The chloroplast ClpP complex in Chlamydomonas reinhardtii contains an unusual high molecular mass subunit with a large apical domain

FEBS Journal

Volumn 272, Issue 21, 2005, Pages 5558-5571

  Majeran, Wojciech ^a   Friso, Giulia ^b   Van Wijk, Klaas Jan ^b   Vallon, Olivier ^a  

^a INST DE BIOLOGIE PHYSICO CHIMIQUE   (France)

^b Department of Obstetrics Gynecology   (United States)

Author keywords

Mass spectroscopy; Native gel electrophoresis; Protein complex; Proteolysis; Volvocale

Indexed keywords

CHLORAMPHENICOL; ENDOPEPTIDASE CLP;

AMINO ACID SEQUENCE; ARTICLE; CHLAMYDOMONAS REINHARDTII; CHLOROPLAST; MOLECULAR WEIGHT; NONHUMAN; PHYLOGENY; PLASTID; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN INTERACTION;

AMINO ACID SEQUENCE; ANIMALS; CELL NUCLEUS; CHLAMYDOMONAS REINHARDTII; CHLOROPLASTS; ENDOPEPTIDASE CLP; ENZYME STABILITY; MOLECULAR SEQUENCE DATA; MOLECULAR WEIGHT; PHYLOGENY; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; PROTEIN SUBUNITS; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID;

ALGAE; CHLAMYDOMONAS REINHARDTII; CHLOROPHYTA; CYANOBACTERIA; EMBRYOPHYTA;

EID: 27644450421     PISSN: 1742464X     EISSN: 17424658     Source Type: Journal    
DOI: 10.1111/j.1742-4658.2005.04951.x     Document Type: Article

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