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Human von Willebrand Factor and the Problems in Sequence Analysis of a 280 K Dalton Protein

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Methods in Protein Sequence Analysis · 1986

Part of the book series: Experimental Biology and Medicine ((EBAM,volume 14))

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Abstract

While it is true that DNA sequencing technology probably provides the simplest and fastest prediction of the raw polypeptide backbone structure of proteins, such predicted sequences should be correlated with those of the mature protein products to avoid frame shift errors, to correct for intron excisions, and to identify the sites of a variety of processing events, any of which may influence expression of function.

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Author information

Authors and Affiliations

  1. Department of Biochemistry, SJ-70, University of Washington, Seattle, Washington, 98195, USA

    Koiti Titani

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  1. Koiti Titani
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Editor information

Editors and Affiliations

  1. Department of Biochemistry, University of Washington, Seattle, Washington, USA

    Kenneth A. Walsh (Chairman) (Chairman)

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© 1987 Springer Science+Business Media New York

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Titani, K. (1987). Human von Willebrand Factor and the Problems in Sequence Analysis of a 280 K Dalton Protein. In: Walsh, K.A. (eds) Methods in Protein Sequence Analysis · 1986. Experimental Biology and Medicine, vol 14. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-480-1_12

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  • DOI: https://doi.org/10.1007/978-1-59259-480-1_12

  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-4757-5826-9

  • Online ISBN: 978-1-59259-480-1

  • eBook Packages: Springer Book Archive

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