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7AH0

Crystal structure of the de novo designed two-heme binding protein, 4D2

Summary for 7AH0
Entry DOI10.2210/pdb7ah0/pdb
Descriptor4D2, PROTOPORPHYRIN IX CONTAINING FE (3 entities in total)
Functional Keywordsheme, maquette, de novo protein
Biological sourcesynthetic construct
Total number of polymer chains1
Total formula weight13885.12
Authors
Hutchins, G.H.,Parnell, A.E.,Anderson, J.L.R. (deposition date: 2020-09-23, release date: 2021-10-06, Last modification date: 2024-06-19)
Primary citationHutchins, G.H.,Noble, C.E.M.,Bunzel, H.A.,Williams, C.,Dubiel, P.,Yadav, S.K.N.,Molinaro, P.M.,Barringer, R.,Blackburn, H.,Hardy, B.J.,Parnell, A.E.,Landau, C.,Race, P.R.,Oliver, T.A.A.,Koder, R.L.,Crump, M.P.,Schaffitzel, C.,Oliveira, A.S.F.,Mulholland, A.J.,Anderson, J.L.R.
An expandable, modular de novo protein platform for precision redox engineering.
Proc.Natl.Acad.Sci.USA, 120:e2306046120-e2306046120, 2023
Cited by
PubMed Abstract: The electron-conducting circuitry of life represents an as-yet untapped resource of exquisite, nanoscale biomolecular engineering. Here, we report the characterization and structure of a de novo diheme "maquette" protein, 4D2, which we subsequently use to create an expanded, modular platform for heme protein design. A well-folded monoheme variant was created by computational redesign, which was then utilized for the experimental validation of continuum electrostatic redox potential calculations. This demonstrates how fundamental biophysical properties can be predicted and fine-tuned. 4D2 was then extended into a tetraheme helical bundle, representing a 7 nm molecular wire. Despite a molecular weight of only 24 kDa, electron cryomicroscopy illustrated a remarkable level of detail, indicating the positioning of the secondary structure and the heme cofactors. This robust, expressible, highly thermostable and readily designable modular platform presents a valuable resource for redox protein design and the future construction of artificial electron-conducting circuitry.
PubMed: 37487099
DOI: 10.1073/pnas.2306046120
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.91 Å)
Structure validation

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数据于2024-11-06公开中

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