Activation of α-keto acid-dependent dioxygenases: Application of an {FeNo} 7/{FeO 2} 8 methodology for characterizing the initial steps of o 2 activation

Journal of the American Chemical Society

Volumn 133, Issue 45, 2011, Pages 18148-18160

  Diebold, Adrienne R ^a   Brown Marshall, Christina D ^a   Neidig, Michael L ^a   Brownlee, June M ^c   Moran, Graham R ^c   Solomon, Edward I ^a,b  

^a STANFORD UNIVERSITY   (United States)

^b SLAC NATIONAL ACCELERATOR LABORATORY   (United States)

^c UNIVERSITY OF WISCONSIN MILWAUKEE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4-HYDROXYPHENYLPYRUVATE DIOXYGENASE; ACTIVATION STEPS; COMPUTATIONAL MODEL; DIOXYGENASES; DONOR LIGANDS; FERROUS ENZYMES; KETO ACIDS; MAGNETIC CIRCULAR DICHROISMS; NON-HEME IRON ENZYMES; NONHEME; REACTION COORDINATES; SPECTROSCOPIC FEATURES; TRANSFER OF CHARGES; UV-VIS ABSORPTIONS; VARIABLE TEMPERATURE;

ABSORPTION SPECTROSCOPY; CATALYSTS; COMPLEXATION; DICHROISM; ELECTRON SPIN RESONANCE SPECTROSCOPY; ENZYMES; IRON; IRON OXIDES;

CHEMICAL ACTIVATION;

2 OXOACID; 4 HYDROXYPHENYLPYRUVATE DIOXYGENASE; FERROUS ION; LIGAND; NITRIC OXIDE; OXYGEN;

ARTICLE; BINDING KINETICS; CHEMICAL ANALYSIS; CHEMICAL BINDING; CHEMICAL INTERACTION; CIRCULAR DICHROISM; CONTROLLED STUDY; ELECTRON SPIN RESONANCE; SPECTROSCOPY; ULTRAVIOLET SPECTROSCOPY;

3-METHYL-2-OXOBUTANOATE DEHYDROGENASE (LIPOAMIDE); FERRIC COMPOUNDS; FERROUS COMPOUNDS; MOLECULAR STRUCTURE; OXYGEN;

EID: 80755126617     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja202549q     Document Type: Article

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