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?:abstract
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A way to study the mutation pattern is to convert a 20-letter protein sequence into a scalar protein sequence, because the 20-letter protein sequence is neither vector nor scalar while a promising way to study patterns is in numerical domain. In this study, we use the amino-acid pair predictability to convert α-galactosidase A with its 137 mutations into scalar sequences, and analyse which amino-acid pairs are more sensitive to mutation. Our results show that the unpredictable amino-acid pairs are more sensitive to mutation, and the mutation trend is to narrow the difference between predicted and actual frequency of amino-acid pairs.
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?:creator
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?:doi
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?:doi
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10.1007/s11030-009-9158-4
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?:journal
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?:license
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document_parses/pdf_json/b1e02833bf7b2d8db0c1c82d9f5186392f14ae24.json
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?:pmid
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?:pmid
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?:publication_isRelatedTo_Disease
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?:source
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?:title
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Mutation patterns in human α-galactosidase A
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?:year
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