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New page: left|200px<br /><applet load="2fpg" size="450" color="white" frame="true" align="right" spinBox="true" caption="2fpg, resolution 2.960Å" /> '''Crystal structure o...
 
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[[Image:2fpg.gif|left|200px]]<br /><applet load="2fpg" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2fpg.gif|left|200px]]<br /><applet load="2fpg" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2fpg, resolution 2.960&Aring;" />
caption="2fpg, resolution 2.960&Aring;" />
'''Crystal structure of pig GTP-specific succinyl-CoA synthetase in complex with GDP'''<br />
'''Crystal structure of pig GTP-specific succinyl-CoA synthetase in complex with GDP'''<br />


==Overview==
==Overview==
Two isoforms of succinyl-CoA synthetase exist in mammals, one specific for, ATP and the other for GTP. The GTP-specific form of pig succinyl-CoA, synthetase has been crystallized in the presence of GTP and the structure, determined to 2.1 A resolution. GTP is bound in the ATP-grasp domain, where interactions of the guanine base with a glutamine residue, (Gln-20beta) and with backbone atoms provide the specificity. The, gamma-phosphate interacts with the side chain of an arginine residue, (Arg-54beta) and with backbone amide nitrogen atoms, leading to tight, interactions between the gamma-phosphate and the protein. This contrasts, with the structures of ATP bound to other members of the family of, ATP-grasp proteins where the gamma-phosphate is exposed, free to react, with the other substrate. To test if GDP would interact with GTP-specific, succinyl-CoA synthetase in the same way that ADP interacts with other, members of the family of ATP-grasp proteins, the structure of GDP bound to, GTP-specific succinyl-CoA synthetase was also determined. A comparison of, the conformations of GTP and GDP shows that the bases adopt the same, position but that changes in conformation of the ribose moieties and the, alpha- and beta-phosphates allow the gamma-phosphate to interact with the, arginine residue and amide nitrogen atoms in GTP, while the beta-phosphate, interacts with these residues in GDP. The complex of GTP with succinyl-CoA, synthetase shows that the enzyme is able to protect GTP from hydrolysis, when the active-site histidine residue is not in position to be, phosphorylated.
Two isoforms of succinyl-CoA synthetase exist in mammals, one specific for ATP and the other for GTP. The GTP-specific form of pig succinyl-CoA synthetase has been crystallized in the presence of GTP and the structure determined to 2.1 A resolution. GTP is bound in the ATP-grasp domain, where interactions of the guanine base with a glutamine residue (Gln-20beta) and with backbone atoms provide the specificity. The gamma-phosphate interacts with the side chain of an arginine residue (Arg-54beta) and with backbone amide nitrogen atoms, leading to tight interactions between the gamma-phosphate and the protein. This contrasts with the structures of ATP bound to other members of the family of ATP-grasp proteins where the gamma-phosphate is exposed, free to react with the other substrate. To test if GDP would interact with GTP-specific succinyl-CoA synthetase in the same way that ADP interacts with other members of the family of ATP-grasp proteins, the structure of GDP bound to GTP-specific succinyl-CoA synthetase was also determined. A comparison of the conformations of GTP and GDP shows that the bases adopt the same position but that changes in conformation of the ribose moieties and the alpha- and beta-phosphates allow the gamma-phosphate to interact with the arginine residue and amide nitrogen atoms in GTP, while the beta-phosphate interacts with these residues in GDP. The complex of GTP with succinyl-CoA synthetase shows that the enzyme is able to protect GTP from hydrolysis when the active-site histidine residue is not in position to be phosphorylated.


==About this Structure==
==About this Structure==
2FPG is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Sus_scrofa Sus scrofa] with K, PO4 and GDP as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Succinate--CoA_ligase_(GDP-forming) Succinate--CoA ligase (GDP-forming)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=6.2.1.4 6.2.1.4] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2FPG OCA].  
2FPG is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Sus_scrofa Sus scrofa] with <scene name='pdbligand=K:'>K</scene>, <scene name='pdbligand=PO4:'>PO4</scene> and <scene name='pdbligand=GDP:'>GDP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Succinate--CoA_ligase_(GDP-forming) Succinate--CoA ligase (GDP-forming)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=6.2.1.4 6.2.1.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FPG OCA].  


==Reference==
==Reference==
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[[Category: Succinate--CoA ligase (GDP-forming)]]
[[Category: Succinate--CoA ligase (GDP-forming)]]
[[Category: Sus scrofa]]
[[Category: Sus scrofa]]
[[Category: Fraser, M.E.]]
[[Category: Fraser, M E.]]
[[Category: GDP]]
[[Category: GDP]]
[[Category: K]]
[[Category: K]]
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[[Category: active site histidine residue]]
[[Category: active site histidine residue]]


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