Aldehyde dehydrogenase

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A cysteine-thiol at the active site of GAPDH plays a role in catalysis.
A cysteine-thiol at the active site of GAPDH plays a role in catalysis.
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*<scene name='44/447036/Cv/5'>Active site</scene>. Water molecules shown as red spheres.
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*<scene name='44/447036/Cv/9'>Active site</scene>. Water molecules shown as red spheres.
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*<scene name='44/447036/Cv/7'>Dithiothreitol binding</scene>.
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*<scene name='44/447036/Cv/10'>Dithiothreitol binding</scene>.
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*<scene name='44/447036/Cv/8'>Dimercaptobutane-diol binding</scene>.
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*<scene name='44/447036/Cv/11'>Dimercaptobutane-diol binding</scene>.
</StructureSection>
</StructureSection>
== 3D Structures of Aldehyde dehydrogenase ==
== 3D Structures of Aldehyde dehydrogenase ==

Revision as of 11:51, 29 April 2018

Aldehyde hydrogenase class 1 tetramer complex with NAD, dithiothreitol and dimercaptobutane-diol, 1o9j

Drag the structure with the mouse to rotate

3D Structures of Aldehyde dehydrogenase

Updated on 29-April-2018

References

  1. Keller, Markus A.; Zander, Ulrich; Fuchs, Julian E.; Kreutz, Christoph; Watschinger, Katrin et al. (2014). A gatekeeper helix determines the substrate specificity of Sjögren–Larsson Syndrome enzyme fatty aldehyde dehydrogenase. Nature Communications vol. 5.

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky, Joel L. Sussman

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