contribute the affinity of the interactions. We represented known protein-RNA interfaces using graphs and then identify common subgraphs enriched in the interfaces. Comparison of the discovered graph patterns with UniProt annotations showed that the graph patterns had a significant overlap with residue sites that had been proven by experimental methods to be crucial for RNA bindings. Using 200 patterns as input features, a Support Vector Machine method was able to classify protein surface patches into RNA-binding sites and non-RNA-biding sites with 84.0% accuracy and 88.9% precision. We built a simple scoring function that calculated the total number of the graph patterns that occurred in a protein-RNA interface. That scoring function was able to discriminate near native protein-RNA complexes from docking decoys with a performance comparable with a state-of-the-art complex scoring function.