HIV-1 Nef employs two distinct mechanisms to modulate Lck subcellular localization and TCR induced actin remodeling

PLoS ONE

Volumn 2, Issue 11, 2007, Pages

  Haller, Claudia ^a   Rauch, Susanne ^a   Fackler, Oliver T ^a  

^a UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

NEF PROTEIN; P21 ACTIVATED KINASE 2; PROTEIN KINASE LCK; T LYMPHOCYTE RECEPTOR; ACTIN; LYMPHOCYTE ANTIGEN RECEPTOR; TYROSINE;

ACTIN FILAMENT; ACTIN POLYMERIZATION; ARTICLE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; ENDOSOME; HUMAN; HUMAN CELL; HUMAN IMMUNODEFICIENCY VIRUS 1; LEUKEMIA CELL LINE; MICROTUBULE; MUTAGENESIS; PROTEIN AGGREGATION; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; SYNAPTIC TRANSMISSION; VIRUS CELL INTERACTION; VIRUS INFECTIVITY; VIRUS PATHOGENESIS; VIRUS REPLICATION; CELL FRACTIONATION; ENZYMOLOGY; GENETICS; METABOLISM; PHOSPHORYLATION; SITE DIRECTED MUTAGENESIS;

HUMAN IMMUNODEFICIENCY VIRUS 1;

ACTINS; GENE PRODUCTS, NEF; HIV-1; HUMANS; JURKAT CELLS; LYMPHOCYTE SPECIFIC PROTEIN TYROSINE KINASE P56(LCK); MUTAGENESIS, SITE-DIRECTED; PHOSPHORYLATION; RECEPTORS, ANTIGEN, T-CELL; SUBCELLULAR FRACTIONS; TYROSINE;

EID: 43249085765     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0001212     Document Type: Article

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