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      CASTp 3.0: computed atlas of surface topography of proteins

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          Abstract

          Geometric and topological properties of protein structures, including surface pockets, interior cavities and cross channels, are of fundamental importance for proteins to carry out their functions. Computed Atlas of Surface Topography of proteins (CASTp) is a web server that provides online services for locating, delineating and measuring these geometric and topological properties of protein structures. It has been widely used since its inception in 2003. In this article, we present the latest version of the web server, CASTp 3.0. CASTp 3.0 continues to provide reliable and comprehensive identifications and quantifications of protein topography. In addition, it now provides: (i) imprints of the negative volumes of pockets, cavities and channels, (ii) topographic features of biological assemblies in the Protein Data Bank, (iii) improved visualization of protein structures and pockets, and (iv) more intuitive structural and annotated information, including information of secondary structure, functional sites, variant sites and other annotations of protein residues. The CASTp 3.0 web server is freely accessible at http://sts.bioe.uic.edu/castp/.

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          CASTp: computed atlas of surface topography of proteins with structural and topographical mapping of functionally annotated residues

          Cavities on a proteins surface as well as specific amino acid positioning within it create the physicochemical properties needed for a protein to perform its function. CASTp () is an online tool that locates and measures pockets and voids on 3D protein structures. This new version of CASTp includes annotated functional information of specific residues on the protein structure. The annotations are derived from the Protein Data Bank (PDB), Swiss-Prot, as well as Online Mendelian Inheritance in Man (OMIM), the latter contains information on the variant single nucleotide polymorphisms (SNPs) that are known to cause disease. These annotated residues are mapped to surface pockets, interior voids or other regions of the PDB structures. We use a semi-global pair-wise sequence alignment method to obtain sequence mapping between entries in Swiss-Prot, OMIM and entries in PDB. The updated CASTp web server can be used to study surface features, functional regions and specific roles of key residues of proteins.
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            The interpretation of protein structures: estimation of static accessibility.

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              3Dmol.js: molecular visualization with WebGL

              Summary: 3Dmol.js is a modern, object-oriented JavaScript library that uses the latest web technologies to provide interactive, hardware-accelerated three-dimensional representations of molecular data without the need to install browser plugins or Java. 3Dmol.js provides a full featured API for developers as well as a straightforward declarative interface that lets users easily share and embed molecular data in websites. Availability and implementation: 3Dmol.js is distributed under the permissive BSD open source license. Source code and documentation can be found at http://3Dmol.csb.pitt.edu Contact: dkoes@pitt.edu
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                Author and article information

                Journal
                Nucleic Acids Res
                Nucleic Acids Res
                nar
                Nucleic Acids Research
                Oxford University Press
                0305-1048
                1362-4962
                02 July 2018
                01 June 2018
                01 June 2018
                : 46
                : Web Server issue
                : W363-W367
                Affiliations
                [1 ]Department of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, USA
                [2 ]Institut National de Recherche en Informatique et en Automatique, Paris 75012, France
                Author notes
                To whom correspondence should be addressed. Tel: +1 312 355 1789; Fax: +1 312 413 2 18; Email: jliang@ 123456uic.edu

                The authors wish it to be known that, in their opinion, the second and third authors should be regarded as Joint Second Authors.

                Article
                gky473
                10.1093/nar/gky473
                6031066
                29860391
                0fef3506-bd2e-45a4-bdb7-d62ab74a0a23
                © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@ 123456oup.com

                History
                : 17 May 2018
                : 04 May 2018
                : 01 March 2018
                Page count
                Pages: 5
                Funding
                Funded by: National Institutes of Health 10.13039/100000002
                Award ID: R01CA204962
                Categories
                Web Server Issue

                Genetics
                Genetics

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