Prediction and identification of sequences coding for orphan enzymes using genomic and metagenomic neighbours
-
- Takuji Yamada
- Structural and Computational Biology Unit, European Molecular Biology Laboratory Heidelberg Germany
-
- Alison S Waller
- Structural and Computational Biology Unit, European Molecular Biology Laboratory Heidelberg Germany
-
- Jeroen Raes
- Molecular and Cellular Interactions Department, VIB Brussels Belgium
-
- Aleksej Zelezniak
- Structural and Computational Biology Unit, European Molecular Biology Laboratory Heidelberg Germany
-
- Nadia Perchat
- Commissariat à l'Energie Atomique Evry France
-
- Alain Perret
- Commissariat à l'Energie Atomique Evry France
-
- Marcel Salanoubat
- Commissariat à l'Energie Atomique Evry France
-
- Kiran R Patil
- Structural and Computational Biology Unit, European Molecular Biology Laboratory Heidelberg Germany
-
- Jean Weissenbach
- Commissariat à l'Energie Atomique Evry France
-
- Peer Bork
- Structural and Computational Biology Unit, European Molecular Biology Laboratory Heidelberg Germany
書誌事項
- 公開日
- 2012-01
- 権利情報
-
- http://creativecommons.org/licenses/by-nc-sa/3.0/
- DOI
-
- 10.1038/msb.2012.13
- 公開者
- Springer Science and Business Media LLC
この論文をさがす
説明
Despite the current wealth of sequencing data, one-third of all biochemically characterized metabolic enzymes lack a corresponding gene or protein sequence, and as such can be considered orphan enzymes. They represent a major gap between our molecular and biochemical knowledge, and consequently are not amenable to modern systemic analyses. As 555 of these orphan enzymes have metabolic pathway neighbours, we developed a global framework that utilizes the pathway and (meta)genomic neighbour information to assign candidate sequences to orphan enzymes. For 131 orphan enzymes (37% of those for which (meta)genomic neighbours are available), we associate sequences to them using scoring parameters with an estimated accuracy of 70%, implying functional annotation of 16,345 gene sequences in numerous (meta)genomes. As a case in point, two of these candidate sequences were experimentally validated to encode the predicted activity. In addition, we augmented the currently available genome-scale metabolic models with these new sequence-function associations and were able to expand the models by on average 8%, with a considerable change in the flux connectivity patterns and improved essentiality prediction.
収録刊行物
-
- Molecular Systems Biology
-
Molecular Systems Biology 8 (1), 581-, 2012-01
Springer Science and Business Media LLC
関連未分類成果物
- Tweet
キーワード
- Medicine (General)
- QH301-705.5
- neighbourhood information
- [SDV]Life Sciences [q-bio]
- [SDV.BBM]Life Sciences [q-bio]/Biochemistry
- [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry
- Models, Biological
- Article
- R5-920
- [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN]
- Databases, Genetic
- genomics
- metabolic pathways
- Humans
- [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology
- Biology (General)
- Molecular Biology
- Molecular Biology/Genomics [q-bio.GN]
- metagenomics
- Systems Biology
- Chromosome Mapping
- Sequence Analysis, DNA
- genomics metabolic pathways metagenomics neighbourhood information orphan enzymes
- Enzymes
- Cardiovascular and Metabolic Diseases
- orphan enzymes
- Metagenome
- Metagenomics
- Metabolic Networks and Pathways
詳細情報 詳細情報について
-
- CRID
- 1363670321106487296
-
- ISSN
- 17444292
-
- PubMed
- 22569339
-
- データソース種別
-
- Crossref
- OpenAIRE
- IRDB

