1p84
From Proteopedia
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- | [[Image:1p84.gif|left|200px]] | + | [[Image:1p84.gif|left|200px]] |
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- | '''HDBT inhibited Yeast Cytochrome bc1 Complex''' | + | {{Structure |
+ | |PDB= 1p84 |SIZE=350|CAPTION= <scene name='initialview01'>1p84</scene>, resolution 2.50Å | ||
+ | |SITE= | ||
+ | |LIGAND= <scene name='pdbligand=HEM:PROTOPORPHYRIN+IX+CONTAINING+FE'>HEM</scene>, <scene name='pdbligand=FES:FE2/S2+(INORGANIC)+CLUSTER'>FES</scene>, <scene name='pdbligand=DBT:5-HEPTYL-6-HYDROXY-1,3-BENZOTHIAZOLE-4,7-DIONE'>DBT</scene>, <scene name='pdbligand=UQ6:5-(3,7,11,15,19,23-HEXAMETHYL-TETRACOSA-2,6,10,14,18,22-HEXAENYL)-2,3-DIMETHOXY-6-METHYL-BENZENE-1,4-DIOL'>UQ6</scene>, <scene name='pdbligand=3PE:1,2-DIACYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE'>3PE</scene>, <scene name='pdbligand=3PH:1,2-DIACYL-GLYCEROL-3-SN-PHOSPHATE'>3PH</scene>, <scene name='pdbligand=PC1:1,2-DIACYL-SN-GLYCERO-3-PHOSPHOCHOLINE'>PC1</scene>, <scene name='pdbligand=UMQ:UNDECYL-MALTOSIDE'>UMQ</scene> and <scene name='pdbligand=CDL:CARDIOLIPIN'>CDL</scene> | ||
+ | |ACTIVITY= [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] | ||
+ | |GENE= | ||
+ | }} | ||
+ | |||
+ | '''HDBT inhibited Yeast Cytochrome bc1 Complex''' | ||
+ | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
- | 1P84 is a [ | + | 1P84 is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] and [http://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1P84 OCA]. |
==Reference== | ==Reference== | ||
- | Structure of the yeast cytochrome bc1 complex with a hydroxyquinone anion Qo site inhibitor bound., Palsdottir H, Lojero CG, Trumpower BL, Hunte C, J Biol Chem. 2003 Aug 15;278(33):31303-11. Epub 2003 Jun 2. PMID:[http:// | + | Structure of the yeast cytochrome bc1 complex with a hydroxyquinone anion Qo site inhibitor bound., Palsdottir H, Lojero CG, Trumpower BL, Hunte C, J Biol Chem. 2003 Aug 15;278(33):31303-11. Epub 2003 Jun 2. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/12782631 12782631] |
[[Category: Mus musculus]] | [[Category: Mus musculus]] | ||
[[Category: Protein complex]] | [[Category: Protein complex]] | ||
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[[Category: ubiquinol]] | [[Category: ubiquinol]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 13:21:08 2008'' |
Revision as of 11:21, 20 March 2008
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, resolution 2.50Å | |||||||
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Ligands: | , , , , , , , and | ||||||
Activity: | Ubiquinol--cytochrome-c reductase, with EC number 1.10.2.2 | ||||||
Coordinates: | save as pdb, mmCIF, xml |
HDBT inhibited Yeast Cytochrome bc1 Complex
Overview
Bifurcated electron transfer during ubiquinol oxidation is the key reaction of cytochrome bc1 complex catalysis. Binding of the competitive inhibitor 5-n-heptyl-6-hydroxy-4,7-dioxobenzothiazole to the Qo site of the cytochrome bc1 complex from Saccharomyces cerevisiae was analyzed by x-ray crystallography. This alkylhydroxydioxobenzothiazole is bound in its ionized form as evident from the crystal structure and confirmed by spectroscopic analysis, consistent with a measured pKa = 6.1 of the hydroxy group in detergent micelles. Stabilizing forces for the hydroxyquinone anion inhibitor include a polarized hydrogen bond to the iron-sulfur cluster ligand His181 and on-edge interactions via weak hydrogen bonds with cytochrome b residue Tyr279. The hydroxy group of the latter contributes to stabilization of the Rieske protein in the b-position by donating a hydrogen bond. The reported pH dependence of inhibition with lower efficacy at alkaline pH is attributed to the protonation state of His181 with a pKa of 7.5. Glu272, a proposed primary ligand and proton acceptor of ubiquinol, is not bound to the carbonyl group of the hydroxydioxobenzothiazole ring but is rotated out of the binding pocket toward the heme bL propionate A, to which it is hydrogen-bonded via a single water molecule. The observed hydrogen bonding pattern provides experimental evidence for the previously proposed proton exit pathway involving the heme propionate and a chain of water molecules. Binding of the alkyl-6-hydroxy-4,7-dioxobenzothiazole is discussed as resembling an intermediate step of ubiquinol oxidation, supporting a single occupancy model at the Qo site.
About this Structure
1P84 is a Protein complex structure of sequences from Mus musculus and Saccharomyces cerevisiae. Full crystallographic information is available from OCA.
Reference
Structure of the yeast cytochrome bc1 complex with a hydroxyquinone anion Qo site inhibitor bound., Palsdottir H, Lojero CG, Trumpower BL, Hunte C, J Biol Chem. 2003 Aug 15;278(33):31303-11. Epub 2003 Jun 2. PMID:12782631
Page seeded by OCA on Thu Mar 20 13:21:08 2008
Categories: Mus musculus | Protein complex | Saccharomyces cerevisiae | Ubiquinol--cytochrome-c reductase | Hunte, C. | Lojero, C G. | Palsdottir, H. | Trumpower, B L. | 3PE | 3PH | CDL | DBT | FES | HEM | PC1 | UMQ | UQ6 | Complex iii | Cytochrome bc1 complex | Cytochrome c oxidoreductase | Hhdbt | Hydroxyquinone | Membrane protein | Phospholipid | Qo site | Ubiquinol