DatabasedbOGAP - An Integrated Bioinformatics Resource for Protein O-GlcNAcylation
2011

dbOGAP: A Database for Protein O-GlcNAcylation

Sample size: 1163 publication 10 minutes Evidence: moderate

Author Information

Author(s): Wang Jinlian, Torii Manabu, Liu Hongfang, Hart Gerald W, Hu Zhang-Zhi

Primary Institution: Georgetown University Medical Center

Hypothesis

The study aims to develop a comprehensive database for O-GlcNAcylated proteins and a prediction tool for O-GlcNAcylation sites.

Conclusion

The dbOGAP database is the first public resource providing systematic access to O-GlcNAcylated proteins and related functional information.

Supporting Evidence

  • The database contains ~800 proteins with experimental O-GlcNAcylation information.
  • 172 proteins have a total of ~400 O-GlcNAcylation sites identified.
  • The OGlcNAcScan tool achieved an area under ROC curve of 74.3% in five-fold cross-validation.
  • About 22% of known O-GlcNAcylated proteins have identified O-GlcNAcylation sites.
  • O-GlcNAcylated proteins are primarily nucleocytoplasmic and involved in various biological processes.
  • 141 annotated GeneGO pathways are significantly enriched for O-GlcNAcylated human proteins.
  • O-GlcNAcylation is implicated in diseases such as type II diabetes and neurodegenerative diseases.
  • The dbOGAP resource facilitates research on O-GlcNAcylation and its proteomic identification.

Takeaway

Scientists created a database to help find proteins that have a special sugar added to them, which is important for many body functions.

Methodology

The database was developed using literature review and includes a prediction system based on Support Vector Machine.

Potential Biases

Potential false positives from mass spectrometry data.

Limitations

Many O-GlcNAcylated proteins were identified through mass spectrometry and require further validation.

Participant Demographics

About 61% of the identified O-GlcNAcylated proteins are from humans.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1471-2105-12-91

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