8BMW
SsoCsm
Summary for 8BMW
Entry DOI | 10.2210/pdb8bmw/pdb |
EMDB information | 16126 16174 16175 16176 16177 2420 |
Descriptor | CRISPR-associated small subunit protein (Type III-D), CRISPR-associated Cas7 paralog (Type III-D), RNA (48-MER), ... (9 entities in total) |
Functional Keywords | sulfolobus, type iii crispr, rna binding protein |
Biological source | Saccharolobus solfataricus More |
Total number of polymer chains | 15 |
Total formula weight | 424274.72 |
Authors | Spagnolo, L.,White, M.F. (deposition date: 2022-11-11, release date: 2023-03-01, Last modification date: 2024-10-23) |
Primary citation | Cannone, G.,Kompaniiets, D.,Graham, S.,White, M.F.,Spagnolo, L. Structure of the Saccharolobus solfataricus type III-D CRISPR effector. Curr Res Struct Biol, 5:100098-100098, 2023 Cited by PubMed Abstract: CRISPR-Cas is a prokaryotic adaptive immune system, classified into six different types, each characterised by a signature protein. Type III systems, classified based on the presence of a Cas10 subunit, are rather diverse multi-subunit assemblies with a range of enzymatic activities and downstream ancillary effectors. The broad array of current biotechnological CRISPR applications is mainly based on proteins classified as Type II, however recent developments established the feasibility and efficacy of multi-protein Type III CRISPR-Cas effector complexes as RNA-targeting tools in eukaryotes. The crenarchaeon has two type III system subtypes (III-B and III-D). Here, we report the cryo-EM structure of the Csm Type III-D complex from (SsoCsm), which uses CRISPR RNA to bind target RNA molecules, activating the Cas10 subunit for antiviral defence. The structure reveals the complex organisation, subunit/subunit connectivity and protein/guide RNA interactions of the SsoCsm complex, one of the largest CRISPR effectors known. PubMed: 36843655DOI: 10.1016/j.crstbi.2023.100098 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (3.5 Å) |
Structure validation
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