1cg6: Difference between revisions

New page: left|200px<br /> <applet load="1cg6" size="450" color="white" frame="true" align="right" spinBox="true" caption="1cg6, resolution 1.7Å" /> '''STRUCTURE OF HUMAN 5...
 
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[[Image:1cg6.gif|left|200px]]<br /><applet load="1cg6" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1cg6" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1cg6, resolution 1.7&Aring;" />
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'''STRUCTURE OF HUMAN 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE COMPLEXED WITH 5'-DEOXY-5'-METHYLTHIOADENOSINE AND SULFATE AT 1.7 A RESOLUTION'''<br />
'''STRUCTURE OF HUMAN 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE COMPLEXED WITH 5'-DEOXY-5'-METHYLTHIOADENOSINE AND SULFATE AT 1.7 A RESOLUTION'''<br />


==Overview==
==Overview==
BACKGROUND: 5'-Deoxy-5'-methylthioadenosine phosphorylase (MTAP) catalyzes, the reversible phosphorolysis of 5'-deoxy-5'-methylthioadenosine (MTA) to, adenine and 5-methylthio-D-ribose-1-phosphate. MTA is a by-product of, polyamine biosynthesis, which is essential for cell growth and, proliferation. This salvage reaction is the principle source of free, adenine in human cells. Because of its importance in coupling the purine, salvage pathway to polyamine biosynthesis MTAP is a potential, chemotherapeutic target. RESULTS: We have determined the crystal structure, of MTAP at 1.7 A resolution using multiwavelength anomalous diffraction, phasing techniques. MTAP is a trimer comprised of three identical, subunits. Each subunit consists of a single alpha/beta domain containing a, central eight-stranded mixed beta sheet, a smaller five-stranded mixed, beta sheet and six alpha helices. The native structure revealed the, presence of an adenine molecule in the purine-binding site. The structure, of MTAP with methylthioadenosine and sulfate ion soaked into the active, site was also determined using diffraction data to 1.7 A resolution., CONCLUSIONS: The overall quaternary structure and subunit topology of MTAP, are similar to mammalian purine nucleoside phosphorylase (PNP). The, structures of the MTAP-ligand complexes provide a map of the active site, and suggest possible roles for specific residues in substrate binding and, catalysis. Residues accounting for the differences in substrate, specificity between MTAP and PNP are also identified. Detailed information, about the structure and chemical nature of the MTAP active site will aid, in the rational design of inhibitors of this potential chemotherapeutic, target. The MTAP structure represents the first structure of a mammalian, PNP that is specific for 6-aminopurines.
BACKGROUND: 5'-Deoxy-5'-methylthioadenosine phosphorylase (MTAP) catalyzes the reversible phosphorolysis of 5'-deoxy-5'-methylthioadenosine (MTA) to adenine and 5-methylthio-D-ribose-1-phosphate. MTA is a by-product of polyamine biosynthesis, which is essential for cell growth and proliferation. This salvage reaction is the principle source of free adenine in human cells. Because of its importance in coupling the purine salvage pathway to polyamine biosynthesis MTAP is a potential chemotherapeutic target. RESULTS: We have determined the crystal structure of MTAP at 1.7 A resolution using multiwavelength anomalous diffraction phasing techniques. MTAP is a trimer comprised of three identical subunits. Each subunit consists of a single alpha/beta domain containing a central eight-stranded mixed beta sheet, a smaller five-stranded mixed beta sheet and six alpha helices. The native structure revealed the presence of an adenine molecule in the purine-binding site. The structure of MTAP with methylthioadenosine and sulfate ion soaked into the active site was also determined using diffraction data to 1.7 A resolution. CONCLUSIONS: The overall quaternary structure and subunit topology of MTAP are similar to mammalian purine nucleoside phosphorylase (PNP). The structures of the MTAP-ligand complexes provide a map of the active site and suggest possible roles for specific residues in substrate binding and catalysis. Residues accounting for the differences in substrate specificity between MTAP and PNP are also identified. Detailed information about the structure and chemical nature of the MTAP active site will aid in the rational design of inhibitors of this potential chemotherapeutic target. The MTAP structure represents the first structure of a mammalian PNP that is specific for 6-aminopurines.


==About this Structure==
==About this Structure==
1CG6 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 SO4 and MTA as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/S-methyl-5-thioadenosine_phosphorylase S-methyl-5-thioadenosine phosphorylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.2.28 2.4.2.28] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1CG6 OCA].  
1CG6 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=SO4:'>SO4</scene> and <scene name='pdbligand=MTA:'>MTA</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/S-methyl-5-thioadenosine_phosphorylase S-methyl-5-thioadenosine phosphorylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.2.28 2.4.2.28] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CG6 OCA].  


==Reference==
==Reference==
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[[Category: S-methyl-5-thioadenosine phosphorylase]]
[[Category: S-methyl-5-thioadenosine phosphorylase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Appleby, T.C.]]
[[Category: Appleby, T C.]]
[[Category: Ealick, S.E.]]
[[Category: Ealick, S E.]]
[[Category: Erion, M.D.]]
[[Category: Erion, M D.]]
[[Category: MTA]]
[[Category: MTA]]
[[Category: SO4]]
[[Category: SO4]]
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[[Category: sulfate]]
[[Category: sulfate]]


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