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      CPPsite 2.0: a repository of experimentally validated cell-penetrating peptides

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          Abstract

          CPPsite 2.0 ( http://crdd.osdd.net/raghava/cppsite/) is an updated version of manually curated database (CPPsite) of cell-penetrating peptides (CPPs). The current version holds around 1850 peptide entries, which is nearly two times than the entries in the previous version. The updated data were curated from research papers and patents published in last three years. It was observed that most of the CPPs discovered/ tested, in last three years, have diverse chemical modifications (e.g. non-natural residues, linkers, lipid moieties, etc.). We have compiled this information on chemical modifications systematically in the updated version of the database. In order to understand the structure-function relationship of these peptides, we predicted tertiary structure of CPPs, possessing both modified and natural residues, using state-of-the-art techniques. CPPsite 2.0 also maintains information about model systems ( in vitro/ in vivo) used for CPP evaluation and different type of cargoes (e.g. nucleic acid, protein, nanoparticles, etc.) delivered by these peptides. In order to assist a wide range of users, we developed a user-friendly responsive website, with various tools, suitable for smartphone, tablet and desktop users. In conclusion, CPPsite 2.0 provides significant improvements over the previous version in terms of data content.

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          Most cited references29

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          Identification of common molecular subsequences.

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            Cell-penetrating peptides: classes, origin, and current landscape.

            With more than ten new FDA approvals since 2001, peptides are emerging as an important therapeutic alternative to small molecules. However, unlike small molecules, peptides on the market today are limited to extracellular targets. By contrast, cell-penetrating peptides (CPPs) can target intracellular proteins and also carry other cargoes (e.g. other peptides, small molecules or proteins) into the cell, thus offering great potential as future therapeutics. In this review I present a classification scheme for CPPs based on their physical-chemical properties and origin, and I provide a general framework for understanding and discovering new CPPs. Copyright © 2012 Elsevier Ltd. All rights reserved.
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              The RCSB Protein Data Bank: views of structural biology for basic and applied research and education

              The RCSB Protein Data Bank (RCSB PDB, http://www.rcsb.org) provides access to 3D structures of biological macromolecules and is one of the leading resources in biology and biomedicine worldwide. Our efforts over the past 2 years focused on enabling a deeper understanding of structural biology and providing new structural views of biology that support both basic and applied research and education. Herein, we describe recently introduced data annotations including integration with external biological resources, such as gene and drug databases, new visualization tools and improved support for the mobile web. We also describe access to data files, web services and open access software components to enable software developers to more effectively mine the PDB archive and related annotations. Our efforts are aimed at expanding the role of 3D structure in understanding biology and medicine.
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                Author and article information

                Journal
                Nucleic Acids Res
                Nucleic Acids Res
                nar
                nar
                Nucleic Acids Research
                Oxford University Press
                0305-1048
                1362-4962
                04 January 2016
                19 November 2015
                19 November 2015
                : 44
                : Database issue , Database issue
                : D1098-D1103
                Affiliations
                Bioinformatics Centre, CSIR-Institute of Microbial Technology, Chandigarh 160036, India
                Author notes
                [* ]To whom correspondence should be addressed. Tel: +91 172 2690557; Fax: +91 172 2690632; Email: raghava@ 123456imtech.res.in
                Correspondence may also be addressed to Ankur Gautam. Tel: +91 172 2690557; Fax: +91 172 2690632; Email: ankurgautam@ 123456imtech.res.in
                []These authors contributed equally to the paper as first authors.
                Article
                10.1093/nar/gkv1266
                4702894
                26586798
                4bdea877-c555-454f-9bc8-99b46617935a
                © The Author(s) 2015. 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 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
                : 03 November 2015
                : 29 October 2015
                : 07 September 2015
                Page count
                Pages: 6
                Categories
                Database Issue
                Custom metadata
                04 January 2016

                Genetics
                Genetics

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