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Protein Engineering vol. 3 no. 5 pp. 433-442, 1990
© 1990 Oxford University Press


RESEARCH-ARTICLE

Sequence differences between glycosylated and non-glycosylated Asn-X-Thr/Ser acceptor sites: implications for protein engineering

Ylva Gavel and Gunnar von Heijne1

Research Group for Theoretical Biophysics, Department of Theoretical Physics, Royal Institute of Technology S-100 44 Stockholm 1Department of Molecular Biology, Karolinska Institute, Centre for Biotechnology NOVUM, S-141 52 Huddinge, Sweden

In N-glycosylated glycoproteins, carbohydrate is attached to Asn in the sequence Asn-X-Ser/Thr, where X denotes any amino acid. However, the presence of this consensus peptide does not always lead to glycosylation. We have compiled an extensive collection of glycosylated and non-glycosylated Asn-X-Thr/Ser sites and present a statistical study based on this data set. Our results indicate that non-glycosylated sites tend to be found more frequently towards the C termini of glycoproteins, and that proline residues in positions X and Y in the consensus Asn-X-Thr/Ser-Y strongly reduce the likelihood of N-linked glycosylation. Beyond this, there are no obvious local sequence features that seem to correlate with the absence or presence of N-linked glycosylation. These findings are discussed in terms of the prediction and engineering of glycosylation sites in secretory proteins.

Keywords: glycoproteins/N-glycosylation/statistical study

Received October 27, 1989; accepted January 15, 1990.


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The Ost1p Subunit of Yeast Oligosaccharyl Transferase Recognizes the Peptide Glycosylation Site Sequence, -Asn-X-Ser/Thr-
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Human Leptin Receptor. DETERMINATION OF DISULFIDE STRUCTURE AND N-GLYCOSYLATION SITES OF THE EXTRACELLULAR DOMAIN
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Protein N-Glycosylation: Molecular Genetics and Functional Significance
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C. M. Elvin, T. Vuocolo, R. D. Pearson, I. J. East, G. A. Riding, C. H. Eisemann, and R. L. Tellam
Characterization of a Major Peritrophic Membrane Protein, Peritrophin-44, from the Larvae of Lucilia cuprina
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The Amino Acid at the X Position of an Asn-X-Ser Sequon Is an Important Determinant of N-Linked Core-glycosylation Efficiency
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N- and O-Glycosylation and Phosphorylation of the Bar Secretion Leader Derived from the Barrier Protease of Saccharomyces cerevisiae
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C. G.ía Rodríguez, D. R. Cundell, E. I. Tuomanen, L. F. Kolakowski , Jr., C. Gerard, and N. P. Gerard
The Role of N-Glycosylation for Functional Expression of the Human Platelet-activating Factor Receptor
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C. A. Power, A. Meyer, K. Nemeth, K. B. Bacon, A. J. Hoogewerf, A. E. I. Proudfoot, and T. N. C. Wells
Molecular Cloning and Functional Expression of a Novel CC Chemokine Receptor cDNA from a Human Basophilic Cell Line
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L. H. Philipson, A. Kuznetsov, P. T. Toth, J. F. Murphy, G. Szabo, G. H. Ma, and R. J. Miller
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The Hydroxy Amino Acid in an Asn-X-Ser/Thr Sequon Can Influence N-Linked Core Glycosylation Efficiency and the Level of Expression of a Cell Surface Glycoprotein
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Z. G. Wo and R. E. Oswald
A Topological Analysis of Goldfish Kainate Receptors Predicts Three Transmembrane Segments
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DevelopmentHome page
S Heller, T. Finn, J Huber, R Nishi, M Geissen, A. Puschel, and H Rohrer
Analysis of function and expression of the chick GPA receptor (GPAR alpha) suggests multiple roles in neuronal development
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I. Nilsson and G. von Heijne
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Roles of Individual N-Glycans for ATP Potency and Expression of the Rat P2X1 Receptor
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J. Dubuisson, S. Duvet, J.-C. Meunier, A. Op De Beeck, R. Cacan, C. Wychowski, and L. Cocquerel
Glycosylation of the Hepatitis C Virus Envelope Protein E1 Is Dependent on the Presence of a Downstream Sequence on the Viral Polyprotein
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Translation Rate of Human Tyrosinase Determines Its N-Linked Glycosylation Level
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R. J. Fernandes, S. Hirohata, J. M. Engle, A. Colige, D. H. Cohn, D. R. Eyre, and S. S. Apte
Procollagen II Amino Propeptide Processing by ADAMTS-3. INSIGHTS ON DERMATOSPARAXIS
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