The crystal structure of flap endonuclease-1 from Methanococcus jannaschii

Authors
Hwang, KYBaek, KKim, HYCho, Y
Issue Date
1998-08
Publisher
NATURE AMERICA INC
Citation
NATURE STRUCTURAL BIOLOGY, v.5, no.8, pp.707 - 713
Abstract
Flap endonuclease-1 (FEN-1), a structure specific nuclease, is an essential enzyme for eukaryotic DNA replication and repair. The crystal structure of FEN-1 from Methanococcus jannaschii, determined at 2.0 Angstrom resolution, reveals an active site with two metal ions residing on top of a deep cleft where several conserved acidic residues are clustered. Near the active site, a long flexible loop comprised of many basic and aromatic residues forms a hole large enough to accommodate the DNA substrate. Deletion mutations in this loop significantly decreased the nuclease activity and specificity of FEN-1, suggesting that the loop is critical for recognition and cleavage of the junction between single and double-stranded regions of flap DNA.
Keywords
COLI DNA-POLYMERASE; EXONUCLEASE; REPLICATION; REPAIR; 5' -EXONUCLEASE; CLEAVAGE; SEQUENCE; HOMOLOGY; DOMAIN; FEN-1; COLI DNA-POLYMERASE; EXONUCLEASE; REPLICATION; REPAIR; 5' -EXONUCLEASE; CLEAVAGE; SEQUENCE; HOMOLOGY; DOMAIN; FEN-1
ISSN
1072-8368
URI
https://pubs.kist.re.kr/handle/201004/142940
DOI
10.1038/1406
Appears in Collections:
KIST Article > Others
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