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6XNS

C3_crown-05

Summary for 6XNS
Entry DOI10.2210/pdb6xns/pdb
DescriptorC3_crown-05 (1 entity in total)
Functional Keywordshelical bundle repeat protein, de novo protein
Biological sourcesynthetic construct
Total number of polymer chains6
Total formula weight228933.80
Authors
Bick, M.J.,Hsia, Y.,Sankaran, B.,Baker, D. (deposition date: 2020-07-04, release date: 2020-12-23, Last modification date: 2024-04-03)
Primary citationHsia, Y.,Mout, R.,Sheffler, W.,Edman, N.I.,Vulovic, I.,Park, Y.J.,Redler, R.L.,Bick, M.J.,Bera, A.K.,Courbet, A.,Kang, A.,Brunette, T.J.,Nattermann, U.,Tsai, E.,Saleem, A.,Chow, C.M.,Ekiert, D.,Bhabha, G.,Veesler, D.,Baker, D.
Design of multi-scale protein complexes by hierarchical building block fusion.
Nat Commun, 12:2294-2294, 2021
Cited by
PubMed Abstract: A systematic and robust approach to generating complex protein nanomaterials would have broad utility. We develop a hierarchical approach to designing multi-component protein assemblies from two classes of modular building blocks: designed helical repeat proteins (DHRs) and helical bundle oligomers (HBs). We first rigidly fuse DHRs to HBs to generate a large library of oligomeric building blocks. We then generate assemblies with cyclic, dihedral, and point group symmetries from these building blocks using architecture guided rigid helical fusion with new software named WORMS. X-ray crystallography and cryo-electron microscopy characterization show that the hierarchical design approach can accurately generate a wide range of assemblies, including a 43 nm diameter icosahedral nanocage. The computational methods and building block sets described here provide a very general route to de novo designed protein nanomaterials.
PubMed: 33863889
DOI: 10.1038/s41467-021-22276-z
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.19 Å)
Structure validation

237735

数据于2025-06-18公开中

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