2012
DOI: 10.1002/bip.22040
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Reply to “comment on ‘binding free energies of inhibitors to iron porphyrin complex as a model for cytochrome P450’”

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(2 citation statements)
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“…Importantly, iron porphine maintained its sensitivity for most of the measured gases, owing to its two strong axial coordination sites. These different behaviors between zinc and iron porphines can be supported by two separate studies by Schalk [ 35 ] and Kang [ 42 ]. They calculated the binding energies of water molecules to zinc and iron porphyrinic systems and showed that zinc porphine has a higher affinity to water molecules than that of iron porphine.…”
Section: Resultsmentioning
confidence: 70%
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“…Importantly, iron porphine maintained its sensitivity for most of the measured gases, owing to its two strong axial coordination sites. These different behaviors between zinc and iron porphines can be supported by two separate studies by Schalk [ 35 ] and Kang [ 42 ]. They calculated the binding energies of water molecules to zinc and iron porphyrinic systems and showed that zinc porphine has a higher affinity to water molecules than that of iron porphine.…”
Section: Resultsmentioning
confidence: 70%
“…Among the three metalloporphines, iron porphine showed the highest intensity to all the measured gases, especially to propionic acid ( Figure 4 ). This was expected as the central iron atom can bind to two extra axial ligands to form octahedral hexadentate coordination [ 42 ]. This was in agreement with the literature reporting higher ligand binding of iron porphyrin than that of zinc and nickel derivatives [ 43 ].…”
Section: Resultsmentioning
confidence: 99%