Author:
Jendele Lukas,Krivak Radoslav,Skoda Petr,Novotny Marian,Hoksza David
Abstract
ABSTRACTPrankWeb is an online resource providing an interface to P2Rank, a state-of-the-art ligand binding site prediction method. P2Rank is a template-free machine learning method which is based on the prediction of ligandability of local chemical neighborhoods centered on points placed on a solvent accessible surface of a protein. Points with high ligandability score are then clustered to form the resulting ligand binding sites. On top of that, PrankWeb then provides a web interface enabling users to easily carry out the prediction and visually inspect the predicted binding sites via an integrated sequence-structure view. Moreover, PrankWeb can determine sequence conservation for the input molecule and use it in both the prediction and results visualization steps. Alongside its online visualization options, PrankWeb also offers the possibility to export the results as a PyMOL script for offline visualization. The web frontend communicates with the serer side via a REST API. Therefore, in high-throughput scenarios users can utilize the server API directly, bypassing the need for a webbased front end or installation of the P2Rank application. PrankWeb is available at http://prankweb.cz/. The source code of the web application and the P2Rank method can be accessed at https://github.com/jendelel/PrankWebApp and https://github.com/rdk/p2rank, respectively.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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