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New page: left|200px<br /><applet load="1knf" size="450" color="white" frame="true" align="right" spinBox="true" caption="1knf, resolution 1.9Å" /> '''Crystal Structure of ...
 
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[[Image:1knf.gif|left|200px]]<br /><applet load="1knf" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1knf.gif|left|200px]]<br /><applet load="1knf" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1knf, resolution 1.9&Aring;" />
caption="1knf, resolution 1.9&Aring;" />
'''Crystal Structure of 2,3-dihydroxybiphenyl 1,2-dioxygenase Complexed with 3-methyl Catechol under Anaerobic Condition'''<br />
'''Crystal Structure of 2,3-dihydroxybiphenyl 1,2-dioxygenase Complexed with 3-methyl Catechol under Anaerobic Condition'''<br />


==Overview==
==Overview==
The steady-state cleavage of catechols by 2,3-dihydroxybiphenyl 1, 2-dioxygenase (DHBD), the extradiol dioxygenase of the biphenyl, biodegradation pathway, was investigated using a highly active, anaerobically purified preparation of enzyme. The kinetic data obtained, using 2,3-dihydroxybiphenyl (DHB) fit a compulsory order ternary complex, mechanism in which substrate inhibition occurs. The Km for dioxygen was, 1280 +/- 70 microM, which is at least 2 orders of magnitude higher than, that reported for catechol 2,3-dioxygenases. Km and Kd for DHB were 22 +/-, 2 and 8 +/- 1 microM, respectively. DHBD was subject to reversible, substrate inhibition and mechanism-based inactivation. In air-saturated, buffer, the partition ratios of catecholic substrates substituted at C-3, were inversely related to their apparent specificity constants. Small, organic molecules that stabilized DHBD most effectively also inhibited the, cleavage reaction most strongly. The steady-state kinetic data and, crystallographic results suggest that the stabilization and inhibition are, due to specific interactions between the organic molecule and the active, site of the enzyme. t-Butanol stabilized the enzyme and inhibited the, cleavage of DHB in a mixed fashion, consistent with the distinct binding, sites occupied by t-butanol in the crystal structures of the, substrate-free form of the enzyme and the enzyme-DHB complex. In contrast, crystal structures of complexes with catechol and 3-methylcatechol, revealed relationships between the binding of these smaller substrates and, t-butanol that are consistent with the observed competitive inhibition.
The steady-state cleavage of catechols by 2,3-dihydroxybiphenyl 1, 2-dioxygenase (DHBD), the extradiol dioxygenase of the biphenyl biodegradation pathway, was investigated using a highly active, anaerobically purified preparation of enzyme. The kinetic data obtained using 2,3-dihydroxybiphenyl (DHB) fit a compulsory order ternary complex mechanism in which substrate inhibition occurs. The Km for dioxygen was 1280 +/- 70 microM, which is at least 2 orders of magnitude higher than that reported for catechol 2,3-dioxygenases. Km and Kd for DHB were 22 +/- 2 and 8 +/- 1 microM, respectively. DHBD was subject to reversible substrate inhibition and mechanism-based inactivation. In air-saturated buffer, the partition ratios of catecholic substrates substituted at C-3 were inversely related to their apparent specificity constants. Small organic molecules that stabilized DHBD most effectively also inhibited the cleavage reaction most strongly. The steady-state kinetic data and crystallographic results suggest that the stabilization and inhibition are due to specific interactions between the organic molecule and the active site of the enzyme. t-Butanol stabilized the enzyme and inhibited the cleavage of DHB in a mixed fashion, consistent with the distinct binding sites occupied by t-butanol in the crystal structures of the substrate-free form of the enzyme and the enzyme-DHB complex. In contrast, crystal structures of complexes with catechol and 3-methylcatechol revealed relationships between the binding of these smaller substrates and t-butanol that are consistent with the observed competitive inhibition.


==About this Structure==
==About this Structure==
1KNF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Burkholderia_cepacia Burkholderia cepacia] with FE2, MBD and TBU as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Biphenyl-2,3-diol_1,2-dioxygenase Biphenyl-2,3-diol 1,2-dioxygenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.13.11.39 1.13.11.39] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1KNF OCA].  
1KNF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Burkholderia_cepacia Burkholderia cepacia] with <scene name='pdbligand=FE2:'>FE2</scene>, <scene name='pdbligand=MBD:'>MBD</scene> and <scene name='pdbligand=TBU:'>TBU</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Biphenyl-2,3-diol_1,2-dioxygenase Biphenyl-2,3-diol 1,2-dioxygenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.13.11.39 1.13.11.39] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1KNF OCA].  


==Reference==
==Reference==
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[[Category: Burkholderia cepacia]]
[[Category: Burkholderia cepacia]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Bolin, J.T.]]
[[Category: Bolin, J T.]]
[[Category: Han, S.]]
[[Category: Han, S.]]
[[Category: FE2]]
[[Category: FE2]]
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[[Category: oxidoreductase]]
[[Category: oxidoreductase]]


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