Adrenodoxin reductase

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
 +
<StructureSection load='1e1k' size='350' side='right' scene='' caption='Fig. 1. Structure of adrenodoxin reductase with FAD and NADP. PDB ID: 1e1k.'>
 +
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>
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>
Line 30: Line 32:
AR has two main domains. The N terminal domain contains a [[Rossmann fold]] that binds FAD and a central domain that binds NADPH.
AR has two main domains. The N terminal domain contains a [[Rossmann fold]] that binds FAD and a central domain that binds NADPH.
- 
-
<Structure load='1e1k' size='350' frame='true' align='left' caption='Fig. 1. Structure of adrenodoxin reductase with FAD and NADP. PDB ID: 1e1k.' scene='' />
 
The following scenes illustrate some aspects of the structure.
The following scenes illustrate some aspects of the structure.
Line 47: Line 47:
<scene name='70/702915/Fad_rossmann_fold/1'>Rossmann fold of FAD</scene>
<scene name='70/702915/Fad_rossmann_fold/1'>Rossmann fold of FAD</scene>
{{clear}}
{{clear}}
-
 
+
</StructureSection>
==3D Structures of Adrenodoxin reductase==
==3D Structures of Adrenodoxin reductase==

Revision as of 14:33, 10 January 2016

Fig. 1. Structure of adrenodoxin reductase with FAD and NADP. PDB ID: 1e1k.

Drag the structure with the mouse to rotate

3D Structures of Adrenodoxin reductase

Updated on 10-January-2016

1e1k, 1e1l, 1e1m – bADR+FAD+NADP – bovine
1e1n, 1cjc – bADR+FAD
1e6e – bADR + adrenodoxin

References

  1. 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

Proteopedia Page Contributors and Editors (what is this?)

Alexander Berchansky, Israel Hanukoglu, Michal Harel, Joel L. Sussman

Personal tools