Structural modeling and analysis of dengue-mediated inhibition of interferon signaling pathway

Genetics and Molecular Research

Volumn 14, Issue 2, 2015, Pages 4215-4237

  Aslam, B ^a   Ahmad, J ^a   Ali, A ^a   Paracha, R Z ^a   Tareen, S ^a   Khusro, S ^b   Ahmad, T ^c   Muhammad, S A ^d   Niazi, U ^e   Azevedo, V ^f  

^a NATIONAL UNIVERSITY OF SCIENCES AND TECHNOLOGY   (Pakistan)

^b UNIVERSITY OF PESHAWAR   (Pakistan)

^c Shifa Tameer e Millat University   (Pakistan)

^d BAHAUDDIN ZAKARIYA UNIVERSITY   (Pakistan)

^e ABERYSTWYTH UNIVERSITY   (United Kingdom)

^f FEDERAL UNIVERSITY OF MINAS GERAIS   (Brazil)

Author keywords

Dengue virus; Interface residues; Non structural protein 5; Protein protein interactions; Seven in absentia homologue; Signal transducer and activator of transcription 2

Indexed keywords

BINDING PROTEIN; INTERFERON; NONSTRUCTURAL PROTEIN 5; PROTEIN SIAH2; STAT2 PROTEIN; UNCLASSIFIED DRUG; NS5 PROTEIN, DENGUE VIRUS; NUCLEAR PROTEIN; SEVEN IN ABSENTIA PROTEINS; STAT1 PROTEIN; STAT1 PROTEIN, HUMAN; STAT2 PROTEIN, HUMAN; UBIQUITIN PROTEIN LIGASE; VIRAL PROTEIN;

ARTICLE; DENGUE VIRUS; MATHEMATICAL COMPUTING; MATHEMATICAL MODEL; MOLECULAR DOCKING; NONHUMAN; PHYSICAL CHEMISTRY; PROTEIN BINDING; PROTEIN DEGRADATION; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; SIGNAL TRANSDUCTION; AMINO ACID SEQUENCE; ANTAGONISTS AND INHIBITORS; CHEMICAL PHENOMENA; CHEMICAL STRUCTURE; DENGUE; HUMAN; IMMUNOLOGY; METABOLISM; PATHOGENICITY; PATHOLOGY; PROTEIN SECONDARY STRUCTURE; SEQUENCE ALIGNMENT; STATIC ELECTRICITY; UBIQUITINATION; ULTRASTRUCTURE;

DENGUE VIRUS; FLAVIVIRIDAE;

AMINO ACID SEQUENCE; DENGUE; DENGUE VIRUS; HUMANS; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; INTERFERON TYPE I; MODELS, MOLECULAR; MOLECULAR DOCKING SIMULATION; NUCLEAR PROTEINS; PROTEIN INTERACTION MAPS; PROTEIN STRUCTURE, SECONDARY; SEQUENCE ALIGNMENT; SIGNAL TRANSDUCTION; STAT1 TRANSCRIPTION FACTOR; STAT2 TRANSCRIPTION FACTOR; STATIC ELECTRICITY; UBIQUITIN-PROTEIN LIGASES; UBIQUITINATION; VIRAL NONSTRUCTURAL PROTEINS;

EID: 84928663252     PISSN: None     EISSN: 16765680     Source Type: Journal    
DOI: 10.4238/2015.April.28.4     Document Type: Article

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