2MJZ
Capsid model of M13 bacteriophage virus from Magic-angle spinning NMR and Rosetta modeling
Summary for 2MJZ
Entry DOI | 10.2210/pdb2mjz/pdb |
NMR Information | BMRB: 19747 |
Descriptor | Capsid protein G8P (1 entity in total) |
Functional Keywords | molecular assembly, viral protein |
Biological source | Enterobacteria phage M13 |
Cellular location | Virion: P69541 |
Total number of polymer chains | 35 |
Total formula weight | 183505.49 |
Authors | Morag, O.,Sgourakis, N.G.,Baker, D.,Goldbourt, A. (deposition date: 2014-01-22, release date: 2015-01-07, Last modification date: 2024-05-01) |
Primary citation | Morag, O.,Sgourakis, N.G.,Baker, D.,Goldbourt, A. The NMR-Rosetta capsid model of M13 bacteriophage reveals a quadrupled hydrophobic packing epitope. Proc.Natl.Acad.Sci.USA, 112:971-976, 2015 Cited by PubMed Abstract: Filamentous phage are elongated semiflexible ssDNA viruses that infect bacteria. The M13 phage, belonging to the family inoviridae, has a length of ∼1 μm and a diameter of ∼7 nm. Here we present a structural model for the capsid of intact M13 bacteriophage using Rosetta model building guided by structure restraints obtained from magic-angle spinning solid-state NMR experimental data. The C5 subunit symmetry observed in fiber diffraction studies was enforced during model building. The structure consists of stacked pentamers with largely alpha helical subunits containing an N-terminal type II β-turn; there is a rise of 16.6-16.7 Å and a tilt of 36.1-36.6° between consecutive pentamers. The packing of the subunits is stabilized by a repeating hydrophobic stacking pocket; each subunit participates in four pockets by contributing different hydrophobic residues, which are spread along the subunit sequence. Our study provides, to our knowledge, the first magic-angle spinning NMR structure of an intact filamentous virus capsid and further demonstrates the strength of this technique as a method of choice to study noncrystalline, high-molecular-weight molecular assemblies. PubMed: 25587134DOI: 10.1073/pnas.1415393112 PDB entries with the same primary citation |
Experimental method | SOLID-STATE NMR |
Structure validation
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