2019
DOI: 10.1101/709899
|View full text |Cite
Preprint
|
Sign up to set email alerts
|

Enzyme annotation in UniProtKB using Rhea

Abstract: Motivation: To provide high quality computationally tractable enzyme annotation in UniProtKB using Rhea, a comprehensive expert-curated knowledgebase of biochemical reactions which describes reaction participants using the ontology ChEBI (Chemical Entities of Biological Interest). Results:We replaced existing textual descriptions of biochemical reactions in UniProtKB with their equivalents from Rhea, which is now the standard for annotation of enzymatic reactions in UniProtKB. We developed improved search and … Show more

Help me understand this report
View published versions

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2019
2019
2023
2023

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 8 publications
(2 citation statements)
references
References 36 publications
0
2
0
Order By: Relevance
“…The lytic module of vB_HmeY_H4907 comprises only two ORFs. P51770 is a member of the spanin complex, homologous to ORF 32, and plays a crucial role in disrupting the host outer membrane during viral efflux and causing cell lysis ( 36 ). The spanin complex completes host lysis by rupturing the outer membrane after the actions of holin and endolysin penetrate the inner membrane and break down the host peptidoglycan.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The lytic module of vB_HmeY_H4907 comprises only two ORFs. P51770 is a member of the spanin complex, homologous to ORF 32, and plays a crucial role in disrupting the host outer membrane during viral efflux and causing cell lysis ( 36 ). The spanin complex completes host lysis by rupturing the outer membrane after the actions of holin and endolysin penetrate the inner membrane and break down the host peptidoglycan.…”
Section: Resultsmentioning
confidence: 99%
“…We manually screened the start and end sites repeated in multiple programs and the sequences with start and stop codons to determine the open reading frame. The conserved domain was detected by finding homologs in the non-redundant database ( http://blast.ncbi.nlm.nih.gov/ ), the InterPro database ( 57 ), the Conserved Domain Database Suite (CDD/SPARCLE) ( 58 ), the UniProtKB database ( 36 ), the Pfam database ( http://pfam.xfam.org/ ), and the HHpred server ( 59 ). To identify the start and end of the phage genome’s replication, the cumulative GC skew ( https://genskew.csb.univie.ac.at/webskew ) analysis was applied ( 29 ).…”
Section: Methodsmentioning
confidence: 99%