Cargando…

PvaxDB: a comprehensive structural repository of Plasmodium vivax proteome

The severity of malaria caused by Plasmodium vivax worldwide and its resistance against the available general antimalarial drugs has created an urgent need for a comprehensive insight into its biology and biochemistry for developing some novel potential vaccines and therapeutics. P.vivax comprises 5...

Descripción completa

Detalles Bibliográficos
Autores principales: Singh, Ankita, Kaushik, Rahul, Kuntal, Himani, Jayaram, B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852996/
https://www.ncbi.nlm.nih.gov/pubmed/29688373
http://dx.doi.org/10.1093/database/bay021
_version_ 1783306684055158784
author Singh, Ankita
Kaushik, Rahul
Kuntal, Himani
Jayaram, B
author_facet Singh, Ankita
Kaushik, Rahul
Kuntal, Himani
Jayaram, B
author_sort Singh, Ankita
collection PubMed
description The severity of malaria caused by Plasmodium vivax worldwide and its resistance against the available general antimalarial drugs has created an urgent need for a comprehensive insight into its biology and biochemistry for developing some novel potential vaccines and therapeutics. P.vivax comprises 5392 proteins mostly predicted, out of which 4211 are soluble proteins and 2205 of these belong to blood and liver stages of malarial cycle. Presently available public resources report functional annotation (gene ontology) of only 28% (627 proteins) of the enzymatic soluble proteins and experimental structures are determined for only 42 proteins P. vivax proteome. In this milieu of severe paucity of structural and functional data, we have generated structures of 2205 soluble proteins, validated them thoroughly, identified their binding pockets (including active sites) and annotated their function increasing the coverage from the existing 28% to 100%. We have pooled all this information together and created a database christened as PvaxDB, which furnishes extensive sequence, structure, ligand binding site and functional information. We believe PvaxDB could be helpful in identifying novel protein drug targets, expediting development of new drugs to combat malaria. This is also the first attempt to create a reliable comprehensive computational structural repository of all the soluble proteins of P. vivax. Database URL: http://www.scfbio-iitd.res.in/PvaxDB
format Online
Article
Text
id pubmed-5852996
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-58529962018-03-23 PvaxDB: a comprehensive structural repository of Plasmodium vivax proteome Singh, Ankita Kaushik, Rahul Kuntal, Himani Jayaram, B Database (Oxford) Original Article The severity of malaria caused by Plasmodium vivax worldwide and its resistance against the available general antimalarial drugs has created an urgent need for a comprehensive insight into its biology and biochemistry for developing some novel potential vaccines and therapeutics. P.vivax comprises 5392 proteins mostly predicted, out of which 4211 are soluble proteins and 2205 of these belong to blood and liver stages of malarial cycle. Presently available public resources report functional annotation (gene ontology) of only 28% (627 proteins) of the enzymatic soluble proteins and experimental structures are determined for only 42 proteins P. vivax proteome. In this milieu of severe paucity of structural and functional data, we have generated structures of 2205 soluble proteins, validated them thoroughly, identified their binding pockets (including active sites) and annotated their function increasing the coverage from the existing 28% to 100%. We have pooled all this information together and created a database christened as PvaxDB, which furnishes extensive sequence, structure, ligand binding site and functional information. We believe PvaxDB could be helpful in identifying novel protein drug targets, expediting development of new drugs to combat malaria. This is also the first attempt to create a reliable comprehensive computational structural repository of all the soluble proteins of P. vivax. Database URL: http://www.scfbio-iitd.res.in/PvaxDB Oxford University Press 2018-03-14 /pmc/articles/PMC5852996/ /pubmed/29688373 http://dx.doi.org/10.1093/database/bay021 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Singh, Ankita
Kaushik, Rahul
Kuntal, Himani
Jayaram, B
PvaxDB: a comprehensive structural repository of Plasmodium vivax proteome
title PvaxDB: a comprehensive structural repository of Plasmodium vivax proteome
title_full PvaxDB: a comprehensive structural repository of Plasmodium vivax proteome
title_fullStr PvaxDB: a comprehensive structural repository of Plasmodium vivax proteome
title_full_unstemmed PvaxDB: a comprehensive structural repository of Plasmodium vivax proteome
title_short PvaxDB: a comprehensive structural repository of Plasmodium vivax proteome
title_sort pvaxdb: a comprehensive structural repository of plasmodium vivax proteome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852996/
https://www.ncbi.nlm.nih.gov/pubmed/29688373
http://dx.doi.org/10.1093/database/bay021
work_keys_str_mv AT singhankita pvaxdbacomprehensivestructuralrepositoryofplasmodiumvivaxproteome
AT kaushikrahul pvaxdbacomprehensivestructuralrepositoryofplasmodiumvivaxproteome
AT kuntalhimani pvaxdbacomprehensivestructuralrepositoryofplasmodiumvivaxproteome
AT jayaramb pvaxdbacomprehensivestructuralrepositoryofplasmodiumvivaxproteome