6opm | pdb_00006opm

Casposase bound to integration product

spinqualitylabelsall models 6opm, resolution 3.10Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 6opm is a 8 chain structure with sequence from methanococcus_frisius_blotevogel_et_al._1986 Atcc 43340 methanococcus frisius blotevogel et al. 1986. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Ligands: CA NonStd Res: MSE, UNK Gene: cas1, DU30_01425, DU33_00735, DU42_16395, DU43_06520, DU45_00060, DU52_05410, DU56_00015, DU57_15540, DU59_17660, DU64_01200, DU66_03140, DU67_00910, DU68_00045, DU71_17290, DU72_02185, DU87_01695 (ATCC 43340 Methanococcus frisius Blotevogel et al. 1986) Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function [A0A0F8IEL4_METMZ] CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette.[HAMAP-Rule:MF_01470] Publication Abstract from PubMed Key to CRISPR-Cas adaptive immunity is maintaining an ongoing record of invading nucleic acids, a process carried out by the Cas1-Cas2 complex that integrates short segments of foreign genetic material (spacers) into the CRISPR locus. It is hypothesized that Cas1 evolved from casposases, a novel class of transposases. We show here that the Methanosarcina mazei casposase can integrate varied forms of the casposon end in vitro, and recapitulates several properties of CRISPR-Cas integrases including site-specificity. The X-ray structure of the casposase bound to DNA representing the product of integration reveals a tetramer with target DNA bound snugly between two dimers in which single-stranded casposon end binding resembles that of spacer 3'-overhangs. The differences between transposase and CRISPR-Cas integrase are largely architectural, and it appears that evolutionary change involved changes in protein-protein interactions to favor Cas2 binding over tetramerization; this in turn led to preferred integration of single spacers over two transposon ends. Casposase structure and the mechanistic link between DNA transposition and spacer acquisition by CRISPR-Cas.,Hickman AB, Kailasan S, Genzor P, Haase AD, Dyda F Elife. 2020 Jan 8;9. pii: 50004. doi: 10.7554/eLife.50004. PMID:31913120 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See Also Endonuclease 3D structures

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