Abstract
BackgroundRNA regulates a variety of biological functions by interacting with other molecules. The ligand often binds in the RNA pocket to trigger structural changes or functions. Thus, it is essential to explore and visualize the RNA pocket to elucidate the structural and recognition mechanism for the RNA-ligand complex formation.ResultsIn this work, we developed one user-friendly bioinformatics tool, RPocket. This database provides geometrical size, centroid, shape, secondary structure element for RNA pocket, RNA-ligand interaction information, and functional sites. We extracted 240 RNA pockets from 94 non-redundant RNA-ligand complex structures. We developed RPDescriptor to calculate the pocket geometrical property quantitatively. The geometrical information was then subjected to RNA-ligand binding analysis by incorporating the sequence, secondary structure, and geometrical combinations. This new approach takes advantage of both the atom-level precision of the structure and the nucleotide-level tertiary interactions. The results show that the higher-level topological pattern indeed improves the tertiary structure prediction. We also proposed a potential mechanism for RNA-ligand complex formation. The electrostatic interactions are responsible for long-range recognition, while the Van der Waals and hydrophobic contacts for short-range binding and optimization. These interaction pairs can be considered as distance constraints to guide complex structural modeling and drug design.ConclusionRPocket database would facilitate RNA-ligand engineering to regulate the complex formation for biological or medical applications. RPocket is available at http://zhaoserver.com.cn/RPocket/RPocket.html.
Highlights
IntroductionThe ligand often binds in the RNA pocket to trigger structural changes or functions
RNA regulates a variety of biological functions by interacting with other molecules
(F) We developed RPDescriptor (RNA Pocket Descriptor) to calculate the pocket geometric characteristics for RNA molecules
Summary
The ligand often binds in the RNA pocket to trigger structural changes or functions. RNA regulates a variety of biological functions by interacting with other molecules. It is currently recognized that more than 70% of the human genome is transcribed into noncoding RNAs [1]. Of the human genome has been identified as protein-targeted for drug development. A human probably produces more than 15,000 long non-coding RNAs [1]. Zhou et al BMC Bioinformatics (2021) 22:428 part of these non-coding RNAs may eventually prove to be disease-related drug targets. A very recent study shows the nucleotide analog inhibitors in one essential molecule for the pathogenesis of COVID-19 by binding with virus-dependent RNA polymerase [4]. It is believed that RNA is more widely involved in the various regulatory processes
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