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| ==Putative methyltransferase yhhF from Escherichia coli.== | | ==Putative methyltransferase yhhF from Escherichia coli.== |
- | <StructureSection load='2fpo' size='340' side='right' caption='[[2fpo]], [[Resolution|resolution]] 2.05Å' scene=''> | + | <StructureSection load='2fpo' size='340' side='right'caption='[[2fpo]], [[Resolution|resolution]] 2.05Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[2fpo]] is a 6 chain structure with sequence from [http://en.wikipedia.org/wiki/Ecoli Ecoli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FPO OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2FPO FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[2fpo]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Escherichia_coli_K-12 Escherichia coli K-12]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FPO OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2FPO FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</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]] 2.05Å</td></tr> |
- | <tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr> |
- | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">yhhF ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=83333 ECOLI])</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=2fpo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2fpo OCA], [https://pdbe.org/2fpo PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2fpo RCSB], [https://www.ebi.ac.uk/pdbsum/2fpo PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2fpo ProSAT], [https://www.topsan.org/Proteins/MCSG/2fpo TOPSAN]</span></td></tr> |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2fpo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2fpo OCA], [http://pdbe.org/2fpo PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2fpo RCSB], [http://www.ebi.ac.uk/pdbsum/2fpo PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=2fpo ProSAT], [http://www.topsan.org/Proteins/MCSG/2fpo TOPSAN]</span></td></tr> | + | |
| </table> | | </table> |
| == Function == | | == Function == |
- | [[http://www.uniprot.org/uniprot/RSMD_ECOLI RSMD_ECOLI]] Specifically methylates the guanine in position 966 of 16S rRNA in the assembled 30S particle.<ref>PMID:17189261</ref> | + | [https://www.uniprot.org/uniprot/RSMD_ECOLI RSMD_ECOLI] Specifically methylates the guanine in position 966 of 16S rRNA in the assembled 30S particle.<ref>PMID:17189261</ref> |
| == Evolutionary Conservation == | | == Evolutionary Conservation == |
| [[Image:Consurf_key_small.gif|200px|right]] | | [[Image:Consurf_key_small.gif|200px|right]] |
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| <jmolCheckbox> | | <jmolCheckbox> |
| <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/fp/2fpo_consurf.spt"</scriptWhenChecked> | | <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/fp/2fpo_consurf.spt"</scriptWhenChecked> |
- | <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked> | + | <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview03.spt</scriptWhenUnchecked> |
| <text>to colour the structure by Evolutionary Conservation</text> | | <text>to colour the structure by Evolutionary Conservation</text> |
| </jmolCheckbox> | | </jmolCheckbox> |
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| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
- | [[Category: Ecoli]] | + | [[Category: Escherichia coli K-12]] |
- | [[Category: Edwards, A]] | + | [[Category: Large Structures]] |
- | [[Category: Evdokimova, E]] | + | [[Category: Edwards A]] |
- | [[Category: Joachimiak, A]] | + | [[Category: Evdokimova E]] |
- | [[Category: Kim, Y]] | + | [[Category: Joachimiak A]] |
- | [[Category: Structural genomic]]
| + | [[Category: Kim Y]] |
- | [[Category: Osipiuk, J]] | + | [[Category: Osipiuk J]] |
- | [[Category: Sanishvili, R]] | + | [[Category: Sanishvili R]] |
- | [[Category: Savchenko, A]] | + | [[Category: Savchenko A]] |
- | [[Category: Skarina, T]] | + | [[Category: Skarina T]] |
- | [[Category: Mcsg]]
| + | |
- | [[Category: PSI, Protein structure initiative]]
| + | |
- | [[Category: Putative methyltransferase]]
| + | |
- | [[Category: Transferase]]
| + | |
| Structural highlights
Function
RSMD_ECOLI Specifically methylates the guanine in position 966 of 16S rRNA in the assembled 30S particle.[1]
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
N(2)-Methylguanine 966 is located in the loop of Escherichia coli 16 S rRNA helix 31, forming a part of the P-site tRNA-binding pocket. We found yhhF to be a gene encoding for m(2)G966 specific 16 S rRNA methyltransferase. Disruption of the yhhF gene by kanamycin resistance marker leads to a loss of modification at G966. The modification could be rescued by expression of recombinant protein from the plasmid carrying the yhhF gene. Moreover, purified m(2)G966 methyltransferase, in the presence of S-adenosylomethionine (AdoMet), is able to methylate 30 S ribosomal subunits that were purified from yhhF knock-out strain in vitro. The methylation is specific for G966 base of the 16 S rRNA. The m(2)G966 methyltransferase was crystallized, and its structure has been determined and refined to 2.05A(.) The structure closely resembles RsmC rRNA methyltransferase, specific for m(2)G1207 of the 16 S rRNA. Structural comparisons and analysis of the enzyme active site suggest modes for binding AdoMet and rRNA to m(2)G966 methyltransferase. Based on the experimental data and current nomenclature the protein expressed from the yhhF gene was renamed to RsmD. A model for interaction of RsmD with ribosome has been proposed.
Methyltransferase that modifies guanine 966 of the 16 S rRNA: functional identification and tertiary structure.,Lesnyak DV, Osipiuk J, Skarina T, Sergiev PV, Bogdanov AA, Edwards A, Savchenko A, Joachimiak A, Dontsova OA J Biol Chem. 2007 Feb 23;282(8):5880-7. Epub 2006 Dec 21. PMID:17189261[2]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Lesnyak DV, Osipiuk J, Skarina T, Sergiev PV, Bogdanov AA, Edwards A, Savchenko A, Joachimiak A, Dontsova OA. Methyltransferase that modifies guanine 966 of the 16 S rRNA: functional identification and tertiary structure. J Biol Chem. 2007 Feb 23;282(8):5880-7. Epub 2006 Dec 21. PMID:17189261 doi:10.1074/jbc.M608214200
- ↑ Lesnyak DV, Osipiuk J, Skarina T, Sergiev PV, Bogdanov AA, Edwards A, Savchenko A, Joachimiak A, Dontsova OA. Methyltransferase that modifies guanine 966 of the 16 S rRNA: functional identification and tertiary structure. J Biol Chem. 2007 Feb 23;282(8):5880-7. Epub 2006 Dec 21. PMID:17189261 doi:10.1074/jbc.M608214200
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