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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/43186
Title: MANORAA (Mapping Analogous Nuclei Onto Residue And Affinity) for identifying protein-ligand fragment interaction, pathways and SNPs
Authors: Duangrudee Tanramluk
Lalita Narupiyakul
Ruj Akavipat
Sungsam Gong
Varodom Charoensawan
Mahidol University
Kasetsart University
University of Cambridge
Keywords: Biochemistry, Genetics and Molecular Biology
Issue Date: 1-Jan-2016
Citation: Nucleic Acids Research. Vol.44, No.W1 (2016), W514-W521
Abstract: © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. Protein-ligand interaction analysis is an important step of drug design and protein engineering in order to predict the binding affinity and selectivity between ligands to the target proteins. To date, there are more than 100 000 structures available in the Protein Data Bank (PDB), of which ∼30% are protein-ligand (MW below 1000 Da) complexes. We have developed the integrative web server MANORAA (Mapping Analogous Nuclei Onto Residue And Affinity) with the aim of providing a user-friendly web interface to assist structural study and design of protein-ligand interactions. In brief, the server allows the users to input the chemical fragments and present all the unique molecular interactions to the target proteins with available three-dimensional structures in the PDB. The users can also link the ligands of interest to assess possible off-target proteins, human variants and pathway information using our all-in-one integrated tools. Taken together, we envisage that the server will facilitate and improve the study of protein-ligand interactions by allowing observation and comparison of ligand interactions with multiple proteins at the same time.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85020843009&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/43186
ISSN: 13624962
03051048
Appears in Collections:Scopus 2016-2017

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