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PDBsum entry 6tjh
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De novo protein
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PDB id
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6tjh
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DOI no:
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FEBS J
288:530-545
(2021)
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PubMed id:
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Structural plasticity of a designer protein sheds light on β-propeller protein evolution.
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B.Mylemans,
I.Laier,
K.Kamata,
S.Akashi,
H.Noguchi,
J.R.H.Tame,
A.R.D.Voet.
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ABSTRACT
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β-propeller proteins are common in nature, where they are observed to adopt 4-
to 10-fold internal rotational pseudo-symmetry. This size diversity can be
explained by the evolutionary process of gene duplication and fusion. In this
study, we investigated a distorted β-propeller protein, an apparent
intermediate between two symmetries. From this template, we created a perfectly
symmetric 9-bladed β-propeller named Cake, using computational design and
ancestral sequence reconstruction. The designed repeat sequence was found to be
capable of generating both 8-fold and 9-fold propellers which are highly stable.
Cake variants with 2-10 identical copies of the repeat sequence were
characterised by X-ray crystallography and in solution. They were found to be
highly stable, and to self-assemble into 8- or 9-fold symmetrical propellers.
These findings show that the β-propeller fold allows sufficient structural
plasticity to permit a given blade to assemble different forms, a transition
from even to odd changes in blade number, and provide a potential explanation
for the wide diversity of repeat numbers observed in natural propeller proteins.
DATABASE: Structural data are available in Protein Data Bank database under the
accession numbers 6TJB, 6TJC, 6TJD, 6TJE, 6TJF, 6TJG, 6TJH and 6TJI.
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');
}
}
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