Modulation of the axial water hydrogen-bonding properties by chemical modification of the substrate in resting state, substrate-bound heme oxygenase from Neisseria meningitidis; coupling to the distal H-bond network via ordered water molecules

Journal of the American Chemical Society

Volumn 128, Issue 19, 2006, Pages 6391-6399

  Ma, Li Hua ^a   Liu, Yangzhong ^a   Zhang, Xuhong ^b   Yoshida, Tadashi ^b   Langry, Kevin C ^a   Smith, Kevin M ^c   La Mar, Gerd N ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b YAMAGATA UNIVERSITY   (Japan)

^c LOUISIANA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AXIAL ANISOTROPY; FIELD STRENGTH; NEISSERIA MENINGITIDIS; PARAMAGNETIC ANISOTROPY;

ANISOTROPY; CHEMICAL REACTIONS; COMPLEXATION; ENZYMES; MUTAGENESIS; NUCLEAR MAGNETIC RESONANCE; PARAMAGNETISM; PERTURBATION TECHNIQUES; SUBSTRATES;

HYDROGEN BONDS;

FERRIC ION; FORMYL GROUP; FUNCTIONAL GROUP; GLUTAMINE; HEME OXYGENASE; HEMIN; HISTIDINE; IRON; METHYL GROUP; UNCLASSIFIED DRUG; VINYL DERIVATIVE; WATER;

ANISOTROPY; ARTICLE; CHEMICAL BOND; CHEMICAL MODIFICATION; DIPOLE; ELECTRON; ENZYME SUBSTRATE COMPLEX; HYDROGEN BOND; LIGAND BINDING; MAGNETIC FIELD; MAGNETISM; MUTAGENESIS; NEISSERIA MENINGITIDIS; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE;

ANISOTROPY; HEME OXYGENASE (DECYCLIZING); HYDROGEN BONDING; MAGNETIC RESONANCE SPECTROSCOPY; NEISSERIA MENINGITIDIS; SUBSTRATE SPECIFICITY; WATER;

EID: 33646571239     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0578505     Document Type: Article

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