1pgq: Difference between revisions

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New page: left|200px<br /><applet load="1pgq" size="450" color="white" frame="true" align="right" spinBox="true" caption="1pgq, resolution 3.17Å" /> '''CRYSTALLOGRAPHIC STU...
 
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[[Image:1pgq.jpg|left|200px]]<br /><applet load="1pgq" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1pgq.jpg|left|200px]]<br /><applet load="1pgq" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1pgq, resolution 3.17&Aring;" />
caption="1pgq, resolution 3.17&Aring;" />
'''CRYSTALLOGRAPHIC STUDY OF COENZYME, COENZYME ANALOGUE AND SUBSTRATE BINDING IN 6-PHOSPHOGLUCONATE DEHYDROGENASE: IMPLICATIONS FOR NADP SPECIFICITY AND THE ENZYME MECHANISM'''<br />
'''CRYSTALLOGRAPHIC STUDY OF COENZYME, COENZYME ANALOGUE AND SUBSTRATE BINDING IN 6-PHOSPHOGLUCONATE DEHYDROGENASE: IMPLICATIONS FOR NADP SPECIFICITY AND THE ENZYME MECHANISM'''<br />


==Overview==
==Overview==
BACKGROUND: The nicotinamide adenine dinucleotide phosphate, (NADP)-dependent oxidative decarboxylase, 6-phosphogluconate, dehydrogenase, is a major source of reduced coenzyme for synthesis., Enzymes later in the pentose phosphate pathway convert the reaction, product, ribulose 5-phosphate, to ribose 5-phosphate. Crystallographic, study of complexes with coenzyme and substrate explain the NADP dependence, which determines the enzyme's metabolic role and support the proposed, general base-general acid mechanism. RESULTS: The refined structures of, binary coenzyme/analogue complexes show that Arg33 is ordered by binding, the 2'-phosphate, and provides one face of the adenine site. The, nicotinamide, while less tightly bound, is more extended when reduced than, when oxidized. All substrate binding residues are conserved; the, 3-hydroxyl of 6-phosphogluconate is hydrogen bonded to N zeta of Lys183, and the 3-hydrogen points towards the oxidized nicotinamide. The, 6-phosphate replaces a tightly bound sulphate in the apo-enzyme., CONCLUSIONS: NADP specificity is achieved primarily by Arg33 which binds, the 2'-phosphate but, in its absence, obscures the adenine pocket. The, bound oxidized nicotinamide is syn; hydride transfer from bound substrate, to the nicotinamide si- face is achieved with a small movement of the, nicotinamide nucleotide. Lys183 may act as general base. A water bound to, Gly130 in the coenzyme domain is the most likely acid required in, decarboxylation. The dihydronicotinamide ring of NADPH competes for, ligands with the 1-carboxyl of 6-phosphogluconate.
BACKGROUND: The nicotinamide adenine dinucleotide phosphate (NADP)-dependent oxidative decarboxylase, 6-phosphogluconate dehydrogenase, is a major source of reduced coenzyme for synthesis. Enzymes later in the pentose phosphate pathway convert the reaction product, ribulose 5-phosphate, to ribose 5-phosphate. Crystallographic study of complexes with coenzyme and substrate explain the NADP dependence which determines the enzyme's metabolic role and support the proposed general base-general acid mechanism. RESULTS: The refined structures of binary coenzyme/analogue complexes show that Arg33 is ordered by binding the 2'-phosphate, and provides one face of the adenine site. The nicotinamide, while less tightly bound, is more extended when reduced than when oxidized. All substrate binding residues are conserved; the 3-hydroxyl of 6-phosphogluconate is hydrogen bonded to N zeta of Lys183 and the 3-hydrogen points towards the oxidized nicotinamide. The 6-phosphate replaces a tightly bound sulphate in the apo-enzyme. CONCLUSIONS: NADP specificity is achieved primarily by Arg33 which binds the 2'-phosphate but, in its absence, obscures the adenine pocket. The bound oxidized nicotinamide is syn; hydride transfer from bound substrate to the nicotinamide si- face is achieved with a small movement of the nicotinamide nucleotide. Lys183 may act as general base. A water bound to Gly130 in the coenzyme domain is the most likely acid required in decarboxylation. The dihydronicotinamide ring of NADPH competes for ligands with the 1-carboxyl of 6-phosphogluconate.


==About this Structure==
==About this Structure==
1PGQ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Ovis_aries Ovis aries] with SO4 and 2AM as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Phosphogluconate_dehydrogenase_(decarboxylating) Phosphogluconate dehydrogenase (decarboxylating)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.44 1.1.1.44] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1PGQ OCA].  
1PGQ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Ovis_aries Ovis aries] with <scene name='pdbligand=SO4:'>SO4</scene> and <scene name='pdbligand=2AM:'>2AM</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Phosphogluconate_dehydrogenase_(decarboxylating) Phosphogluconate dehydrogenase (decarboxylating)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.44 1.1.1.44] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PGQ OCA].  


==Reference==
==Reference==
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[[Category: Phosphogluconate dehydrogenase (decarboxylating)]]
[[Category: Phosphogluconate dehydrogenase (decarboxylating)]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Adams, M.J.]]
[[Category: Adams, M J.]]
[[Category: Gover, S.]]
[[Category: Gover, S.]]
[[Category: Phillips, C.]]
[[Category: Phillips, C.]]
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[[Category: oxidoreductase (choh(d)-nadp+(a))]]
[[Category: oxidoreductase (choh(d)-nadp+(a))]]


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