Structural highlights
Function
T2CX_CITFR Recognizes the double-stranded sequence RCCGGY and cleaves after R-1.
Publication Abstract from PubMed
The X-ray crystal structure of Citrobacter freundii restriction endonuclease Cfr10I has been determined at a resolution of 2.15 A 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.
Crystal structure of Citrobacter freundii restriction endonuclease Cfr10I at 2.15 A resolution.,Bozic D, Grazulis S, Siksnys V, Huber R J Mol Biol. 1996 Jan 12;255(1):176-86. PMID:8568865[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Bozic D, Grazulis S, Siksnys V, Huber R. Crystal structure of Citrobacter freundii restriction endonuclease Cfr10I at 2.15 A resolution. J Mol Biol. 1996 Jan 12;255(1):176-86. PMID:8568865 doi:http://dx.doi.org/S0022-2836(96)90015-7