The conserved His-144 in the PsbP protein is important for the interaction between the PsbP N-terminus and the Cyt b559 subunit of photosystem II

Journal of Biological Chemistry

Volumn 287, Issue 31, 2012, Pages 26377-26387

  Ido, Kunio ^a   Kakiuchi, Shusuke ^a   Uno, Chihiro ^b   Nishimura, Taishi ^a   Fukao, Yoichiro ^c   Noguchi, Takumi ^b   Sato, Fumihiko ^a   Ifuku, Kentaro ^a,d  

^a KYOTO UNIVERSITY   (Japan)

^b NAGOYA UNIVERSITY   (Japan)

^c NARA INSTITUTE OF SCIENCE AND TECHNOLOGY   (Japan)

^d JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING CHARACTERISTICS; BINDING PROPERTIES; C-TERMINAL DOMAINS; CONFORMATIONAL CHANGE; DIRECT INTERACTIONS; DOUBLE MUTATION; FTIR DIFFERENCE SPECTROSCOPY; FUNCTIONAL INTERACTION; GREEN PLANTS; MASS SPECTROMETRIC ANALYSIS; METAL BINDING; METAL BINDING SITES; MN CLUSTERS; PHOTOSYSTEM II; SALT BRIDGES;

BINDING ENERGY; CHLORINE COMPOUNDS; FOURIER TRANSFORM INFRARED SPECTROSCOPY; MANGANESE; MANGANESE COMPOUNDS; RESTORATION;

PROTEINS;

ASPARTIC ACID; ASPARTIC ACID 165; CYTOCHROME B559; HISTIDINE; HISTIDINE 144; MANGANESE; PSBP PROTEIN; UNCLASSIFIED DRUG; VEGETABLE PROTEIN;

ARTICLE; BINDING AFFINITY; BINDING SITE; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; GENETIC CONSERVATION; INFRARED SPECTROSCOPY; METAL BINDING; MOLECULAR DYNAMICS; MOLECULAR EVOLUTION; NONHUMAN; PHASE TRANSITION; PHOTOSYSTEM II; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN CROSS LINKING; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; RESIDUE ANALYSIS;

AMINO ACID MOTIFS; AMINO ACID SUBSTITUTION; CALCIUM; CARBODIIMIDES; CHLORIDES; COMPUTER SIMULATION; CONSERVED SEQUENCE; CROSS-LINKING REAGENTS; HISTIDINE; KINETICS; MODELS, MOLECULAR; MUTAGENESIS, SITE-DIRECTED; OXYGEN; PEPTIDE FRAGMENTS; PHOTOSYSTEM II PROTEIN COMPLEX; PROTEIN BINDING; PROTEIN INTERACTION DOMAINS AND MOTIFS; PROTEIN SUBUNITS; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; SPINACIA OLERACEA;

VIRIDIPLANTAE;

EID: 84864381355     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.385286     Document Type: Article

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