5DLJ

Crystal Structure of Cas-DNA-N1 complex

Summary for 5DLJ

• Entry DOI: 10.2210/pdb5dlj/pdb
• Related: 5DQT 5DQU 5DQZ
• Descriptor: CRISPR-associated endonuclease Cas1, 39-mer DNA N1-F, 39-mer DNA N1-R, ... (5 entities in total)
• Functional Keywords: protein-dna complex, hydrolase-dna complex, hydrolase/dna
• Biological source: Escherichia coli K12; More
• Cellular location: Cytoplasm : Q46896
• Total number of polymer chains: 8
• Total formula weight: 164304.00

Authors

Wang, J.,Li, J.,Zhao, H.,Sheng, G.,Wang, M.,Yin, M.,Wang, Y. (deposition date: 2015-09-05, release date: 2015-11-11, Last modification date: 2024-03-20)

Primary citation

Wang, J.,Li, J.,Zhao, H.,Sheng, G.,Wang, M.,Yin, M.,Wang, Y.
Structural and Mechanistic Basis of PAM-Dependent Spacer Acquisition in CRISPR-Cas Systems.
Cell, 163:840-853, 2015

PubMed Abstract: Bacteria acquire memory of viral invaders by incorporating invasive DNA sequence elements into the host CRISPR locus, generating a new spacer within the CRISPR array. We report on the structures of Cas1-Cas2-dual-forked DNA complexes in an effort toward understanding how the protospacer is sampled prior to insertion into the CRISPR locus. Our study reveals a protospacer DNA comprising a 23-bp duplex bracketed by tyrosine residues, together with anchored flanking 3' overhang segments. The PAM-complementary sequence in the 3' overhang is recognized by the Cas1a catalytic subunits in a base-specific manner, and subsequent cleavage at positions 5 nt from the duplex boundary generates a 33-nt DNA intermediate that is incorporated into the CRISPR array via a cut-and-paste mechanism. Upon protospacer binding, Cas1-Cas2 undergoes a significant conformational change, generating a flat surface conducive to proper protospacer recognition. Here, our study provides important structure-based mechanistic insights into PAM-dependent spacer acquisition.

PubMed: 26478180
DOI: 10.1016/j.cell.2015.10.008

Experimental method

X-RAY DIFFRACTION (2.6 Å)