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Timothy E. Machonkin

Showing results (1-10 of 14) with videos related to

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Biochemistry|September 28, 2011
Substrate specificity of Sphingobium chlorophenolicum 2,6-dichlorohydroquinone 1,2-dioxygenaseTimothy E Machonkin, Amy E Doerner
Journal of the American Chemical Society|April 29, 2004
Strategy for the study of paramagnetic proteins with slow electronic relaxation rates by nmr spectroscopy: application to oxidized human [2Fe-2S] ferredoxinTimothy E Machonkin, William M Westler, John L Markley
Journal of the American Chemical Society|March 28, 2002
(13)C[(13)C] 2D NMR: a novel strategy for the study of paramagnetic proteins with slow electronic relaxation ratesTimothy E Machonkin, William M Westler, John L Markley
Inorganic Chemistry|April 30, 2005
Paramagnetic NMR spectroscopy and density functional calculations in the analysis of the geometric and electronic structures of iron-sulfur proteinsTimothy E Machonkin, William M Westler, John L Markley
Chemical Reviews|November 7, 1996
Multicopper Oxidases and OxygenasesEdward I. Solomon, Uma M. Sundaram, Timothy E. Machonkin
Journal of Biological Inorganic Chemistry : JBIC : a Publication of the Society of Biological Inorganic Chemistry|February 17, 2025
Characterization of the substrate specificity and regioselectivity of ring-cleavage of Pseudomonas putida DLL-E4 hydroquinone 1,2-dioxygenase (PnpC1C2)Timothy E Machonkin, Madeleine S Maker, Nandin Ganjoloo, et al.
Inorganic Chemistry|November 10, 2010
Solution and structural characterization of iron(II) complexes with ortho-halogenated phenolates: insights into potential substrate binding modes in hydroquinone dioxygenasesSara S Rocks, William W Brennessel, Timothy E Machonkin, et al.
Journal of Biological Inorganic Chemistry : JBIC : a Publication of the Society of Biological Inorganic Chemistry|May 16, 2019
The role of halogen substituents and substrate pK<sub>a</sub> in defining the substrate specificity of 2,6-dichlorohydroquinone 1,2-dioxygenase (PcpA)Julia E Burrows, Monica Q Paulson, Emma R Altman, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 4, 2005
Changes in hydrogen-bond strengths explain reduction potentials in 10 rubredoxin variantsI-Jin Lin, Erika B Gebel, Timothy E Machonkin, et al.
Journal of the American Chemical Society|February 6, 2003
Correlation between hydrogen bond lengths and reduction potentials in Clostridium pasteurianum rubredoxinI-Jin Lin, Erika B Gebel, Timothy E Machonkin, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Biochemistry|September 28, 2011
Substrate specificity of Sphingobium chlorophenolicum 2,6-dichlorohydroquinone 1,2-dioxygenaseTimothy E Machonkin, Amy E Doerner
Journal of the American Chemical Society|April 29, 2004
Strategy for the study of paramagnetic proteins with slow electronic relaxation rates by nmr spectroscopy: application to oxidized human [2Fe-2S] ferredoxinTimothy E Machonkin, William M Westler, John L Markley
Journal of the American Chemical Society|March 28, 2002
(13)C[(13)C] 2D NMR: a novel strategy for the study of paramagnetic proteins with slow electronic relaxation ratesTimothy E Machonkin, William M Westler, John L Markley
Inorganic Chemistry|April 30, 2005
Paramagnetic NMR spectroscopy and density functional calculations in the analysis of the geometric and electronic structures of iron-sulfur proteinsTimothy E Machonkin, William M Westler, John L Markley
Chemical Reviews|November 7, 1996
Multicopper Oxidases and OxygenasesEdward I. Solomon, Uma M. Sundaram, Timothy E. Machonkin
Journal of Biological Inorganic Chemistry : JBIC : a Publication of the Society of Biological Inorganic Chemistry|February 17, 2025
Characterization of the substrate specificity and regioselectivity of ring-cleavage of Pseudomonas putida DLL-E4 hydroquinone 1,2-dioxygenase (PnpC1C2)Timothy E Machonkin, Madeleine S Maker, Nandin Ganjoloo, et al.
Inorganic Chemistry|November 10, 2010
Solution and structural characterization of iron(II) complexes with ortho-halogenated phenolates: insights into potential substrate binding modes in hydroquinone dioxygenasesSara S Rocks, William W Brennessel, Timothy E Machonkin, et al.
Journal of Biological Inorganic Chemistry : JBIC : a Publication of the Society of Biological Inorganic Chemistry|May 16, 2019
The role of halogen substituents and substrate pK<sub>a</sub> in defining the substrate specificity of 2,6-dichlorohydroquinone 1,2-dioxygenase (PcpA)Julia E Burrows, Monica Q Paulson, Emma R Altman, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 4, 2005
Changes in hydrogen-bond strengths explain reduction potentials in 10 rubredoxin variantsI-Jin Lin, Erika B Gebel, Timothy E Machonkin, et al.
Journal of the American Chemical Society|February 6, 2003
Correlation between hydrogen bond lengths and reduction potentials in Clostridium pasteurianum rubredoxinI-Jin Lin, Erika B Gebel, Timothy E Machonkin, et al.
Pageof 2