Molecular mechanism and functional role of brefeldin A-mediated ADP-ribosylation of CtBP1/BARS

Proceedings of the National Academy of Sciences of the United States of America

Volumn 110, Issue 24, 2013, Pages 9794-9799

  Colanzi, Antonino ^a   Grimaldi, Giovanna ^a   Catara, Giuliana ^a   Valente, Carmen ^a   Cericola, Claudia ^b   Liberali, Prisca ^b,j   Ronci, Maurizio ^c,k   Lalioti, Vasiliki S ^d   Bruno, Agostino ^e   Beccari, Andrea R ^e,f   Urbani, Andrea ^c,g   De Florah, Antonio ^h   Nardini, Marco ⁱ   Bolognesi, Martino ⁱ   Luini, Alberto ^a   Corda, Daniela ^a  

^a INSTITUTE OF PROTEIN BIOCHEMISTRY   (Italy)

^b Consorzio Mario Negri Sud ^*  (Italy)

^c UNIVERSITY OF ROME TOR VERGATA   (Italy)

^d UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

^e UNIVERSITY OF PARMA   (Italy)

^f Chemistry Section   (Italy)

^g IRCCS FONDAZIONE SANTA LUCIA   (Italy)

^h UNIVERSITY OF GENOA   (Italy)

ⁱ UNIVERSITY OF MILAN   (Italy)

^j UNIVERSITY OF ZURICH   (Switzerland)

^k UNIVERSITY OF SOUTH AUSTRALIA   (Australia)

more..

Author keywords

Anticancer molecules; Cell signaling; Golgi fragmentation; Mitosis

Indexed keywords

ADENOSINE DIPHOSPHATE; ADENOSINE DIPHOSPHATE RIBOSYL CYCLASE; ADP RIBOSYL CYCLASE CD38; BREFELDIN A; CTBP1 PROTEIN; DIMER; NICOTINAMIDE ADENINE DINUCLEOTIDE; PROTEIN; UNCLASSIFIED DRUG;

ADENOSINE DIPHOSPHATE RIBOSYLATION; ARTICLE; BINDING SITE; CELL CYCLE ARREST; CELL CYCLE G2 PHASE; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; COVALENT BOND; FISSION NEUTRON; GOLGI COMPLEX; HUMAN; HUMAN CELL; MOLECULAR MECHANICS; OLIGOMERIZATION; PRIORITY JOURNAL;

ANTICANCER MOLECULES; CELL SIGNALING; GOLGI FRAGMENTATION; MITOSIS;

ADENOSINE DIPHOSPHATE RIBOSE; ADP-RIBOSYL CYCLASE; ALCOHOL OXIDOREDUCTASES; ANIMALS; ANTIGENS, CD38; BINDING SITES; BINDING, COMPETITIVE; BLOTTING, WESTERN; BREFELDIN A; CYTOSOL; DNA-BINDING PROTEINS; HELA CELLS; HUMANS; MEMBRANE GLYCOPROTEINS; MODELS, MOLECULAR; NAD; PROTEIN BINDING; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEIN STRUCTURE, TERTIARY; RATS;

EID: 84878981905     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1222413110     Document Type: Article

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