Adrenodoxin reductase
From Proteopedia
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| - | Adrenodoxin reductase (AR) is an FAD containing flavoprotein that functions as an electron transfer protein in the mitochondrial P450 systems that catalyze essential steps in the biosynthesis of steroid hormones.<ref name="HI-review">PMID:22217824</ref> | + | <StructureSection load='' size='450' side='right' scene='70/702915/Cv/1' caption='Structure of adrenodoxin reductase with FAD and NADP. PDB ID: [[1e1k]].'> |
| + | __TOC__ | ||
| + | ==Function== | ||
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| + | '''Adrenodoxin reductase''' (AR) is an FAD containing flavoprotein that functions as an electron transfer protein in the mitochondrial P450 systems that catalyze essential steps in the biosynthesis of steroid hormones.<ref name="HI-review">PMID:22217824</ref> | ||
The enzyme nomenclature code of AR is [http://www.chem.qmul.ac.uk/iubmb/enzyme/EC1/18/1/6.html 1.18.1.6]. | The enzyme nomenclature code of AR is [http://www.chem.qmul.ac.uk/iubmb/enzyme/EC1/18/1/6.html 1.18.1.6]. | ||
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==Structure of adrenodoxin reductase== | ==Structure of adrenodoxin reductase== | ||
| - | AR has two main domains. The N terminal domain contains a Rossmann fold that binds FAD and a | + | AR has two main domains. The N terminal domain contains a [[Rossmann fold]] that binds FAD and a central domain that binds NADPH.<ref>PMID:29177972</ref> |
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The following scenes illustrate some aspects of the structure. | The following scenes illustrate some aspects of the structure. | ||
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Click the following green links for the action indicated: | Click the following green links for the action indicated: | ||
| - | <scene name='70/702915/ | + | <scene name='70/702915/Cv/14'>Ball and stick repsentation of NADP and FAD in AR</scene> |
| - | <scene name='70/702915/ | + | <scene name='70/702915/Cv/15'>Spacefill repsentation of NADP and FAD in AR</scene> |
| + | <scene name='70/702915/Cv/16'>FAD binding site in AR</scene> (water molecules shown as red spheres) | ||
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| + | <scene name='70/702915/Cv/17'>NADP binding site in AR</scene> (water molecules shown as red spheres) (PDB entry [[1e1k]])<ref>PMID:10998235</ref> | ||
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| + | <scene name='70/702915/Fad_rossmann_fold/2'>Rossmann fold of FAD</scene> | ||
{{clear}} | {{clear}} | ||
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| + | ==3D Structures of Adrenodoxin reductase== | ||
| + | [[Adrenodoxin reductase 3D structures]] | ||
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| + | </StructureSection> | ||
==References== | ==References== | ||
<references /> | <references /> | ||
| - | + | [[Category: Oxidoreductase]] | |
| - | [[ | + | [[Category: Rossmann fold]] |
| + | [[Category:Topic Page]] | ||
Current revision
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References
- ↑ 1.0 1.1 Hanukoglu I. Steroidogenic enzymes: structure, function, and role in regulation of steroid hormone biosynthesis. J Steroid Biochem Mol Biol. 1992 Dec;43(8):779-804. doi:, 10.1016/0960-0760(92)90307-5. PMID:22217824 doi:http://dx.doi.org/10.1016/0960-0760(92)90307-5
- ↑ Hanukoglu I. Conservation of the Enzyme-Coenzyme Interfaces in FAD and NADP Binding Adrenodoxin Reductase-A Ubiquitous Enzyme. J Mol Evol. 2017 Dec;85(5-6):205-218. doi: 10.1007/s00239-017-9821-9. Epub 2017, Nov 24. PMID:29177972 doi:http://dx.doi.org/10.1007/s00239-017-9821-9
- ↑ Ziegler GA, Schulz GE. Crystal structures of adrenodoxin reductase in complex with NADP+ and NADPH suggesting a mechanism for the electron transfer of an enzyme family. Biochemistry. 2000 Sep 12;39(36):10986-95. PMID:10998235
Proteopedia Page Contributors and Editors (what is this?)
Alexander Berchansky, Israel Hanukoglu, Michal Harel, Joel L. Sussman

