Domain 3 of NS5A protein from the hepatitis C virus has intrinsic α-helical propensity and is a substrate of cyclophilin A

Journal of Biological Chemistry

Volumn 286, Issue 23, 2011, Pages 20441-20454

  Verdegem, Dries ^a,b   Badillo, Aurélie ^c   Wieruszeski, Jean Michel ^a,b   Landrieu, Isabelle ^a,b   Leroy, Arnaud ^d   Bartenschlager, Ralf ^e   Penin, François ^c   Lippens, Guy ^a,b   Hanoulle, Xavier ^a,b  

^a UNIV LILLE   (France)

^b UNIVERSITÉ DES SCIENCES ET TECHNOLOGIES DE LILLE   (France)

^c University Lyon i   (France)

^d UNIVERSITÉ PARIS SACLAY   (France)

^e UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; VIRUSES;

ANTI-VIRAL DRUGS; FUNCTIONAL INTERACTION; HEPATITIS C VIRUS; MEMBRANE ANCHORS; MOLECULAR CHARACTERIZATION; MOLECULAR RECOGNITION ELEMENT; NONSTRUCTURAL PROTEINS; STRUCTURAL FEATURE;

PROTEINS;

CYCLOPHILIN A; NONSTRUCTURAL PROTEIN 5A;

ALPHA HELIX; ARTICLE; CHEMICAL BOND; COMPARATIVE STUDY; CONTROLLED STUDY; ENZYME INHIBITION; GENOTYPE; HEPATITIS C VIRUS; HETERONUCLEAR NUCLEAR MAGNETIC RESONANCE; IN VITRO STUDY; MOLECULAR MODEL; MOLECULAR RECOGNITION; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN DOMAIN; PROTEIN FOLDING; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; VIRUS STRAIN;

HEPATITIS C VIRUS;

EID: 79958018094     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.182436     Document Type: Article

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