Aromatic amine dehydrogenase

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Current revision (08:26, 20 March 2019) (edit) (undo)
 
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==3D structures of aromatic amine dehydrogenase==
 
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Updated on {{REVISIONDAY2}}-{{MONTHNAME|{{REVISIONMONTH}}}}-{{REVISIONYEAR}}
 
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[[2ah1]] – AfAADH – ''Alcaligenes faecalis''<br />
 
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[[2i0r]], [[2iup]], [[2iur]], [[2iuv]], [[2iot]], [[2oiz]] – AfAADH + TTQ derivative<br />
 
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[[2agl]] – AfAADH + TTQ derivative + phenylhydrazine <br />
 
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[[2agw]], [[2iuq]] – AfAADH + TTQ derivative + tryptamine<br />
 
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[[2agx]], [[2agy]] – AfAADH + TTQ derivative + indol ethanimine<br />
 
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[[2ojy]] – AfAADH + TTQ derivative + indol acetamide<br />
 
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[[2agz]], [[2ah0]] – AfAADH + TTQ derivative + indol aminoethanol<br />
 
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[[2ok6]] – AfAADH + TTQ derivative + formyl amino tryptophan<br />
 
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[[2hxc]] – AfAADH + TTQ + benzylamine<br />
 
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[[2hj4]], [[2hjb]] – AfAADH + TTQ derivative + benzylamine derivative<br />
 
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[[2i0s]] – AfAADH + TTQ + phenylacetaldehyde<br />
 
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[[2i0t]] – AfAADH + TTQ + phenyl alcohol<br />
 
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[[2ok4]] – AfAADH + TTQ derivative + phenylacetaldehyde<br />
 
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[[2q7q]] – AfAADH + TTQ derivative + phenyl methanamine<br />
 
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[[2hkm]] – AfAADH + TTQ derivative + phenyl ethyl amine<br />
 
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[[2hkr]] – AfAADH + TTQ derivative + methoxyphenyl ethanamide + methoxyphenyl acetamide<br />
 
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[[2h3x]], [[2h47]], [[2iaa]] – AfAADH + TTQ derivative + azurin<br />
 
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== References ==
== References ==

Current revision

Structure of aromatic amine dehydrogenase large subunit (cyan and green) and small subunit (magenta and salmon) with cofactor TTQ complex with phenylacetaldehyde (PDB code 2i0s).

Drag the structure with the mouse to rotate

References

  1. Govindaraj S, Eisenstein E, Jones LH, Sanders-Loehr J, Chistoserdov AY, Davidson VL, Edwards SL. Aromatic amine dehydrogenase, a second tryptophan tryptophylquinone enzyme. J Bacteriol. 1994 May;176(10):2922-9. PMID:8188594
  2. Roujeinikova A, Hothi P, Masgrau L, Sutcliffe MJ, Scrutton NS, Leys D. New insights into the reductive half-reaction mechanism of aromatic amine dehydrogenase revealed by reaction with carbinolamine substrates. J Biol Chem. 2007 Aug 17;282(33):23766-77. Epub 2007 May 1. PMID:17475620 doi:10.1074/jbc.M700677200

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Alexander Berchansky, Michal Harel

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