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6S97

Fragment transplantation onto a hyperstable ancestor of haloalkane dehalogenases and Renilla luciferase (Anc-FT)

Summary for 6S97
Entry DOI10.2210/pdb6s97/pdb
Related6S6E
DescriptorFragment transplantation onto hyperstable ancestor of haloalkane dehalogenases and Renilla luciferase (Anc-FT) (2 entities in total)
Functional Keywordsfragment transplantation, ancestral enzyme, bioluminscence, coelenterazine-utilizing enzyme, luminescent protein
Biological sourceRenilla reniformis
Total number of polymer chains1
Total formula weight33877.28
Authors
Schenkmayerova, A.,Damborsky, J.,Marek, M. (deposition date: 2019-07-11, release date: 2020-08-26, Last modification date: 2024-06-19)
Primary citationSchenkmayerova, A.,Pinto, G.P.,Toul, M.,Marek, M.,Hernychova, L.,Planas-Iglesias, J.,Daniel Liskova, V.,Pluskal, D.,Vasina, M.,Emond, S.,Dorr, M.,Chaloupkova, R.,Bednar, D.,Prokop, Z.,Hollfelder, F.,Bornscheuer, U.T.,Damborsky, J.
Engineering the protein dynamics of an ancestral luciferase.
Nat Commun, 12:3616-3616, 2021
Cited by
PubMed Abstract: Protein dynamics are often invoked in explanations of enzyme catalysis, but their design has proven elusive. Here we track the role of dynamics in evolution, starting from the evolvable and thermostable ancestral protein Anc which catalyses both dehalogenase and luciferase reactions. Insertion-deletion (InDel) backbone mutagenesis of Anc challenged the scaffold dynamics. Screening for both activities reveals InDel mutations localized in three distinct regions that lead to altered protein dynamics (based on crystallographic B-factors, hydrogen exchange, and molecular dynamics simulations). An anisotropic network model highlights the importance of the conformational flexibility of a loop-helix fragment of Renilla luciferases for ligand binding. Transplantation of this dynamic fragment leads to lower product inhibition and highly stable glow-type bioluminescence. The success of our approach suggests that a strategy comprising (i) constructing a stable and evolvable template, (ii) mapping functional regions by backbone mutagenesis, and (iii) transplantation of dynamic features, can lead to functionally innovative proteins.
PubMed: 34127663
DOI: 10.1038/s41467-021-23450-z
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.953 Å)
Structure validation

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