Nuclear import of isoforms of the cytomegalovirus kinase pUL97 is mediated by differential activity of NLS1 and NLS2 both acting through classical importin-α binding

Journal of General Virology

Volumn 93, Issue 8, 2012, Pages 1756-1768

  Webel, Rike ^a   Solbak, Sara M Ø ^b   Held, Christian ^c   Milbradt, Jens ^a   Groß, Andrea ^a   Eichler, Jutta ^a   Wittenberg, Thomas ^c   Jardin, Christophe ^a   Sticht, Heinrich ^a   Fossen, Torgils ^b   Marschall, Manfred ^a  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^b UNIVERSITY OF BERGEN   (Norway)

^c FRAUNHOFER INSTITUTE FOR INTEGRATED CIRCUITS IIS   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; KARYOPHERIN ALPHA; NLS1 PROTEIN; NLS2 PROTEIN; PROTEIN KINASE; UNCLASSIFIED DRUG; VIRUS PROTEIN;

ALPHA HELIX; AMINO TERMINAL SEQUENCE; ARTICLE; BIOINFORMATICS; CELLULAR DISTRIBUTION; FIBROBLAST; HELA CELL; HUMAN CYTOMEGALOVIRUS; IN VITRO STUDY; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN LOCALIZATION; SURFACE PLASMON RESONANCE;

ALPHA KARYOPHERINS; AMINO ACID SEQUENCE; CELLS, CULTURED; COMPUTER SIMULATION; CYTOMEGALOVIRUS; FIBROBLASTS; GENE EXPRESSION REGULATION, VIRAL; HUMANS; MODELS, MOLECULAR; NUCLEAR LOCALIZATION SIGNALS; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN ISOFORMS;

CYTOMEGALOVIRUS; HUMAN HERPESVIRUS 5;

EID: 84864062825     PISSN: 00221317     EISSN: 14652099     Source Type: Journal    
DOI: 10.1099/vir.0.040592-0     Document Type: Article

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