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Uncovering of cytochrome P450 anatomy by SecStrAnnotator

Protein structural families are groups of homologous proteins defined by the organization of secondary structure elements (SSEs). Nowadays, many families contain vast numbers of structures, and the SSEs can help to orient within them. Communities around specific protein families have even developed...

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Autores principales: Midlik, Adam, Navrátilová, Veronika, Moturu, Taraka Ramji, Koča, Jaroslav, Svobodová, Radka, Berka, Karel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196199/
https://www.ncbi.nlm.nih.gov/pubmed/34117311
http://dx.doi.org/10.1038/s41598-021-91494-8
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author Midlik, Adam
Navrátilová, Veronika
Moturu, Taraka Ramji
Koča, Jaroslav
Svobodová, Radka
Berka, Karel
author_facet Midlik, Adam
Navrátilová, Veronika
Moturu, Taraka Ramji
Koča, Jaroslav
Svobodová, Radka
Berka, Karel
author_sort Midlik, Adam
collection PubMed
description Protein structural families are groups of homologous proteins defined by the organization of secondary structure elements (SSEs). Nowadays, many families contain vast numbers of structures, and the SSEs can help to orient within them. Communities around specific protein families have even developed specialized SSE annotations, always assigning the same name to the equivalent SSEs in homologous proteins. A detailed analysis of the groups of equivalent SSEs provides an overview of the studied family and enriches the analysis of any particular protein at hand. We developed a workflow for the analysis of the secondary structure anatomy of a protein family. We applied this analysis to the model family of cytochromes P450 (CYPs)—a family of important biotransformation enzymes with a community-wide used SSE annotation. We report the occurrence, typical length and amino acid sequence for the equivalent SSE groups, the conservation/variability of these properties and relationship to the substrate recognition sites. We also suggest a generic residue numbering scheme for the CYP family. Comparing the bacterial and eukaryotic part of the family highlights the significant differences and reveals a well-known anomalous group of bacterial CYPs with some typically eukaryotic features. Our workflow for SSE annotation for CYP and other families can be freely used at address https://sestra.ncbr.muni.cz.
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spelling pubmed-81961992021-06-15 Uncovering of cytochrome P450 anatomy by SecStrAnnotator Midlik, Adam Navrátilová, Veronika Moturu, Taraka Ramji Koča, Jaroslav Svobodová, Radka Berka, Karel Sci Rep Article Protein structural families are groups of homologous proteins defined by the organization of secondary structure elements (SSEs). Nowadays, many families contain vast numbers of structures, and the SSEs can help to orient within them. Communities around specific protein families have even developed specialized SSE annotations, always assigning the same name to the equivalent SSEs in homologous proteins. A detailed analysis of the groups of equivalent SSEs provides an overview of the studied family and enriches the analysis of any particular protein at hand. We developed a workflow for the analysis of the secondary structure anatomy of a protein family. We applied this analysis to the model family of cytochromes P450 (CYPs)—a family of important biotransformation enzymes with a community-wide used SSE annotation. We report the occurrence, typical length and amino acid sequence for the equivalent SSE groups, the conservation/variability of these properties and relationship to the substrate recognition sites. We also suggest a generic residue numbering scheme for the CYP family. Comparing the bacterial and eukaryotic part of the family highlights the significant differences and reveals a well-known anomalous group of bacterial CYPs with some typically eukaryotic features. Our workflow for SSE annotation for CYP and other families can be freely used at address https://sestra.ncbr.muni.cz. Nature Publishing Group UK 2021-06-11 /pmc/articles/PMC8196199/ /pubmed/34117311 http://dx.doi.org/10.1038/s41598-021-91494-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Midlik, Adam
Navrátilová, Veronika
Moturu, Taraka Ramji
Koča, Jaroslav
Svobodová, Radka
Berka, Karel
Uncovering of cytochrome P450 anatomy by SecStrAnnotator
title Uncovering of cytochrome P450 anatomy by SecStrAnnotator
title_full Uncovering of cytochrome P450 anatomy by SecStrAnnotator
title_fullStr Uncovering of cytochrome P450 anatomy by SecStrAnnotator
title_full_unstemmed Uncovering of cytochrome P450 anatomy by SecStrAnnotator
title_short Uncovering of cytochrome P450 anatomy by SecStrAnnotator
title_sort uncovering of cytochrome p450 anatomy by secstrannotator
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196199/
https://www.ncbi.nlm.nih.gov/pubmed/34117311
http://dx.doi.org/10.1038/s41598-021-91494-8
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