The SH3 domain-binding surface and an acidic motif in HIV-1 Nef regulate trafficking of class I MHC complexes

EMBO Journal

Volumn 17, Issue 10, 1998, Pages 2777-2789

  Greenberg, Michael E ^a   Lafrate, A John ^a   Skowronski, Jacek ^a  

^a Howard Hughes Medical Institute Cold Spring Harbor Laboratory Cold Spring Harbor   (United States)

Author keywords

Class I MHC; HIV; Nef; SH3; trans Golgi network

Indexed keywords

ADAPTOR PROTEIN; CD4 ANTIGEN; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1; MEMBRANE ANTIGEN; NEF PROTEIN; VIRUS PROTEIN;

AMINO ACID SEQUENCE; ANTIGEN EXPRESSION; ARTICLE; CELL MEMBRANE; CONTROLLED STUDY; ENDOCYTOSIS; FIBROBLAST; FLOW CYTOMETRY; GENE EXPRESSION REGULATION; GOLGI COMPLEX; HOST CELL; HUMAN; HUMAN CELL; HUMAN IMMUNODEFICIENCY VIRUS 1; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN LOCALIZATION; PROTEIN TARGETING; PROTEIN TRANSPORT; SIGNAL TRANSDUCTION; T LYMPHOCYTE;

ADAPTOR PROTEIN COMPLEX ALPHA SUBUNITS; ADAPTOR PROTEINS, VESICULAR TRANSPORT; ANTIGENS, CD4; BINDING SITES; CELL MEMBRANE; CELLS, CULTURED; DOWN-REGULATION; GENE EXPRESSION; GENE PRODUCTS, NEF; GOLGI APPARATUS; HISTOCOMPATIBILITY ANTIGENS CLASS I; HIV-1; HLA-B7 ANTIGEN; HUMANS; JURKAT CELLS; MEMBRANE PROTEINS; RECOMBINANT FUSION PROTEINS; SRC HOMOLOGY DOMAINS; TYROSINE;

EID: 0032525137     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1093/emboj/17.10.2777     Document Type: Article

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