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PDBsum entry 5g2h
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References listed in PDB file
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Key reference
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Title
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Structural and functional innovations in the real-Time evolution of new (βα)8 barrel enzymes.
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Authors
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M.S.Newton,
X.Guo,
A.Söderholm,
J.Näsvall,
P.Lundström,
D.I.Andersson,
M.Selmer,
W.M.Patrick.
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Ref.
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Proc Natl Acad Sci U S A, 2017,
114,
4727-4732.
[DOI no: ]
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PubMed id
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Abstract
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New genes can arise by duplication and divergence, but there is a fundamental
gap in our understanding of the relationship between these genes, the evolving
proteins they encode, and the fitness of the organism. Here we used
crystallography, NMR dynamics, kinetics, and mass spectrometry to explain the
molecular innovations that arose during a previous real-time evolution
experiment. In that experiment, the (βα)8 barrel enzyme HisA was under
selection for two functions (HisA and TrpF), resulting in duplication and
divergence of the hisA gene to encode TrpF specialists, HisA specialists, and
bifunctional generalists. We found that selection affects enzyme structure and
dynamics, and thus substrate preference, simultaneously and sequentially.
Bifunctionality is associated with two distinct sets of loop conformations, each
essential for one function. We observed two mechanisms for functional
specialization: structural stabilization of each loop conformation and
substrate-specific adaptation of the active site. Intracellular enzyme
performance, calculated as the product of catalytic efficiency and relative
expression level, was not linearly related to fitness. Instead, we observed
thresholds for each activity above which further improvements in catalytic
efficiency had little if any effect on growth rate. Overall, we have shown how
beneficial substitutions selected during real-time evolution can lead to
manifold changes in enzyme function and bacterial fitness. This work emphasizes
the speed at which adaptive evolution can yield enzymes with sufficiently high
activities such that they no longer limit the growth of their host organism, and
confirms the (βα)8 barrel as an inherently evolvable protein scaffold.
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