<p>(A) shows the H-bonding network between the propionate groups of heme <i>a</i> and the amino acids/water surrounding it in fully oxidized bC<i>c</i>O (PDB: 3ABL). The red spheres indicate water molecules. (B) shows the comparison of heme <i>a</i> in the fully oxidized enzyme (PDB: 3ABL) and fully reduced enzyme (PDB: 2EIJ), which are highlighted in green and yellow, respectively. The dotted lines indicate the H-bonds present in the fully oxidized state; the red arrows indicate the structural changes induced by heme reduction. The structural alignment was made by superimposing the heme iron atoms. The structures were drawn with the PyMol Molecular Graphics System, Schrodinger, LLC.</p
Heme oxygenase from Leptospira interrogans is an important virulence factor. During catalysis, redox...
<p>Residues identified as belonging to heme-binding networks were mapped to the molecular structures...
Heme-substituted horseradish peroxidases and myoglobins were reconstituted from the apoenzyme using ...
In this paper, a clustering method was used to find out why the heme cofactor exhibits different pot...
Heme binds selectively to the 3′-terminal G-quartet (G6 G-quartet) of an all parallel-stranded tetra...
<p>A) Cartoon representation of the LepHO-C26S-stop structure. B) Arrangement of the most relevant a...
While ubiquitous in the biological realm, heme enzymes exhibit numerous functions, including protect...
Heme proteins are a class of biological molecules that contain iron-porphyrin derivatives as prosthe...
Hemes are common elements of biological redox cofactor chains involved in rapid electron transfer. W...
Hemoproteidy to białka zawierające w swojej budowie hem, który koordynuje jon żelaza. Są to bardzo w...
A correlation between the stereochemical geometry around the metal ion in heme enzymes and their cat...
(A) Three-dimensional structure of the heme domain of the CYP BM3 M11 mutant (without organic ligand...
Heme oxygenase from Leptospira interrogans is an important virulence factor. During catalysis, redox...
Thesis (Ph. D.)--University of Rochester. Dept. of Chemistry, 2012.Cytochromes c (cyts c) are excell...
Bio-inorganic chemistry is the basic backbone of human body. Human body consist of several numbers o...
Heme oxygenase from Leptospira interrogans is an important virulence factor. During catalysis, redox...
<p>Residues identified as belonging to heme-binding networks were mapped to the molecular structures...
Heme-substituted horseradish peroxidases and myoglobins were reconstituted from the apoenzyme using ...
In this paper, a clustering method was used to find out why the heme cofactor exhibits different pot...
Heme binds selectively to the 3′-terminal G-quartet (G6 G-quartet) of an all parallel-stranded tetra...
<p>A) Cartoon representation of the LepHO-C26S-stop structure. B) Arrangement of the most relevant a...
While ubiquitous in the biological realm, heme enzymes exhibit numerous functions, including protect...
Heme proteins are a class of biological molecules that contain iron-porphyrin derivatives as prosthe...
Hemes are common elements of biological redox cofactor chains involved in rapid electron transfer. W...
Hemoproteidy to białka zawierające w swojej budowie hem, który koordynuje jon żelaza. Są to bardzo w...
A correlation between the stereochemical geometry around the metal ion in heme enzymes and their cat...
(A) Three-dimensional structure of the heme domain of the CYP BM3 M11 mutant (without organic ligand...
Heme oxygenase from Leptospira interrogans is an important virulence factor. During catalysis, redox...
Thesis (Ph. D.)--University of Rochester. Dept. of Chemistry, 2012.Cytochromes c (cyts c) are excell...
Bio-inorganic chemistry is the basic backbone of human body. Human body consist of several numbers o...
Heme oxygenase from Leptospira interrogans is an important virulence factor. During catalysis, redox...
<p>Residues identified as belonging to heme-binding networks were mapped to the molecular structures...
Heme-substituted horseradish peroxidases and myoglobins were reconstituted from the apoenzyme using ...