Structural parsimony in endonuclease active sites:: should the number of homing endonuclease families be redefined?

被引:95
作者
Kühlmann, UC
Moore, GR
James, R
Kleanthous, C [1 ]
Hemmings, AM
机构
[1] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
[2] Univ E Anglia, Sch Chem Sci, Norwich NR4 7TJ, Norfolk, England
关键词
colicin E9; nuclease active site motif; homing endonuclease;
D O I
10.1016/S0014-5793(99)01499-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Homing endonucleases are classified into four families based on active site sequence motifs, Through structural comparisons we have found structural similarities between the endonuclease domain of colicin E9, an H-N-H motif-containing enzyme, acid both the non-specific nuclease from Serratia and I-PpoI, a His-Cys box-containing homing endonuclease. Our comparison identifies conservation at the heart of all three enzyme active sites and so argues for a re-classification of H-NH and His-Cys box homing endonucleases as a single family. We suggest the 'beta beta alpha-Me family' of homing enzymes to reflect the three elements of secondary structure and the metal ion that define the motif. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:1 / 2
页数:2
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