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Volumn 43, Issue 3, 2014, Pages 973-981
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A dominant homolytic O-Cl bond cleavage with low-spin triplet-state Fe(IV)=O formed is revealed in the mechanism of heme-dependent chlorite dismutase
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Author keywords
[No Author keywords available]
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Indexed keywords
B3LYP DENSITY FUNCTIONAL;
BOND DISSOCIATION;
BOND FORMATION;
CHEMICAL MODEL;
DISPERSION INTERACTION;
ENERGY DIFFERENCES;
REACTION MECHANISM;
X RAY CRYSTAL STRUCTURES;
CHLORINE;
CHLORINE COMPOUNDS;
ENZYMES;
PORPHYRINS;
CHEMICAL BONDS;
CHLORIDE;
CHLORITE DISMUTASE;
HEME;
IRON;
OXIDOREDUCTASE;
OXYGEN;
ARTICLE;
CHEMISTRY;
ENZYME ACTIVE SITE;
METABOLISM;
QUANTUM THEORY;
THERMODYNAMICS;
X RAY CRYSTALLOGRAPHY;
CATALYTIC DOMAIN;
CHLORIDES;
CRYSTALLOGRAPHY, X-RAY;
HEME;
IRON;
OXIDOREDUCTASES;
OXYGEN;
QUANTUM THEORY;
THERMODYNAMICS;
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EID: 84890480905
PISSN: 14779226
EISSN: 14779234
Source Type: Journal
DOI: 10.1039/c3dt52171k Document Type: Article |
Times cited : (23)
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References (88)
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