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Published July 17, 1990 | public
Journal Article

Orientation of the putative recognition helix in the DNA-binding domain of Hin recombinase complexed with the hix site


On the basis of sequence similarity with other known DNA-binding proteins, the DNA-binding domain of Hin recombinase, residues 139-190, is thought to bind DNA by a helix-turn-helix motif. Two models can be considered that differ in the orientation of the recognition helix in the major groove of DNA. One is based on the orientation of the recognition helix found in the 434 repressor (1-69) and lambda repressor-DNA cocrystals, and the other is based on the NMR studies of lac repressor headpiece. Cleavage by EDTA.Fe attached to a lysine side chain (Ser^(183) → Lys^(183)) near the COOH terminus of Hin(139-184) reveals that the putative recognition helix is oriented toward the center of the inverted repeats in a manner similar to that seen in the 434 and λ repressor-DNA cocrystals.

Additional Information

© 1990 American Chemical Society. Received January 5, 1990; Revised Manuscript Received March 6, 1990. Supported by grants from the DARPA University Research Initiation Program, the National Foundation for Cancer Research, and the NSF and by National Research Service Awards from NIGMS to D.P.M., J.P.S., and J.A.S.

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