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- W1966454970 abstract "Determinants of the Fe−CO and C−O stretching frequencies in (imidazole)heme−CO adducts have been investigated via density functional theory (DFT) analysis, in connection with puzzling characteristics of the heme sensor protein CooA and of the H−NOX (Heme−Nitric Oxide and/or OXygen binding) family of proteins, including soluble guanylate cyclase (sGC). The computations show that two mechanisms of Fe−histidine bond weakening have opposite effects on the νFeC/νCO pattern. Mechanical tension is expected to raise νFeC with little change in νCO whereas the weakening of H-bond donation from the imidazole ligand has the opposite effect. Data on CooA indicate imidazole H-bond weakening associated with heme displacement, as part of the activation mechanism. The computations also reveal that protein-induced distortion of the porphyrin ring, a prominent structural feature of the H−NOX protein TtTar4H (Thermoanaerobacter tengcongensis Tar4 protein heme domain), has surprisingly little effect on νFeC or νCO. However, another structural feature, strong H-bonding to the propionates, is suggested to account for the weakened back bonding that is evident in sGC. TtTar4H−CO itself has an elevated νFeC, which is successfully modeled as a compression effect, resulting from steric crowding in the distal pocket. νFeC/νCO data, in conjunction with modeling, can provide valuable insight into mechanisms for heme-protein modulation." @default.
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- W1966454970 date "2008-01-25" @default.
- W1966454970 modified "2023-10-10" @default.
- W1966454970 title "DFT Analysis of Axial and Equatorial Effects on Heme−CO Vibrational Modes: Applications to CooA and H−NOX Heme Sensor Proteins" @default.
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- W1966454970 doi "https://doi.org/10.1021/bi702254y" @default.
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