1f17: Difference between revisions
New page: left|200px<br /> <applet load="1f17" size="450" color="white" frame="true" align="right" spinBox="true" caption="1f17, resolution 2.30Å" /> '''L-3-HYDROXYACYL-COA... |
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[[Image:1f17.gif|left|200px]]<br /> | [[Image:1f17.gif|left|200px]]<br /><applet load="1f17" size="350" color="white" frame="true" align="right" spinBox="true" | ||
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caption="1f17, resolution 2.30Å" /> | caption="1f17, resolution 2.30Å" /> | ||
'''L-3-HYDROXYACYL-COA DEHYDROGENASE COMPLEXED WITH NADH'''<br /> | '''L-3-HYDROXYACYL-COA DEHYDROGENASE COMPLEXED WITH NADH'''<br /> | ||
==Overview== | ==Overview== | ||
l-3-Hydroxyacyl-CoA dehydrogenase reversibly catalyzes the conversion of | l-3-Hydroxyacyl-CoA dehydrogenase reversibly catalyzes the conversion of l-3-hydroxyacyl-CoA to 3-ketoacyl-CoA concomitant with the reduction of NAD(+) to NADH as part of the beta-oxidation spiral. In this report, crystal structures have been solved for the apoenzyme, binary complexes of the enzyme with reduced cofactor or 3-hydroxybutyryl-CoA substrate, and an abortive ternary complex of the enzyme with NAD(+) and acetoacetyl-CoA. The models illustrate positioning of cofactor and substrate within the active site of the enzyme. Comparison of these structures with the previous model of the enzyme-NAD(+) complex reveals that although significant shifting of the NAD(+)-binding domain relative to the C-terminal domain occurs in the ternary and substrate-bound complexes, there are few differences between the apoenzyme and cofactor-bound complexes. Analysis of these models clarifies the role of key amino acids implicated in catalysis and highlights additional critical residues. Furthermore, a novel charge transfer complex has been identified in the course of abortive ternary complex formation, and its characterization provides additional insight into aspects of the catalytic mechanism of l-3-hydroxyacyl-CoA dehydrogenase. | ||
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
1F17 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with NAI as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/3-hydroxyacyl-CoA_dehydrogenase 3-hydroxyacyl-CoA dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.35 1.1.1.35] Full crystallographic information is available from [http:// | 1F17 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=NAI:'>NAI</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/3-hydroxyacyl-CoA_dehydrogenase 3-hydroxyacyl-CoA dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.35 1.1.1.35] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1F17 OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Banaszak, L | [[Category: Banaszak, L J.]] | ||
[[Category: Barycki, J | [[Category: Barycki, J J.]] | ||
[[Category: Brien, L | [[Category: Brien, L K.O.]] | ||
[[Category: Strauss, A | [[Category: Strauss, A W.]] | ||
[[Category: NAI]] | [[Category: NAI]] | ||
[[Category: l-3-hydroxyacyl-coa dehydrogenase complexed with nadh]] | [[Category: l-3-hydroxyacyl-coa dehydrogenase complexed with nadh]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:33:41 2008'' |