1bx4: Difference between revisions

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==Overview==
==Overview==
Adenosine kinase (AK) is a key enzyme in the regulation of extracellular, adenosine and intracellular adenylate levels. Inhibitors of adenosine, kinase elevate adenosine to levels that activate nearby adenosine, receptors and produce a wide variety of therapeutically beneficial, activities. Accordingly, AK is a promising target for new analgesic, neuroprotective, and cardioprotective agents. We determined the structure, of human adenosine kinase by X-ray crystallography using MAD phasing, techniques and refined the structure to 1.5 A resolution. The enzyme, structure consisted of one large alpha/beta domain with nine beta-strands, eight alpha-helices, and one small alpha/beta-domain with five, beta-strands and two alpha-helices. The active site is formed along the, edge of the beta-sheet ... [[http://ispc.weizmann.ac.il/pmbin/getpm?9843365 (full description)]]
Adenosine kinase (AK) is a key enzyme in the regulation of extracellular, adenosine and intracellular adenylate levels. Inhibitors of adenosine, kinase elevate adenosine to levels that activate nearby adenosine, receptors and produce a wide variety of therapeutically beneficial, activities. Accordingly, AK is a promising target for new analgesic, neuroprotective, and cardioprotective agents. We determined the structure, of human adenosine kinase by X-ray crystallography using MAD phasing, techniques and refined the structure to 1.5 A resolution. The enzyme, structure consisted of one large alpha/beta domain with nine beta-strands, eight alpha-helices, and one small alpha/beta-domain with five, beta-strands and two alpha-helices. The active site is formed along the, edge of the beta-sheet in the large domain while the small domain acts as, a lid to cover the upper face of the active site. The overall structure is, similar to the recently reported structure of ribokinase from Escherichia, coli [Sigrell et al. (1998) Structure 6, 183-193]. The structure of, ribokinase was determined at 1.8 A resolution and represents the first, structure of a new family of carbohydrate kinases. Two molecules of, adenosine were present in the AK crystal structure with one adenosine, molecule located in a site that matches the ribose site in ribokinase and, probably represents the substrate-binding site. The second adenosine site, overlaps the ADP site in ribokinase and probably represents the ATP site., A Mg2+ ion binding site is observed in a trough between the two adenosine, sites. The structure of the active site is consistent with the observed, substrate specificity. The active-site model suggests that Asp300 is an, important catalytic residue involved in the deprotonation of the, 5'-hydroxyl during the phosphate transfer.


==About this Structure==
==About this Structure==
1BX4 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 CL, MG and ADN as [[http://en.wikipedia.org/wiki/ligands ligands]]. Active as [[http://en.wikipedia.org/wiki/Adenosine_kinase Adenosine kinase]], with EC number [[http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.20 2.7.1.20]]. Structure known Active Sites: ADA and ADB. Full crystallographic information is available from [[http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1BX4 OCA]].  
1BX4 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 CL, MG and ADN as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Adenosine_kinase Adenosine kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.20 2.7.1.20] Structure known Active Sites: ADA and ADB. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1BX4 OCA].  


==Reference==
==Reference==
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[[Category: human adenosine kinase]]
[[Category: human adenosine kinase]]


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