A novel class of PTEN protein in Arabidopsis displays unusual phosphoinositide phosphatase activity and efficiently binds phosphatidic acid

Biochemical Journal

Volumn 441, Issue 1, 2012, Pages 161-171

  Pribat, Anne ^a   Sormani, Rodnay ^a,b   Rousseau Gueutin, Mathieu ^a,e   Julkowska, Magdalena M ^c   Testerink, Christa ^c   Joubès, Jerôme ^a   Castroviejo, Michel ^d   Laguerre, Michel ^a   Meyer, Christian ^b   Germain, Véronique ^a   Rothan, Christophe ^a  

^a UNIVERSITÉ DE BORDEAUX   (France)

^b INSTITUT JEAN PIERRE BOURGIN   (France)

^c UNIVERSITY OF AMSTERDAM   (Netherlands)

^d University Victor Segalen   (France)

^e UNIVERSITY OF ADELAIDE   (Australia)

Author keywords

Expression in planta; Phosphatidic acid (PA) binding; Phosphoinositide phosphatase; Phylogenetics; Site directed mutagenesis

Indexed keywords

ALANINE; ARABIDOPSIS PROTEIN; BETA GLUCURONIDASE; GLYCINE; LYSINE; METHIONINE; PHOSPHATIDIC ACID; PHOSPHATIDYLINOSITIDE; PHOSPHATIDYLINOSITOL 3 PHOSPHATE; PHOSPHATIDYLINOSITOL 3,4 BISPHOSPHATE; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE 2; PHOSPHATIDYLINOSITOL 3,5 BISPHOSPHATE; PHOSPHOINOSITIDE PHOSPHATASE; PROTEIN TYROSINE PHOSPHATASE; RECOMBINANT PROTEIN; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARABIDOPSIS; ARTICLE; CATALYSIS; CONTROLLED STUDY; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ENZYME BINDING; LIPID TRANSPORT; MOLECULAR MODEL; NONHUMAN; OSMOTIC STRESS; PHYLOGENY; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN DEPHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; PROTEIN PURIFICATION; SIGNAL TRANSDUCTION; SITE DIRECTED MUTAGENESIS; TRANSCRIPTION REGULATION; UBIQUITINATION;

ARABIDOPSIS; ARABIDOPSIS PROTEINS; ESCHERICHIA COLI; GENE EXPRESSION REGULATION, PLANT; MODELS, MOLECULAR; PHOSPHATIDIC ACIDS; PHOSPHORIC MONOESTER HYDROLASES; PHYLOGENY; PROTEIN BINDING; PROTEIN CONFORMATION; PTEN PHOSPHOHYDROLASE; SIGNAL TRANSDUCTION; SUBSTRATE SPECIFICITY;

EID: 84055213714     PISSN: 02646021     EISSN: 14708728     Source Type: Journal    
DOI: 10.1042/BJ20110776     Document Type: Article

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