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New page: left|200px<br /><applet load="2e0x" size="450" color="white" frame="true" align="right" spinBox="true" caption="2e0x, resolution 1.950Å" /> '''Crystal Structure o...
 
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[[Image:2e0x.gif|left|200px]]<br /><applet load="2e0x" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2e0x.gif|left|200px]]<br /><applet load="2e0x" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2e0x, resolution 1.950&Aring;" />
caption="2e0x, resolution 1.950&Aring;" />
'''Crystal Structure of Gamma-glutamyltranspeptidase from Escherichia coli (monoclinic form)'''<br />
'''Crystal Structure of Gamma-glutamyltranspeptidase from Escherichia coli (monoclinic form)'''<br />


==Overview==
==Overview==
Gamma-glutamyltranspeptidase (GGT) is a heterodimic enzyme that is, generated from the precursor protein through posttranslational processing, and catalyzes the hydrolysis of gamma-glutamyl bonds in gamma-glutamyl, compounds such as glutathione and/or the transfer of the gamma-glutamyl, group to other amino acids and peptides. We have determined the crystal, structure of GGT from Escherichia coli K-12 at 1.95 A resolution. GGT has, a stacked alphabetabetaalpha fold comprising the large and small subunits, similar to the folds seen in members of the N-terminal nucleophile, hydrolase superfamily. The active site Thr-391, the N-terminal residue of, the small subunit, is located in the groove, from which the pocket for, gamma-glutamyl moiety binding follows. We have further determined the, structure of the gamma-glutamyl-enzyme intermediate trapped by flash, cooling the GGT crystal soaked in glutathione solution and the structure, of GGT in complex with l-glutamate. These structures revealed how the, gamma-glutamyl moiety and l-glutamate are recognized by the enzyme. A, water molecule was seen on the carbonyl carbon of the, gamma-glutamyl-Thr-391 Ogamma bond in the intermediate that is to be, hydrolyzed. Notably the residues essential for GGT activity (Arg-114, Asp-433, Ser-462, and Ser-463 in E. coli GGT) shown by site-directed, mutagenesis of human GGT are all involved in the binding of the, gamma-glutamyl moiety. The structure of E. coli GGT presented here, together with sequence alignment of GGTs, may be applicable to interpret, the biochemical and genetic data of other GGTs.
Gamma-glutamyltranspeptidase (GGT) is a heterodimic enzyme that is generated from the precursor protein through posttranslational processing and catalyzes the hydrolysis of gamma-glutamyl bonds in gamma-glutamyl compounds such as glutathione and/or the transfer of the gamma-glutamyl group to other amino acids and peptides. We have determined the crystal structure of GGT from Escherichia coli K-12 at 1.95 A resolution. GGT has a stacked alphabetabetaalpha fold comprising the large and small subunits, similar to the folds seen in members of the N-terminal nucleophile hydrolase superfamily. The active site Thr-391, the N-terminal residue of the small subunit, is located in the groove, from which the pocket for gamma-glutamyl moiety binding follows. We have further determined the structure of the gamma-glutamyl-enzyme intermediate trapped by flash cooling the GGT crystal soaked in glutathione solution and the structure of GGT in complex with l-glutamate. These structures revealed how the gamma-glutamyl moiety and l-glutamate are recognized by the enzyme. A water molecule was seen on the carbonyl carbon of the gamma-glutamyl-Thr-391 Ogamma bond in the intermediate that is to be hydrolyzed. Notably the residues essential for GGT activity (Arg-114, Asp-433, Ser-462, and Ser-463 in E. coli GGT) shown by site-directed mutagenesis of human GGT are all involved in the binding of the gamma-glutamyl moiety. The structure of E. coli GGT presented here, together with sequence alignment of GGTs, may be applicable to interpret the biochemical and genetic data of other GGTs.


==About this Structure==
==About this Structure==
2E0X is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with CA as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Gamma-glutamyltransferase Gamma-glutamyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.2.2 2.3.2.2] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2E0X OCA].  
2E0X is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=CA:'>CA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Gamma-glutamyltransferase Gamma-glutamyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.2.2 2.3.2.2] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2E0X OCA].  


==Reference==
==Reference==
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[[Category: ggt]]
[[Category: ggt]]


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