2iid: Difference between revisions

New page: left|200px<br /><applet load="2iid" size="450" color="white" frame="true" align="right" spinBox="true" caption="2iid, resolution 1.80Å" /> '''Structure of L-amino...
 
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caption="2iid, resolution 1.80&Aring;" />
caption="2iid, resolution 1.80&Aring;" />
'''Structure of L-amino acid oxidase from Calloselasma rhodostoma in complex with L-phenylalanine'''<br />
'''Structure of L-amino acid oxidase from Calloselasma rhodostoma in complex with L-phenylalanine'''<br />


==Overview==
==Overview==
L-Amino acid oxidase is a dimeric glycosylated flavoenzyme, a major, constituent of the venom-from the snake Calloselasma rhodostoma. The, enzyme exhibits apoptosis inducing effects as well as antibacterial and, anti-HIV activities. The structure of l-amino acid oxidase with its, substrate (L-phenylalanine) has been refined to a resolution of 1.8 A. The, complex structure reveals the substrate bound to the reduced flavin, (FADred). Alternative conformations for the key residues His223 and Arg322, are evident, suggesting a dynamic active site. Furthermore, conformational, changes are apparent for the isoalloxazine ring; the three-ring system, exhibits more bending around the N5-N10 axis compared to the oxidized, flavin. The implications of the observed dynamics on the mechanism of, catalysis are discussed. Inspection of buried surfaces in the enzyme, reveals a Y-shaped channel system extending from the external surface of, the protein to the active site. One portion of this channel may serve as, the entry path for O2 during the oxidative half-reaction. The second, region, separated from the proposed O2 channel by the N terminus (residues, 8-16) of the protein, may play a role in H2O2 release. Interestingly, the, latter portion of the channel would direct the H2O2 product to the, exterior surface of the protein, near the glycan moiety, thought to anchor, the enzyme to the host cell. This channel location may explain the ability, of the enzyme to localize H2O2 to the targeted cell and thus induce the, apoptotic effect.
L-Amino acid oxidase is a dimeric glycosylated flavoenzyme, a major constituent of the venom-from the snake Calloselasma rhodostoma. The enzyme exhibits apoptosis inducing effects as well as antibacterial and anti-HIV activities. The structure of l-amino acid oxidase with its substrate (L-phenylalanine) has been refined to a resolution of 1.8 A. The complex structure reveals the substrate bound to the reduced flavin (FADred). Alternative conformations for the key residues His223 and Arg322 are evident, suggesting a dynamic active site. Furthermore, conformational changes are apparent for the isoalloxazine ring; the three-ring system exhibits more bending around the N5-N10 axis compared to the oxidized flavin. The implications of the observed dynamics on the mechanism of catalysis are discussed. Inspection of buried surfaces in the enzyme reveals a Y-shaped channel system extending from the external surface of the protein to the active site. One portion of this channel may serve as the entry path for O2 during the oxidative half-reaction. The second region, separated from the proposed O2 channel by the N terminus (residues 8-16) of the protein, may play a role in H2O2 release. Interestingly, the latter portion of the channel would direct the H2O2 product to the exterior surface of the protein, near the glycan moiety, thought to anchor the enzyme to the host cell. This channel location may explain the ability of the enzyme to localize H2O2 to the targeted cell and thus induce the apoptotic effect.


==About this Structure==
==About this Structure==
2IID is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Calloselasma_rhodostoma Calloselasma rhodostoma] with NAG, PHE and FAD as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/L-amino-acid_oxidase L-amino-acid oxidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.4.3.2 1.4.3.2] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2IID OCA].  
2IID is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Calloselasma_rhodostoma Calloselasma rhodostoma] with <scene name='pdbligand=NAG:'>NAG</scene>, <scene name='pdbligand=PHE:'>PHE</scene> and <scene name='pdbligand=FAD:'>FAD</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/L-amino-acid_oxidase L-amino-acid oxidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.4.3.2 1.4.3.2] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2IID OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Foster, S.]]
[[Category: Foster, S.]]
[[Category: Lyubimov, A.Y.]]
[[Category: Lyubimov, A Y.]]
[[Category: Moustafa, I.M.]]
[[Category: Moustafa, I M.]]
[[Category: Vrielink, A.]]
[[Category: Vrielink, A.]]
[[Category: FAD]]
[[Category: FAD]]
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[[Category: sustrate binding]]
[[Category: sustrate binding]]


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