Crystal Structure of Citrobacter freundiiRestriction Endonuclease Cfr10I at 2.15 Å Resolution
The X-ray crystal structure of Citrobacter freundiirestriction endonuclease Cfr10I has been determined at a resolution of 2.15 Å by multiple isomorphous replacement methods and refined to an R-factor of 19.64%. The structure of Cfr10I represents the first structure of a restriction endonuclease reco...
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Veröffentlicht in: | Journal of molecular biology 1996, Vol.255 (1), p.176-186 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The X-ray crystal structure of
Citrobacter freundiirestriction endonuclease
Cfr10I has been determined at a resolution of 2.15 Å by multiple isomorphous replacement methods and refined to an
R-factor of 19.64%. The structure of
Cfr10I represents the first structure of a restriction endonuclease recognizing a degenerated nucleotide sequence. Structural comparison of
Cfr10I with previously solved structures of other restriction enzymes suggests that recognition of specific sequence occurs through contacts in the major and the minor grooves of DNA. The arrangement of the putative active site residues shows some striking differences from previously described restriction endonucleases and supports a two-metal- ion mechanism of catalysis. |
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ISSN: | 0022-2836 1089-8638 |
DOI: | 10.1006/jmbi.1996.0015 |