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| ==Stable A-state hairpin of T4 fibritin foldon== | | ==Stable A-state hairpin of T4 fibritin foldon== |
- | <StructureSection load='1u0p' size='340' side='right'caption='[[1u0p]], [[NMR_Ensembles_of_Models | 10 NMR models]]' scene=''> | + | <StructureSection load='1u0p' size='340' side='right'caption='[[1u0p]]' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[1u0p]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Bpox2 Bpox2]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1U0P OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1U0P FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[1u0p]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Enterobacteria_phage_Ox2 Enterobacteria phage Ox2]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1U0P OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1U0P FirstGlance]. <br> |
- | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat"><div style='overflow: auto; max-height: 3em;'>[[1rfo|1rfo]]</div></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'>[https://proteopedia.org/fgij/fg.htm?mol=1u0p FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1u0p OCA], [https://pdbe.org/1u0p PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1u0p RCSB], [https://www.ebi.ac.uk/pdbsum/1u0p PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1u0p 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=1u0p FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1u0p OCA], [https://pdbe.org/1u0p PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1u0p RCSB], [https://www.ebi.ac.uk/pdbsum/1u0p PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1u0p ProSAT]</span></td></tr> |
| </table> | | </table> |
| + | == Function == |
| + | [https://www.uniprot.org/uniprot/Q38650_BPOX2 Q38650_BPOX2] |
| <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
- | [[Category: Bpox2]] | + | [[Category: Enterobacteria phage Ox2]] |
| [[Category: Large Structures]] | | [[Category: Large Structures]] |
- | [[Category: Grzesiek, S]] | + | [[Category: Grzesiek S]] |
- | [[Category: Guthe, S]] | + | [[Category: Guthe S]] |
- | [[Category: Kiefhaber, T]] | + | [[Category: Kiefhaber T]] |
- | [[Category: Meier, S]] | + | [[Category: Meier S]] |
- | [[Category: Beta-hairpin]]
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- | [[Category: Folding nucleus]]
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- | [[Category: Hairpin]]
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- | [[Category: Structural protein]]
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| Structural highlights
Function
Q38650_BPOX2
Publication Abstract from PubMed
The C-terminal domain of T4 fibritin (foldon) is obligatory for the formation of the fibritin trimer structure and can be used as an artificial trimerization domain. Its native structure consists of a trimeric beta-hairpin propeller. At low pH, the foldon trimer disintegrates into a monomeric (A-state) form that has similar properties as that of an early intermediate of the trimer folding pathway. The formation of this A-state monomer from the trimer, its structure, thermodynamic stability, equilibrium association and folding dynamics have been characterized to atomic detail by modern high-resolution NMR techniques. The foldon A-state monomer forms a beta-hairpin with intact and stable H-bonds that is similar to the monomer in the foldon trimer, but lacks a defined structure in its N and C-terminal parts. Its thermodynamic stability in pure water is comparable to designed hairpins stabilized in alcohol/water mixtures. Details of the thermal unfolding of the foldon A-state have been characterized by chemical shifts and residual dipolar couplings (RDCs) detected in inert, mechanically stretched polyacrylamide gels. At the onset of the thermal transition, uniform relative changes in RDC values indicate a uniform decrease of local N-HN and Calpha-Halpha order parameters for the hairpin strand residues. In contrast, near-turn residues show particular thermal stability in RDC values and hence in local order parameters. This coincides with increased transition temperatures of the beta-turn residues observed by chemical shifts. At high temperatures, the RDCs converge to non-zero average values consistent with predictions from random chain polymer models. Residue-specific deviations above the unfolding transition reveal the persistence of residual order around proline residues, large hydrophobic residues and at the beta-turn.
Foldon, the natural trimerization domain of T4 fibritin, dissociates into a monomeric A-state form containing a stable beta-hairpin: atomic details of trimer dissociation and local beta-hairpin stability from residual dipolar couplings.,Meier S, Guthe S, Kiefhaber T, Grzesiek S J Mol Biol. 2004 Dec 3;344(4):1051-69. PMID:15544812[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Meier S, Guthe S, Kiefhaber T, Grzesiek S. Foldon, the natural trimerization domain of T4 fibritin, dissociates into a monomeric A-state form containing a stable beta-hairpin: atomic details of trimer dissociation and local beta-hairpin stability from residual dipolar couplings. J Mol Biol. 2004 Dec 3;344(4):1051-69. PMID:15544812 doi:http://dx.doi.org/S0022-2836(04)01235-5
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