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New page: left|200px<br /> <applet load="2iag" size="450" color="white" frame="true" align="right" spinBox="true" caption="2iag, resolution 2.15Å" /> '''Crystal structure o...
 
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[[Image:2iag.gif|left|200px]]<br />
[[Image:2iag.gif|left|200px]]<br /><applet load="2iag" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="2iag" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2iag, resolution 2.15&Aring;" />
caption="2iag, resolution 2.15&Aring;" />
'''Crystal structure of human prostacyclin synthase'''<br />
'''Crystal structure of human prostacyclin synthase'''<br />


==Overview==
==Overview==
Prostacyclin synthase (PGIS) catalyzes an isomerization of prostaglandin, H(2) to prostacyclin, a potent mediator of vasodilation and anti-platelet, aggregation. Here, we report the crystal structure of human PGIS at 2.15 A, resolution, which represents the first three-dimensional structure of a, class III cytochrome P450. While notable sequence divergence has been, recognized between PGIS and other P450s, PGIS exhibits the typical, triangular prism-shaped P450 fold with only moderate structural, differences. The conserved acid-alcohol pair in the I helix of P450s is, replaced by residues G286 and N287 in PGIS, but the distinctive disruption, of the I helix and the presence of a nearby water channel remain, conserved. The side-chain of N287 appears to be positioned to facilitate, the endoperoxide bond cleavage, suggesting a functional conservation of, this residue in O-O bond cleavage. A combination of bent I helix and, tilted B' helix creates a channel extending from the heme distal pocket, which seemingly allows binding of various ligands; however, residue W282, placed in this channel at a distance of 8.4 A from the iron with its, indole side-chain lying parallel with the porphyrin plane, may serve as a, threshold to exclude most ligands from binding. Additionally, a long, "meander" region protruding from the protein surface may impede electron, transfer. Although the primary sequence of the PGIS cysteine ligand loop, diverges significantly from the consensus, conserved tertiary structure, and hydrogen bonding pattern are observed for this region. The, substrate-binding model was constructed and the structural basis for, prostacyclin biosynthesis is discussed.
Prostacyclin synthase (PGIS) catalyzes an isomerization of prostaglandin H(2) to prostacyclin, a potent mediator of vasodilation and anti-platelet aggregation. Here, we report the crystal structure of human PGIS at 2.15 A resolution, which represents the first three-dimensional structure of a class III cytochrome P450. While notable sequence divergence has been recognized between PGIS and other P450s, PGIS exhibits the typical triangular prism-shaped P450 fold with only moderate structural differences. The conserved acid-alcohol pair in the I helix of P450s is replaced by residues G286 and N287 in PGIS, but the distinctive disruption of the I helix and the presence of a nearby water channel remain conserved. The side-chain of N287 appears to be positioned to facilitate the endoperoxide bond cleavage, suggesting a functional conservation of this residue in O-O bond cleavage. A combination of bent I helix and tilted B' helix creates a channel extending from the heme distal pocket, which seemingly allows binding of various ligands; however, residue W282, placed in this channel at a distance of 8.4 A from the iron with its indole side-chain lying parallel with the porphyrin plane, may serve as a threshold to exclude most ligands from binding. Additionally, a long "meander" region protruding from the protein surface may impede electron transfer. Although the primary sequence of the PGIS cysteine ligand loop diverges significantly from the consensus, conserved tertiary structure and hydrogen bonding pattern are observed for this region. The substrate-binding model was constructed and the structural basis for prostacyclin biosynthesis is discussed.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
2IAG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with NA and HEM as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Prostaglandin-I_synthase Prostaglandin-I synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.99.4 5.3.99.4] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2IAG OCA].  
2IAG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=NA:'>NA</scene> and <scene name='pdbligand=HEM:'>HEM</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Prostaglandin-I_synthase Prostaglandin-I synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.99.4 5.3.99.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2IAG OCA].  


==Reference==
==Reference==
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[[Category: Prostaglandin-I synthase]]
[[Category: Prostaglandin-I synthase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Chan, N.L.]]
[[Category: Chan, N L.]]
[[Category: Chiang, C.W.]]
[[Category: Chiang, C W.]]
[[Category: Wang, L.H.]]
[[Category: Wang, L H.]]
[[Category: Yeh, H.C.]]
[[Category: Yeh, H C.]]
[[Category: HEM]]
[[Category: HEM]]
[[Category: NA]]
[[Category: NA]]
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[[Category: prostacyclin synthase]]
[[Category: prostacyclin synthase]]


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