|
|
(One intermediate revision not shown.) |
Line 1: |
Line 1: |
| | | |
| ==Solution structure of Thermus thermophilus HB8 TTHA1718 protein in living E. coli cells== | | ==Solution structure of Thermus thermophilus HB8 TTHA1718 protein in living E. coli cells== |
- | <StructureSection load='2rog' size='340' side='right'caption='[[2rog]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | + | <StructureSection load='2rog' size='340' side='right'caption='[[2rog]]' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[2rog]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/"flavobacterium_thermophilum"_yoshida_and_oshima_1971 "flavobacterium thermophilum" yoshida and oshima 1971]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2ROG OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=2ROG FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[2rog]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Thermus_thermophilus Thermus thermophilus]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2ROG OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2ROG FirstGlance]. <br> |
- | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2roe|2roe]]</td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr> |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=2rog FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2rog OCA], [http://pdbe.org/2rog PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2rog RCSB], [http://www.ebi.ac.uk/pdbsum/2rog PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=2rog 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=2rog FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2rog OCA], [https://pdbe.org/2rog PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2rog RCSB], [https://www.ebi.ac.uk/pdbsum/2rog PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2rog ProSAT]</span></td></tr> |
| </table> | | </table> |
| + | == Function == |
| + | [https://www.uniprot.org/uniprot/Q5SHL2_THET8 Q5SHL2_THET8] |
| == Evolutionary Conservation == | | == Evolutionary Conservation == |
| [[Image:Consurf_key_small.gif|200px|right]] | | [[Image:Consurf_key_small.gif|200px|right]] |
Line 30: |
Line 32: |
| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
- | [[Category: Flavobacterium thermophilum yoshida and oshima 1971]] | |
| [[Category: Large Structures]] | | [[Category: Large Structures]] |
- | [[Category: Guentert, P]] | + | [[Category: Thermus thermophilus]] |
- | [[Category: Hamatsu, J]] | + | [[Category: Guentert P]] |
- | [[Category: Ikeya, T]] | + | [[Category: Hamatsu J]] |
- | [[Category: Ito, Y]] | + | [[Category: Ikeya T]] |
- | [[Category: Koyama, H]] | + | [[Category: Ito Y]] |
- | [[Category: Mikawa, T]] | + | [[Category: Koyama H]] |
- | [[Category: Mishima, M]] | + | [[Category: Mikawa T]] |
- | [[Category: Sakakibara, D]] | + | [[Category: Mishima M]] |
- | [[Category: Sasaki, A]] | + | [[Category: Sakakibara D]] |
- | [[Category: Shirakawa, M]] | + | [[Category: Sasaki A]] |
- | [[Category: Smith, B O]] | + | [[Category: Shirakawa M]] |
- | [[Category: Waelchli, M]] | + | [[Category: Smith BO]] |
- | [[Category: Metal binding protein]]
| + | [[Category: Waelchli M]] |
- | [[Category: Protein]]
| + | |
| Structural highlights
Function
Q5SHL2_THET8
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
Investigating proteins 'at work' in a living environment at atomic resolution is a major goal of molecular biology, which has not been achieved even though methods for the three-dimensional (3D) structure determination of purified proteins in single crystals or in solution are widely used. Recent developments in NMR hardware and methodology have enabled the measurement of high-resolution heteronuclear multi-dimensional NMR spectra of macromolecules in living cells (in-cell NMR). Various intracellular events such as conformational changes, dynamics and binding events have been investigated by this method. However, the low sensitivity and the short lifetime of the samples have so far prevented the acquisition of sufficient structural information to determine protein structures by in-cell NMR. Here we show the first, to our knowledge, 3D protein structure calculated exclusively on the basis of information obtained in living cells. The structure of the putative heavy-metal binding protein TTHA1718 from Thermus thermophilus HB8 overexpressed in Escherichia coli cells was solved by in-cell NMR. Rapid measurement of the 3D NMR spectra by nonlinear sampling of the indirectly acquired dimensions was used to overcome problems caused by the instability and low sensitivity of living E. coli samples. Almost all of the expected backbone NMR resonances and most of the side-chain NMR resonances were observed and assigned, enabling high quality (0.96 angstrom backbone root mean squared deviation) structures to be calculated that are very similar to the in vitro structure of TTHA1718 determined independently. The in-cell NMR approach can thus provide accurate high-resolution structures of proteins in living environments.
Protein structure determination in living cells by in-cell NMR spectroscopy.,Sakakibara D, Sasaki A, Ikeya T, Hamatsu J, Hanashima T, Mishima M, Yoshimasu M, Hayashi N, Mikawa T, Walchli M, Smith BO, Shirakawa M, Guntert P, Ito Y Nature. 2009 Mar 5;458(7234):102-5. PMID:19262674[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Sakakibara D, Sasaki A, Ikeya T, Hamatsu J, Hanashima T, Mishima M, Yoshimasu M, Hayashi N, Mikawa T, Walchli M, Smith BO, Shirakawa M, Guntert P, Ito Y. Protein structure determination in living cells by in-cell NMR spectroscopy. Nature. 2009 Mar 5;458(7234):102-5. PMID:19262674 doi:10.1038/nature07814
|