Role of the RING-CH domain of viral ligase mK3 in ubiquitination of non-lysine and lysine MHC I residues

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Volumn 10, Issue 9, 2009, Pages 1301-1317

  Herr, Roger A ^a   Harris, Jennifer ^a   Fang, Shengyun ^b   Wang, Xiaoli ^a   Hansen, Ted H ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MARYLAND   (United States)

Author keywords

MHCI; mK3; Non lysine; Ubiquitination

Indexed keywords

ESTER; GAMMA HERPESVIRUS 68 LIGASE MK3; LIGASE; LYSINE; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1; MEMBRANE ASSOCIATED RING CH LIGASE; SERINE; THREONINE; TRYPTOPHAN; UBIQUITIN; UNCLASSIFIED DRUG; VIRUS ENZYME;

ANIMAL CELL; ARTICLE; CARBOXY TERMINAL SEQUENCE; CHEMICAL BOND; CONJUGATION; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; ENZYME DEGRADATION; ENZYME MECHANISM; ENZYME SPECIFICITY; ENZYME STRUCTURE; ENZYME SUBSTRATE; HUMAN; HUMAN CELL; HUMAN HERPESVIRUS 8; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FUNCTION; UBIQUITINATION;

AMINO ACID SEQUENCE; ANIMALS; CELL LINE; DIRECTED MOLECULAR EVOLUTION; ENDOPLASMIC RETICULUM; GAMMAHERPESVIRINAE; HISTOCOMPATIBILITY ANTIGENS CLASS I; HUMANS; IMMUNOPRECIPITATION; MEMBRANE PROTEINS; MICE; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; PHYLOGENY; PROTEIN STRUCTURE, TERTIARY; SEQUENCE ALIGNMENT; SUBSTRATE SPECIFICITY; UBIQUITIN; UBIQUITIN-PROTEIN LIGASES; VIRAL PROTEINS;

EID: 68549119002     PISSN: 13989219     EISSN: 16000854     Source Type: Journal    
DOI: 10.1111/j.1600-0854.2009.00946.x     Document Type: Article

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