Summary information and primary citation

PDB-id
6gcd; SNAP-derived features in text and JSON formats; DNAproDB
Class
DNA binding protein
Method
X-ray (1.8 Å)
Summary
DNA binding domain of restriction endonuclease mcrbc in complex with 5-hydroxymethylcytosine DNA
Reference
Zagorskaite E, Manakova E, Sasnauskas G (2018): "Recognition of modified cytosine variants by the DNA-binding domain of methyl-directed endonuclease McrBC." FEBS Lett., 592, 3335-3345. doi: 10.1002/1873-3468.13244.
Abstract
Cytosine modifications expand the information content of genomic DNA in both eukaryotes and prokaryotes, providing means for epigenetic regulation and self versus non-self discrimination. For example, the methyl-directed restriction endonuclease McrBC recognizes and cuts invading bacteriophage DNA containing 5-methylcytosine (5mC), 5-hydroxymethylcytosine (5hmC) and N4-methylcytosine (4mC), leaving unmodified host DNA intact. Here, we present co-crystal structures of McrB-N bound to DNA oligoduplexes containing 5hmC, 5-formylcytosine (5fC) and 4mC, and characterise the relative affinity of McrB-N to various cytosine variants. We find that McrB-N flips out modified bases into a protein pocket and binds cytosine derivatives in the order of descending affinity: 4mC>5mC>5hmC≫5fC. We also show that pocket mutations alter the relative preference of McrB-N to 5mC, 5hmC and 4mC. This article is protected by copyright. All rights reserved.

Cartoon-block schematics in six views (download the tarball)

PyMOL session file Download PDB file View in 3Dmol.js