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New page: left|200px<br /><applet load="1omo" size="450" color="white" frame="true" align="right" spinBox="true" caption="1omo, resolution 2.32Å" /> '''alanine dehydrogenas...
 
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[[Image:1omo.gif|left|200px]]<br /><applet load="1omo" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1omo.gif|left|200px]]<br /><applet load="1omo" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1omo, resolution 2.32&Aring;" />
caption="1omo, resolution 2.32&Aring;" />
'''alanine dehydrogenase dimer w/bound NAD (archaeal)'''<br />
'''alanine dehydrogenase dimer w/bound NAD (archaeal)'''<br />


==Overview==
==Overview==
The hyperthermophilic archaeon Archaeoglobus fulgidus contains an L-Ala, dehydrogenase (AlaDH, EC 1.4.1.1) that is not homologous to known, bacterial dehydrogenases and appears to represent a previously, unrecognized archaeal group of NAD-dependent dehydrogenases. The gene, (Genbank; TIGR AF1665) was annotated initially as an ornithine, cyclodeaminase (OCD) on the basis of strong homology with the mu, crystallin/OCD protein family. We report the structure of the NAD-bound, AF1665 AlaDH (AF-AlaDH) at 2.3 A in a C2 crystal form with the 70 kDa, dimer in the asymmetric unit, as the first structural representative of, this family. Consistent with its lack of homology to bacterial AlaDH, proteins, which are mostly hexameric, the archaeal dimer has a novel, structure. Although both types of AlaDH enzyme include a Rossmann-type, NAD-binding domain, the arrangement of strands in the C-terminal half of, this domain is novel, and the other (catalytic) domain in the archaeal, protein has a new fold. The active site presents a cluster of conserved, Arg and Lys side-chains over the pro-R face of the cofactor. In addition, the best ordered of the 338 water molecules in the structure is positioned, well for mechanistic interaction. The overall structure and active site, are compared with other dehydrogenases, including the AlaDH from, Phormidium lapideum. Implications for the catalytic mechanism and for the, structures of homologs are considered. The archaeal AlaDH represents an, ancient and previously undescribed subclass of Rossmann-fold proteins that, includes bacterial ornithine and lysine cyclodeaminases, marsupial lens, proteins and, in man, a thyroid hormone-binding protein that exhibits 30%, sequence identity with AF1665.
The hyperthermophilic archaeon Archaeoglobus fulgidus contains an L-Ala dehydrogenase (AlaDH, EC 1.4.1.1) that is not homologous to known bacterial dehydrogenases and appears to represent a previously unrecognized archaeal group of NAD-dependent dehydrogenases. The gene (Genbank; TIGR AF1665) was annotated initially as an ornithine cyclodeaminase (OCD) on the basis of strong homology with the mu crystallin/OCD protein family. We report the structure of the NAD-bound AF1665 AlaDH (AF-AlaDH) at 2.3 A in a C2 crystal form with the 70 kDa dimer in the asymmetric unit, as the first structural representative of this family. Consistent with its lack of homology to bacterial AlaDH proteins, which are mostly hexameric, the archaeal dimer has a novel structure. Although both types of AlaDH enzyme include a Rossmann-type NAD-binding domain, the arrangement of strands in the C-terminal half of this domain is novel, and the other (catalytic) domain in the archaeal protein has a new fold. The active site presents a cluster of conserved Arg and Lys side-chains over the pro-R face of the cofactor. In addition, the best ordered of the 338 water molecules in the structure is positioned well for mechanistic interaction. The overall structure and active site are compared with other dehydrogenases, including the AlaDH from Phormidium lapideum. Implications for the catalytic mechanism and for the structures of homologs are considered. The archaeal AlaDH represents an ancient and previously undescribed subclass of Rossmann-fold proteins that includes bacterial ornithine and lysine cyclodeaminases, marsupial lens proteins and, in man, a thyroid hormone-binding protein that exhibits 30% sequence identity with AF1665.


==About this Structure==
==About this Structure==
1OMO is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Archaeoglobus_fulgidus Archaeoglobus fulgidus] with NA and NAD as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Alanine_dehydrogenase Alanine dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.4.1.1 1.4.1.1] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1OMO OCA].  
1OMO is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Archaeoglobus_fulgidus Archaeoglobus fulgidus] with <scene name='pdbligand=NA:'>NA</scene> and <scene name='pdbligand=NAD:'>NAD</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Alanine_dehydrogenase Alanine dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.4.1.1 1.4.1.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1OMO OCA].  


==Reference==
==Reference==
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[[Category: Archaeoglobus fulgidus]]
[[Category: Archaeoglobus fulgidus]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Gallagher, D.T.]]
[[Category: Gallagher, D T.]]
[[Category: Holden, M.J.]]
[[Category: Holden, M J.]]
[[Category: Monbouquette, H.G.]]
[[Category: Monbouquette, H G.]]
[[Category: Schroeder, I.]]
[[Category: Schroeder, I.]]
[[Category: Smith, N.N.]]
[[Category: Smith, N N.]]
[[Category: NA]]
[[Category: NA]]
[[Category: NAD]]
[[Category: NAD]]
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[[Category: two-domain]]
[[Category: two-domain]]


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