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novPTMenzy: a database for enzymes involved in novel post-translational modifications

With the recent discoveries of novel post-translational modifications (PTMs) which play important roles in signaling and biosynthetic pathways, identification of such PTM catalyzing enzymes by genome mining has been an area of major interest. Unlike well-known PTMs like phosphorylation, glycosylatio...

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Detalles Bibliográficos
Autores principales: Khater, Shradha, Mohanty, Debasisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414956/
https://www.ncbi.nlm.nih.gov/pubmed/25931459
http://dx.doi.org/10.1093/database/bav039
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author Khater, Shradha
Mohanty, Debasisa
author_facet Khater, Shradha
Mohanty, Debasisa
author_sort Khater, Shradha
collection PubMed
description With the recent discoveries of novel post-translational modifications (PTMs) which play important roles in signaling and biosynthetic pathways, identification of such PTM catalyzing enzymes by genome mining has been an area of major interest. Unlike well-known PTMs like phosphorylation, glycosylation, SUMOylation, no bioinformatics resources are available for enzymes associated with novel and unusual PTMs. Therefore, we have developed the novPTMenzy database which catalogs information on the sequence, structure, active site and genomic neighborhood of experimentally characterized enzymes involved in five novel PTMs, namely AMPylation, Eliminylation, Sulfation, Hydroxylation and Deamidation. Based on a comprehensive analysis of the sequence and structural features of these known PTM catalyzing enzymes, we have created Hidden Markov Model profiles for the identification of similar PTM catalyzing enzymatic domains in genomic sequences. We have also created predictive rules for grouping them into functional subfamilies and deciphering their mechanistic details by structure-based analysis of their active site pockets. These analytical modules have been made available as user friendly search interfaces of novPTMenzy database. It also has a specialized analysis interface for some PTMs like AMPylation and Eliminylation. The novPTMenzy database is a unique resource that can aid in discovery of unusual PTM catalyzing enzymes in newly sequenced genomes. Database URL: http://www.nii.ac.in/novptmenzy.html
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spelling pubmed-44149562015-05-06 novPTMenzy: a database for enzymes involved in novel post-translational modifications Khater, Shradha Mohanty, Debasisa Database (Oxford) Original Article With the recent discoveries of novel post-translational modifications (PTMs) which play important roles in signaling and biosynthetic pathways, identification of such PTM catalyzing enzymes by genome mining has been an area of major interest. Unlike well-known PTMs like phosphorylation, glycosylation, SUMOylation, no bioinformatics resources are available for enzymes associated with novel and unusual PTMs. Therefore, we have developed the novPTMenzy database which catalogs information on the sequence, structure, active site and genomic neighborhood of experimentally characterized enzymes involved in five novel PTMs, namely AMPylation, Eliminylation, Sulfation, Hydroxylation and Deamidation. Based on a comprehensive analysis of the sequence and structural features of these known PTM catalyzing enzymes, we have created Hidden Markov Model profiles for the identification of similar PTM catalyzing enzymatic domains in genomic sequences. We have also created predictive rules for grouping them into functional subfamilies and deciphering their mechanistic details by structure-based analysis of their active site pockets. These analytical modules have been made available as user friendly search interfaces of novPTMenzy database. It also has a specialized analysis interface for some PTMs like AMPylation and Eliminylation. The novPTMenzy database is a unique resource that can aid in discovery of unusual PTM catalyzing enzymes in newly sequenced genomes. Database URL: http://www.nii.ac.in/novptmenzy.html Oxford University Press 2015-04-29 /pmc/articles/PMC4414956/ /pubmed/25931459 http://dx.doi.org/10.1093/database/bav039 Text en © The Author(s) 2015. 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
Khater, Shradha
Mohanty, Debasisa
novPTMenzy: a database for enzymes involved in novel post-translational modifications
title novPTMenzy: a database for enzymes involved in novel post-translational modifications
title_full novPTMenzy: a database for enzymes involved in novel post-translational modifications
title_fullStr novPTMenzy: a database for enzymes involved in novel post-translational modifications
title_full_unstemmed novPTMenzy: a database for enzymes involved in novel post-translational modifications
title_short novPTMenzy: a database for enzymes involved in novel post-translational modifications
title_sort novptmenzy: a database for enzymes involved in novel post-translational modifications
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414956/
https://www.ncbi.nlm.nih.gov/pubmed/25931459
http://dx.doi.org/10.1093/database/bav039
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