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Prediction and characterization of enzymatic activities guided by sequence similarity and genome neighborhood networks
Metabolic pathways in eubacteria and archaea often are encoded by operons and/or gene clusters (genome neighborhoods) that provide important clues for assignment of both enzyme functions and metabolic pathways. We describe a bioinformatic approach (genome neighborhood network; GNN) that enables larg...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113996/ https://www.ncbi.nlm.nih.gov/pubmed/24980702 http://dx.doi.org/10.7554/eLife.03275 |
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author | Zhao, Suwen Sakai, Ayano Zhang, Xinshuai Vetting, Matthew W Kumar, Ritesh Hillerich, Brandan San Francisco, Brian Solbiati, Jose Steves, Adam Brown, Shoshana Akiva, Eyal Barber, Alan Seidel, Ronald D Babbitt, Patricia C Almo, Steven C Gerlt, John A Jacobson, Matthew P |
author_facet | Zhao, Suwen Sakai, Ayano Zhang, Xinshuai Vetting, Matthew W Kumar, Ritesh Hillerich, Brandan San Francisco, Brian Solbiati, Jose Steves, Adam Brown, Shoshana Akiva, Eyal Barber, Alan Seidel, Ronald D Babbitt, Patricia C Almo, Steven C Gerlt, John A Jacobson, Matthew P |
author_sort | Zhao, Suwen |
collection | PubMed |
description | Metabolic pathways in eubacteria and archaea often are encoded by operons and/or gene clusters (genome neighborhoods) that provide important clues for assignment of both enzyme functions and metabolic pathways. We describe a bioinformatic approach (genome neighborhood network; GNN) that enables large scale prediction of the in vitro enzymatic activities and in vivo physiological functions (metabolic pathways) of uncharacterized enzymes in protein families. We demonstrate the utility of the GNN approach by predicting in vitro activities and in vivo functions in the proline racemase superfamily (PRS; InterPro IPR008794). The predictions were verified by measuring in vitro activities for 51 proteins in 12 families in the PRS that represent ∼85% of the sequences; in vitro activities of pathway enzymes, carbon/nitrogen source phenotypes, and/or transcriptomic studies confirmed the predicted pathways. The synergistic use of sequence similarity networks(3) and GNNs will facilitate the discovery of the components of novel, uncharacterized metabolic pathways in sequenced genomes. DOI: http://dx.doi.org/10.7554/eLife.03275.001 |
format | Online Article Text |
id | pubmed-4113996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41139962014-08-22 Prediction and characterization of enzymatic activities guided by sequence similarity and genome neighborhood networks Zhao, Suwen Sakai, Ayano Zhang, Xinshuai Vetting, Matthew W Kumar, Ritesh Hillerich, Brandan San Francisco, Brian Solbiati, Jose Steves, Adam Brown, Shoshana Akiva, Eyal Barber, Alan Seidel, Ronald D Babbitt, Patricia C Almo, Steven C Gerlt, John A Jacobson, Matthew P eLife Biochemistry Metabolic pathways in eubacteria and archaea often are encoded by operons and/or gene clusters (genome neighborhoods) that provide important clues for assignment of both enzyme functions and metabolic pathways. We describe a bioinformatic approach (genome neighborhood network; GNN) that enables large scale prediction of the in vitro enzymatic activities and in vivo physiological functions (metabolic pathways) of uncharacterized enzymes in protein families. We demonstrate the utility of the GNN approach by predicting in vitro activities and in vivo functions in the proline racemase superfamily (PRS; InterPro IPR008794). The predictions were verified by measuring in vitro activities for 51 proteins in 12 families in the PRS that represent ∼85% of the sequences; in vitro activities of pathway enzymes, carbon/nitrogen source phenotypes, and/or transcriptomic studies confirmed the predicted pathways. The synergistic use of sequence similarity networks(3) and GNNs will facilitate the discovery of the components of novel, uncharacterized metabolic pathways in sequenced genomes. DOI: http://dx.doi.org/10.7554/eLife.03275.001 eLife Sciences Publications, Ltd 2014-06-30 /pmc/articles/PMC4113996/ /pubmed/24980702 http://dx.doi.org/10.7554/eLife.03275 Text en Copyright © 2014, Zhao et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Zhao, Suwen Sakai, Ayano Zhang, Xinshuai Vetting, Matthew W Kumar, Ritesh Hillerich, Brandan San Francisco, Brian Solbiati, Jose Steves, Adam Brown, Shoshana Akiva, Eyal Barber, Alan Seidel, Ronald D Babbitt, Patricia C Almo, Steven C Gerlt, John A Jacobson, Matthew P Prediction and characterization of enzymatic activities guided by sequence similarity and genome neighborhood networks |
title | Prediction and characterization of enzymatic activities guided by sequence similarity and genome neighborhood networks |
title_full | Prediction and characterization of enzymatic activities guided by sequence similarity and genome neighborhood networks |
title_fullStr | Prediction and characterization of enzymatic activities guided by sequence similarity and genome neighborhood networks |
title_full_unstemmed | Prediction and characterization of enzymatic activities guided by sequence similarity and genome neighborhood networks |
title_short | Prediction and characterization of enzymatic activities guided by sequence similarity and genome neighborhood networks |
title_sort | prediction and characterization of enzymatic activities guided by sequence similarity and genome neighborhood networks |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113996/ https://www.ncbi.nlm.nih.gov/pubmed/24980702 http://dx.doi.org/10.7554/eLife.03275 |
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