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

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Article
English
1990

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

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English
1990
Protein Engineering Design and Selection
Vol 3 (5)
DOI: 10.1093/protein/3.5.433

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Gunnar Von Heijne
Gunnar Von Heijne

Stockholm University

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Ylva Gavel
Gunnar Von Heijne

Abstract

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.

How to cite this publication

Ylva Gavel, Gunnar Von Heijne (1990). Sequence differences between glycosylated and non-glycosylated Asn-X-Thr/Ser acceptor sites: implications for protein engineering. Protein Engineering Design and Selection, 3(5), pp. 433-442, DOI: 10.1093/protein/3.5.433.

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Publication Details

Type

Article

Year

1990

Authors

2

Datasets

0

Total Files

0

Language

English

Journal

Protein Engineering Design and Selection

DOI

10.1093/protein/3.5.433

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