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Building and rebuilding N-glycans in protein structure models
- Source :
- Acta Crystallographica Section D Structural Biology, Acta Crystallographica. Section D, Structural Biology
- Publication Year :
- 2019
- Publisher :
- International Union of Crystallography (IUCr), 2019.
-
Abstract
- Carbohydrates are automatically built and rebuilt using Coot in the PDB-REDO pipeline.<br />N-Glycosylation is one of the most common post-translational modifications and is implicated in, for example, protein folding and interaction with ligands and receptors. N-Glycosylation trees are complex structures of linked carbohydrate residues attached to asparagine residues. While carbohydrates are typically modeled in protein structures, they are often incomplete or have the wrong chemistry. Here, new tools are presented to automatically rebuild existing glycosylation trees, to extend them where possible, and to add new glycosylation trees if they are missing from the model. The method has been incorporated in the PDB-REDO pipeline and has been applied to build or rebuild 16 452 carbohydrate residues in 11 651 glycosylation trees in 4498 structure models, and is also available from the PDB-REDO web server. With better modeling of N-glycosylation, the biological function of this important modification can be better and more easily understood.
- Subjects :
- Models, Molecular
Glycan
Glycosylation
Protein Conformation
Computer science
carbohydrates
Coot
N-glycans
macromolecular substances
Computational biology
Crystallography, X-Ray
PDB-REDO
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Protein structure
Polysaccharides
Structural Biology
Carbohydrate Conformation
Humans
Asparagine
Databases, Protein
crystallography
Hardware_REGISTER-TRANSFER-LEVELIMPLEMENTATION
Glycoproteins
030304 developmental biology
validation
0303 health sciences
biology
model building
InformationSystems_DATABASEMANAGEMENT
Research Papers
carbohydrates (lipids)
Carbohydrate Sequence
chemistry
030220 oncology & carcinogenesis
biology.protein
lipids (amino acids, peptides, and proteins)
Protein folding
Subjects
Details
- ISSN :
- 20597983
- Volume :
- 75
- Database :
- OpenAIRE
- Journal :
- Acta Crystallographica Section D Structural Biology
- Accession number :
- edsair.doi.dedup.....ecca77434f9ca8dfbd375c44eeac2583
- Full Text :
- https://doi.org/10.1107/s2059798319003875