1wvp: Difference between revisions
New page: left|200px<br /><applet load="1wvp" size="450" color="white" frame="true" align="right" spinBox="true" caption="1wvp, resolution 1.53Å" /> '''Structure of chemica... |
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[[Image:1wvp.gif|left|200px]]<br /><applet load="1wvp" size=" | [[Image:1wvp.gif|left|200px]]<br /><applet load="1wvp" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1wvp, resolution 1.53Å" /> | caption="1wvp, resolution 1.53Å" /> | ||
'''Structure of chemically modified myoglobin with distal N-tetrazolyl-histidine E7(64)'''<br /> | '''Structure of chemically modified myoglobin with distal N-tetrazolyl-histidine E7(64)'''<br /> | ||
==Overview== | ==Overview== | ||
Tetrazole-myoglobin (Tet-Mb), a site selectively modified myoglobin with | Tetrazole-myoglobin (Tet-Mb), a site selectively modified myoglobin with tetrazole anion (-CN4-) covalently attached to the imidazole N epsilon of the distal histidine 64(E7) (see Fig. 1; Kamiya, N., Shiro, Y., Iwata, T., Iizuka, T., and Iwasaki, H. (1991) J. Am. Chem. Soc. 113, 1826-1829), exhibited unique properties in the reduction from ferric to ferrous states and in the reaction of its deoxy form with O2. The redox potential of Tet-Mb is obtained to be -193 mV, which is much lower than that of unmodified (native) myoglobin (50 mV), possibly due to the electrostatic interaction between the heme iron and the tetrazole group. The ferrous deoxy form of Tet-Mb was rapidly oxidized to its ferric form in the reaction with O2 at room temperature through an intermediary formation of its oxy form and with the generation of O2-. The oxy form of Tet-Mb can be detected by the optical spectral measurement at -12 degrees C, the rapid scan measurement at room temperature, and the electron spin resonance measurement of its cobalt-substituted derivative (Tet-Mb(Co2+)) at 77 K. In the kinetic measurement of the O2 binding reaction to Tet-Mb, its association and dissociation rate constants in the bimolecular reaction were 6.1 x 10(7) M-1 s-1 and 2200 s-1, respectively, showing that the tetrazole modification of His-64 extremely accelerates its association and dissociation rates. Taken together with the extremely fast autoxidation rate (53 h-1) obtained, these kinetic results suggested that the channel of O2 from the solvent region to the protein interior is open enough to pass the external ligand. The structure is discussed in relation to those of some genetic mutants. Taking these properties, we demonstrated that Tet-Mb can catalyze O2 consumption to generate O2-, coupled with the NADH-supported enzymatic reduction system of cytochrome P-450cam under an aerobic condition. | ||
==About this Structure== | ==About this Structure== | ||
1WVP is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Physeter_catodon Physeter catodon] with SO4 and HEM as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http:// | 1WVP is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Physeter_catodon Physeter catodon] with <scene name='pdbligand=SO4:'>SO4</scene> and <scene name='pdbligand=HEM:'>HEM</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1WVP OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Kamiya, N.]] | [[Category: Kamiya, N.]] | ||
[[Category: Makino, M.]] | [[Category: Makino, M.]] | ||
[[Category: RSGI, RIKEN | [[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]] | ||
[[Category: Shiro, Y.]] | [[Category: Shiro, Y.]] | ||
[[Category: Sugimoto, H.]] | [[Category: Sugimoto, H.]] | ||
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[[Category: tetrazole]] | [[Category: tetrazole]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:48:35 2008'' |