Abstract
A P1 mutation (Arg-444-->Leu) was identified in a dysfunctional C1 inhibitor from a patient with type 2 hereditary angioneurotic edema. The mutation was defined at the level of the protein (by sequence analysis of the Pseudomonas aeruginosa elastase-derived reactive center peptide), and the mRNA (CGC-->CTC) (by sequence analysis of PCR-amplified DNA).
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Sequence
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Angioedema / genetics*
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Arginine
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Binding Sites / genetics
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Complement C1 Inactivator Proteins / genetics*
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Humans
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Leucine
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Molecular Sequence Data
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Mutation
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Peptide Fragments / genetics
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Polymerase Chain Reaction
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Serpins / genetics*
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Structure-Activity Relationship
Substances
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Complement C1 Inactivator Proteins
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Peptide Fragments
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Serpins
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Arginine
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Leucine