Dephosphorylation of the core clock protein KaiC in the cyanobacterial KaiABC circadian oscillator proceeds via an ATP synthase mechanism

Biochemistry

Volumn 51, Issue 8, 2012, Pages 1547-1558

  Egli, Martin ^a   Mori, Tetsuya ^a   Pattanayek, Rekha ^a   Xu, Yao ^a   Qin, Ximing ^a   Johnson, Carl H ^a  

^a VANDERBILT UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVE SITE; ATP SYNTHASE; ATP-ASE ACTIVITY; ATPASE REACTION; C-TERMINAL DOMAINS; CIRCADIAN CLOCK; CLOCK PERIOD; CORE CLOCK; CYANOBACTERIUM; DEPHOSPHORYLATIONS; EXPERIMENTAL DATA; F1-ATPASE; GENERAL BASE; HETERODIMERS; HEXAMERS; IN-VITRO; ION-DEPENDENCE; N-TERMINALS; PHOSPHORYLATION SITES; PHOSPHOTRANSFERASES; RELATIVE ACTIVITIES; SEQUENCE MOTIFS; SITE DIRECTED MUTAGENESIS; SMALL ANGLE X-RAY SCATTERING; STRUCTURAL WORKS; SUBUNIT INTERFACES; SYNECHOCOCCUS ELONGATUS; WILD TYPES;

AMINO ACIDS; METAL IONS; PHOSPHATASES;

PHOSPHORYLATION;

ADENOSINE DIPHOSPHATE; ADENOSINE TRIPHOSPHATASE; AUTOKINASE; AUTOPHOSPHATASE; GLUTAMIC ACID; NUCLEIC ACID BINDING PROTEIN; PHOSPHATASE; PHOSPHOTRANSFERASE; PROTEIN KAIA; PROTEIN KAIB; PROTEIN KAIC; PROTEIN KAICII; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE; SERINE; THREONINE; TRANSCRIPTION FACTOR CLOCK; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; BINDING SITE; CIRCADIAN RHYTHM; CRYSTAL STRUCTURE; CYANOBACTERIUM; ENZYME ACTIVE SITE; ENZYME ACTIVITY; HYDROLYSIS; NONHUMAN; OSCILLATOR; PRIORITY JOURNAL; PROTEIN DEPHOSPHORYLATION; PROTEIN DOMAIN; PROTEIN MOTIF; PROTEIN PHOSPHORYLATION; SITE DIRECTED MUTAGENESIS; SYNECHOCOCCUS ELONGATUS; X RAY CRYSTALLOGRAPHY;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; BACTERIAL PROTEINS; CATALYTIC DOMAIN; CIRCADIAN RHYTHM SIGNALING PEPTIDES AND PROTEINS; CLOCK PROTEINS; CRYSTALLOGRAPHY, X-RAY; CYANOBACTERIA; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION; PHOSPHORYLATION;

CYANOBACTERIA; IXODIDA; KAIA; SYNECHOCOCCUS ELONGATUS; SYNECHOCOCCUS ELONGATUS PCC 6301;

EID: 84863275177     PISSN: 00062960     EISSN: 15204995     Source Type: Journal    
DOI: 10.1021/bi201525n     Document Type: Article

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