View source for 1grf

[[Image:1grf.jpg|left|200px]]<br /><applet load="1grf" size="350" color="white" frame="true" align="right" spinBox="true" 
caption="1grf, resolution 2.0&Aring;" />
'''SUBSTRATE BINDING AND CATALYSIS BY GLUTATHIONE REDUCTASE AS DERIVED FROM REFINED ENZYME: SUBSTRATE CRYSTAL STRUCTURES AT 2 ANGSTROMS RESOLUTION'''<br />

==Overview==
The X-ray structure analyses of four glutathione reductase complexes and, derivatives have been extended to 2 A resolution and refined. The results, are discussed in conjunction with the structure of the oxidized native, enzyme known at 1.54 A resolution. While the residual co-ordinate errors, are around 0.2 A, some significant shifts even in this range could be, established. Points of particular interest are the 3.2 A approach of C4N, of nicotinamide to N5F of flavin in hydride transfer geometry, the, hydrogen bond geometries of the 2'-phosphate of NADPH as compared to, inferior geometries for an inorganic phosphate binding together with NADH, the differential mobilities of parts of the substrates as derived from, refined atomic temperature factors, and the stabilization of the thiolate, of the proximal Cys63 by conformational changes of neighboring residues as, well as by flavin. In addition, catalytically competent His467' is seen to, interact more optimally with the sulfur of glutathione-I than with the, distal sulfur of Cys58. The observed participation of water molecules for, both NADPH and glutathione binding is so extensive that a prediction of, the binding mode merely from the polypeptide structure would be very, difficult. The accurately known geometries allowed us to draw some, conclusions on the enzyme mechanism and suggest a possible scenario of the, catalysis.

==Disease==
Known diseases associated with this structure: Hemolytic anemia due to glutathione reductase deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138300 138300]], Mental retardation, autosomal recessive, 6 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138244 138244]]

==About this Structure==
1GRF 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=PO4:'>PO4</scene>, <scene name='pdbligand=FAD:'>FAD</scene> and <scene name='pdbligand=ACM:'>ACM</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Glutathione-disulfide_reductase Glutathione-disulfide reductase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.8.1.7 1.8.1.7] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1GRF OCA]. 

==Reference==
Substrate binding and catalysis by glutathione reductase as derived from refined enzyme: substrate crystal structures at 2 A resolution., Karplus PA, Schulz GE, J Mol Biol. 1989 Nov 5;210(1):163-80. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=2585516 2585516]
[[Category: Glutathione-disulfide reductase]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Karplus, P.A.]]
[[Category: Schulz, G.E.]]
[[Category: ACM]]
[[Category: FAD]]
[[Category: PO4]]
[[Category: oxidoreductase(flavoenzyme)]]

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