1l0n

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(New page: 200px<br /><applet load="1l0n" size="450" color="white" frame="true" align="right" spinBox="true" caption="1l0n, resolution 2.60&Aring;" /> '''native structure of ...)
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[[Image:1l0n.gif|left|200px]]<br /><applet load="1l0n" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1l0n.gif|left|200px]]<br /><applet load="1l0n" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1l0n, resolution 2.60&Aring;" />
caption="1l0n, resolution 2.60&Aring;" />
'''native structure of bovine mitochondrial cytochrome bc1 complex'''<br />
'''native structure of bovine mitochondrial cytochrome bc1 complex'''<br />
==Overview==
==Overview==
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Ubiquinol cytochrome c oxido-reductase (EC. 1.10.2.2, bc1) is an integral, membrane protein complex essential to cellular respiration. Structures of, the 11-subunit mitochondrial bc1 complex were determined with and without, the fungicide famoxadone. Specific inhibition by famoxadone is achieved, through a coordinated optimization of aromatic-aromatic interactions where, conformational rearrangements in famoxadone and in residues lining the, inhibitor-binding pocket produce a network of aromatic-aromatic, interactions that mimic the crystal lattice of benzene. The profound, aromatic-aromatic interactions as supported by prior mutagenesis provide a, structural basis for specific protein-ligand interaction in a hydrophobic, environment. Dramatic conformational changes, both in cyt. b and ISP, subunits in the inhibitor-protein complex, confer experimental evidence, for a functional role of cytochrome b in the induced conformational arrest, of ISP and allow the identification of a possible intrasubunit signal, transduction pathway that controls the movement of ISP. These results, support an inhibitory mechanism that is consistent with the requirement, for ISP movement in the electron transfer of this complex.
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Ubiquinol cytochrome c oxido-reductase (EC. 1.10.2.2, bc1) is an integral membrane protein complex essential to cellular respiration. Structures of the 11-subunit mitochondrial bc1 complex were determined with and without the fungicide famoxadone. Specific inhibition by famoxadone is achieved through a coordinated optimization of aromatic-aromatic interactions where conformational rearrangements in famoxadone and in residues lining the inhibitor-binding pocket produce a network of aromatic-aromatic interactions that mimic the crystal lattice of benzene. The profound aromatic-aromatic interactions as supported by prior mutagenesis provide a structural basis for specific protein-ligand interaction in a hydrophobic environment. Dramatic conformational changes, both in cyt. b and ISP subunits in the inhibitor-protein complex, confer experimental evidence for a functional role of cytochrome b in the induced conformational arrest of ISP and allow the identification of a possible intrasubunit signal transduction pathway that controls the movement of ISP. These results support an inhibitory mechanism that is consistent with the requirement for ISP movement in the electron transfer of this complex.
==About this Structure==
==About this Structure==
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1L0N is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with HEM and FES as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Ubiquinol--cytochrome-c_reductase Ubiquinol--cytochrome-c reductase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.10.2.2 1.10.2.2] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1L0N OCA].
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1L0N is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with <scene name='pdbligand=HEM:'>HEM</scene> and <scene name='pdbligand=FES:'>FES</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Ubiquinol--cytochrome-c_reductase Ubiquinol--cytochrome-c reductase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.10.2.2 1.10.2.2] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1L0N OCA].
==Reference==
==Reference==
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[[Category: Wen, X.]]
[[Category: Wen, X.]]
[[Category: Xia, D.]]
[[Category: Xia, D.]]
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[[Category: Yu, C.A.]]
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[[Category: Yu, C A.]]
[[Category: Yu, L.]]
[[Category: Yu, L.]]
[[Category: Zhang, L.]]
[[Category: Zhang, L.]]
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[[Category: mpp]]
[[Category: mpp]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 20:08:28 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:39:59 2008''

Revision as of 11:40, 21 February 2008


1l0n, resolution 2.60Å

Drag the structure with the mouse to rotate

native structure of bovine mitochondrial cytochrome bc1 complex

Overview

Ubiquinol cytochrome c oxido-reductase (EC. 1.10.2.2, bc1) is an integral membrane protein complex essential to cellular respiration. Structures of the 11-subunit mitochondrial bc1 complex were determined with and without the fungicide famoxadone. Specific inhibition by famoxadone is achieved through a coordinated optimization of aromatic-aromatic interactions where conformational rearrangements in famoxadone and in residues lining the inhibitor-binding pocket produce a network of aromatic-aromatic interactions that mimic the crystal lattice of benzene. The profound aromatic-aromatic interactions as supported by prior mutagenesis provide a structural basis for specific protein-ligand interaction in a hydrophobic environment. Dramatic conformational changes, both in cyt. b and ISP subunits in the inhibitor-protein complex, confer experimental evidence for a functional role of cytochrome b in the induced conformational arrest of ISP and allow the identification of a possible intrasubunit signal transduction pathway that controls the movement of ISP. These results support an inhibitory mechanism that is consistent with the requirement for ISP movement in the electron transfer of this complex.

About this Structure

1L0N is a Protein complex structure of sequences from Bos taurus with and as ligands. Active as Ubiquinol--cytochrome-c reductase, with EC number 1.10.2.2 Full crystallographic information is available from OCA.

Reference

The crystal structure of mitochondrial cytochrome bc1 in complex with famoxadone: the role of aromatic-aromatic interaction in inhibition., Gao X, Wen X, Yu C, Esser L, Tsao S, Quinn B, Zhang L, Yu L, Xia D, Biochemistry. 2002 Oct 1;41(39):11692-702. PMID:12269811

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