1u31

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(New page: 200px<br /> <applet load="1u31" size="450" color="white" frame="true" align="right" spinBox="true" caption="1u31, resolution 2.20&Aring;" /> '''recombinant human h...)
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[[Image:1u31.gif|left|200px]]<br />
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[[Image:1u31.gif|left|200px]]<br /><applet load="1u31" size="350" color="white" frame="true" align="right" spinBox="true"
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<applet load="1u31" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1u31, resolution 2.20&Aring;" />
caption="1u31, resolution 2.20&Aring;" />
'''recombinant human heart transhydrogenase dIII bound with NADPH'''<br />
'''recombinant human heart transhydrogenase dIII bound with NADPH'''<br />
==Overview==
==Overview==
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Transhydrogenase couples the redox (hydride-transfer) reaction between, NAD(H) and NADP(H) to proton translocation across a membrane. The redox, reaction is catalyzed at the interface between two components (dI and, dIII) which protrude from the membrane. A complex formed from recombinant, dI and dIII (the dI(2)dIII(1) complex) from Rhodospirillum rubrum, transhydrogenase catalyzes fast single-turnover hydride transfer between, bound nucleotides. In this report we describe three new crystal structures, of the dI(2)dIII(1) complex in different nucleotide-bound forms. The, structures reveal an asymmetry in nucleotide binding that complements, results from solution studies and supports the notion that intact, transhydrogenase functions by an alternating site mechanism. In one, structure, the redox site is occupied by NADH (on dI) and NADPH (on dIII)., The dihydronicotinamide rings take up positions which may approximate to, the ground state for hydride transfer: the redox-active C4(N) atoms are, separated by only 3.6 A, and the perceived reaction stereochemistry, matches that observed experimentally. The NADH conformation is different, in the two dI polypeptides of this form of the dI(2)dIII(1) complex., Comparisons between a number of X-ray structures show that a, conformational change in the NADH is driven by relative movement of the, two domains which comprise dI. It is suggested that an equivalent, conformational change in the intact enzyme is important in gating the, hydride-transfer reaction. The observed nucleotide conformational change, in the dI(2)dIII(1) complex is accompanied by rearrangements in the, orientation of local amino acid side chains which may be responsible for, sealing the site from the solvent and polarizing hydride transfer.
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Transhydrogenase couples the redox (hydride-transfer) reaction between NAD(H) and NADP(H) to proton translocation across a membrane. The redox reaction is catalyzed at the interface between two components (dI and dIII) which protrude from the membrane. A complex formed from recombinant dI and dIII (the dI(2)dIII(1) complex) from Rhodospirillum rubrum transhydrogenase catalyzes fast single-turnover hydride transfer between bound nucleotides. In this report we describe three new crystal structures of the dI(2)dIII(1) complex in different nucleotide-bound forms. The structures reveal an asymmetry in nucleotide binding that complements results from solution studies and supports the notion that intact transhydrogenase functions by an alternating site mechanism. In one structure, the redox site is occupied by NADH (on dI) and NADPH (on dIII). The dihydronicotinamide rings take up positions which may approximate to the ground state for hydride transfer: the redox-active C4(N) atoms are separated by only 3.6 A, and the perceived reaction stereochemistry matches that observed experimentally. The NADH conformation is different in the two dI polypeptides of this form of the dI(2)dIII(1) complex. Comparisons between a number of X-ray structures show that a conformational change in the NADH is driven by relative movement of the two domains which comprise dI. It is suggested that an equivalent conformational change in the intact enzyme is important in gating the hydride-transfer reaction. The observed nucleotide conformational change in the dI(2)dIII(1) complex is accompanied by rearrangements in the orientation of local amino acid side chains which may be responsible for sealing the site from the solvent and polarizing hydride transfer.
==About this Structure==
==About this Structure==
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1U31 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, NAP and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/NAD(P)(+)_transhydrogenase_(AB-specific) NAD(P)(+) transhydrogenase (AB-specific)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.6.1.2 1.6.1.2] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1U31 OCA].
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1U31 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>, <scene name='pdbligand=NAP:'>NAP</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/NAD(P)(+)_transhydrogenase_(AB-specific) NAD(P)(+) transhydrogenase (AB-specific)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.6.1.2 1.6.1.2] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1U31 OCA].
==Reference==
==Reference==
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[[Category: NAD(P)(+) transhydrogenase (AB-specific)]]
[[Category: NAD(P)(+) transhydrogenase (AB-specific)]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Boxel, G.I.van.]]
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[[Category: Boxel, G I.van.]]
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[[Category: Jackson, J.B.]]
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[[Category: Jackson, J B.]]
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[[Category: Mather, O.C.]]
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[[Category: Mather, O C.]]
[[Category: Singh, A.]]
[[Category: Singh, A.]]
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[[Category: White, S.A.]]
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[[Category: White, S A.]]
[[Category: GOL]]
[[Category: GOL]]
[[Category: NAP]]
[[Category: NAP]]
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[[Category: oxidoreductase]]
[[Category: oxidoreductase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 19:30:44 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:20:04 2008''

Revision as of 13:20, 21 February 2008


1u31, resolution 2.20Å

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recombinant human heart transhydrogenase dIII bound with NADPH

Overview

Transhydrogenase couples the redox (hydride-transfer) reaction between NAD(H) and NADP(H) to proton translocation across a membrane. The redox reaction is catalyzed at the interface between two components (dI and dIII) which protrude from the membrane. A complex formed from recombinant dI and dIII (the dI(2)dIII(1) complex) from Rhodospirillum rubrum transhydrogenase catalyzes fast single-turnover hydride transfer between bound nucleotides. In this report we describe three new crystal structures of the dI(2)dIII(1) complex in different nucleotide-bound forms. The structures reveal an asymmetry in nucleotide binding that complements results from solution studies and supports the notion that intact transhydrogenase functions by an alternating site mechanism. In one structure, the redox site is occupied by NADH (on dI) and NADPH (on dIII). The dihydronicotinamide rings take up positions which may approximate to the ground state for hydride transfer: the redox-active C4(N) atoms are separated by only 3.6 A, and the perceived reaction stereochemistry matches that observed experimentally. The NADH conformation is different in the two dI polypeptides of this form of the dI(2)dIII(1) complex. Comparisons between a number of X-ray structures show that a conformational change in the NADH is driven by relative movement of the two domains which comprise dI. It is suggested that an equivalent conformational change in the intact enzyme is important in gating the hydride-transfer reaction. The observed nucleotide conformational change in the dI(2)dIII(1) complex is accompanied by rearrangements in the orientation of local amino acid side chains which may be responsible for sealing the site from the solvent and polarizing hydride transfer.

About this Structure

1U31 is a Single protein structure of sequence from Homo sapiens with , and as ligands. Active as NAD(P)(+) transhydrogenase (AB-specific), with EC number 1.6.1.2 Full crystallographic information is available from OCA.

Reference

Active-site conformational changes associated with hydride transfer in proton-translocating transhydrogenase., Mather OC, Singh A, van Boxel GI, White SA, Jackson JB, Biochemistry. 2004 Aug 31;43(34):10952-64. PMID:15323555

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