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| <StructureSection load='1b0y' size='340' side='right'caption='[[1b0y]], [[Resolution|resolution]] 0.93Å' scene=''> | | <StructureSection load='1b0y' size='340' side='right'caption='[[1b0y]], [[Resolution|resolution]] 0.93Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[1b0y]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/"bacillus_vinosus"_(ehrenberg_1838)_trevisan_1889 "bacillus vinosus" (ehrenberg 1838) trevisan 1889]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1B0Y OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1B0Y FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[1b0y]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Allochromatium_vinosum Allochromatium vinosum]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1B0Y OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1B0Y FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=SF4:IRON/SULFUR+CLUSTER'>SF4</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]] 0.93Å</td></tr> |
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=SF4:IRON/SULFUR+CLUSTER'>SF4</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=1b0y FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1b0y OCA], [https://pdbe.org/1b0y PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1b0y RCSB], [https://www.ebi.ac.uk/pdbsum/1b0y PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1b0y 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=1b0y FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1b0y OCA], [https://pdbe.org/1b0y PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1b0y RCSB], [https://www.ebi.ac.uk/pdbsum/1b0y PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1b0y ProSAT]</span></td></tr> |
| </table> | | </table> |
| == Function == | | == Function == |
- | [[https://www.uniprot.org/uniprot/HIP_ALLVD HIP_ALLVD]] Specific class of high-redox-potential 4Fe-4S ferredoxins. Functions in anaerobic electron transport in most purple and in some other photosynthetic bacteria and in at least one genus (Paracoccus) of halophilic, denitrifying bacteria.
| + | [https://www.uniprot.org/uniprot/HIP_ALLVD HIP_ALLVD] Specific class of high-redox-potential 4Fe-4S ferredoxins. Functions in anaerobic electron transport in most purple and in some other photosynthetic bacteria and in at least one genus (Paracoccus) of halophilic, denitrifying bacteria. |
| == Evolutionary Conservation == | | == Evolutionary Conservation == |
| [[Image:Consurf_key_small.gif|200px|right]] | | [[Image:Consurf_key_small.gif|200px|right]] |
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| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
| + | [[Category: Allochromatium vinosum]] |
| [[Category: Large Structures]] | | [[Category: Large Structures]] |
- | [[Category: Sheldrick, G M]] | + | [[Category: Sheldrick GM]] |
- | [[Category: Atomic resolution]]
| + | |
- | [[Category: Direct methods iron-sulphur cluster]]
| + | |
- | [[Category: Electron transfer protein]]
| + | |
- | [[Category: Electron transport]]
| + | |
- | [[Category: Metalloprotein]]
| + | |
| Structural highlights
Function
HIP_ALLVD Specific class of high-redox-potential 4Fe-4S ferredoxins. Functions in anaerobic electron transport in most purple and in some other photosynthetic bacteria and in at least one genus (Paracoccus) of halophilic, denitrifying bacteria.
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
The crystal structure of the reduced high-potential iron protein (HiPIP) from Chromatium vinosum has been redetermined in a new orthorhombic crystal modification, and the structure of its H42Q mutant has been determined in orthorhombic (H42Q-1) and cubic (H42Q-2) modifications. The first two were solved by ab initio direct methods using data collected to atomic resolution (1.20 and 0. 93 A, respectively). The recombinant wild type (rc-WT) with two HiPIP molecules in the asymmetric unit has 1264 protein atoms and 335 solvent sites, and is the second largest structure reported so far that has been solved by pure direct methods. The solutions were obtained in a fully automated way and included more than 80% of the protein atoms. Restrained anisotropic refinement for rc-WT and H42Q-1 converged to R(1) = summation operator||F(o)| - |F(c)|| / summation operator|F(o)| of 12.0 and 13.6%, respectively [data with I > 2sigma(I)], and 12.8 and 15.5% (all data). H42Q-2 contains two molecules in the asymmetric unit and diffracted only to 2.6 A. In both molecules of rc-WT and in the single unique molecule of H42Q-1 the [Fe(4)S(4)](2+) cluster dimensions are very similar and show a characteristic tetragonal distortion with four short Fe-S bonds along four approximately parallel cube edges, and eight long Fe-S bonds. The unique protein molecules in H42Q-2 and rc-WT are also very similar in other respects, except for the hydrogen bonding around the mutated residue that is at the surface of the protein, supporting the hypothesis that the difference in redox potentials at lower pH values is caused primarily by differences in the charge distribution near the surface of the protein rather than by structural differences in the cluster region.
Ab initio solution and refinement of two high-potential iron protein structures at atomic resolution.,Parisini E, Capozzi F, Lubini P, Lamzin V, Luchinat C, Sheldrick GM Acta Crystallogr D Biol Crystallogr. 1999 Nov;55(Pt 11):1773-84. PMID:10531472[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Parisini E, Capozzi F, Lubini P, Lamzin V, Luchinat C, Sheldrick GM. Ab initio solution and refinement of two high-potential iron protein structures at atomic resolution. Acta Crystallogr D Biol Crystallogr. 1999 Nov;55(Pt 11):1773-84. PMID:10531472
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