A Proposal for a Structural Model of the Feline Calicivirus Protease Bound to the Substrate Peptide under Physiological Conditions.

Yokoyama, Masaru; Oka, Tomoichiro; Takagi, Hirotaka; Kojima, Hirotatsu; Okabe, Takayoshi; Nagano, Tetsuo; Tohya, Yukinobu; Sato, Hironori

Yokoyama, Masaru; Oka, Tomoichiro; Takagi, Hirotaka; Kojima, Hirotatsu; Okabe, Takayoshi; Nagano, Tetsuo; Tohya, Yukinobu; Sato, Hironori.

Afiliación

Yokoyama M; Pathogen Genomics Center, National Institute of Infectious DiseasesTokyo, Japan.
Oka T; Department of Virology II, National Institute of Infectious DiseasesTokyo, Japan.
Takagi H; Division of Biosafety Control and Research, National Institute of Infectious DiseasesTokyo, Japan.
Kojima H; Drug Discovery Initiative, The University of TokyoTokyo, Japan.
Okabe T; Drug Discovery Initiative, The University of TokyoTokyo, Japan.
Nagano T; Drug Discovery Initiative, The University of TokyoTokyo, Japan.
Tohya Y; Department of Veterinary Medicine, Nihon UniversityFujisawa, Japan.
Sato H; Pathogen Genomics Center, National Institute of Infectious DiseasesTokyo, Japan.

Front Microbiol ; 8: 1383, 2017.

Article en En | MEDLINE | ID: mdl-28790989

Palabras clave

3-D pharmacophore; BRET technology; MD simulation; feline calicivirus; in silico screening; protease

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Microbiol Año: 2017 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Suiza

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