PDBsum entry 3wwa

De novo protein

PDB id: 3wwa

Contents

Protein chain

251 a.a.

Ligands

IPA

Waters ×93

PDB id:

3wwa

Name:

De novo protein

Title:

Crystal structure of the computationally designed pizza7 protein after heat treatment

Structure:

Pizza7h protein. Chain: a. Engineered: yes

Source:

Synthetic: yes. Other_details: the protein was designed.

Resolution:

1.99Å R-factor: 0.197 R-free: 0.259

Authors:

A.R.D.Voet,H.Noguchi,C.Addy,D.Simoncini,D.Terada,S.Unzai,S.Y.Park, K.Y.J.Zhang,J.R.H.Tame

Key ref:

A.R.Voet et al. (2014). Computational design of a self-assembling symmetrical β-propeller protein. Proc Natl Acad Sci U S A, 111, 15102-15107. PubMed id: 25288768 DOI: 10.1073/pnas.1412768111

Date:

17-Jun-14 Release date: 08-Oct-14

Protein chain

No UniProt id for this chain

Struc: 251 a.a.

DOI no: 10.1073/pnas.1412768111

Proc Natl Acad Sci U S A 111:15102-15107 (2014)

PubMed id: 25288768

Computational design of a self-assembling symmetrical β-propeller protein.

A.R.Voet, H.Noguchi, C.Addy, D.Simoncini, D.Terada, S.Unzai, S.Y.Park, K.Y.Zhang, J.R.Tame.

ABSTRACT

The modular structure of many protein families, such as β-propeller proteins, strongly implies that duplication played an important role in their evolution, leading to highly symmetrical intermediate forms. Previous attempts to create perfectly symmetrical propeller proteins have failed, however. We have therefore developed a new and rapid computational approach to design such proteins. As a test case, we have created a sixfold symmetrical β-propeller protein and experimentally validated the structure using X-ray crystallography. Each blade consists of 42 residues. Proteins carrying 2-10 identical blades were also expressed and purified. Two or three tandem blades assemble to recreate the highly stable sixfold symmetrical architecture, consistent with the duplication and fusion theory. The other proteins produce different monodisperse complexes, up to 42 blades (180 kDa) in size, which self-assemble according to simple symmetry rules. Our procedure is suitable for creating nano-building blocks from different protein templates of desired symmetry.