2hm6: Difference between revisions
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< | ==Nematocyst outer wall antigen, NW1 G11V K21P== | ||
<StructureSection load='2hm6' size='340' side='right'caption='[[2hm6]]' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[2hm6]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Hydra_vulgaris Hydra vulgaris]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2HM6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2HM6 FirstGlance]. <br> | |||
</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=2hm6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2hm6 OCA], [https://pdbe.org/2hm6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2hm6 RCSB], [https://www.ebi.ac.uk/pdbsum/2hm6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2hm6 ProSAT]</span></td></tr> | |||
</table> | |||
== Function == | |||
[https://www.uniprot.org/uniprot/Q8IT70_HYDVU Q8IT70_HYDVU] | |||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Protein structures cluster into families of folds that can result from extremely different amino acid sequences [1]. Because the enormous amount of genetic information generates a limited number of protein folds [2], a particular domain structure often assumes numerous functions. How new protein structures and new functions evolve under these limitations remains elusive. Molecular evolution may be driven by the ability of biomacromolecules to adopt multiple conformations as a bridge between different folds [3-6]. This could allow proteins to explore new structures and new tasks while part of the structural ensemble retains the initial conformation and function as a safeguard [7]. Here we show that a global structural switch can arise from single amino acid changes in cysteine-rich domains (CRD) of cnidarian nematocyst proteins. The ability of these CRDs to form two structures with different disulfide patterns from an identical cysteine pattern is distinctive [8]. By applying a structure-based mutagenesis approach, we demonstrate that a cysteine-rich domain can interconvert between two natively occurring domain structures via a bridge state containing both structures. Comparing cnidarian CRD sequences leads us to believe that the mutations we introduced to stabilize each structure reflect the birth of new protein folds in evolution. | |||
Continuous molecular evolution of protein-domain structures by single amino acid changes.,Meier S, Jensen PR, David CN, Chapman J, Holstein TW, Grzesiek S, Ozbek S Curr Biol. 2007 Jan 23;17(2):173-8. PMID:17240343<ref>PMID:17240343</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
</div> | |||
<div class="pdbe-citations 2hm6" style="background-color:#fffaf0;"></div> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
== | |||
== | |||
[[Category: Hydra vulgaris]] | [[Category: Hydra vulgaris]] | ||
[[Category: | [[Category: Large Structures]] | ||
[[Category: Grzesiek | [[Category: Grzesiek S]] | ||
[[Category: Jensen | [[Category: Jensen PR]] | ||
[[Category: Meier | [[Category: Meier S]] | ||
[[Category: Oezbek | [[Category: Oezbek S]] | ||
Latest revision as of 16:06, 26 July 2023
Nematocyst outer wall antigen, NW1 G11V K21PNematocyst outer wall antigen, NW1 G11V K21P
Structural highlights
FunctionPublication Abstract from PubMedProtein structures cluster into families of folds that can result from extremely different amino acid sequences [1]. Because the enormous amount of genetic information generates a limited number of protein folds [2], a particular domain structure often assumes numerous functions. How new protein structures and new functions evolve under these limitations remains elusive. Molecular evolution may be driven by the ability of biomacromolecules to adopt multiple conformations as a bridge between different folds [3-6]. This could allow proteins to explore new structures and new tasks while part of the structural ensemble retains the initial conformation and function as a safeguard [7]. Here we show that a global structural switch can arise from single amino acid changes in cysteine-rich domains (CRD) of cnidarian nematocyst proteins. The ability of these CRDs to form two structures with different disulfide patterns from an identical cysteine pattern is distinctive [8]. By applying a structure-based mutagenesis approach, we demonstrate that a cysteine-rich domain can interconvert between two natively occurring domain structures via a bridge state containing both structures. Comparing cnidarian CRD sequences leads us to believe that the mutations we introduced to stabilize each structure reflect the birth of new protein folds in evolution. Continuous molecular evolution of protein-domain structures by single amino acid changes.,Meier S, Jensen PR, David CN, Chapman J, Holstein TW, Grzesiek S, Ozbek S Curr Biol. 2007 Jan 23;17(2):173-8. PMID:17240343[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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