Proceedings of the National Academy of Sciences · 2017 · 99 citations · 41 references
Life SciencesBiochemistryMolecular BiologyEnzymologyGlycobiologyPost-translational ModificationGlycan DegradationGlycan RecognitionGlycan StructureGlycan-protein InteractionsO-linked GlycosylationProtein GlycosylationGlycopeptide AnalysisN-glycan RecognitionO-glycan AnalysisO-glycan DegradationO-glycan RecognitionPeptidase ActivityProtein Glycosylation AnalysisSubstrate Specificity Of Glycan-degrading Enzymes
The vast majority of proteins are posttranslationally altered, with the addition of covalently linked sugars (glycosylation) being one of the most abundant modifications. However, despite the hydrolysis of protein peptide bonds by peptidases being a process essential to all life on Earth, the fundamental details of how peptidases accommodate posttranslational modifications, including glycosylation, has not been addressed. Through biochemical analyses and X-ray crystallographic structures we show that to hydrolyze their substrates, three structurally related metallopeptidases require the specific recognition of O-linked glycan modifications via carbohydrate-specific subsites immediately adjacent to their peptidase catalytic machinery. The three peptidases showed selectivity for different glycans, revealing protein-specific adaptations to particular glycan modifications, yet always cleaved the peptide bond immediately preceding the glycosylated residue. This insight builds upon the paradigm of how peptidases recognize substrates and provides a molecular understanding of glycoprotein degradation.
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<i>Phaser</i>crystallographic software
Airlie J. McCoy, Ralf W. Grosse‐Kunstleve, Paul D. Adams et al. · Journal of Applied Crystallography · 2007 · 20.9K citations · Full text
Wolfgang Kabsch · Acta Crystallographica Section D Biological Crystallography · 2010 · 16.9K citations · Full text