Abstract
Hepatitis C virus (HCV) infection remains a major health problem worldwide. HCV entry into host cells and membrane fusion are achieved by two envelope glycoproteins, E1 and E2. We report here the 3.5-Å resolution crystal structure of the N-terminal domain of the HCV E1 ectodomain, which reveals a complex network of covalently linked intertwined homodimers that do not harbour the expected truncated class II fusion protein fold.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Crystallography, X-Ray
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Gene Expression
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HEK293 Cells
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Hepacivirus / chemistry*
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Humans
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Molecular Sequence Data
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Protein Folding
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Protein Multimerization
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Protein Structure, Secondary
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Protein Structure, Tertiary
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Recombinant Proteins / chemistry
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Recombinant Proteins / genetics
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Viral Envelope Proteins / chemistry*
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Viral Envelope Proteins / genetics
Substances
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E1 protein, Hepatitis C virus
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Recombinant Proteins
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Viral Envelope Proteins