1skm
From Proteopedia
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HhaI methyltransferase in complex with DNA containing an abasic south carbocyclic sugar at its target site
Overview
Rotation of a DNA or RNA nucleotide out of the double helix and into a, protein pocket ('base flipping') is a mechanistic feature common to some, DNA/RNA-binding proteins. Here, we report the structure of HhaI, methyltransferase in complex with DNA containing a south-constrained, abasic carbocyclic sugar at the target site in the presence of the methyl, donor byproduct AdoHcy. Unexpectedly, the locked south pseudosugar appears, to be trapped in the middle of the flipping pathway via the DNA major, groove, held in place primarily through Van der Waals contacts with a set, of invariant amino acids. Molecular dynamics simulations indicate that the, structural stabilization observed with the south-constrained pseudosugar, will not occur with a north-constrained pseudosugar, which explains its, lowered binding affinity. Moreover, comparison of structural transitions, of the sugar and phosphodiester backbone observed during computational, studies of base flipping in the M.HhaI-DNA-AdoHcy ternary complex indicate, that the south-constrained pseudosugar induces a conformation on the, phosphodiester backbone that corresponds to that of a discrete, intermediate of the base-flipping pathway. As previous crystal structures, of M.HhaI ternary complex with DNA displayed the flipped sugar moiety in, the antipodal north conformation, we suggest that conversion of the sugar, pucker from south to north beyond the middle of the pathway is an, essential part of the mechanism through which flipping must proceed to, reach its final destination. We also discuss the possibility of the, south-constrained pseudosugar mimicking a transition state in the, phosphodiester and sugar moieties that occurs during DNA base flipping in, the presence of M.HhaI.
About this Structure
1SKM is a Single protein structure of sequence from Haemophilus haemolyticus with SAH as ligand. Active as DNA (cytosine-5-)-methyltransferase, with EC number 2.1.1.37 Full crystallographic information is available from OCA.
Reference
Caught in the act: visualization of an intermediate in the DNA base-flipping pathway induced by HhaI methyltransferase., Horton JR, Ratner G, Banavali NK, Huang N, Choi Y, Maier MA, Marquez VE, MacKerell AD Jr, Cheng X, Nucleic Acids Res. 2004 Jul 23;32(13):3877-86. Print 2004. PMID:15273274
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