1aqv

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(New page: 200px<br /> <applet load="1aqv" size="450" color="white" frame="true" align="right" spinBox="true" caption="1aqv, resolution 1.94&Aring;" /> '''GLUTATHIONE S-TRANS...)
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<applet load="1aqv" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1aqv, resolution 1.94&Aring;" />
'''GLUTATHIONE S-TRANSFERASE IN COMPLEX WITH P-BROMOBENZYLGLUTATHIONE'''<br />
'''GLUTATHIONE S-TRANSFERASE IN COMPLEX WITH P-BROMOBENZYLGLUTATHIONE'''<br />
==Overview==
==Overview==
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The three-dimensional structure of human class pi glutathione, S-transferase from placenta (hGSTP1-1), a homodimeric enzyme, has been, solved by Patterson search methods and refined at 2.8 A resolution to a, final crystallographic R-factor of 19.6% (8.0 to 2.8 A resolution)., Subunit folding topology, subunit overall structure and subunit, association closely resembles the structure of porcine class pi, glutathione S-transferase. The binding site of a competitive inhibitor, S-hexylglutathione, is analyzed and the locations of the binding regions, for glutathione (G-site) and electrophilic substrates (H-site) are, determined. The specific interactions between protein and the inhibitor's, glutathione peptide are the same as those observed between glutathione, sulfonate and the porcine isozyme. The H-site is located adjacent to the, G-site, with the hexyl moiety lying above a segment (residues 8 to 10), connecting strand beta 1 and helix alpha A where it is in hydrophobic, contact with Tyr7, Phe8, Val10, Val35 and Tyr106. Catalytic models are, discussed on the basis of the molecular structure.
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The three-dimensional structure of human class pi glutathione S-transferase from placenta (hGSTP1-1), a homodimeric enzyme, has been solved by Patterson search methods and refined at 2.8 A resolution to a final crystallographic R-factor of 19.6% (8.0 to 2.8 A resolution). Subunit folding topology, subunit overall structure and subunit association closely resembles the structure of porcine class pi glutathione S-transferase. The binding site of a competitive inhibitor, S-hexylglutathione, is analyzed and the locations of the binding regions for glutathione (G-site) and electrophilic substrates (H-site) are determined. The specific interactions between protein and the inhibitor's glutathione peptide are the same as those observed between glutathione sulfonate and the porcine isozyme. The H-site is located adjacent to the G-site, with the hexyl moiety lying above a segment (residues 8 to 10) connecting strand beta 1 and helix alpha A where it is in hydrophobic contact with Tyr7, Phe8, Val10, Val35 and Tyr106. Catalytic models are discussed on the basis of the molecular structure.
==About this Structure==
==About this Structure==
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1AQV 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 MES as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Glutathione_transferase Glutathione transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.18 2.5.1.18] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1AQV OCA].
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1AQV 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=MES:'>MES</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Glutathione_transferase Glutathione transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.18 2.5.1.18] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1AQV OCA].
==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Fahl, W.E.]]
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[[Category: Fahl, W E.]]
[[Category: Huber, R.]]
[[Category: Huber, R.]]
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[[Category: Manoharan, T.H.]]
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[[Category: Manoharan, T H.]]
[[Category: Prade, L.]]
[[Category: Prade, L.]]
[[Category: Reuter, W.]]
[[Category: Reuter, W.]]
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[[Category: complex (transferase/peptide)]]
[[Category: complex (transferase/peptide)]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 16:01:18 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 11:47:21 2008''

Revision as of 09:47, 21 February 2008


1aqv, resolution 1.94Å

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GLUTATHIONE S-TRANSFERASE IN COMPLEX WITH P-BROMOBENZYLGLUTATHIONE

Overview

The three-dimensional structure of human class pi glutathione S-transferase from placenta (hGSTP1-1), a homodimeric enzyme, has been solved by Patterson search methods and refined at 2.8 A resolution to a final crystallographic R-factor of 19.6% (8.0 to 2.8 A resolution). Subunit folding topology, subunit overall structure and subunit association closely resembles the structure of porcine class pi glutathione S-transferase. The binding site of a competitive inhibitor, S-hexylglutathione, is analyzed and the locations of the binding regions for glutathione (G-site) and electrophilic substrates (H-site) are determined. The specific interactions between protein and the inhibitor's glutathione peptide are the same as those observed between glutathione sulfonate and the porcine isozyme. The H-site is located adjacent to the G-site, with the hexyl moiety lying above a segment (residues 8 to 10) connecting strand beta 1 and helix alpha A where it is in hydrophobic contact with Tyr7, Phe8, Val10, Val35 and Tyr106. Catalytic models are discussed on the basis of the molecular structure.

About this Structure

1AQV is a Single protein structure of sequence from Homo sapiens with as ligand. Active as Glutathione transferase, with EC number 2.5.1.18 Full crystallographic information is available from OCA.

Reference

Three-dimensional structure of class pi glutathione S-transferase from human placenta in complex with S-hexylglutathione at 2.8 A resolution., Reinemer P, Dirr HW, Ladenstein R, Huber R, Lo Bello M, Federici G, Parker MW, J Mol Biol. 1992 Sep 5;227(1):214-26. PMID:1522586

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