|
|
| Line 3: |
Line 3: |
| | <StructureSection load='2ccw' size='340' side='right'caption='[[2ccw]], [[Resolution|resolution]] 1.13Å' scene=''> | | <StructureSection load='2ccw' size='340' side='right'caption='[[2ccw]], [[Resolution|resolution]] 1.13Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[2ccw]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Alcaligenes_xylosoxydans Alcaligenes xylosoxydans]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2CCW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2CCW FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[2ccw]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Achromobacter_xylosoxidans Achromobacter xylosoxidans]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2CCW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2CCW FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CU1:COPPER+(I)+ION'>CU1</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.13Å</td></tr> |
| - | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat"><div style='overflow: auto; max-height: 3em;'>[[1dyz|1dyz]], [[1dz0|1dz0]]</div></td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CU1:COPPER+(I)+ION'>CU1</scene></td></tr> |
| | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2ccw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ccw OCA], [https://pdbe.org/2ccw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ccw RCSB], [https://www.ebi.ac.uk/pdbsum/2ccw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ccw ProSAT]</span></td></tr> | | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2ccw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ccw OCA], [https://pdbe.org/2ccw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ccw RCSB], [https://www.ebi.ac.uk/pdbsum/2ccw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ccw ProSAT]</span></td></tr> |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[https://www.uniprot.org/uniprot/AZUR2_ALCXX AZUR2_ALCXX]] Transfers electrons from cytochrome c551 to cytochrome oxidase.
| + | [https://www.uniprot.org/uniprot/AZUR2_ALCXX AZUR2_ALCXX] Transfers electrons from cytochrome c551 to cytochrome oxidase. |
| | == Evolutionary Conservation == | | == Evolutionary Conservation == |
| | [[Image:Consurf_key_small.gif|200px|right]] | | [[Image:Consurf_key_small.gif|200px|right]] |
| Line 36: |
Line 36: |
| | __TOC__ | | __TOC__ |
| | </StructureSection> | | </StructureSection> |
| - | [[Category: Alcaligenes xylosoxydans]] | + | [[Category: Achromobacter xylosoxidans]] |
| | [[Category: Large Structures]] | | [[Category: Large Structures]] |
| - | [[Category: Eady, R R]] | + | [[Category: Eady RR]] |
| - | [[Category: Hasnain, S S]] | + | [[Category: Hasnain SS]] |
| - | [[Category: Hough, M A]] | + | [[Category: Hough MA]] |
| - | [[Category: Paraskevopoulos, K]] | + | [[Category: Paraskevopoulos K]] |
| - | [[Category: Alcaligenes xylosoxidan]]
| + | |
| - | [[Category: Azurin ii]]
| + | |
| - | [[Category: Copper]]
| + | |
| - | [[Category: Cupredoxin]]
| + | |
| - | [[Category: Cuproprotein]]
| + | |
| - | [[Category: Electron transfer]]
| + | |
| - | [[Category: Electron transport]]
| + | |
| - | [[Category: Metal- binding]]
| + | |
| - | [[Category: Periplasmic]]
| + | |
| Structural highlights
Function
AZUR2_ALCXX Transfers electrons from cytochrome c551 to cytochrome oxidase.
Evolutionary Conservation
Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf.
Publication Abstract from PubMed
Understanding how the active site structures of blue copper proteins determine their redox properties is the central structure-function relationship question of this important class of protein, also referred to as cupredoxins. We here describe both experimental and computational studies of azurin, plastocyanin and stellacyanin designed to define more accurately the geometric structures of the active site of the reduced and oxidized species, and thus to understand how these structures determine the redox potentials of these proteins. To this end the crystal structure of reduced azurin II has been determined at an atomic resolution of 1.13 Angstrom and is presented here. Co-ordinates and structure factors have been deposited in the RCSB Protein Data Bank with accession codes 2ccw and r2ccwsf respectively. The improved accuracy provided by the atomic resolution for the metal stereochemistry are utilised in conjunction with the EXAFS data for theoretical calculations. Multilevel calculations involving density functional theory and molecular mechanical potentials are used to predict both the geometric and electronic structure of the active sites of azurin, plastocyanin and stellacyanin and to estimate the relative redox potentials of these three proteins. We have also compared the relative energies of the structures obtained from experiment at varying resolutions, and from the isolated and embedded cluster calculations. We find significant energy differences between low and high (atomic) resolution structures arising primarily due to inaccuracies in the Cu-ligand distances in the lower resolution structures, emphasising the importance of accurate, very high resolution structural information. QM/MM structures are only approximately 1 kcal mol(-1) lower in energy than the 1.13 Angstrom structure while the optimized gas phase structure is 13.0 kcal mol(-1) lower in energy.
Active site structures and the redox properties of blue copper proteins: atomic resolution structure of azurin II and electronic structure calculations of azurin, plastocyanin and stellacyanin.,Paraskevopoulos K, Sundararajan M, Surendran R, Hough MA, Eady RR, Hillier IH, Hasnain SS Dalton Trans. 2006 Jul 7;(25):3067-76. Epub 2006 Feb 23. PMID:16786065[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Paraskevopoulos K, Sundararajan M, Surendran R, Hough MA, Eady RR, Hillier IH, Hasnain SS. Active site structures and the redox properties of blue copper proteins: atomic resolution structure of azurin II and electronic structure calculations of azurin, plastocyanin and stellacyanin. Dalton Trans. 2006 Jul 7;(25):3067-76. Epub 2006 Feb 23. PMID:16786065 doi:10.1039/b513942b
|