Evidence map›Paper›PMID 27892693›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2017

A Graph Approach to Mining Biological Patterns in the Binding Interfaces.

Wen Cheng, Changhui Yan

Abstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Wen ChengDepartment of Computer Science, North Dakota State University , Fargo, North Dakota.
Changhui YanDepartment of Computer Science, North Dakota State University , Fargo, North Dakota.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein-RNA interactions play important roles in the biological systems. Searching for regular patterns in the Protein-RNA binding interfaces is important for understanding how protein and RNA recognize each other and bind to form a complex. Herein, we present a graph-mining method for discovering biological patterns in the protein-RNA interfaces. We represented known protein-RNA interfaces using graphs and then discovered graph patterns 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 crucial for the RNA binding by experimental methods. 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-binding 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 that of a state-of-the-art complex scoring function. Our work also revealed possible patterns that might be important for binding affinity.

Indexed as

Support Vector MachineAmino Acid MotifsAnimalsBinding SitesComputational BiologyComputer GraphicsData MiningHumansMolecular Docking SimulationProtein BindingProtein ConformationProtein Interaction Domains and MotifsProteinsRNARNA-Binding ProteinsProteinsRNARNA-Binding Proteinsbinding sitescommon subgraphsgraph patternsprotein–RNA interactionsrecurrent patternsscoring functions

Identifiers

PMID27892693
PMCPMC5220573

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.