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1 t in the crystal structure of wild type (wt) deoxymyoglobin.
2 gen average distances close to the value for deoxymyoglobin (2.05 +/- 0.01 A), while the distance fro
4 ron porphyrin; (5) ferrous high-spin (S = 2) deoxymyoglobin and deoxyhemoglobin; and (6) ferric high
5 the difference between the static spectra of deoxymyoglobin and MbNO, showing the formation of an int
7 ns at the E7 position (His64) of sperm whale deoxymyoglobin (deoxyMb) are used as a probe of distal p
10 ntaining diamagnetic analogue of sperm whale deoxymyoglobin has been measured as a function of oxygen
11 ate to the solvent from which they rebind to deoxymyoglobin in a bimolecular process with a second-or
13 ne (PCr)/ATP was determined with 31P NMR and deoxymyoglobin (Mb-delta) with 1H NMR in myocardium remo
16 is and characterization of six new high-spin deoxymyoglobin models (imidazole(tetraarylporphyrinato)i
17 a second order reaction that is dependent on deoxymyoglobin, nitrite and proton concentration, with a
18 chemiluminescent measurements show that the deoxymyoglobin-nitrite reaction produces NO in a second
19 ket, perhaps accompanying rehydration of the deoxymyoglobin photoproduct or accommodation of protein
21 mal structural decomposition of the hemes in deoxymyoglobins reveals a predominantly dom heme deforma
23 t O(2), and we have previously reported that deoxymyoglobin traps free HNO to form a stable adduct.
25 l histidine residue (13)C NMR assignments in deoxymyoglobin which are confirmed by new quantitative N
26 aracterize the nitrite reductase activity of deoxymyoglobin, which reduces nitrite approximately 36 t
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